June - Respiratory Care
Transcription
June - Respiratory Care
JUNE 1 998 VOLUME 43 NUMBER 6 ISSN 0020-1324-RECACP RE/PIRATORy A MONTHLY SCIENCE JOURNAL YEAR— ESTABLISHED 1956 43RD CASE REPORTS Acute Pulmonary Edema following Upper Airway Obstruction REVIEWS, OVERVIEWS & UPDATES Leukotriene Modifiers in the Treatment of Asttima 1997 PHILIP KITTREDGE MEMORIAL LECTURE Mechanical Ventilation: The Next 50 Years "Three weeks aqo, Andrew was struqqlinq to breathe'. "Thanks to Ohmeda, resuscitation wasn't a stinjqqle for us." Ki'Uy ^:._, Hendmm. R.N., St^ Nmye/NlC. U. Hetrhey Medical Caiter/Pmn State Geisinger Health Systmi tei^ In the often-hectic environment of a I typical resuscitation, the last thing you need are scattered components to deal with. why That's the Ohmeda Infant Resuscitation System combines all of the necessary equipment into one .„,,,,„ Ohmeda miant module. eas\'-to-use The Ohmeda ."" . Infant Resuscitanon tie ResuSCltatlOn System Can System combines everything imo one compact, versatile imit. be used on all incubators and warmers. 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For more information visit our web site at www.aarc.org. »-. "pp^^^^^ ^^^H You'd be surprised what new EasiVent" will hold. And so will your patients. Any holding chamber will hold a dose of respiratory Chamber Or any medication. But only the EasiVent'" Valved Holding is designed to hold the complete MDI kit inside. other personal treasure of modest size. ' Physicians, respiratory therapists, , and patients indicate a preference for the unique design of EasiVent™.* Since EasiVent'" improves the portability of asthma treatment, it encourages patient compliance. NAEPP a guidelines also recommend that holding chamber to maximize dose delivery. all patients using corticosteroids use Which is exactly what EasiVent'" is designed to do. EasiVent'" instructions improves medication delivery and simplifies patient advanced features such as a dual, low-resistance printed on the unit, and built-in coaching signal. valve, universal MDI EasiVent'" Valved Holding Chamber. advanced design also helps the patient •Data on medication. And that's no fish story. training, with port, graphic Help your patients with compliance. Specify the It not only holds the complete get maximum MDI benefit from their kit inside, its fiie. Circle 102 on reader service card l*M-755-55(iO ©1998 DEY All righls reserved, 09-527-00 5m ALSO IN THIS ISSUE All systems go. The expressway to Ki,si'in\rnin ( aiu; is now open. Be access to a host of coiiNciiicril features like word seareiies of all a\aiiai)le contact the editorial stafK \ iew issues. llie Dont tlie sure to hookiiiark www.rejoiiriial.eom for fast author guide foi' inaiiuscript preparation, phis key- forget to check out the Oidine Resources page: you can annual indexes for 1997, or e-mail vour 1998 Open Fori m abstract. RE/PIRiSJORy QiRE oil line Browse safely. EDITORIAL OFFICE EDITOR ; 600 Ninth Avenue. Suite 702 WA 98 Seattle David 1 04 Fax (206) 223-0563 MD | fc Seattle. Wasliinglon '; (206) 223-0558 CHIEF IN Pierson Hiirbotview Medical Center University of Washington ^ J ' www.rcjoumal.com ASSOCIATE EDITORS D RichartJ Branson RRT R Dean PhD RRT Hess Massachusetts General Hospital University of Cincinnati Harvard University Ohio Cincinnati. Boston. Massachusetts G MD MD University of Virginia K Stoller The Cleveland Clinic Foundation Charlottesville. Virginia Cleveland, Ohio Charles Durbin Jr James EDITORIAL BOARD A Thomas EdD RRT Barnes Leonard D Hudson MD Northeastern University University of Washington Boston. Massachusetts Seattle, Michael J MD Bishop Robert M Augusta. Georgia Kacmarek PhD RRT Washington PhD RRT Joseph L Rau Massachusetts General Hospital University of Wasliinglon Seattle. C Mishoe PhD RRT Shelley Medical College of Georgia Washington Georgia State University Harx'ard University Atlanta, Georgia Boston. Massachusetts Bartolome Tiifis R Celli MD Toshihiko Koga University Catherine MD SH Sassoon Long Beach. Kurume. Japan California L Chatbum RRT Robert H MD Arthur S Slutsky University Hospitals of Cleveland Marin Case Western Resen'e University Washington University University of Toronto St Louis. Missouri Toronto. Ontario, Cleveland. Ohio Luciano Gattinoni MD Kollef Patrick Leger MD Martin University of Milan Clinique Medicale Edouard Rist Milan. Italy Paris. E John Heffner MD Neil J Mavwood. Maclntyre MD Canada MD Tobin Loyola University France R MD University of California In'ine Koga Hospital Boston. Mas.^achusetts Illinois MD Duke University Durham. North Carolina University of Arizona Phoenix. Arizona STATISTICAL CONSULTANT Mark MD J Heulitt John University of Arkansas Little RE,SPIRATORY CARE ISSN I 0020-1.124. USPS 0489- is published monthly by Daedalus Enterprises Inc. at 1030 Abies Une. Dallas TX 75229-4593. tor the American Association for Respiratory Care. One volume is 190) Rock. Arkansas J Marini MD Gordon D Rubenfeld University of Minnesota University of Washington St Paul, Minnesota Seattle. MD Washington SECTION EDITORS 1 published per year beginning each January. Subscription $75 per year in the US; $90 airmail, add $94). rates are ffor The contents of in all other countries Robert MS R the Journal are indexed in Hospital and Hugh S Mathewson Drug Capsule MD Library Edition. Abridged versions of RESPIRA- Giaphics Charles G Irvin PhD Gregg L Ruppel Richard MEd RRT RPFT PFT Comer PhD RRT Ken Hargett RRT Robert Harwood MSA ing and Allied Health Literature. Excerpta Medica. and RNdex MS RRT MD Jon Nilsestuen Health Administration Index, Cumulative Index to Nurs- TORY Care Fluck Jr Jastremski Blood Gas Corner RRT Patricia Ann Doorley Charles G Durbin Jr D Ktttredge MS RRT Barbara Wilson MD Jon Mcliones '.v RRT RRT Comer MEd RRT MD John Palmisano Test Your Radiologic Skill Comer Branson Robert S Campbell RRT Cardiorespiratory Interactions are also published in Italian. French, and Japanese, with permission from Daedalus Enterprises Inc. Periodicals postage paid at Dallas TX and at additional POSTMASTER: Send address changes to RE.SPIRATORY CARE. Membership Office. Daedalus Enmailing offices. terprises Inc. 1 1030 Abies Lane. Dallas TX 75229-4593. Printed in the United States of America Copyright © 199S, by Daedalus Enterprises Inc. CONSULTING EDITORS Frank \l Howard Biondo J RRT Bircnbaum Donald R Elton MD MD MD Ronald B George James M Hurst MD Michael McPeck RRT John Shigeoka Jeffrey J MD Ward MEd RKT Abstracts Summaries of Pertinent Articles in Other Journals Commentaries, Editorials, & Reviews To Note Gastric Rupture after Inadvertent Esophageal Intubation with a Jet Ventilation Catheter — TB. Aneslhesiology 1998;88(2):537-538. Gilbert —Clarke M, Chalmers Meta-Analyses, Multivariate Analyses, and Coping with the Play of Chance Lancet 1998;351(9108):I062-1063. I. PEEP: More than Just Support? 1998:24(1): I — Femandez-Mondejar E, Vazquez-Mata G. Intensive Care Med -2. Ethics Review and Clinical Trials— Madder H. Myles P. McRae R. Lancet 1 998:35 1(9 08): 10651 1066. Use of the Breathing Reserve To Interpret Submaximal Exercise Responses — Mahler DA. Chest 1998:1 13(4):858-859. Ventilator-Induced Am J Saumon G. Lung Injury: Lessons from Experimental Med I998:I57( ):294-323. Respir Crit Care — Dreyfuss D, Studies (Review) I The Health Care Costs of Smoking (Letter)— Fries JF. N Engl J Med I998:338(7):470-47L The Health Care Costs of Smoking (Letter)— Hodgson TA. N Engl J Med 1998:338(7):470. Women, Smoking, and Lung Cancer (Editorial)— Stover DE. Chest 1998:1 13( 1-2. 1 Vena Caval J Med Pulmonary Embolism Filters for the Prevention of ( Editorial ) N Engl J Med Protective Ventilation for Patients with Acute Respiratory Distress N son LD. Engl J Med 1 Skin Vasomotor Reflex Predicts Circulatory SVmR amplitude had decreased to < 0. Responses to Laryngoscopy and Intubation control group (n — Sakamoto M. Terasaki H. Anesthesiology 1998:88(2):297. = 15), intubation regardless of changes in the In Study reactivity may to intubation. evaluation of autonomic help to predict circulatory responses The relation between the magnitude of the skin vasomotor reflex (SVmR) immediately before laryngoscopy and the circulatory respon.ses to intubation was examined. METHODS: Forty- MAC (n = 9) or SVmR was and heart rate nificantly (p lanyl 11) were fen- and thiamylal and maintained with nitrous oxide and sevoflurane. The by an electroslimulus SVmR was evoked to the ulnar nerve, and de- In [he SVmR amplitude. was maintained at Study 1, inten- the blood pressure of the control group increased sig) after laryngoscopy. The blood SVmR amplitude and the systolic blood pres- lation (p < showed 0.(X)l ). In a significant linear corre- Study 2, the relation the electric intensity and Ihe showed 0.01 ) a weak in the I between SVmR amplitude but significant correlation (p < MAC group. CONCLUSION: The SVmR Helium Versus Oxygen for Tracheal Gas sufflation zov R, Oppenheim A, Eidelman LA, Weiss Spmng CL, Cotev S. Crit Care Med ferent physical properties, in patients with respiratory intensive care unit in a tertiary university medical center. PATIENTS: Seven etiologies. All patients 446 14), were studied. In the monitored group laryngoscopy was perlormed when Ihe vidual palienls. in indi- in the vol- mode (Vx 5-7 mL/kg). Inclusion criwere Pacch of > 50 torr (> 6.7 kPa), together teria cm HiO and respiratory rate INTERVENTIONS: All pa- lienls = were ventilated ume-control depth for laryngoscopy and intubation patients sedated and par- alyzed patients with respiratory failure of various of > 14 breaths/min. (n DESIGN: Prx> SETTING: General failure. spective, intervention study. mation lor determining the optimal anesthetic (if helium and oxygen, as an adjunct to conventional mechanical ventilation iaser-Doppler flow meter. In Study provides useful infor- the effect of tracheal gas insufflation using 2 gases with dif- evaluation of the 2 groups Pi- YG, 1998:26(2): 290. OBJECTTVE: To evaluate and compare creases in skin blood flow were detected using a I, In- — during Mechanical Ventilation I pressure of the monitored group did not increase. sure changes or 1 . was performed by changing the elecuic In < O.OI The I 998:35 1(9098):277-282. MAC (n = 6) for 5 min. The .3 tested four adult patients (classified as American Soci- was induced with 1 RESULTS: sity. ety of Anesthesiok)gists physical stanis studied. General anesthesia —Hud- induction, the end-tidal con- 2. after centration of sevoflurane BACKGROUND: An l998:338(4):239-247. Syndrome (Editorial) 1998:338(6):385-387. Cystic Fibrosis (Review)— Rosenstein BJ, Zeitlin PL. Lancet Ikula Y, —Haire WD. N Engl 1998:338(7):463-464. Respiratory Function of Hemoglobin (Review)— Hsia CC. Shimoda O, ): wilh Pimax of > 35 that were intubated with an endotracheal tube had an additional lumen opening RESPIRATORY CARE • at its dis- JUNE 1998 VOL 43 NO 6 IIRIENTHTION HNO COMPETENCY flSSURHNCE MflMUHL EOR RESPIRRTOfiY CflRll Garner some applause of your own! With the Orientation and Competency Assurance Manual for Respiratory Care, you can ensure that your staff receives a structured orientation and that competence is periodically assessed and documented. The Manual provides you with a resource and examples to create a customized orien- and competency assurance system tation And, to it for respiratory care services. provides the information, assessment tools, and models necessary demonstrate that the competence of employees according to JCAHO documented is requirements. "The Clinical Performance Evaluations in the manual were a great way to get all my staff working at the same performance level, regardless of where they went to school. Consistency of care are key words in health care today, and everything I needed to develop a staff-leveling program was right there." - John H. R/ggs, PhD, RRT The Only Orientation and Competency Assurance Manual that Gives You All This. . . ' team for meetm Initial Assessment and Document Employee of Experience, Education, and Credentials ' Competency Validation in Critical Organizational Competency Checklists • Construction of Clinical • Improvement of Competency Assessment Congruency • Reporting of Competence Patterns and Trends System Safety Practices • Integration of ' Competency Assessments with Departmental Orientation In-Services and Continuing Education mJ/exceeMnj ' Orientation and Competency Validation for General • Respiratory, Adult Critical, Neonatal/Pediatric mtmmzuJts" • ' Orientee Progress Evaluations ' Preceptor Training and Competency Validation > System • for the Selection, Ongoing Assessment, PhD, RRT Appendix-Self-Learning Module for Critical Appendix-Orientation and Competency Validation for Multi-Skilling and Cross-Training in Perinatal Care Skills, • and Competency H. Riggs, Linkage of Job Description, Competency Organizational System Safety Practices Maintenance, Improvement of John for Annual Performance Evaluation, and Performance Improvement and Age-Specific Patient Populations tkeir System Level, Respiratory Care, Diagnostic Testing, Appendix-Sample Performance Evaluation Instrument By Daniel Grady, MEd, RRT; Valerie Lawrence, RRT; Tammy Caliri, RRT; and Mitzi Johnson, RNC, MSN. 258 Pages, Binder. 1997 $65 for AARC members, $90 for nonmembers-ltem BK55 Cadd $8 for shipping and handling] Texas customers only, please add 8.25% sales tax Oncluding shipping charges). Texas customers that are exempt from sales tax must supply an exemption certificate. MasterCard, Visa, Institutional Purchase Order, or check payable to: Daedalus Enterprises, 11030 Abies Lane / Inc. ATTN: Order Fulfillment Department Dallas, Texas 75229 / Phone (972] 243-2272 / Fax [972] 484-6010 Abstracts tal end. through which tracheal gas insufflation was administered. The tracheal gas insufflation was applied continuously throughout the respi- and 6 L/niin) with ratory cycle at 3 flow rates (2. 4. 2 gases, oxygen and helium, while the ventilatory .sellings MEASURE- were maintained constant. MENTS & RESULTS: In addiuon airway pres- lo have demonstrated significant improvements outcomes patient ical ventilation, (eg. shorter durations in of mechan- lower incidence of ventilator-asso- ciated pneumonia, fewer patient complications) as a result of implementing formal Our hope tocols. is weaning pro- tha[ these data will assist other own hospitals in developing their systematic guide- and protocols for weaning patients from sures and arterial hlood gases, the relative effi- lines cacy of tracheal gas insufflation with each gas was mechanical ventilation. as the change Paco^/Pinm) compared in with baseline measurements. Tracheal gas insufflation with both gases < 0.05) decreased Paco; signifi- flow rates. This effect was accompanied by an increase in Pa„, with both ga.ses cantly (p at all (o.xygen and helium). However, at flow rates of 6 L/min. tracheal gas insufflation with helium re- sulted in lower Pi„,a, than with oxygen. Tracheal gas insufflation with helium was more effective (as estimated by the coeftlcieni of efficiency) than with oxygen at SION: all tilated patients CONCLU- flow rates (p < 0.05 ). In volume-controlled, mechanically ven- with respiratory failure, tracheal were measured during acute in 15 patients respiratory failure, within 24 hours of the institution of mechanical ventilation, when during recovery, and in ume [fk/Vx]); rapid shallow breathing-occlusion (ROP = P,, x fR^r; Pi i Questions Crucial the 1998:1 — Fein AM. Chest Suppl):277S. 1.3(4 spiratory time (n = 1 Patients [t|]). who failed to had a similar ROP.fRA'r and Pu 1 ) significandy reduced Po i/VtAi, the value of which Emphysema and other forms of chronic obstructive pulmonary diseazse (COPD) are not only common, but also have a poor prognosis. Mortality with severe COPD may be as high as 60% at 5 years and associated with a significant is degree of disability and cost to the health care sys- Dr Otto Brantigan's experience when multiple-wedge resections of tem. Building on 1950s, in the emphysematous lung were performed to decrease failed to who weaned who wean was similar to that of patients who weaned successfully. was comparable successfully (n of patients to that = 38). The Pimax of patients We conclude that patients who failed to wean had a breathing lar to that pattern simi- during acute respiratory failure, despite a reduced mechanical load on the respiratory muscles and a relatively adequate inspiratory mus- cle strength. This suggests that strategies that enhance respiratory muscle endurance itate lizing L, Brock WA. New Horst. HM. Prang mon is one of the most com- medical therapies administered within ICUs. Similarly, the "weaning" or "liberation" of patients from mechanical ventilation is a common and extremely important task performed in ICUs and emphysema to treat There a Better Right-Sided Tube for OneLung Ventilation? A Comparison of the RightSided Double-Lumen Tube with the Single- lo the treat- known as lung vol- reduction surgery (LVRS), pneumectomy. Is Lumen Tube — Campos JH. Anesth Analg 1998:86 (4):696. for a 20 to 30% reduction in lung volume and may be performed by stapler or laser resec- aim tion, or both. The mechanisms of benefit have enhanced Anatomic between tracheal carina and variation the take-off of the right upper bronchus often makes the use of a right-sided (R-DLT) rection ness to be liberated from mechanical ventilation improved efficiency of respiratory musculature, vent) undesirable. This study and for conducting the weaning process. Clini- and improved with the ICUs frequently develop (heir that to of ventilation remain elastic recoil, cor- perfusion mismatch, right ventricular filling. Questions to be answered include duration of benefits, safety, and cost of LVRS. The National double-lumen tube or a single-lumen tube with right-sided ious methods exist for assessing a patient's readi- personal preferences regarding the best Massa EC. and reduction pneumoplasty. These operations been attributed own Enclosed Right-Sided with Bronchial Blocker specialized ventilator units within hospitals. Var- cians working in facil- include excision of large bullae (bul- ment of emphysema. The operations used ume may weaning. improved surgical and anesthetic technique, have redeveloped a surgical approach tous lung and are variously Mechanical ventilation uti- lectomy) and resection of diffusely emphysema- Horiz 1998:6:52. wean |/Pin,ax to those with acute respiratory failure despite a reducing hyperinflation, recent investigators, Care Unit— Kollef MH. i/Pimax); and effective inspiratory impedance (Pu i/Vj/in- Lung Volume Reduction Surgery: Answering lung volume, thereby improving airflow and sive fol- breathing index (respiratory frequency/tidal vol- as an alternative to oxygen. Reducing the Duration of Mechanical VentiThree Examples of Change in the Inten- patients The lowing indices were calculated: rapid shallow gas insufflation with helium might be suggested lation: 49 they were ready for discon- tinuation from mechanical ventilation. pressure index estimated using a "coefficient of efficiency" (which we defined (Pimax) enclosed bronchial blocker tube R-UBB to (R-UBB) (Uni- compared the R-DLT determine whether there was any advantage of one over the other during anesthesia with one-lung ventilation (OLV) for right- approach to weaning patients from ventilatory sup- Heart. Lung, and Blood Institute and the Health sided thoracic surgeries. Forty patients requiring of wean- Care Financing Administration have responded right lung deflation port. Therefore, variability in the practice ing patients from mechanical ventilation is fre- to the demand quently demonstrated, even within a single ICU. tion about Recently, several randomized clinical registry trials have more access for LVRS to and informa- by organizing both a national and conffolled clinical trial of these pro- produced conflicting results regarding the best cedures over a 7-year period. This multicenter technique for carrying out the weaning process trial (eg. spontaneous breathing mandatory lation). intermittent trials, ventilation, pressure-support venti- Such conflicting findings have trated the the difficulties in identifying the "besf medical " practices for carrying out this endeavor. However, other investigations have suggested that the selec- weaning employing a systematic approach lo this medical process. Prolocol-guided weaning of mechanical ventilation in the ICU setting, often perfomied by non-physicians, has gained in tance as a result of these invesligalions. scribe Ihc recent experience of three 448 LVRS to to compare methods of bilateral maximal medical therapy. accep- Wc de- ICUs which to one of two groups. Twenty patients received a right-sided BronchoCalh double-lumen tube, and 20 received a Univent tube with a bronchial blocker placed in the right mainstem bronchus. The lowing were studied: ( 1 ) tion each tube until satisfactory achieved; (2) fol- time required to posi- number of times placement was that fiberoptic bron- choscopy was required (including one with the Breathing Pattern during Acute Respiratory Failure and Recovery — Del Rosario N. Sassoon CS. Chctty KG. Gruer SE. Mahutte CK. Eur RespirJ iy97;l()( 1 1 patient supine and one in lateral decubitus position); (.3) number of malpositions of tubes per case. The objccfive of (his study was to compare the breathing pattern of patients from mechanical ventilation ing acute respiratory failure. who failed to wean to the pattern dur- We hypothesized that a similar breathing pattern occurs under both conditions. Breathing pattern, sure (Pii |), and mouth occlusion maximum after initial con- fimiation of tube placement; (4) time required until lung collapse; (5) surgical exposure: and (6) cost ):2.560. patients from mechanical ventilation may not be as important as emphysema further illus- complexity of the weaning process and tion of an individual technique for intends to enroll patients with end-stage were randomly assigned No dil lercnccs were any of these variables except sition overall the was R-DLT. No served in the radiograph in tliat greater for the right found with the cost of acqui- R-UBB than for upper lobe collapse was ob- postoperative period in the chest any of the patients studied. We con- pres- clude that either tube can be used safely and effec- inspiratory pressure tively for right-sided thoracic surgeries that requins RHSPIRATORY CARE • JUNE 1998 VOL 43 NO 6 A...cfa<ion for Rtn>in.loi>' C»B (AARC) is J p»»ssioi.»J m(mb<Btuf es«WKJ> lot «hM»,»l prq.w«»n .,.^ ""S TV AARC <..KO>u»g« ptof«s».»l .x«llM>c<. m wpmlov «. Iv «»«"=' "V'uy. -*««"« P'l^T ''^ '"^-'^ ^'''' "^ •''^^ c"W.u,ri V^nxms lo--.mv* «s.^-l> M«l <rf™^t < scop< of pnctw ocioss p»>!« Cortautf <« »«"»«« iftfonvi4»K'i^ «k1 i»sow:<'3 for h^akKc r pio(i'3sion»l3 AARC m«mb»K. at y our Put the AAJ^ Fingertips Mid ^ all the best links to other slated Do you have tarnivorous Informati^m insfanfaneous now? Right now?! — the need for information , Today we have all the information you heed right at your fingertips. Do you need the full complement of Clinical Practice Guidelines? They're there, on our website, at ^ ost-effectiveness of www.aarc.org. ? Do you want to reference your State Practice Do you hove a question you want input on— from RCPs around the world? Want to find a job? Need a tips sheet for a patient on websites? What's the -i^M-i®" °" verbal orders? Do you neecyti pffl^fen RCPs as multiskilled health care proxnd^ASee www.aarc.org. Go Check us oti^We're to www.aarc.org. right at your fingertips. Act? AARC Online http://v9iv.aarc.org asthma? Check www.aarc.org. Need to know who sells CPAP head straps? for^^AARC Members Only area on AARC Online, E-maifM^age to webmaster@aarc.org with your To register send an nber number. 4 Abstracts OLV. anesthesia for Implications: In this study, right-sided double-lumen tubes were compared with the Univent with right-sided bronchial blockers. The results indicate that either tube can be used Oxide Production during Sepsis Docs Not Prevent Lung Inflam- — Aaron mation Mullen JB, .SD, Valenza Volgyesi G. F. AS, Stewart TE. Slut.sky was worse significantly Crit Med Care L-NAME did not. in rats that from to originate the lungs of rats after .septic lung injury. The aim of this study was to investigate whether treatment NO synthase inhibitor N-nitro-L-arginine (L-NAME) would prevent methyl ester lipopoly- saccharide (LPS)-induced increases in exhaled and whether L-NAME had more in- would have an this lung inflammation. DESIGN: effect on septic Prospective, ran- SUBJECTS: SETTING: University laboratory. Male, anesthetized, paralyzed, and mechanically ventilated Sprague-Dawley = 27). INTERVENTIONS: Rats were mechan- 40 breaths/min, Vt 3 mL, (expiratory rate tive end-expiratory pressure 0. Fio, 0.21 were then randomized jections of either = 1 1 ) = 10). of saline 5 min was collected in later. 1 NO from the lungs exhaled but that this inhibition does not rats, may worsen Thereafter, exhaled gas polyethylene bags for measure- ments of NO concentration. After 4 hours, the were killed amined To examine the effect of and LPS on mean arterial blood pres- histologically. L-NAME sure, rats and the lungs were preserved and ex- 6 additional rats underwent the same ven- Preventable Adverse Drug Events in Hospi- A Comparative Study of Inten- Care and General Care Units Sweitzer BJ, Bates DW. A, Leape LL. Crit Care with Upper Respiratory Tract in Children Infections: A — Comparison with Endotracheal Intubation AR, Pandit UA. Voepel-Lewis T. Munro HM, Anesth Analg 1998;86(4):706. S. DJ, Med 1997;25(8):I289. it. Tait Malviya —Cullen Burdick E, Edmondson OBJECTIVES: To compare Use of the Laryngeal Mask Airway a suitable alter- native to the endotracheal tube. sive hibit the increase in proceed with anesthesia for the mask airway provides laryngeal talized Patients: that the frequency and preventability of adverse drug events and potential adverse drug events in intensive care units (ICUs) and non-ICUs.To evaluate systems factors involving the individual caregivers, care unit- teams, and patients involved each adverse drug in event by comparing ICUs with non-ICUs and Several studies suggest tracheal tube ( ETT) piratory infection plications. laryngeal placement of an endo- tliat a child with an upper res- in (URl) increases the However, risk of com- development of the the mask airway (LMA) has provided thesiologists with an alternative to 1 to compare it The study (3 mo for elective surgery with a URI. Patients with URIs were randomly LMA (n = 41 ) ETT = 41 or (n ) a and were followed for the appear- ance and severity of any perioperative complications. The two groups were to age, gender, anesthesia ber of attempts ing at adult admissions to a stratified, 1 1 all random sam- medical and surgical units in 2 tertiary ical and 2 surgical general care Two tertiary care hospitals: 1 units. gical units, including 2 medical and 3 surgical PATIENTS: Adult admissions ICUs. INTERVENTIONS: None. SETTING: medical and sur- 1 (n = 4,03 1 ). MEASUREMENTS & MAIN RESULTS: Rate of preventable adverse drug events and potential adverse drug events, length of stay, charges, costs, and measures of the were detected by unit's environment. Incidents similar with respect stimulated self-report by nurses and pharmacists and surgery times, num- and by daily review of all charts by nurse inves- lube placement, and present- URl symptoms. There were no between groups 1 ple of cluded 2 medical and 3 surgical ICUs and 4 med- with the ETT. allocated to receive either an 4,03 care hospitals over a 6-month period. Units in- LMA in children with 6 yr of age) who presented Pros- anes- management. This study was therefore designed to evaluate the u.se of the DESIGN: medical ICUs with surgical ICUs. pective cohort study. Participants included means of airway sample consisted of 82 pediatric patients dose) or an equal vol- to L-NAME can in- conclude URIs and LPS (Salmonella made is CLUSION: We posi- mg/kg/h x 4 h) sion child with an upper respiratory infection, then the L-NAME. CON- They Both groups were again to receive either typhosa: 20 mg/kg I.V. x ume ). to receive intravenous in- L-NAME (25 or saline (n randomized NO with air filtered to remove ically ventilated (n rats (n piratory infections. Results suggest that if the deci- treated rats that did not receive NO domized, placebo-controlled animal laboratory investigation. LPS- did not receive LPS; however, Increases in exhaled nitric oxide (NO) have been demonstrated with the that did not cause lung inflammation reduce lung inflammation, and OBJECTIVES: 2 groups of rats flammatory interstitial infiltrate (p < 0.05) and a trend toward worse lung injury than did LPS- of septic 1998:26(2):309. in the which received LPS compared with the 2 treated rats that received for right-sided thoracic surgery. Inhibition of Exhaled Nitric tion differences tigators. Incidents were subsequently classified by 2 independent reviewers as whether they to incidence of cough, breath- represented adverse drug events or potential ad- holding, excessive secretions, or arrhythmias. verse drug events and as to severity and preventa- in the Although one patient ETT group required in the bility. Those individuals involved in the prevent- inter- a muscle relaxant for laryngospasm, the overall able adverse drug event and potential adverse drug nal carotid artery so that systemic arterial pressures incidence of laryngospasm was similar between event underwent detailed interviews by peer case- tilation protocol with cannulation of the right could be measured. SULTS: Exhaled ments of NO MEASUREMENTS & RE- gas was collected and measure- concentrations were made using chemilumine.scence every 20 min for 240 min during ventilation. A total lung injury score was cal- culated by determining the extent of cellular infiltrate, exudate and hemorrhage. pressure was recorded every 5 min Mean for arterial 20 min and then at 20-min periods for 120 min. Exhaled concentrations increased in that did not receive all the LPS-treated rats L-NAME by was reached by 190 min teau LPS (p < 0.(K)1 L-NAME and LPS exhaled NO. ). 20 min; 1 that mately 4 times greater than control with rats not treated show an Administration of pressure in 2 rats treated with by LPS. This increase in with increase in L-NAME induced a lO-min nonsustained increa.se in was a pla- was approxi- In contrast, rats treated did not NO mean arterial L-NAME followed mean arterial pressure not seen in 2 placebo and 2 LPS-treated rats thai did not receive i50 L-NAME. Lung intlamma- the two groups. There was, however, a bronchospasm greater incidence of mild ETT group compared with significantly the LMA group in the ( 1 2.2% investigators. was 19 events/ 10(X) 0%, p < 0.05). The incidence of major arterial oxygen desaturation events (SpOj < 90%) during rate of placement of the airway device was also (p vs signif- ETT group (12.5% vs 0%, icantly increased in the p < 0.05). Furthermore, the total number of episodes of respiratory complications, ie, all breath- holding, laryngospasm, bronchospasm, and major oxygen desaturation, was the all ETT group (35 vs 1 9. non-ICUs (25 events/ events/ 1 000 in the easily managed, LMA offers a suitable alterin children with URIs. compares the use ol the ICU rate ( 1 for the previous 24 hours ICUs and non-ICUs. ferences in rates between ICU were rate significantly When adjusted verse drug event were greater this, controversial, results from this ETT for use surgical p < 0.05). Despite mask airway with the endotracheal tube for airway management in children with upper reslaryngeal patient days). number of drugs used acuity, length of stay, and severity of the adin ICUs than non- ICUs, but there were no differences between med- ICU and interviews Implications: This study 000 patient days) was or ordered since admission, there were no dif- ical native to the The medical ICU ) risks associated with anesthetizing a child with study suggest that the (p 0.01 ). significantly greater in respiratory complications URl remain 1 ICUs patient days, nearly twice that < 0.05 higher than the and there were no adverse sequelae. Although the an The rate of preventable adverse drug events and potential adverse drug events in surgical indicated ICU patients. Structured almost between ICUs and non-ICUs teristics many charac- of the patient, patient care team, systems, and individual caregivers. rate no differences for CONCLUSIONS: The of preventable and potential adverse drug events was twice as high in ICUs compared with non-ICUs. However, when adjusted for the num- RESPIRATORY CARE • JUNE 1998 VOL 43 NO 6 Abstracts A detailed understanding ber of drugs ordered, there was no greater like- comparability of studies. lihood for preventable adverse drug events and of the methods and limitations of economic anal- potential adverse drug events to occur in ICUs yses is essential to clinicians challenged by a grow- number of articles and manufacturers' claims than in non-ICUs. Preventable adverse drug events ing and potential adverse drug events occurred regarding the cost-effectiveness of critical care. that functioned who in units cumstances, not at the stress, or a difficult cir- extremes of workload, Elevation of Peak Expiratory Flow by a "Spitting" Maneuver: Measured with Five Peak Flowmeters environment. — Strayhom V. Leeper K, Tolley Self T. Chest 1998;l 13(4): Horiz I998;6:33. The ICU, perhaps more than any other modem area medicine, brings the conflicting issues of high cost and live-saving technology into stark relief Cost-effectiveness analysis offers a quantitative method for selecting among treatments to optimize outcomes for any given financial outlay. Impediments to developing and using cost- using incorrect 68.2% above the PEF with the subject using correct technique. SION: Each of the five had a significant elevation ters was CONCLU- marketed peak flowmein PEF when a "spit- used. Clinicians need to instruct patients carefully regarding correct technique when using peak flowmeters. Physical Therapy on Expectoration in Patients OBJECTIVE: To flow (PEE) in 2.4 to Chest Wall Oscillation and Conventional Chest Cost-EfTectiveness Considerations in Critical Care— Rubenfeld CD. New 1 E, 134. 1 PEF for elevation in technique was ling action" normally and involved caregivers were working under reasonably normal The range determine if peak expiratory is higher using incorrect technique ver- with Stable Cy.stic Hbrosis dun J, —Scherer TA, Baran- Martinez E, Wanner A, Rubin sus correct technique with five marketed peak 1998; 113(4):1019. DESIGN: Randomized, nonblinded SETTING: University pulmonary medicine clinic. PATIENTS: Twenty adults with clinically OBJECTIVE: To compare EM. Chest flowmeters. study. stable asthma. INTERVENTIONS: After inhal- ing 2 puffs of albuterol via a valved aerosol hold- ing chamber (Aerochamber), patients min were in- and quency chest wall oscillation, ical tum, pulmonary function, and oxygen saturation with stable cystic fibrosis (CF). structed over the next 15 sions include the lack of accurate estimates or incorrect (a "spitting" action) technique treatment effectiveness and reliable cost measures; peak flowmeters. Order of use of five peak flow- Pediattic variations in assumptions used in different cost- meters and correct vs incorrect technique was ran- ter. PATIENTS: effectiveness analyses; and lack of an ethical or dom. MEASUREMENTS & RESULTS: PEF ble CF regulatory construct to ensure that the decisions (percentage of personal best will be carried out fairly. Recently, standards for of three attempts with correct and incorrect tech- performing cost-effectiveness analyses have been nique. proposed which should enhance the quality and nificant elevation in ) when using was recorded Each peak flowmeter had a PEF with for best statisfically sig- incorrect technique. ^ and conventional chest phys- therapy (CPT) on weight of expectorated spu- effectiveness analysis to guide medical care deci- in correct the effect of high-fre- oral airway oscillation, high-frequency in outpatients SIGN: Prospective randomized pulmonary division of a 1 : recruited from the tertiary care cen- CF center. ratio 9: 1 2: airway oscillation frequency 14 Hz; I;E of chest wall oscillation (1: sta- INTER- frequency 8 Hz; inspiratory to expiratory ; DE- SETTING: Fourteen outpatients with VENTIONS: Two modes of oral ( Uial. 8: 1 ), |I:E] two modes frequency 3 Hz; I:E IngMar Medical Expand Your Vision with a Spontaneously Breathing Lung Model Imagine having a L realistic rentdering of the spontaneously breathing patient for ventilator instruction, ow WATC H FOR you can. Introducing the Spontaneous Breathing (SB 2000) CRCE Module THROUGH for the IngMar Medical Adult/Pediatric THE JOURNAL Lung Model. RESPIRATORY CARE AUGUST 1998 IngMar Medical ... Expanding the Care Vision of Respiratory; Tel: 800-583-9910 Fax: 412-683-8404 http://www.ingmarmed.com Internet: Email: info(g)ingmarmed.com RESPIRATORY CARE • JUNE 1998 VOL 43 NO 6 Circle 96 on reader service card 451 Abstracts 16Hz;I:E 4:1; 2: frequency frequency 1 Hz, 1:E .5 6: 1), 1 1 : alternating with between processes of care and 30-day mortality should be instructed to continue taking inhaled CPT were determined with steroids . and (clapping, and encouraged vibration, postural drainage, coughing) were applied during the first 20 min MEASUREMENTS & of 4 consecutive hours. RESULTS: Sputum was collected on an hourly basis for a total of 6 consecutive hours. During the first and the last hour, patients collected spu- tum without having any treatment and underwent pulmonary function was measured ration ing hours ond at Oxygen (PFTs). first To Hours 2 to care performance were antibiotic administration within 8 hours of hospital arrival, 75.5% (95% con- fidence interval (CI), 73.1-77.9); blood cultures 57.3% (95% CI, before antibiotics, (95% and initial 54.5-60. 68.7% (95% when Used doses. ini- 1 ); CI. 66.2- Dissemination in Japanese Hospitals of Strains of Staphylococcus Aureus Heterogeneously CI, 87.5-90.9). Lower 30-day mortality was Resistant to 95% CI. 0.75-0.96) and blood culture collection within 24 hours of arrival (OR, 0.90; 95% CI, 0.81- (9092): 1670. first 1 .00). State and territory varied from 49.0%' to performance estimates 89.7% for antibiotics given 45.6% within 8 hours and from drawn within 24 hours. to 82.6% for blood CONCLUSIONS: cultures mean sputum dry and wet weights ranged between 122% and 185% of baseline. There was no sta- Administering antibiotics within 8 hours of hos- among pital arrival and collecting blood cultures within Fukuchi Y, Kobayashi BACKGROUND: Since the discovery of the vanMu50 (minimum strain [MIC| 8 mg/L), ment modalities. As measured by sputum wet The fact that states varied widely in the performance of these measures suggests that opportu- and dry weight, oral an I:E of 9: 1 = As measured by (p airway oscillation at 8 Hz with and 0.15). CPT tended to ble = 0.57). treatment modalities had an effect on PFTs and oxygen erated. saturation CONCLUSION: CF, high-frequency and tients improve hospital care of elderiy pa- all were well tol- oscillation applied via the CPT have Long-Acting Inhaled /3-2 Agonists in Therapy— Moore RH, Khan A, 1998:1 1 Asthma Dickey BE. Chest 3(4): 1095. OBJECTIVE: To review long-acting inhaled the pharmacology of the /3-2 agonists, salmeterol and sputum weight without changing PFTs or oxygen als, oral tri- evaluate their safety records, and discuss their roles in the treatment of asthma. DATA airway and chest wall oscillations are self-admin- SOURCES: istered, thereby containing health-care expenses. ing salmeterol or formoterol were identified by a Quality of Care, Process, and Outcomes in Elderly Patients with Mockalis JT, Fine JM. — Meehan TP, Pneumonia HM, DH, Weber GF, Petrillo MK, Houck PM, Fine MJ, Krumholz JAMA Scinto JD, Galusha CONTEXT: Pneumonia is a frequent cause of hospitalization and death among elderly the relationships quality patients, but between processes of care pneumonia and outcomes are uncertain, for making improvement a challenge. OBJECTIVES: To assess quality of care pitalized with for Medicare patients hos- pneumonia and to process of care performance lower 30-day mortality. determine whether associated with is DESIGN: Multicenler ret- rospective cohort study with medical record review. SETTING: A pitals throughout the United Slates. A total total of 4,(J69 patients 1 of 3,555 acute care hos- at least PATIENTS: 65 years old ho.s- MAIN OUTCOME and Preclinical MEDLINE search, erature updates, and SYNTHESIS: clinical studies involv- weekly computerized lit- manual searches. Studies of were chosen for review. satisfactory quality DATA Salmeterol and formoterol are potent and selective /J-2-adrenoceptor agonists with durations of action I997;278(23):2080. is the prevalence of > 1 2 hours. Their major dif- VRSA, re- METHODS: The vancomycin sus- of 3 methicillin-resistant strains (Mu50. Mu3, and HI S. ) aureus and the aureus type strain FDA209P were compared by MIC determinations Mu3 (MIC 3 mg/L) was and population analysis. monia formoterol, summarize results of their clinical CPT, high-frequency sistance occur. ceptibilities from the sputum of a patient with pneu- isolated comparable augmenting effects on expectorated saturation. In contrast to important questions need to what ( 1 ) methicillin-susceptible S. In outpatients with sta- airway opening or via the chest wall and been concern about the by what mechanism does vancomycin (2) (MRSA) with pneumonia. be more effec- tive than the other treatment modalities (p None of the nities exist to there has Two anese hospitals. be answered: CPT (VRSA) inhibitory concentration potential spread of such strains throughout Jap- 24 hours were associated with improved survival. oscillatory devices tended to be less Hosoda Y, Hori Lancet 1997:350 I. comycin-resistant Staphylococcus aureus the treat- all — Hiramatsu K, Ari- one of the hour (baseline). For the 5 treatment modalities. weight, Vancomycin S, 6 was averaged and expressed as per- effective than properiy, they are effective and safe adjunctive agents in the treatment of asthma. 8 hours of hospital arrival (odds ratio [OR], 0.85; centage of the weight expectorated during the to not take long- acting /3-2 agonists between regularly scheduled sec- assess the effect of the interven- tisfically significant difference long-acting /J-2 agonists are admin- on a regular schedule and oxygenation assessment, 89.3% Ual blood culture collection. 71.2); istered taka N. Hanaki H, Kawasaki S. weight of expectorated sputum during tion, the National estimates of process-of- associated with antibiotic administration within 20 min of the to the fifth hour, patients received treatments. satu- 30-minute intervals dur- For the to 6. 1 tests RESULTS: sis. logistic regression analy- after surgery H (MIC 2 therapy. 1 who had failed mg/L), which sponded favourably clones of Mu3 to with increased resistance against vancomycin and their mined. The prevalence of strains in re- vancomycin therapy. Sub- vancomycin were selected with serial concentra- MICs were deter- VRSA and Mu3-like Japanese hospitals was estimated by pop- ulation analysis from 1,149 clinical lates a represent- from a patient with pneumonia who isolated tions of vancomycin is MRSA strain, was ative vancomycin-susceptible MRSA iso- obtained from 203 hospitals throughout Japan. The genetic traits of the Mu3 and Mu50 strains were compared with clonolypes of MRSA from Mu3 Mu50 ferences are that formoterol has a rapid onset of around the worid. FINDINGS: action and had an identical pulsed-field gel electrophoresis is a partial agonist of high intrinsic effi- cacy, whereas salmeterol has a delayed onset and is a partial agonist of low intrinsic efficacy. Twice daily use of either drug results in symptoms, and a function, reduced ity of life. improved lung better qual- These agents protect against exercise- banding ium, pattern. Mu3 and When grown in a drug-free med- produced subpopulation of cells with varying degrees of vancomycin resistance, thus demonstrating natural heterogeneity, or variability, vancomycin. in susceptibility to Mu3 In the presence induced asthma for 12 hours and eliminate night- of vancomycin, time awakening resistance roughly proportional to the concentra- in most patients. Limited tolerance develops, especially to their bronchoprotective effects, but their is sustained. improvement of lung function CONCLUSIONS: Regular use of sal- tions of 8 mg/L vancomycin used. Selection of Mu3 with more of vancomycin gave or rise to sub- clones with vancomycin resistance equal to that Mu50 (MIC meterol or formoterol provides subjective and of objective amelioration of asthma in patients expe- 1,()0(),(KH). symptoms or physiologic im- produced subclones with no 8 mg/lj at a frequency of During screening of Japanese 1/ MRSA VRSA additional to Mu50 was pitalized with pneumonia. MEASURES: Four processes of care: time from pairment despite the regular administration of low hospital arrival to initial antibiotic administration: doses of inhaled corticosteroids (equivalent to ap- The prevalence of MRSA isolates heterogeneously resistant to vancomycin was 20% in blood culture collection before proximately 500 //g/d of beclomethasone). Inter- Juntendo University Hospital, 9.3% biotics; initial hospital anti- blood culture collection within 24 hours riencing excessive mittent use of either long-acting ^2 agonist can sfrains, strain of found. of hospital arrival; and oxygenation assessment provide prolonged protection against exercise- sity ho.spitals within 24 hours of hospital arrival. Associations induced asthma or nighttime symptoms. Patients erogeneously resistant 4.52 in the other 7 university hospitals, and 1.3% in non-univer- RESPIRATORY CARE or clinics. • INTERPRETATION: Het- VRSA is a preliminary stage JUNE 1998 VOL 43 NO 6 ABSTRACTS THE ULTIMATE SEAL™ For Standard Type Nasal iri^ InyWfifinnrii'r.l'Wr'^'^ lliriririi'Filirii llilllia'ril'igl CPAP Masks, The AirSep® Nasal CPAP Masks For Rudolph Full Face Masks & Patient Assessment Course {(2 W — — Dallas,TX mT^ Atlanta, Chicago, II GA April 17-19, 1998 June 12-14, 1998 — September 1998 11 -13, Summer Forum Naples, — Fl 1^ 17-19, 1998 July National Respiratory Care ^ that allows Fit Provides Ideal Environment for Wound Face Masks Full Healing or Prevention of Mate with Sealing Surface of Masks Home Care or Hospital Environment Easy to Apply to Masks Unique Hydrogel Material Will Not Dry Out Patent Pending For OEM, 44th International Respiratory Congress GA Dealer & Custom Sizes Available HANS RUDOLPH, — 1938 TEL: (816) FAX: 816-822-1414 E-Mail: hri@rudolphkc.com 7205 CENTRAL, KANSAS Circle 104 VRSA upon expo- INC. MAKERS OF RESPIRATORY VALVES SINCE 363-5522 U.S.A. & CANADA (800) 456-6695 I November 7-10, 1998 development into CPAP & with Nasal tVlolded to Week October 4-10, 1998 Atlanta, For Leak-Free Comfortable Wounds Specific leukotriene receptor antagonists and syn- CITY, MISSOURI 64114 U.S.A. on reader service card tion or prevention of hypoxemia a priority, and is have been developed and are cur- long-term oxygen therapy supplementation pro- one longs survival in hypoxemic patients. With only sure to vancomycin. Heterogeneously resistant thesis inhibitors VRSA was found in fiospitals throughout Japan. rently This finding could explain, leukouiene receptor antagonist (zafirlukast) and limited data quent therapeutic failure of MRS A infection with one 5-lipoxygenase inhibitor zileuton were the objectives of hospitalization, the published vancomycin cently approved by the United States at least partly, the fre- in Japan. showing promise ( Drug Administration New Approaches to apy for Asthma in clinical trials; ) re- Food and for the treaunent of asthma. SB. Am J Med Standards for the Optimal Management of COPD: 1998:104 (3):287. admission and criteria for hospital standards on the management of COPD include an expert consensus statement on these aspects of hospital care. Surgery, special considerations Anti-Inflammatory Ther- — Wenzel on a summary—Celli BR. Chest 1998:1 13 such as sleep, nutrition, and ical issues are air travel, and eth- discussed. (4Suppl):283S. Tuberculosis Control Policies in Major Met- Currently, corticosteroids are the therapy of choice for the inflammatory component of asthma. This class of drug provides powerful anti-inflammatory effects in most patients; are not specific and in some cases may serious side effects. Also, ficulty however, these effects many result in have patients dif- adhering to therapy with inhaled forms of Tobacco smoking obstructive is the main cause of chronic pulmonary disease (COPD), and en- couragement and support is the best The way in States. VI. Standard of Practice smoking cessation DR. Leff AR. COPD. 156(5):1487. to help the patient three major goals of ropolitan Health Departments in the United COPD with in 1996—Leff Am J Respir Crit Care Med 1997; management are to lessen airflow limitation, to prevent and secondary medical complications, and to Since 1980. we have surveyed at 4-year intervals the metropolitan health departments iniually re- these drugs, which are administered by metered treat dose inhalers up to several times per day. There porting are several other therapies that provide potential decrease respiratory symptoms and improve quality of life. Outpatient pharmacotherapy anti-inflammatory effects, but they are of low effi- should be organized in a stepwise manner accord- control and the factors affecting formulation of definitive anti-inflammatory effect. ing to the severity of disease, the aims being to treatment policies. Between 1992 and 1996, use induce bronchodilation. reduce inflammation, and of supervised short-course (6 to 9 cacy, with While little efforts are currenUy under way to improve although the role of anti- > 250 cases of tuberculosis tent therapy with multiple facilitate expectoration, development of targeted anti-inflammatory agents. inflammatory and mucolytic treatment of COPD niazid, ethambutol, pyrazinamide, For example, the leukotrienes, a family of inflam- has not been clearly established. Pafients whose increased from have been shown to enhance conditions are not well controlled with opfimal Pyrazinamide use for mucus pharmacotherapy are candidates for enrollment has increased substantially and that bronchoconstriction and airway secretion, have been the focus of numerous investigations. RESPIRATORY CARE • in a pulmonary JUNE 1998 VOL 43 NO 6 rehabilitation program. Correc- mo) intermit- drugs including iso- corticosteroid therapy, other directions include the matory mediators to determine the perceived standard of practice for mberculosis and rifampin 43% to 4695- of all new patients. (74.2% of pafients initial in treatment for children now predominates 1996 vs 48.1% of patients 453 , Abstracts mo 1 + Duration of treatment, which was 20 in 1992). 2. in 980. 1 now is 8.00 ± 2.29 mo in 1 996. The incidence of human immunodeficiency virusassociated tuberculosis, which was virtually unrecognized in 1984, has remained the same be- tween 1992 and 1996 (18.0%). As was years, there departments incidence and an over a 20-min period before and after the applicafionof NPPV (inspiratory pressure of 10 to 12 and quality of life, but the routine use of PFM cm HiO and expiratory pressure of 4 to 6 cm HiO). RESULTS: NPPV increased saturation from 88 ± 2% to 90 ± 1% (p < 0.05) and decreased tcco2 trol that education, regular follow-up. guide interventions to is way not the only to accomplish these objectives. among health (< 5% to > 40%) of B7-CD28/CTLA-4 Costimulatory Pathways Are Required for the Development of T Helper HIV-associated tuberculosis. After years of fund- Cell 2-Mediated Allergic Inhaled Antigens Linsley PS, mean budget 1997;158(5):2042. Chen Airway Responses to — Keane-Myers A. Cause WC. ing decreases, there has been an impressive in- crease in resources in the past 4 years. In 1988. allocation for health departments SJ, Wills-Karp M. J Immunol We have previously demonstrated that the devel- allocation after inflation versus 1988. In 1996, opment of allergen-induced airway hyperrespon- change overall in T cell however, funds for treatment increased by 84 ± siveness in a murine model is 33%. This increase dent. In the present study, we examined in funding has been translated expanded use of supervised into the greatly inter- mittent therapy and aggressive screening programs. which likely have resulted in the decreased inci- dence of tuberculosis since the prior of the CD4-I- depen- the role B7/CD28-(7rLA4 costimulatory T cell acti- vation pathway in the pathogenesis of allergen- induced airway hyperresponsiveness in murine this model. Sensifized A/J mice develop significant .survey. (p ± 2 to ventilation decreased ± 0.6 L/min (p = ± 5% 1 8 ± 1 (p < 0.01 ). 34 to ± 5%, p = in NS). In two was a decrease in pressure cm H2O to -1 ± 2 cm HjO and -14 cm H:0 to -7 ± cm HiO. CONCLUSIONS; 1 1 1 1 In patients with stable, severe cystic fibrosis, ) to 4.6 There was no change esophageal pressure measurements were from -2 1 ± 1 Minute from 5.3 ± 0.8 L/min 0.08). also recorded. There ( mL not significant |NS]) and respiratory rate decreased from 24 + + 20 mL to 256 ± 37 increased from 2 1 9 = patients, budget was no Vt duty cycle (32 decreased by 7.9% versus the prior 4 years and, in 1992, there mm Hg to 50 ± 2 mm Hg (p < 0.05). from51 ± 3 previous in a wide variance in the show action plan are effective in improving asthma con- NPPV acutely improves gas exchange, (2) decreases minute ventilation, suggesfing either a reduction in CO2 production or an increase in alveolar ven- and (3) reduces work of breathing. nlation, increases in airway responsiveness, bronchoal- A Randomized Comparing Peak Expi- veolar lavage eosinophils, serum IgE levels, and Symptom Self-Management Th2-associated cytokine production following as- Asthma Attending a Pri- OVA. Administrafion of CTLA4-Ig either before Ag sensitization or before pulmonary Ag challenge abolished Ag-induced Teaching and Community Hospitals. The Southwestern Ontario Critical Care Research airway hyperresponsiveness and pulmonary eosin- Esmail R. Inman KJ, Sibbald WJ. Crit Care Trial ratory Flow and Plans for Patients nith mary Care nett Clinic —Turner MO. Taylor D. Ben- R, Fitzgerald JM. Am J Respir Crit Care Med 1998;157(2):540. piration challenge with ophilia. Great emphasis ics to placed on educating asthmat- is use action plans to achieve better control of symptoms. The use of peak flow meters has been recommended self-management plans. (PFM) as an important part of We studied 92 (47 female) adult patients with asthma in a primary care setting to compare the effectiveness of action plans symptoms using either peak flow monitoring or self-management. Each patient was to guide in- structed in the use of the action plan in the context of a 6-month asthma education program taught by a nurse. Patients were already using inhaled in the Examination of cytokine protein levels Withdrawal and Withholding of Life Support in the Intensive Care Unit: A Comparison of Network— Keenan SP, Busche KD, Chen LM, Med 1998;26(2):245. bronchoalveolar lavage showed a signif- icant decrease in the level of the IL-4, after CTLA4-Ig change cytokine, with no significant concentration of the Thl cytokine, in the IFN-gamma. Th2 treatment either before sen- sitization or before challenge, Further, the Ag-specific IgG and IgE were 1 Ab isotypes significantly decreased in ani- OBJECTIVK: To compare the incidence of withlife support (WD/ drawal or withholding of WHLS), and to identify similarities and differen- ces in the process of the withdrawal of port (WDLS) between teaching and sup- life community hospitals' intensive care units (ICUs). DESIGN: mals treated with CTLA4-Ig before challenge, Prospective cohort study, with while there was no significant change in the by retrospective chart review. SETTING; The Ab that isotype. These data demonstrate isQ^tion of CTLA4-lg is IgG2a admin- effective in ablating aller- gen-induced airway dysfunction concomitant with Th2 response. We B7/CD28-CTLA-4 cosfimulation for the development of many of the ICUs of 3 teaching pitals. hospitals some data obtained and 6 community hos- PATIENTS: All patients who died in these a 6-mo penod. INTERVENTIONS; 9 ICUs over MEASUREMENTS & RESULTS: corticosteroids or were newly prescribed corti- a significant reduction in the None. costeroids by their family physician. Forty-four conclude that on admitting diagnosis, cause of death, mode of were randomized patients 48 to the to the PFM group and symptoms group. Spirometry, symptom .scores, quality of life, medication use, and mea- sures of health care utilization and morbidity (emergency department visits, hospitalizations, uascheduled doctor and days visits, lost from work or school) were recorded at baseline and throughout the study period. sured at the symptoms of and PC20 methacholine was meaat the final visits. There were improvements within groups significant ity first score, PC20 for FEV significant shift /J-agonists (p from higher < 0.008 to A lower daily use of for both groups) and sig- nificant shifts to higher daily do.ses of inhaled steroids (p < 0.(X)1 occurred ) in each group. Adher- ence to the self-management plans wa.s only symptoms in the PI-TVl group antl .52% Outcomes for health care utilization lar in the 65% group. were simi- except for fewer patients making unscheduled doctor 454 visits within the required immunologic and physiologic features of asthma, PFM group. Our findings these initiating and involved in support withdrawn were gathered for possibly by promoting a pathologic type 2-asso- ities patients dying in the of life hundred The Acute Effects of Nasal Positive Pressure Ventilation in Patients with Fibrosis— Granton Advanced Cystic JT, Keslen S. Chest 1998; 292 in community hospitals and teaching hospitals died in their respective ICUs over ence ICU over a 6-mo period. One sixty patients in 6-mo the period. in the distribution community 113(4):1013. WD/WHLS), WDLS, and modal- death (death despite active treatment ciated response. hospitals of We found a differ- mode of death between and teaching hospitals, result- ing from a greater proportion of patients dying as i methacholine. and qual- but no between-group differences. life, is Data OBJECTIVE: To evaluate the acute effects of non- invasive positive pressure vennlanon (NPPV) in patients with .stable chronic respiratory failure sec- ondary to cystic fibrosis. PATIENTS: Eight pa- ± 5 years of age) with severe airtlow limitation (mean FEV|, 24 ± 3% predicted) and chronic re.spiratory failure (PaOj = 67 ± 15 mm Hg and P.,co2 = 50 ± 4 mm Hg) were evaluated. tients (29 METHODS: Tidal volume (Vt), respiratory rate, minute ventilafion, oxygen saturation, and transcutaneous COi (tcco;) measurements were made a result of withholding hospitals p ( 1 1 life support in .9% vs 3.8% withheld, community respectively, = 0.004). Among the 6 community hospitals and we found a difference in the 3 teaching hospitals, proportion of patients dying despite active treat- ment compared with those dying as a result of (p = 0.042 and p = 0.044. respec- WD/WHLS tively). Initiation more frequent at of WDLS by physicians was teaching hospitals (81% vs61%, p = 0.0005). while families more commonly fiated WDLS rfspiratory Care • at community hospitals ini- (34% June 1998 vol 43 No vs 6 Abstracts 19%, p = 0.005). in A the quality was a trend for hospitals (0.74 = + 1 fewer into WDAVHLS hospitals and teaching hospitals; however, with- holding of life support was more The need for more cosmetically oxygen in the home, remain challenges. ogy, of Definitions, Epidemiol- and Factors Influencing Rennard SI. Its — Development Chest 1998:1 13(4 Suppl):235S. in the — Kollef MH. New outcomes of critically amined ill in a systematic care practitioners on the patients has not manner. This been ex- is in contrast which have demons&ated ical care physicians and nurses in the a ICU method setting. on patient Outcomes research outcomes represents for the formal evaluation of various health care provider staffing patterns within the (COPD) ICU. Specific patient outcomes including hospital a heterogeneous collection of conditions that mortality, respiratory complications, lengths of Chronic obstructive pulmonary disease is can affect various sUTictures within the lung in a number of different ways. These various processes COPD—Petty TL.Chest can 1998;113(4Suppl):256S. If all result in limitation of expiratory airflow. severe enough, this physiologic abnormality defines in The impact of respiratory to clinical investigations common in com- ing hospitals. Supportive therapy Care Unit Setting Horiz 1998:6:91. the beneficial influence of specially trained crit- COPD: Overview community between community hospitals and teach- Supportive Therapy in Intensive as a Tool for Defining the COPD through patient funjre directions in providing munity hospitals. The process of WDLS appears to differ coping with advanced pleasing oxygen delivery systems to the nose, and inci- dence of similar in patients with + 0.79 [SD] CONCLUSIONS: The was life in patients with oxygen gain insight support groups. compared with teaching .38 days vs 0.27 0.0028). and length of COPD. Many hospitals and teaching hospitals, community hospitals to have vasopressors withdrawn (56% vs 70%, p = 0.082). The time to death after WDLS had begun was longer days, p this condition. Role of Respiratory Care Practitioners patients in hospitals from Outcomes Researcli respectively), while there community tients suffering of trials vided an effective therapy which improved both vasopressors mechanical ventilation withdrawn (68% and 74%, in 960s and the 1970s, along with additional advances, pro- WDLS. community 1 (76% (99% vs 89%) and 65%) before LTOT dating to the early bolstered by excellent controlled clinical Similar proportions had ventilation vs rich history of greater proportion of patients teaching hospitals were receiving mechanical COPD. The lead to this chronic obstructive pul- various conditions that can syndrome are prevalent and often stay, mine and medical care costs can be used the optimal ICU to deter- staffing strategy for res- piratory care practitioners. Until recently, we have lacked good outcomes data for assessing the role of respiratory practitioners in the ICU. Several barriers have contributed to this deficiency of data monary disease (COPD) includes long-term oxy- relentlessly progressive. In aggregate, they rep- including a lack of funding, absence of a national gen therapy (LTOT) and patient support groups resent an important public health problem. This research initiative aimed at this specific issue, and comprehensive program supplement outlines diagnostic and therapeutic the paucity of clinical investigators in this area as two cornerstones of care known as in a pulmonary rehabilitation. You need it The strategies by which the practitioner can assist pa- of study. Good outcomes research requires appro- now. 19 9 8 LITERARY Not next week. Not next month. AWARDS NOW? Ma(de possible by the American Respiratory Care Foun(dation Allen DeVilbiss Technology Paper Award $2,000 & ARCF Certificate PLUS Airfare & Night's 1 Locjging During the 44th International Respiratory And you can have The fastest it. Congress answers to your questions about products and services advertised in the current issue of are just a "Click" Respiratory Care in November 7-10, 1998 Atlanta, Georgia, Best Original Paper $1,000 & ARCF Certificate away when you go online: Radiometer Awards for Best Features -3 Awardshttp://www.aarc.org/resources/htinl RESPIRATORY CARE • JUNE 1998 VOL 43 NO 6 $333 & ARCF Certificate 455 Abstracts increased intrapulmonary pressures, total pulmonresistance, ;iry Keep abreast of the We inves- and airway abnormalities. tigated the hypothesis that inhalation of nitric oxide (NO) could latest research in maximum exercise capac- and excessive ventilatory response ity in influence the CHF. Fifteen patients in to exercise CHF (mean age 48 + NO inhala- 12 years) underwent a control and a RE/PIRATORy 30 ppni. tion progressive treadmill exercise test with We determined the maximum oxygen consump- CARE CO: tion (peak Vo;). pulmonary ventilation (Ve). respiratory rate, tidal volume (Vj), ( production (Vco;), minute oxygen ventilatory equivalent for Ve/Vq:), ventilatory equivalent for carbon diox- ide (Vg/Vco:). estimated physiologic tidal volume rate, systemic slope, dead space/ (Vi/Vt). Vg/Vco: slope, heart ratio arterial pressure. Vg/exercise time and Vy/exercise time slope during every incremental exercise. Mean maxunum exercise val- ues of heart rate, systolic systemic arterial pressure, diastolic lODM! systemic respiratory rate, peak Vq;. Voj/heart rate. Vg/CO:. maximum exercise time were unchanged by and inhalation of nitric oxide. There was a strong trend toward reduction of Vj/ Vq; from 53 ± Make checks payable ViVVt. arterial pressure, 1 5 to 47 = 0.05 1 and in maximum Ve from 58 ± 2 to 48 ± 17 L min-' (p = 0.059). Maximum Vt decreased from 1639 ± 556 to 1406 ± 479 mL (p = 0.04). The Ve/Vco: slope was reduced from 43 ± 2 to 35 ± 8 (p = 0.01 8). Two patients had signs ± to 1 2 (p (see last page for rates), ^ 1 subscription officejt 1L030 Abies Lane Dallas. Texas 75229-4593 priate levels of funding, adequately trained Vj in response to exercise and during exercise in in CHF. The pathway may be involved mechanisms contributing to hyperventilation CHF. impact on patient in the 13(4): 1028. area ratory lung volume (EELV) and mean methods of outcomes research can be employed and limitations of in normal subjects and patients with severe chronic obstructive pulmonary disease (COPD). DESIGN: Comparative TING: Pulmonary practices. oscillated during high-frequency chest com- (HFCC) study. Oxide Inhalation Reduces Pulmonary TICIPANTS: Tidal Volume during Exercise female) and 6 patients with clinically stable in Severe — Bocchi EA. Auler JO Guimaraes GV. Carmona MJ. Wajngarten M, 997; .M(4):737. I (5 male; 1 female) with hypercapnia. I the effectiveness of mucus from in during COPD HFCC-i-PEEP HFCC in clear- the lungs of patients with airway disease. Preoperative Smoking Habits and Postoper- — Pulmonary Complications Bluman LG, Mosca L. Newman N. Simon DG. Chest 1998; ative I13(4):883. the effect of preop- smoking behavior on postoperative pul- SETTING: The Veterans AdminPAR- Medical Center. Syracuse NY. TICIPANTS: Patients scheduled for noncardiac = 410). MEASUREMENTS & RESULTS: Smoking status was determined by elective surgery (n pulmonary complica- self-report. Postoperative were determined by systematic extraction complications occurred in 31 of 141 (22.0%) current smokers. 24 of 187 (12.8%) past smokers, and cuit spirometer of HFCC- that was 5.5 (OR) smokers versus never smok- (95% confidence interval [CI], 1.9 to 16.2) and 4.2 (95% CI. ment for type of surgery, type of anesthesia, 1.2 to 14.8) after adjust- abnormal chest radiograph, chronic cough, tory of pulmonary disease, ease, history of chronic obstructive disease, education level, body mass index, and his- history of cardiac dis- pulmonary pulmonary function, age. Current smokers who reported reducing cigarette consumption prior to surgery were more likely to develop a com- COPD plication compared with those who did not (adjusted OR = 6.7. 95% CI, system permitted measurement and PEEP-induced changes ers ratio pulmonary com- INTER- VENTIONS: A pneumatic vest system was operated at 10 Hz with a mean chest wall pressure of 16 cm HiO to provide the HFCC. A closed-cir- plain the hyperventilation and the limited exercise including PAR- Six normal subjects (5 male; Multiple mechanisms have been proposed to ex- (CHF) SET- function and lung mechanics laboratory. University of Alberta Hospitals. Nitric capacity in congestive heart failure ing plication for current the effects of pos- end-expiratory pressure (PEEP) on end-expi- pression relates to the role 1 may improve for developing a postoperative piratory care practitioners in the ICU. Similarly, 4,56 on these research goals. Am Heart J patients. This higher Vos,. during RL. Chest 1998;! (Vos^.) BeUotti G, Pileggi F. prevents the VOSC and increases 4 of 82 (4.9%) never smokers. The odds flow rate Jr. EELV in both phases of spontaneous breathing tions — of res- Chronic Heart Failure HFCC amount of PEEP during decrease Flow Rate during High-Frequency Chest Compression Perry RJ. Man GC. Jones itive ICU COPD both inspi- of medical record data. Postoperative pulmonary OBJECTIVE: To investigate other PEEP increased V^sc during (30.5%) and expiration (57.0%) (both, p < O.OI ). CONCLUSIONS: Addition of a modest ration istration and organized and dedicated approach must be to better define the benefits during inspiration (5.1% increase). In the patients, < on V^sc Vt. developed based upon strong research proposals. the significant effect Vg and minor increase Inhalation of nitric oxide attenuated the excessive interest in res- made was no monary complications. DESIGN: Prospective Oscillated it but there ). cohort study. medical sciences), and the support of both local of outcomes research as expiration to increase 14.6% (p Vosc during 0.01 sta- Effects of Positive End-Expiratory Pressure This will allow advances to be 1 slope during incremental exercise were reduced disciplines (eg. statistics, epidemiology, general To accomplish ). by inhalation of nitric oxide, demonstrating a experienced clinical investigators from various outcomes. For the normal sub- ) erative in their RESULTS: HFCC caused a significant decrease in EELV to 82.0% of FRC (p < 0.01 and the addition of 4.8 ± 0.5 cm H2O of PEEP during HFCC increased EELV to 97.5% FRC. In the COPD pauents, HFCC decreased EELV to 92.3% of FRC (p < 0.01 and the addition of 3.7 ± .0 cm H:0 of PEEP increased EELV to 98.4% FRC. For the normal subjects, increasing EELV to near FRC caused The VE/exercise time slope and Vj/exercise time L-arginine-nitric oxide and surement of Vosc OBJECTIVE: To examine increase in piratory care sendees chamber jects. the recovery period with inhalation of nitric oxide. tistically significant and national organizations with an isothermic of pulmonary congestion during peak exercise or aad mail to the ^ (FRO. An connected near the mouthpiece permitted mea- ) 1 Respiratory Care residual capacity in EELV were expressed as percent baseline functional 2.6 to 1 CLUSIONS: Current smoking was with a 7. 1 ). CON- associated nearly 6-fold increase in risk for a postoperative pulmonary complication. Reduction in smoking within 1 month of surgery was not associated with a decreased risk of postoperative pulmonary complications. RESPIRATORY CARE • JUNE 1998 VOL 43 NO 6 Abstracts — ]]lJIJJilJiJiJ Circle 115 Volume Therapy in the Critically — Boldt 111: Is There function were analyzed from arterial blood sam- MuUer M. Mentges D, Papsdorf M, Hempelmann G. Intensive Care Med ples 1998;24(1):28. line" value) a Difference? J. on the day of admission to the ICU and on the day of sepsis diagnosis, respectively ("base- and daily over the following 5 days. Mortality during and after the study did not dif- OBJECTIVE: There are still several concerns fer significantly There were also no differences between the oxyethylstarch solution (HES) in critically dence of pulmonary, patients. The effects of volume replacement with the inci- renal, or hepatic failure in two subgroups. Mean arterial pressure, heart PCWP were similar in both subgroups, HES over 5 days on hemodynamics, laboratory rate, data, and organ function were compared with vol- whereas cardiac index, oxygen delivery index, oxy- and ume therapy using human albumin (HA). DESIGN: Prospective, randomized study. SET- gen consumption index, and the TING: fractional inspired Clinical investigations sive care unit on a surgical inten- (ICU) of a university hospital. PATIENTS: 150 traumatized patients (injury severity score > 15) and 150 postoperative patients partial pressure ratio between the of oxygen in arterial blood and oxygen were higher in the HES- than in the HA-treated groups. Standard coagulation parameters did not differ, albumin con- centration increased significantly in both HA INTERVENTIONS: Either 10% low-molecular weight HES (HEStrauma, n = 75; HES-sepsis, n = 75) or 20% HA groups, and lactate concentrations decreased only (HA-trauma, n = 75; HA-sepsis, n = 75) was given min was with sepsis were analyzed. for 5 days to maintain the pulmonary capillary wedge pressure (PCWP) between 12 and 15 torr. The entire management of therapy of the patients was performed by physicians who were not smdy and blinded involved in the regimen. MEASUREMENTS & RESULTS: In to the infusion in the HES-sepsis patients (from 2.8 ± 0.5 to 1.5 + 0.4 mg/dL). Volume replacement using albusignificantly (p < 0.001 more ) costly than therapy with HES. CONCLUSIONS: Volume therapy with 10% HES for 5 days in the ICU Mahul Viale JP, Duperret S. P, Delpuech C, Weismann D, Arinat G. Crit Med Care — Delafosse B, Am J Respir 1998;157(2):428. Inspiratory muscle unloading decreases ventilatory drive. In this study, course of this effect modes of ventilatory receiving support: pressure support ventilation (PSV), during assisted, the time with chronic ob- (COPD) pulmonary disease structive 2 we examined in patients which each cycle was and biphasic positive airway pressure (BIPAP), set up in such a manner that sponta- 1 neous breath took place between 2 consecutive pressure-assisted breaths. the switch The associated with an increase and a drop (mean per Pj,) liter first breath following from spontaneous breathing in tidal PSV was to volume (Vy) mean ttansdiaphragmatic pressure and inspiratory work (Wi) performed in but with unchanged values of esophageal occlusion pressure at 1 00 ms (Pes 0. 1 ), diaphrag- matic electrical activity (EMGdi), and WI per- formed by breath. The same phenomena were HES may pared with the preceding spontaneous breath. Dur- replacement using even be associated with improved hemodynamics. HES appears to be a valuable and significantly cheaper alterna- several routine laboratory parameters for assess- tive to ing pulmonary, renal, hepatic, and coagulation apy • of Ventilatory Re- sponses to Inspiratory Unloading in Patients showed no disadvantages compared with an infusion regimen using 20% albumin. Volume patient addition to extensive cardiorespiratory monitoring, RESPIRATORY CARE Time Course Evolution between the infusion groups. about the extensive and prolonged use of hydrill on reader service card —even albumin in the critically JUNE 1998 VOL 43 NO 6 for ill prolonged volume ther- patient. observed for the assisted breath of BIPAP as ing the subsequent breaths of PSV, Pes 0. 1 , com- EMGd,, Wi performed per breath decreased progressively up to the sixth to eighth breaths, and Vt re- and turned to pre-PSV values. We conclude that in pa- 457 Abstracts with tienLs COPD the decrease in ventilatory drive PSV associated with takes place from the first breath onwards but requires 6 to 8 breaths to be During BIPAP. as a consequence fully achieved. We analysed data for all patients listed for ODS: USA transplantation in the tic fibrosis, on the waiting of ventilatory drive, assisted breaths following ing, emphysema, cys- pulmonary or interstitial fibrosis in The numbers of patients entered the years 1992-94. of the kinetics of the PSV-induced down regulation for list, post-transplantation, died wait- and currenUy waiting were: emphysema group spontaneous breaths are characterized by an en- 1,274, 843, 143, and 165; cystic fibrosis group hanced 664, 318. 193, and 59; inspiratory efficiency. First Decade of Continuous Monitoring FINDINGS: The group. sis The on the waiting list. from of transplantation com- relative risks pared with waiting were 0.87, 0.61. and 0.61 1 month. 6 months, and = 0.008), year (p I pulmonary at respec- with cerebral perfusion pressure versus outcome tively. responding relative risks were 2.09, 0.71, and 0.67 agement of cerebral perfusion pressure alone (p in = For interstiti;il 0.09). No the of 178 patients underwent continuous monitor- ing 2 years of follow-up. 1 and management of cerebral extraction of oxy- ing gen and cerebral perfusion pressure, while a con- group of 175 patients underwent monitoring trol and management of cerebral perfusion pressure only. INTERVENTIONS: emergency procedures. RESULTS: The Routine neuro- MEASUREMENTS & 2 groups of patients emphysema group. The relative to waiting 1 fibrosis, the cor- was apparent survival benefit DESIGN: Prospective, interventional study. SETTING: Intensive care unit of a university hospital. PATIENTS: Adults (n = 353 w ith severe acute brain tauma. A group I 1.12, at year, respectively, and below 1 . .0 dur- 1 INTERPRETATION: that lung transplantation does not confer a survival benefit end-stage and 1 the relative risk did not decrease to These findings suggest in of transplantation risks were 2.76, month, 6 months, and emphysema by with in patients 2 years of follow-up. Other benefits not accounted for such as improved quality of in this analysis may however, life, were matched Coma Scale vention: Characteristics of Participants hematomas and brain swelling, pupillary Non-Participants — and Abdulwadud O. Abramson abnormalities, early hypotensive events (before M. Forbes A. James A, Light intensive care monitoring), as well as RespirMedl997;9I(9):524. els initial lev- Thien F. L, et al. Outcome nificantly better (p at 6 months postinjury was < 0.00005) in the sig- 178 patients undergoing monitoring and management of cerebral extraction of oxygen along with cerebral per- fusion pressure, than in the control group of 175 patients undergoing monitoring and management of cerebral perfusion pressure alone. CLUSION: CON- In patients with severe acute brain As part of an evaluation of the patient education tal, in 1994/95 clinic of at the The Alfred Hospi- a tertiary referral hospital in Melbourne, Aus- The objective of the study was tralia. Effect of Diagnosis cere- on Survival Benefit of Lung — Limg Disease Bennett LE. Keck BM. Edwards Transplantation for End-Stage Hosenpud JD. EB. Novick RJ. Lancet 1997:351 (9095 ):24. full A total foniis of end- stage lung disea.se are debilitating, whether the a.ssocialed mortality rate tation is unclear. exceeds that of transplan- a.ss of COPD can be attributed to bacterial infection, and antibiotic therapy has been demonstrated improve outcomes and hasten clinical clinical to and physiologic recovery. The major pathogen con- Haemophilus influenzae, and tinues to be resis- tance to /J-lactam antibiotics such as ampicillin can be expected in 20 to 40% of isolated strains. whom the cost of clin- Certain high-risk patients, in ical treatment failure simple clinical is high, can be identified criteria. Patients by with significant cardiopulmonary comorbidity, frequent purulent ministration, long duration of COPD, underlying lung function tend to fail and severe therapy with older drugs, such as ampicillin, and early relapse can be expected. Treatment directed toward resis- may pathogens with potent bactericidal drugs to lead to and overall lower improved clinical outcomes costs, particularly if hospital mine if new therapies have significant clinical, and economic advantages over quality-of-life, older agents. asthma edu- in the pro- Lung Volume Reduction Surgery: An Analysis of Hospital Klontz B, Costs Wan^n WH, —Elpem EH, Behner KG, Szidon JP, Kesten S. Chest 1998; 113(4):896. to immediate, rather than OBJECTIVE: Lung volume nificant predictors of attendance. Subjects ran- were approximately (LVRS) represents a potential breakthrough in the management of advanced emphysema, although likely to attend than conU'ol sub- questions remain about clinical and economic domized to the intervention three times more jects (odds ratio |OR| = 3.3, 95% val |CI| 1.5-7.3). (OR = confidence 6.6, inter- Asthmatics over 60 years old 95% CI likely to attend 2.2- 19.8) than the age group 16-30 years. The increasing trend in attendance across age categories 0.001 liance METH- at compliance with the programme was 43.2%. Allocation of lung transplantation for various types of end-stage lung disease. vis- Approximately one half of all exacerbations delayed, education and age were the only sig- We undertook analysis to clar- ify the survival benefit to investi- of 125 asthmatics aged were approximately 6 times more BACKGROUND: Although certain its. gate which demographic and clinical characteristics gramme, and alone. primary care for a significant proportion of all otics should enroll these high-risk patients to deter- was conducted asthma and allergy oxygen managed and acute respiratory infections account outpatient cation over 16 years agreed to participate outcome than when (COPD) the fifth leading cause of death in the United States, vented. Future studies examining the role of antibi- trial were associated with attendance in better is admissions and respiratory failure can be pre- randomized, controlled cational session. bral perfusion pressure is Chronic obsUTictive pulmonary disease of asthma edu- plan, a monitoring and managing cerebral extraction of pressure result Suppl):249S. component of the Australian Asthma Management with compromised cerebrospinal fluid spaces. conjunction with cerebral perfusion of Antibiotics and the be expected trauma and intracranial hypertension associated in at Outcomes of Therapy in Exacerbations of COPD—Grossman RF. Chest 1998:113(4 tant of intracranial pressure and cerebral perfusion pressure. required to improve par- debility, malnutrition, chronic corticosteroid ad- Attendance at an Asthma Educational Inter- nial is by young and employed asthmatics hospital-based asthma education programs. exacerbations of COPD. advanced age. generalized justify lung transplantation for these patients. with regard to age. postresuscitation Glasgow scores, rates of acute surgical intracra- Over inter- in the cystic fibro- of patients undergoing monitoring and man- severe acute brain trauma. ticipation poor. time-depen- clearest survival benefit lung transplantation occurred comparatively assess outcome alternative strategy Antibiotic tion relative to that for patients OBJECTIVE: To An was who had expressed attend for their educational sessions. est, failed to The Value Management Strategies and Clinical Outcome—Cruz J. Crit Care Med 1998;26(2):344. in attending sessions half of the asthmatics, of mortality after transplanta- to assess the risk agement of cerebral extraction of oxygen along fibro- compliance dent nonproportional hazard analysis was used of Jugular Bulb Oxyhemoglobin Saturation: of patients undergoing monitoring and man- A group 481, 230, 160, and 48. sis The pulmonary interstitial Despite offering incentives and conducting the education sessions at subjects" preferred times, their ). was highly significant (p There was no relationship between < atten- and gender, medication, atopy, smoking sta- tus or the physical accessibility of the hospital. reduction surgery implications of widespread application of we In this report, ing physicians' fees, for pital LVRS. describe hospital costs, exclud- LVRS. DESIGN: Hos- charges were obtained from billing records and converted to costs by applying multiple cost- SETTING: A large, urban academic medical center. PATIENTS: Fifty-two consecutive patients who received bilateral LVRS to-charge ratios. through a median sternotomy between April RESPIRATORY CARE • 1 995 JUNE 1998 VOL 43 NO 6 nEW! Orientation & Competency Manual The Orientation and Competency Assurance Manual for Respiratory Care provides the information, assessment tools, and models necessary to demonstrate that the competence of employees is documented according to JCAHO requirements. Item BK55 S65 ($40 nonmembers) nEW! Respiratory Home Care Procedure Manual The new Respiratory Home Care Procedure Manual is especially designed for the home care setting. And, it is easily adaptable to any alternate care site from subacute to home medical equipment companies and nursing agencies. The manual features five sections of information, forms, and checklists for the patient and practitioner. Item BK3 $80 ($150 nonmembers) nEW! Uniform Reporting Manual for Subacute Care The Uniform Reporting Manual for Subacute Care is tool to determine productivity, track trends in the a care services, assist in determining personnel requirements, measure demand for and intensity of services, and meet the requirements of prospective payment systems. (PPS). utilization of respiratory Item BK2 nEW! $75 ($115 I.V. nonmembers) Sample Curriculum Sample Curriculum is designed for use by respiratory care educational programs in conjunction with their clinical affiliates. A course following this curriculum will augment training programs for respiratory care practitioners with thorough in- The I.V. struction in I.V. -line placement and management. Contains everything needed to establish a complete I.V. -line course: lesson outlines, checklists and references. Item BK18 $25 ($35 nonmembers) how to order Call the American Association for Respiratory Care at (472)243-2272 Here's for your Continuing Education needs 44th -^ ¥ y, :^";W A^^r I sociation for o r y Care Managers and educators from will all across the country gather to exchange more about many ideas and learn meeting the challenges in health care. A vast array of educational opportunities especially designed to help them compete in an increasingly aggressive and business- oriented health industry will be AARC available. Join the and your respiratory care colleagues in Atlanta for a relaxing vacation and learning experience. at Atlanta, Georgia Nov. 7-10, 1998 ) Abstracts and August 1996. was RESULTS: Median hospital stay 14.8 ± 12.8 days; range = = 6 ± 9.2 (mean = 10 days 3 to 48 days), including 2 days (mean = days; range unit (ICU One ). 35 days) to 1 in the intensive care hospital death occurred. Hospital costs per case ranged from $11,712 to $121 .829. mean costs of $30,976 and median with Costs were related significantly to dura- $19,77 1 . tion of ICU who tients costs of and length of hospitalization. Pa- stay accrued the highest costs were sig- remainder of the sample nificantly older than the (69.3 years vs 62.4 years). LVRS CONCLUSIONS: Hos- (HlyA). an important virulence factor NO liberation in isolated endothe- stimulator of lial cells, eration and and in extrain- was found to be a potent testinal E. coli infections, that it also causes thrombtixane gen- related va.soconstriction in rabbit lungs. We investigated the effect of different concentfations of HlyA on pulmonary NO synthesis in buffer-perfused rabbit lungs. NO release into the alveolar as well as the intravascular compartment was NO and by measurement of (per- tion of expired oxy-)nitrite/nitrate release into the perfusate. HlyA induced a pressor respKinse and an immediate dose- lated directly to hospital stay. Identification of fac- dependent increase of exhalative and intravascular of tors associated with vary significantly but are prolonged stays can be used in assessing benefits LVRS and risks of against of health-care dollars. utilization DNase I Acutely Increases Cystic Fibrosis Sputum Elastase Activity and Its Potential To Induce Lung Hemorrhage in Mice Cantin — Am J RespirCritCareMed AM. 1998;157(2):464. NO liberation, further enhanced by the addition sis potential of sputum evaluated. tle in I to increase cystic fibro- and lung damage was Sputum from CF patients lung hemorrhage C57BL/6 when ± .56 vs 3.9 1 1 lit- instilled inlranasally 1 mg/mL bovine DNase showed increased neutrophil (7.97 induced mice. However, sputum treated in by the addition of vitro I DNase elasta,se activity elastase activity ± 0.62 /iM. p < 0.0 1 ) and in- NOS These ). I alone bolism. Intravascular gas was documented within travascular compartments. bition of in- Enhancement of NO NO (L-NMMA) synthesis amplified greatly, the HlyA-elicited vasoconstrictor response. Inhibition of the pressor response by a that marked NO formation. We conclude ( 1 NO biosynthesis occurs in this model of the septic lung, 2 that the signal transduction ( in response to ) HlyA proceeds changes in when that hour of treat- sep- were highest, induced lung hemorrhage DNase I We conclude therapy of patients with CF can acutely increase the elastase activity of sputum and also its potential to induce hemorrhage in the murine lung. and not shear stress, and (3) that approaches using NOS in an Kndotoxin- of Gastric Insufflation and the Risk Position — Latorre F, Eberle B, Weiler N. Mienert R. Stanek A. Goedecke R. W. Anesth Analg Heinrichs 1998;86(4):867. mask airway an incomplete mask seal causing gas- is insufflation or oropharyngeal air leakage. tric objective of the present study incidence of LMA was gastric insufflation age. to assess the malpositions by fiberoptic and oropharyngeal One hundred eight placement tidal sure exceeded Schultc Mayer K, GesslerT. Ruhl M. .SchlaudraH et al. Am J Med 1 J. 998; patients were air leak- .studied after any surgical mask is (NO) is an important vasodilator that produced by constitutive (cNOS) as well as inducible (INOS) isoforms of nitric oxide synthase. The pore-forming hemolysin of Escherichia 162 40 cm HiO. or air leakage from prevented further increases culi incidence of in Wj. erative the effect of preop- smoking behavior on postoperative SETTING: The pul- the and in 90% ( Medical Center. Syracuse NY. istration in = 4 0). MEASUREMENTS & RESULTS: Smoking status was determined by 1 self-report. Postoperative tions pulmonary complica- were determined by systematic extraction of medical record data. Postoperative pulmonary rent smokers, 24 of 87 1 ( 1 1 of 141 (22.0%) cur- 2.8%) past smokers, and 4 of 82 (4.9%) never smokers. The odds was 5.5 (95% confidence 16.2) and 4.2 ment (95% (OR) smokers versus never smok- plication for current ers ratio pulmonary com- for developing a postoperative interval [CI], 1.9 to CI. 1.2 to 14.8) after adjust- for type of surgery, type of anesthesia abnor- mal chest radiograph, chronic cough, history of pulmonary disease, history of cardiac disease, tory of chronic obstructive pulmonary cation level, pulmonary function, and age. Current smokers who his- disease, edu- body mass index, reported reducing were more cigarette consumption prior likely to develop a complication compared with was The over- in 19% 19 of 21) of these patients, 42% and was PAR- Patients scheduled for noncardiac the LMA was malpositioned. Oropharyngeal air leakage occurred Veterans Admin- LMA LMA malpositions was 40% (43 of 108). Gastric air insufllation occurred (21 of 108), step- stomach, airway pres- position in relation to the laryngeal entrance all Nitric oxide .seal LMA volumes (Vx) were increased until air entered the verified using a fiexiblc bronchoscope. I57(2):498. The laryngoscopy, and to determine their influence on Impact on Pulmonary Hemodynamics Burger H, OBJECTIVE: To examine complications occurred in 3 potential risk of the laryngeal wise Rcspir Cril Care 1998:1 13(4):883. elective surgery (n Mask Airway Laryngeal Induced Septic Lung Model: Role oi'cNOS and H. — Pulmonary Complications Bluman LG, Mosca L, Newman N, Simon DG. Chest TICIPANTS: inhibitors in sepsis. the induction of anesthesia, before Oxide Biosynthesis Preoperative Smoking Habits and Postoperative via activation of manipulations. After clinically satisfactory Nitric gas embolism as a complication of arterial mechanical ventilation. have important implications for therapeutic which elastase instilled intranasally in mice. arterial cir- aware of venous human (LMA) levels em- monary complications. DESIGN: Prospective rhDNase on 4 in pulmonary culations. Clinicians need to be gas cohort study. Spumm collected after the cerebral, coronary, and and The next fatal cerebral arterial pulmonary vasoconstriction. These findings may A hour end-expiratory pressure. She sustained an itive thrombox- ane receptor antagonist did not interfere with the exotoxin-elicited therapy levels 24 hours after aerosol treatment. 1 We report a 53-year-old woman with ARDS who NO liberation into both the alveolar and the ment. Elastase levels returned to pre-rhDNase from 2 of 6 patients Morris A. Chest 1998:1 13(4):l 132. phos- (MeOSAAPV-CMK). In vivo administration of 2.5 mg aerosolized recombinant human DNase I to patients with CF resulted in a 2.2-fold increase arate days —Weaver LK, with Positive Pressure Ventilation day she sustained a alanyl-alanyl-prolyl-valine-chloromethylketone I Venous and Arterial Gas Embolism Associated effects neutrophil elastase inhibitor methoxysuccinyl- of sputum elastase activity within gastric air insufflation. this vasodilator release mitigates the HlyA-induced in phate buffer and were suppressed by the of cases. Such mal- positioning considerably increased the risk of dourea-dihydrobromide. blocked the HlyA-evoked to .secondary were not observed with DNase position revealed sub- 40% ciated with cardiovascular instability. cNOS directly related to exotoxin activity vs 44.5 mask acute right ventricular myocardial infarction asso- = 92.8 + 40.7 1 verification of optimal placement in aminoguanidine and 2-(2-aminoethyll-2-thiopseu- mice (broncho- 12.0 /Jg/mL. p < 0.01 tic required positive pressure ventilation with pos- in + not require laryngoscopy. In our study, fiberop- NOS inhibitor N(G)-monomethyl-L-arginine (LNMMA), but not the iNOS selective inhibitors substrate L-arginine. alveolar lavage fluid hemoglobin duced marked lung hemorrhage placement of laryngeal mask airways does tine The nonspecific of the formation (L-arginine) slightly reduced, and inhi- The Rou- factor for gastric air insufflation. Implications: monitored on-line by chemiluminescence detec- re- pital costs LMA position. We conclude that clinically unrecognized LMA malposition is a significant risk independent of those who 2.6 to 17. was 1 ). OR = 6.7, 95% CI, CONCLUSIONS: Current smoking associated with a nearly 6-fold increase in risk for a postoperative Reduction was to surgery did not (adjusted in pulmonary complication. smoking within I month of surgery not as.sociated with a decreased risk of post- operative pulmonary complications. RESPIRATORY CARE • JUNE 1998 VOL 43 NO 6 ABSTRACTS Automatic Actuation of a Dry Powder Inhaler —Bisgaard H. Am a Nonelectrostatic Spacer into J Respir Crit Care Med Reduction in smoking within was not associated with month of surgery 1 a decreased risk of post- operative pulmonary complications. 1998;157(2):5I8. TB CONCLUSIONS: CI. 1.9-9.9) were independent predictors of diagnosed in San Francisco. Timely, adequate medical evaluation and follow- up care of immigranLs and refugees has a relatively This article describes a new '"automatic spacer" device, which has been developed to improve the delivery of inhaled medication to In the device, a dry powder young inhaler (DPI) children. Ventilator-Associated Pneumonia: Clinical Significance and Implications Pneumonia producing an aerosol cloud of fine drug particles comial infection (aerodynamic diameter. < 4.7/jm) with a long The new device combines half- the principal advan- tages of the conventional spacer and the DPI. It den Brande (ll):26.50. coordination or forced inhalation, and it is exposure of the patient and pro- show — Hansson gency and Life-Saving Procedure F. Eyskens E. Eur Respir J I997;I0 pneumonia (VAP) occurs in a pa- with mechanical ventilation, and Lung volume reduction surgery for rigorously selected patients with severe debil- it is a serious problem — with signifi- cant morbidity and mortality rates. Aspiration of bacteria from the oropharynx, leakage of contam- A5 emphysema. itating eralized 1 mothoraces during his first high repeatability of drug delivery owing to the piratory mechanical nature of the actuation (relative stan- important factors dard deviation, 12%). and a prolonged residence Nurses caring for patients treated with mechan- bronchopneumonia and time of the fine particle aerosol (half-life of the ical ventilation must recognize transferred to Belgium. and cros.s-contamination from res- equipment and health care providers are in the development of VAP. and risk factors -year-old emphysema developed inated secretions around the endotracheal tube, should prove advantageous emerg- neither present nor developing at the time of intubation; patient position, s). is ing as a promising and unique therapeutic option (mass median aerodynamic diameter. 2.8 fim). a 82 (LVRS) it a high yield of fine drug particles in the aerosol fallout of the fine particles. B. W. van Jorens PG, van Schil P. van Kerckhoven Intubation and mechanical ventilation greatly in- tient treated halers. Studies with the prototype device United States and the lead- ing cause of death from nosocomial infections. tor-as.sociated pellants used in pressurized metered dose in- noso- crease the risk of bacterial pneumonia. Ventila- lung dose and pharyngeal dose, without need for avoids in the common most the second is has the potential to provide a high ratio between to the additives TB prevention and control programs. Lung Volume Reduction Surgery as an Emer- mech- is high yield and should be a high priority for MJ. Munro CL. Heari Lung 1997;26(6):419. anically actuated into a nonelectrostatic spacer, life. —Grap for Nursing man pneu- holiday abroad. to respiratory insufficiency, intubation anical ventilation with gen- bilateral were necessary. In Due and mech- total. 6 chest tubes were inserted but massive air leak persisted and his respiratory condition deteriorated due sepsis. As The patient to was a last resort, bilateral These features include strategies for reducing these factors as part LVRS was performed through a median treatment of of their nursing care. This article summarizes the omy. The most diseased areas of the upper lobes in the young children with inhaled medication. VAP: sternot- incidence, associ- containing the air leak were resected bilaterally ated factors, diagnosis, and current therapies, with and a pleurectomy was associated. Three months an emphasis on nursing implications in the care after operation, there Pulmonary Complications Bluman LG. Mosca L, Newman N. Simon DG. Chest of these patients. ment 1998:1 13(4):883. Tuberculosis literature related to Preoperative Smoking Habits and Postoper- — ative erative the effect of preop- smoking behavior on postoperative SETTING: The Veterans AdminPAR- cohort study. istration Medical Center. Syracuse NY. TICIPANTS: Patients scheduled for noncardiac elective surgery (n = 410). MEASUREMENTS & RESULTS: Smoking status was determined by self-report. Postoperative pulmonary complica- were determined by systematic extraction tions K. Chin DP. Schecter GF. Reingold AL. Arch Intern Med 1998: I58(7):753. 4 of 82 (4.9%) never smokers. The odds plication for current ers was (OR) smokers versus never smok- 5.5 (95%' confidence interval [CI], 1.9 to and 4.2 (95% CI. 16.2) ment ratio pulmonary com- for developing a postoperative 1.2 to 14.8) after adjust- for type of surgery, type of anesthesia, abnor- (TB) or who foreign-bom individuals after their arrival United States. METHODS: cation level, pulmonary function, body mass index, after a follow- dramatic case, lung vol- reduction surgery proved to be effective and a life saving procedure. United States from July December 1. who arrived 1992. through San 31. 1993. with a destination of Francisco. California, and a referral for further medical evaluation. URES: Time ment MAIN OUTCOME MEAS- to report to the local health depart- after arrival and the yield of active and pre- ventable cases of evaluations. TB from follow-up medical RESULTS: Median United States to Effects of the Prone Position — Mascheroni Pelosi P. Tubiolo D. D. Vicardi P. Crotti S. Valenza F, Gattinoni L. J Respir Crit Care Med Am 1998;157(2):387. in the Retrospective cohort We studied 16 patients with acute lung injury receiving volume-controlled ventilation to assess the relationships between gas exchange and res- piratory mechanics before, during, and after 2 hours in the prone position. expiratory lung We measured the end- volume (EELV. helium the total respiratory system (Csi,rs), dilution), the lung (Cj^l) and the thoracoabdominal cage (Cslw) compliances (end-inspiratory occlusion technique and esoph- time from arrival ageal balloon), the hemodynamics, and gas ex- seeking care in San Fran- change. In the prone position, PaO: increased from in the disease, edu- relies on further medical evaluation and follow-up of cisco was 9 days (range. 1-920 days). pulmonary this Lung Injury are at high risk for tuberculosis mal chest radiograph, chronic cough, history of tory of chronic obstructive ume second of almost who have active TB. The system's effectiveness pulmonary disease, history of cardiac disease, his- up of 8 months. In 1 1 were sustained on Respiratory Mechanics and Gas Exchange during Acute in the of 141 (22.0%)cur- results United States identifies foreign-bom individuals grants and refugees applying for a visa to the complications occurred in .3 1 100%. The Overseas screening of immi- study of 893 immigrants and refugees 24 of 187 (12.8%) past smokers, and was a remarkable improve- spirometric values with an increase in was even BACKGROUND: of medical record data. Postoperative pulmonary rent smokers. and Immigrants pul- monary complications. DESIGN: Prospective in forced expiratory volume in among Refugees— DeRiemer OBJECTIVE: To examine its immigrants and refugees (83.4%) ther medical evaluation, 5 1 who Of 745 sought fur- (6.9%) had active TB 103.2 ± 23.8 to 129.3 ± 32.9 mm Hg (p < 0.05) without significant changes of Csi.rs and EELV. + 97.4 to However. Cs,,w decreased from 204.8 cigarette consumption prior likely to develop a complication compared with dictor of failure to seek further medical evalua- ± 52.5 mL/cm HiO (p < 0.01 and the dewas correlated with the oxygenation increase (r = 0.62. p < 0.05). Furthermore, the greater OR = 6.7, 95% CI, tion in the United States. Class B-1 disease sta- the baseline supine Csi.w, the greater and age. Current smokers those 2.6 to who 1 who did not (adjusted 7. 1). reported reducing to surgery CONCLUSIONS: was associated with were more Current smoking a nearly 6-fold increa.se in risk for a postoperative pulmonary complication. RESPIRATORY CARE • and 296 (39.7%) were candidates for preventive therapy. Being a refugee tus based on overseas [OR], 3.5; was an independent TB 95% confidence NO 6 135.9 ) crease prone posifion = < its decrease Con- screening (odds ratio in the interval (CI), 2.0-6.2) sequently, the oxygenation changes in the prone 95% position were predictable from baseline supine and being from mainland China (OR, 4.4; JUNE 1998 VOL 43 pre- (r 0.82, p 0.01). 46? m MessQfs A New Ou Don't find yourself lost flfly/ids iratory Care in the dark on important issues that involve your career. Tune into "Professor's Rounds," designed to answer your questions about respiratory care. Spotlighted topics: technology, restructuring, reform and regulations, are timely and vital for the operation of your facility and for honing your skills in patient care. 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CALL THE AARC AT FOR MORE INFORMATION (972) 243-2272 1 9 Abstracts Csi.w (r = 0.80, p < 0.01 Returning to the supine ). compared with basehne position, CsLrs increased (42.3 ± 14.4 vs 38.4 ± mUcni HjO; p < 0.01 13.7 ), mainly because of the lung component (57.5 ± 25.1 vs 52.4 ( 1 ) in baseline + 23.3 mUcm H2O; p < 0.01 d.^ and its may changes ). Thus, play a role determining the oxygenation response in the prospective study during a 2-month period in 1993 FVC, and peak expiratory flow with a pulse oximeter available and a compari- paradoxical bronchoconsuiction. son with the same period device delivered significantly more fenoterol to SETTING; An imeter residents ordered their discretion. resumed. PATIENTS; All patients who underwent ABG or SpO: measurements. INTERVENTIONS; During the prospective study, Csu-, and Cstx when is EDof auni- adult medical vereity hospital in France. prone position; (2) the prone position improves the supine position 1992 without the ox- in ABG or SpO; measurements at The reasons Breathing Reserve at the Lactate Threshold a Pulmonary Mechanical from to Differentiate — Medoff BD, Cardiovascular Limit to Exercise DM. Oelberg DA, Kanarek DJ. Systrom Chest mined whether Criteria used to define the respec- of pulmonary mechanics and cardio- vascular disea.se in limiting exercise performance are usually obtained at peak exercise, but are de- pendent on maximal patient tiate heart effort. To from lung disease during a differen- less effort- dependent domain of exercise, the predictive value of the breathing reserve index (BRI [Vpl/maximal tilation = minute voluntary ven- ventilation [MVV]) at the lactate threshold (LT) was evaluated. DESIGN: Thirty-two patients with chronic obstructive pulmonary disease (COPD) and a pulmonary mechanical limit (PML) to exercise de- maximum oxygen fined by classic criteria at uptake (Vo:max) were compared with 29 patients (CVL) and with a cardiovascular limit mal control subjects. Expired gases and Vg were available metabolic cart (Model 2001: Med- Graphics Corp: St Paul MN). Arterial blood gases, lactate were sampled each minute dur- ing exercise, and cardiac output (Q) by tem 77: Baird Corp; Bedford RESULTS; lactate threshold at was measured first-pass radionuclide ventriculography (Sy.s- exercise. For MA) at rest ABG measurements in MEASUREMENTS & RESULTS; The patients who had BRI at (r = < 0.0001 The (0.73 + 0.03, mean 0.85, p ). BRIlt was higher for PML ± SEM) vs CVL (0.27 ± 0.02, p < 0.0001 ), and vs control subjects (0.24 ± 0.03, p < 0.0001 A BRIlt ^ 0.42 predicted a PML at maximum exer). with a sensitivity of 96.9%, a specificity of 95.1%, a positive predictive value of 93.9%, and a negative predictive value of 97.5%. SIONS; The BRI] ing the T, a variable CONCLU- measured dur- submaximal realm of exercise, can tinguish a PML dis- from CVL. Oximeter in an Adult Emergency Department: Impact on the Number of Arterial Blood Gas Analyses Ordered Le BourLIse of a Pulse — delles G, Estagnasie P, Lenoir F, Brun P, Drey- fussD. Chest 1998:1 1.3(4):1042. OBJECTIVES; To assess ABG levels tients. of arterial blood gas the impact of pulse ox- (ABG) were measured The use of SpO; did not in 1 19 pa- result in the order- ABG determinations. One hunABG measurements were justified. There were fewer unjustified ABG detering of fewer useful minations in 1993 when the pulse oximeter was available than in vs 54 of 184: p 1 992 when < 0.001 ) it was not ( 1 4 of 1 1 mainly because fewer ABG determinations were ordered for miscellaneous nonrespiratory indications < 0.01 of 1 84: p ). (1 3 of 1 1 of a pulse oximeter did not affect the ordering of ABG useful measurements but allowed a nificant reduction of unjustified levels ordered in an emergency department (ED). DESIGN; A Aerochamber (39.2% vs The any RESPIMAT alone or an MDl with 9.9% of 11.0%- and metered dose, respectively: p < 0.01). Oropharyngeal deposition of fenoterol from the < 0.0 vs 7 .7%, respectively: p 1 1 ). new MDl (37. % device was lower than that from the 1 The RESPIMAT device deposited significantly more fiunisolide lungs compared with in the MDl (44.6%' vs 26.4%, respectively: p plus spacer < 0.01 ), while resulting in similar oropharyngeal deposition (26.2% vs 31.2%, respectively). Introduction of a baffie into the RESPIMAT system reduced lung deposition of flunisolide to 29.5%, and oropha- < ryngeal deposition to 7.8% (p 0.01). CON- CLUSION; The RESPIMAT device may prove to be an effective alternative to MDIs for the administration of inhaled bronchodilators and corticosteroids. The high lung deposifion and low may lead to improved oropharyngeal deposition efficacy and tolerability of inhaled medications, especially corticosteroids. 9 vs 43 CONCLUSION; The availabiUty sig- ABG measure- Compliance with Peak Expiratory Flow Monitoring in J, Home Management of Asthma Cartier A, Malo JL, Rouleau —Cote M. Boulet LP. Chest 1998:1 13(4);968. ments. Substantial cost savings could be achieved by using SpO: in BACKGROLTVD: The recent consensus reports an ED. on asthma management emphasize the importance Lung Deposition of Eenoterol and Flunisolide of using peak flowmeters to accurately assess the Delivered Using a Novel Device for Inhaled degree of airflow obstruction. However, the opti- Medicines: Comparison of RESPIMAT with Conventional Metered-Dose Inhalers with and without Spacer Devices J, — Newman SP, Brown Steed KP, Reader SJ. Kladders H. Chest 1998:1 13(4);957. mal way to use those devices has not yet termined. with peak expiratory flow (PEF) measurements in the long-term management of asthma and to compliance. OBJECTIVES; To compare fenoterol or lung deposition of f unisolide administered from a novel, SETTING; tertiary-care hospitals. and prospective '\sthma clinics from three DESIGN; A PATIENTS; Twenty-six (RESPIMAT: Boehringer Ingelheim Ltd: Bracknell, UK) or from conventional metered dose inhalers (MDls) with and without spacers. DE- to .severe Patients were asked Two randomized, three-way crossover stud- evening PEF droplets ter INTERVENTIONS; device. In one .study, radiolabeled RESPIMAT device MDl with or without an asthma taking I descriptive -year duration. patients with moderate an asthma education part in MAIN OUTCOME MEASURES; program. ies. SETTING: Clinical research laboratory. PARTICIPANTS; Healthy, nonsmoking volunteers. of study multidose inhalation device delivering liquid SIGN; been de- OBJECTIVES: To assess compliance identify the characteristics of patients with poor measure morning and to using an electronic peak flowme- with a 3-month memory: they were unaware that PEF values were being recorded by this RESULTS; Compliance with PEF mea- aerosols of fenoterol from the surements was relatively good during the and from a conventional month (63% of the measurements done) Aerochamber spacer (Tnidell Medical: London, with regular reinforcement, Ontario, Canada). In the second study, radiola- and to 33% beled aerosols of fluni.solide from a RESPIMAT ning, 8 of RESPIMAT device modified by (< device, from a inclusion of a baffie/impaclor in the mouthpiece, and from a conventional MDl with an Inhacort spacer (Boehringer Ingelheim: Ingelheim, Ger- imetry (SpO;) on the indications and the number 466 study dred and five (88%) many). adult 1992. and peak patients, the all (BRI lt) correlated with the BRI Vojmax (BRImax) cise, The data 12 nor- measured breath by breath using a commercially pH, and choice was justified. were compared with those for 184 consecutive patients: tive roles who deter- included 152 patients. Spo. alone was u.sed in 33 1998:1 13(4):913. OBJECTIVES: their were for their ordering reviewed by two independent experts MDl the lungs than either an rate) to detect MEASUREMENTS & RESULTS; Assessment of the deposition of fenoterol or nisolide in the lung and scintigraphy. oropharynx using flu- gamma Safety was as.sessed based on reported adverse effects and spirometry (FEV|, at 12 fell to first but even 50% at 6 months months. Right from the begin- 26 subjects (30%) never or almost never 5% of the readings done) measured PEF, with seven of these subjects writing fabricated results in their diaries 60% most of the lime. At of the subjects were measuring 1 2 months, PEF < 25% of the time, and most of them continued writing fabricated PEF values in their diaries. None of the subjects' characteristics helped us to identify those who had poor compliance ments. CONCLUSIONS; RESPIRATORY CARE • with these measure- While short-temi com- JUNE 998 VOL 43 NO 6 1 Abstracts pliance with PEF measurements not interested in measuring is good, asthma are PEF twice daily over a prolonged period. In the current of a.sthma. fairly to severe most patients with moderate management PEF measurement devices can be sug- gested to those showing a strong personal interest in using them, but should be limited to short periods of time. Furthermore, this study outlines the usefulness of electronic peak flowmeters when doing clinical research where is PEF improvement an important outcome. both VAIs and their caregivers. INTERVENTION: None. sis ANALYSIS: Confirmatory factor analy- with principal components extraction. lique (oblimin) solution the factor matrices. tors needed was used An ob- for rotation of The number of common to obtain the best fit fac- of the factor model on chronic daily therapy. Total and regional deposition were correlated with breathing pattern, pulmonary function, demographic factors, patient's tion measured lung dose on pulmonary func- was estimated by stopping the drug and ob- was determined with use of maximum-likelihood serving changes in spirometry over a 2-week fol- estimation. Confirmatory factor analysis with low-up period. After discontinuance of the drug, ear structural equation modeling formed. sis RESULTS: was lin- also per- Confirmatory factor analy- did not fully replicate the factor structure proposed by Lawton et al. CONCLUSIONS: The all patients reported worsening of dyspnea and producing sputum. There was a difficulty model proposed by Lawton giving Appraisal Scale for Caregivers of Home- ful foundation for examining the appraisal of fam- patients, as much as ily caregivers of home-based VAIs. Additional was found in the pharynx (range 0.0 — MA, Sereika S, Hoffman LA, Matthews Sevick JT, Chen development work is et al provides a use- — Diot the underlying dimen- tors in Cystic Fibrosis sions of the Caregiving Appraisal Scale (CAS) Smaldone A, DeCelie-Germana with use of data collected ftom caregivers of home- Smaldone GC. based ventilator-assisted individuals (VAIs). DE- 156(5): 1662. SAMPLE: Two hundred seventy-seven primary family caregivers of VAIs. MEASURES: developed by Lawton Twenty-eight-item et al 48% of the deposited to 0.029), and pharyngeal depo- CAS (1989), and an inves- = -0.696. p < 0.006) and age (r volume (r = -0.743, p < Palmer LB. 0.(X)5). Grimson R, 0.16mgand0.78mgofthe 2.5 mg nebulizer dose (mean 0.47 + O.Ot mg) and correlated negatively with FEV % predicted, r = -0.6 1 1 p = 0.0 52 1997: For the lungs, deposition ranged between , However, To aerosol 0.30 mg, J, ( 1 , ). the spirometric decrements following identify factors influencing lung dose of aero- cessation of therapy did not correlate with the lung human deoxyribonuclease dose of the drug. Analysis of regional deposition solized recombinant (rhDNase I), we used gamma camera and filter techniques to measure deposition in 15 clinically tigator-developed instrument to assess physical stable patients with cystic fibrosis health and sociodemographic characteristics of and 10 females, age 6- .31 RESP paUents completed the study. In some P, Am J Respir Crit Care Med SIGN: Cross-sectional survey. SETTING: Residences of home-based VAIs. all sition correlated negatively with fidal rhDNase I Aerosol Deposition and Related Fac- OBJECTIVE: To confirm but mean 0.089 mg ± needed for the CAS. GJ. Heart Lung 1997;26(6):430. sig- FEV| {9c predicted, mean ± SE, 86.9% ± 5.57 to 77.8% ± 5.73. p < 0.005), nificant decrease in A Confirmatory Factor Analysis of the CareBased Ventilator-Assisted Individuals and disease severity. In addition, the effects of each yr. mean (CF) (5 males 16.9) who wen? within the lungs indicated a wide range of distribution between central and peripheral zones. In conclusion, the deposition pattern of I aerosols in patients with CF is largely rhDNase influenced Abstracts by respiratory physiology, which itself depends upon age and severity of lung disease. As the patients grow there is a decrease in upper airway deposition and more particles are presented to the more airways lungs where those patients with dis- ical conditions that suggested the possibility of INTERVENTIONS: inadequate preload. administered rapidly until the Ppa„ rose by one airway deposition of rhDNase days and for different younger patients, I is significant, espe- may be related and to in stroke and Altered Lung Func- to Physical Inactivity tion in COPD Patients—Semes I, Gautier V. Var- ray A. Prefaut C. Chest 1998;1 13(4):900. mine tive ( 1 ) pulmonary disease (COPD) skeletal were to deter- whether patients with chronic obstruc- muscle performance (ie. have impaired maximal strength and endurance) compared with healthy subjects, and whether the (2) level of physical body activity, 14.2 + 3.6 mm Hg; p = 0.001 to baseline RVEDVI mL/m-; p = 0.22). in SV (r = 0.44); in RVEDVI exceeded poor response dict a was not a fluid. Seventeen COPD patients and eight healthy age-matched control subjects performed voluntary contraction and an endurance test (MVC) 20% of MVC an imposed regular pace until exhaustion. The endurance test duration determined the muscle "limit time" (Tum). (PA ± 33 between = 0.58 ). and Pp;,,, A positive As A score of physical activity score) was obtained using an adapted phys- ical activity questionnaire for the elderly, and body 4 of 9 cases CONCLUSION: RESULTS: The results showed that T|,m test. and PA Comparison of Drug Delivery from Conventional versus "Venturi" Nebulizers son SG, Everard — Devada- ML. Linto JM. Le Souef PN. Eur RespirJ1997;IO(lI):2479. Attempts to improve drug delivery from conventional jet nebulizers have included the use of stor- age systems to reduce drug wastage during exhaVenturi nebulizers enhance drug delivery lation. during inhalation, reducing treatment times and ulizer (Acorn) used both with and without a (Ventstream and Pari LC). Filters were ulizers RVEDVI. to is an In indi- best assessed by an empiric fluid challenge. salbutamol. and 18 children with cystic fibrosis ( 3- 6 yr^ inhaled through these devices. The quan- 1 tity ) of drug collected on the filter was assessed using ultraviolet spectrophotometry. Diaphragm Cellular Adaptations in the Chronic Obstructive Pulmonary vine S. Kaiser L. Leferovich Med stor- age chamber (Mizer), compared to 2 Venturi neb- attached to the 4 nebulizer systems, containing J. in — Le- Disea.se N Tikunov B. Engl cle size distribution ulizer The parti- of the aerosol from each neb- system was measured using laser diffrac- tion. Inspiratory filter was lower than 1997;337(25):I799. the deposition using the Acorn Acorn with Mizer. and both Venturi nebulizers. Filter deposition using the BACKGROUND: In patients with severe chronic phragm undergoes physiologic adaptations COPD patients diaphragm, an adap- reliable predictor of the re- obstructive pulmonary disease in in the tation that increases resistance to fatigue. a predictor of fluid respon- impedance method. Symptom-limited oxygen using a maximal incremental exercise of the muscle fibers of age on inhaled dose from a conventional jet neb- vidual patient, adequacy of preload J Severe drug wastage. This study investigated the effect in composition was measured by the bioelectrical uptake (Vo,s|) was also assessed CONCLUSIONS: COPD increases the slow-twitch characteristics in to fluid. was superior siveness. Ppa, forms of these proteins. 138 mL/m-, a thresh- consisting of dynamic con- tractions of the quadriceps against at maximum of the quadriceps dif- 3.4 vs old value that has been suggested to reliably pre- RVEDVI ODS; r was observed sponse to in ( controls had higher percentages of the fast iso- but not with respect the relationship COPD patients. METH- muscle performance ± (105 + 31 vs 119 S V was suonger respon.se to fluid which 10.0 ( RVEDVI and fluid-induced change between change ). SV) There was a moderate corre- composition, and lung function are related to skeletal increase in fered with respect to baseline Ppa„ lation OBJECnVE: The aims of this work Responders (n = 20; volume [SV]) and non- 10% chains, troponins, and tropomyosin, whereas the MEAS- clinical indications. UREMENTS & RESULTS: responders (n = 16; < Impaired Skeletal Muscle Endurance Related at least were given on separate fluid challenge, these > 10% increase laryngeal side effects. was mm Hg. When a patient underwent more than 3 ease have enhanced pulmonary deposition. Upper cially in Thirty- six fluid challenges. Fluid (saline or colloid) acterized by an increa.se in (COPD). the dia- char- Acorn with Mizer was lower than trend with age. height, or weight any nebulizer. Aerosol LC. die Pari No was noted using particle size using the Vent- energy expenditure and stream was lower than the other nebulizer sy.stems. We hypothesized that Drug output from both Venturi nebulizers was relative resistance to fatigue. these physiologic characteristics would be asso- more efficient than from the jet nebulizer, used COPD ciated with structural adaptations consisting of an with and without the storage chamber, during in- patients (p<0.05). Significant positive correla- increased proportion of less-fatigable slow-twitch halation by children with cystic fibrosis. muscle haled dose did not change with the patient's age score were significantly decreased in tions were found and the 0.52; p same and PA in the score < 0.05). and results Vcfesi (r p < 0.05). COPD group between Ti.n, (r = (r = 0.60; p < 0.05), FEV, P^ (r = 0.63; p < 0.05). The were found between the = 0.57; p < 0.05) and FEV, CONCLUSION: cate impaired skeletal PA score = 0.63; patients related to altered lung function volume [ ± standard error] forced expira- and asso- of the various isoforms of myosin heavy chains, indi- tory myosin Volume as a Hemodynamic Response Predictor of the METHODS: We obtained biopsy spec- to a — Wagner JO. Leatherman JW. Fluid Challenge Chest 1998;I13(4):I048. in 1 second. 33 venuicular end-dia.stolic volume index (RVEDVI) and pulmonary artery occlusion pressure as predictors of the right (Pp;n,) hemodynamic response to a DESIGN: Pro.spective cohort SETTING: Medical ICU of a university- in- or size using both types of nebulizer. and tropomyosin light chains, froponin. Pulmonary Function Tests: Comparison of 95th Percentile-Based and Conventional Criteria of Normality WR Jr. — Margolis ML. Monloya South Med J BACKGROUND: FJ. Palma 1997;90(12):1 187. Although 95th peiv;entile-based were determined by sodium dodecyl sulfate-poly- normal limits are recommended instead of con- acrylamide-gel elecQ-ophoresis. We also used im- ventional criteria of nonnality to guide pulmonary munocytochemical techniques to determine the we have found no how the choice of normight influence PFT interpretation. function test (PFT) readings, proportions of the various types of muscle fibers. objective assessment of RESULTS: The diaphragm-biopsy specimens mal limits from the patients had higher percentages of slow OBJECTIVE: To compare thermodilution The imens of the diaphragm from 6 patients with severe COPD (mean COPD in ciated physical inactivity. Right Ventricular End-Dlastolic proteins. and slow isoforms of myofibrillar ± 4 of the predicted value; residual volume. 259 ± 25 of the predicted value) and 10 control subjects. The proportions (r These findings muscle endurance fibers myosin heavy chain I (64 ± 3 vs 45 ± 2, p< 0.(X)1 ). METHODS: We did a retrospective comparison of PFT readings referenced to conventional cri- and lower percentages of fast myosin heavy chains teria lla(29±3vs39±2.p = 0.01)andllb(8± ments influenced by 95th percentile-based nor- 1 7 + 1 . 1 vs p < 0.00 1 ) than the diaphragms of the con- Similar differences were noted when im- of normality versus independent repeat asse.ss- We also conducted a nationwide telephone survey of VA Hospital PFT mal limits in 166 veterans. fiuid challenge. trols. study. munohistcK-hemical techniques were used to com- laboratories. ICU pare the percentages of these fiber types in the 2 curred in only 7.2% of 616 individual PFTs; how- of a community hospital. PATIENTS: Twentywho had one or more clin- groups. In addition, the patients had higher per- ever, these discrepancies could potentially influ- five critically centages of the slow isoforms of myosin light ence affiliated 408 county hospital and medical-surgical ill patients at least RESPIRATORY CARE RESULTS: Discordant readings oc- PFT 1 component of • JUNE 1998 VOL 43 NO the report of 6 A new tool for subacute care... IE Uniform Reporte Manual FDR subacute: care It's a new tool that helps you... Determine productivity Promote standardization of care Benchmarl< and track trends Match resources and demand Prospective payment systems In post-acute care require that respiratory care managers possess the tools to Identify the resources for efficient administration of respiratory care servlces.The Uniform Reporting Manual for Subacute Care Is that tool. The Uniform Reporting Manual n RUSH ME MY COPY oftk for Subacute tool to determine productivity, track trends in Care is a Uniform Reporting Manual for Subacute Can the utilization of respiratory care services, assist in determining personnel requirements, and measure demand for and (Item $75 forAARC Members, $ I 15 for Nonmembers (add $8 for Shipping and Handling) intensity of services. Name The Uniform Reporting Manual for Subacute includes time standards for 126 activities in Care Resident AARC Member Assessments and Documentation, Airway Care, Breathing Institution and Adjunctive Devices, Mechanical Ventilation, Bronchial Address Hygiene, Diagnostic Tests and Resident Monitoring, City No. Zip State Supplemental Oxygen and Continuous Aerosol Therapy, Resident Care, Support, Equipment and Supplies, Management and Supervisory Skills. There are also Payment Enclosed sections on Clinical Activities w^ithoutTime Standards, Card Number Non-Allocated Hours, and an Appendix with worksheets to Signature compute your own workload hours. Binder, 122 Pages, 1998. Z Charge to my Purchase Order No. Please Charge to my: II MasterCard lI Visa (required for Purchase Expiration Date Order and Credit Card) American Association for Respiratory Care Order Department II 030 Abies Une Dallas.TX 75229-4593 Call (972) 243-2272 • Fax (972) 484-2720 BK2/ ATLANTA, GEORGIA Patient June 12-14 Assessment Course To Meet the Demand for the Patient Assessment Course, Respiratory Care Practitioners Are Offered Another Opportunity to Attend this Landmark Course This course has been approved for 12 clock hours for certification maintenance purposes by the Commission for Case Manager Certification Check-in time the last class, will be from noon until 1 :00 PM on Friday afternoon. Following participants will take a 100-item test developed by the NBRC, which should take about one and a half hours to complete, and which will be scored on site. Attendees should be finished with the test at approximately 1 :00 PM Sunday. All activities will course is be conducted limited to at the Atlanta Airport Marriott Hotel. 200 attendees and preregistration is Space at this required. Successful completion of the course will earn participants 16 hours of CRCE credit and a course completion. Each attendee will be given a pocket guide to physical assessment, which will be helpful on the job. certificate of AARC Assessment Course/Examination 1. Obligations of the Respiratory Care Practitioner in the Practice of Patient Assessment A. B. document assessment findings H. Present findings to a physician Appreciate the cost of care Understand the scope and limitations of the practitioners role in patient assessment C. Detailed Content Outline G. Accurately ^ "I truly believe that assessment (total what — not just keep our profession a portion of the health care team." physical) Understand the principle of patient is will vital self-determination D. Appreciate the psychological, social, and physical 3. Assess the Caregivers and caregivers characteristics of wellness/illness A. Identify sites of care E. Recognize the patient's right to confidentiality B. Interview the caregivers F. List the principles of informed consent C. Assess the abilities of caregivers to physical, technological, ^ "Assessment — of the patient isn't purely clinical anymore helped to start the 'Thinking outside the box concept,' that is necessary for continued survival of RT as a profession." 2. D. Assess 4. Review patient records B. Structure an interview C. Conduct an interview Conduct a physical assessment D. needs situations health resources Assess the Patient's Understanding and Compliance with Physician's Orders and Care Plan Perform a Comprehensive Health Assessment A. home manage and emergency A. Review the physician's order with the patient B. Assess the patient's understanding of technique and components ^ "I plan on sending other staff who will be involved in asthma case management to the April '98 course in Dallas" E. Identify F. Identify patients with potential for high-risk medical for referral lohn Kimble, RT Director, Respiratory Care Services ancJ Sleep Disorders Laboratory, Scott complications ALAMO CAR RENTAL FLY DELTA and pay than the fares Delta offers to the general public. Discounts are available only through less Delta's toll-free Call today, or have your number. travel agent call: (800) 241-6760 8:00 am - 11 :30 & White Memorial Hospital, Temple, TX pm, Eastern Time, Daily Refer to Alamo is the official car rental company for the AARC Assessment Course. Special discount rates are available to all AARC attendees. To make your reservation, call Alamo's toll-free number: (800) 732-3232 File #109967A. Request Croup ID #72191 . Rate Code CR. Advanced reservation required. ^ "I traveled ten hours to get here and feel well worth the trip. Your Penny Cagne Plouff, program is it was great." B. Inspect the patient care environment C. Determine the resources available to the patient and RRT Respiratory Rehabilitation family & Therapy, P.A. Portland, ME ^^ ,., Document assessment D. ,. ,. findings C. Assess patient ability to administer treatments, use equipment, monitor changes, interpret and respond to those D. ^ "Bravo for a job well done. I plan to share a lot of this information with staff." changes Document assessment findings Continued Appropriateness of Physician Orders and Care Plan 6. Assess S. Assess the Patient's Environment as it Relates to Health Status and Supporting Physician's Orders A. A. Review physician orders ^- Evaluate the patient's response to physician orders C- Evaluate the appropriateness of the orders Identify barriers to wellness and the care plan "The course was relevant to the changes in health care and my practice. Well worth my time." t Course Registration Atlanta, * Registration will close First and Recommend E. Document assessment findings modification of the treatment plan — Registration Deadline May 25, CA on the date noted or when 200 1998 registrations are received. Name Last AARC Member # Titie Mailing Address (Please indicate which address is D Work D shown above: City ( D. Home) Zip State ) Daytime Phone Specialty Advance Registration Required D AARC Member $250 C Nonmember $325 D Check or money order enclosed D Charge Credit Card # cliecl<, C MasterCard Expiration Date Mail Registration and my: C VISA Signature Form payable to AARC: AARC 11030 Abies Lane Dallas, TX 75229-4593 Phone: (972) 243-2272 If paying by credit card, you may fax your Registration Form to (972) 484-2720. Cancellations must be made in writing. There handling fee for cancellations received 21 days before the course begins. No refunds will be made thereafter. will 30% HOTEL RESERVATIONS The Patient Assessment Course will be conducted at the Atlanta Airport Marriott Hotel 4711 Best Road For reservations June 12-14, 1998 call: • College Park, (404) 766-7900 and AARC Assessment Course • CA 30337 identify yourself as Deadline for Cuaranteed an attendee at the Room Rate is May 25, 1998 be a Abstracts 26.5% of our subjects. The 95th percent! le-based normal hmits were used by only 40% laboratories, without relationship to or hospital size. CONCLUSIONS: of terial V A PFT 56% [95% confidence geography Discrepancies and 95th percentile-based ings, in the majority of used VA PFT laboratories. A New Bronchoscopic Technique for the DiagPneumonia in HIV-Positive Sauleda J, Maimo A. Riera M. Ramirez — Togores B. Pons S, et al. Respir Med commensals, such as nontypable Haemophilus with- was influenzae, cause most bronchial infections by 37-75%] and exploiting deficiencies in the host defenses. 37-75%) and 94% (CI. 86-100%) for mpBAL. When both techniques were assessed together, sensitivity increased to 70% (CI, 53-87%'). The use equilibrium in which the numbers of bacteria are of a single catheter reduced the cost of the orig- When an these figures were pBAL contained by the host defenses but not eliminated. procedure by approxi- an inflammatory response. Neutrophil products mpBAL can improve can further impair the mucosal defenses, favor- TPC bacterial followed by a pneumonia and reduces its ing the bacteria, but symptoms cost. sists, Infection in COPD—Wilson R. Chest 1998:1 13(4 Suppl):242S. to evaluate in HIV-positive patients with bacterial pneumonia, the diagnostic value of a new endoscopic nique that uses a single catheter to perform a scopic plugged catheter ified protected (TPC followed by ) a obstructive pulmonary disease tele- mod- ficult and were included mpBAL in the study. diffuse sponse both Samples from were cultured quantitatively. According symptoms that can vary sponta- overcome, the infection per- may cause lung dam- About half of exacerbanons involve bacteinfection, but these patients are not easy to from those who are uninfected, which that antibiotics is strictly have to be given more often necessary. Further research whom to characterize those patients in infection has a in the short more important needed is bacterial role. Lung Transplantation for COPD and long term. The role of bacterial infection, and thus use of antibiotics, in shows to In appropriately selected patients with chronic that bacterial infection has a significant role in were classified gression group (27 with bac- —Trulock EP. Chest 1998:1 13(4 Suppl);269S. COPD is controversial. The available evidence the clinical and microbiological results, patients in the study chronic inflammation is if rial than are dif- the infection neously, and difficulties in defining clinical re- Standard bronchoalveolar lavage was performed to rule out opportunistic infections. (COPD) if However, age. means because of the heterogeneous nature of COPD, bronchoalveolar lavage (mpBAL). Fifty-eight HIV-positive patients with respiratory infection resolve. differentiate Clinical studies of acute exacerbations of chronic tech- is mately 50%. The use of a single catheter to per- The Role of The aim of the present study was exacerbation occurs, this equilibrium upset and bacterial numbers increa.se, which incites 91(9):530. Trc between exacerbations, which represents an teria the diagnostic yield in FTrV-positive patients with 1997; Some COPD patients are chronically colonized by bac- form a nosis of Bacterial Patients intervals (CI) was 100%: specificity inally described J. 1 (CI, PFT read- criteria are not (3 56% its between 95th percentile-based and conventional normal limits can potentially influence pneumonia) or the control group out bacterial pneumonia). Sensitivity of TPC acute exacerbations, but is less certain. its obstructive role in disease pro- Upper pulmonary disease (COPD) and a-l- antitrypsin deficiency respiratory tract emphysema, lung trans- £ye Shi Protect your eyes with these lightweight, plastic safety glass meet come OSHA guidelines. :^s thai Reusal in assorted colors. Easy- ^sscjrjbl)' directions included. Package o disposable lenses and 5 reusab frames Item R45 ($3 1 JtOmtiembers) Sliipping is$ American Association for Respiratory Care Tr^AOs <mi'iimr, fjiily, All tutuling $25 or 11030 Abies odd 'i.2j% iiws< attadi on /j/foi'y jofei I'M S • Ln., Dallas, iolei (<« (iiKkidirhj ^hifjijimj le-is. TX 75229-^ <:hor<i'i'jj. p/'/) y^Ci-r/l'/ Tyxa: -.uitomcn min/jii'Mi curlilkole. frktu st/d/ec! to diomj ,'ilhoiH llKil ore e>:cmj>l ftom < I -or. {^//'/) 'If;'! 6010 ., nolkr. RESPIRATORY CARE • JUNE 1998 VOL 43 NO 6 Abstracts Volume 42 is bound charge, witti your ^40 for current in a blue-buckrom cover and name or rtie name moy be imprinted, tree of of your organization. Each AARC members end ^80 for volume non-members. Shipping is is in- cluded for U.S. and Conadion residents. hme, ttie '89 and '90 bound volumes ore discounted ^30 (members) ond ^70 (nonmembers). The '92 ttirough '94 volumes ^35 are availoble for (members) and ^75 (nonmembers). Available for a limited to BOUriD — ORDERS MUST BE PREPAID INCLUDE CHECK, INSTITUTIONAL PURCHASE ORDER, OR VALID CREDIT CARD NUMBER. n n D n D respiratory 1997 VOLUME AT MO/580 1996 VOLUME AT 1995 VOLUME AT '40/^80 1994 VOLUME AT '35/''75 CHECK CAUD 0« P0» SIGN4TURe_ Care AVAILABLE AARC MEMBER # D MO/^SO PURCHASE ORDER D 1993VOLUME D 1992VOLUME D 1990VOLUME D 1989 VOLUME D VISA D AT 535/^75 AT 535/^75 AT ^30/^70 AT =30/570 MASTERCARD 2 1 fore investigated prospectively the evolution of a Pressurized Metered-Dose Inhaler Formu- Body weight decreased (from 85 ± 42 LS. Systolic and mean pulmonary arterial pressure decreased in LS and SS. Airway Ob- Right ventricular ejection fraction increased in LS. treated with 1 ABSTRACTS Differences in Bronchodilating Potency of Salbutamol in Turbuhaler as Compared with lation in Patients with Reversible struction — Lofdahl CG, Andersson son E, Carlsson LG, Friberg K, Hedner J 1997:10(1 to 8 ±40 kg) during 1 lishing the via Turbuhaler cluded. nasal CPAP was 64 ± 6 months. Most of the pa- tients (77%) were smokers were increased on admission, whereas plasma ment. ):2474. 1 re- mal. We suggest that in these patients, oedema and via a pressurized metered- sterone-vasopressin and with a normal cardiac out- ratio for salbutamol put. ble-blind, randomized design. Outpatients with lowed a confection of blood gases, associated with mild-to-moderate chronic reversible airway ob- the resolution of were given single doses of salbutamol pMDI. Effi- Noninvasive positive pressure ventilation oedema, a decrease and an increase arterial pressures in al- pulmonary in right ven- after each dose. The including 1 first study 2 padenLs. The salbutamol doses given were: 50, 100 and 2x 1 00 /^ via Turbuhaler and 2x 1 00 /Jg via pMDI (Ventolin). The study showed that 2x 100 ;jg of salbutamol inhaled via Turbuhaler is that via a 2x100 study. study including 50 was a placebo-controlled 5-way Two is at salbutamol inhaled /Jg pMDI. The second patients pMDl, 100 /ig salbutamol via Turbuhaler least as potent as crossover, doses of salbutamol via Turbuhaler, 50 and 2x 1 00 /Jg, and via pMDI, 00 and 2x200 1 /Jg, were given. There was a dose-dependent response (FEV|) in forced expiratory volume in for both inhalers. in baseline FEVi second 1 Adjusted for differences values, the estimated nslative dose potency for Turbuhaler versus A 30 Year Epi- Respiratory Health Status: demiological Study of Workers in Paris mann F, Annesi Chwalow I, J. —Kauff- Eur Respir J 1997; 10(11):2508. pMDI was 1 .98: The validity of scales used for subjective assess- ment of health, is particularly transitional indices, under discussion. The aim of the present study was ity and predictive valid- to assess the concurrent 30 smdy of 9 1 5 workers was conducted over years, with both retrospective self-assessment assessment of the reason for death during the M, Favre H, Kyle Chevrolet JC. Eur Respir Jolliet P, J 1997; assessment of respiratory deterioration over tional lung function values was (FEVi after to investigate the hae- modynamic and endocrinological effects of non- also related to the same FEVi (smoking, risk factors as de- occupational exposure). significantly predictive of death were measured at study |LS1). of To NIPPV and and water handling hormones admission and discharge (long discriminate between the action from all was causes, 1 .5 (Paco2) for the group as a whole increased slighUy, but significantly, from 5.2 mm ± 0.7 kPa (39 ± 5 to 5.4 ± 0.5 kPa (4 ± 4 mm Hg) (p < 0.05). Mean pulmonary artery pressure (Ppa) at rest did not change 16 ± 5 mm Hg vs 17 ± 5 mm Hg; not Hg) 1 patients with was 24 ± t5 (NS). of FEV 5 pulmonary hypertension mm Hg at to versus 20 ± 7 at to, 1 Ppa mm Hg at We conclude that the significant decrease I after 5-year follow-up was related to a and pulmonary artery pressure remained an unselected series of 65 OSA stable in patients treated which increased by a small, but significant, amount Propofol for Sedation in the Intensive Care Unit: Essentials for the Clinician MA. Respir Med — Marinella 1997;91(9):505. Propofol is a short-acting intravenous anesthetic commonly utilized in the intensive care unit (ICU) for sedation of mechanically ventilated patients. The it rapid onset and termination of action make an attractive drug for use in the ICU. The safety However, there are potential adverse reactions associated long-term variability (objective and subjective) with the drug. This review discusses the phar- self- assessment of respiratory health deterioration was significantly related to FEV|. Subjective assess- macology, administration and adverse effects associated with propofol with which clinicians who administer propofol should be familiar. in respiratory health Five- Year Effects of Nasal Continuous Positive Airway Pressure in Obstructive Sleep ApChaouat A, Weitzenblum E, — noea Syndrome Kessler R, Oswald M, Sforza E, Liegeon MN, KriegerJ. Eur Respir J 1997;10(1 1):2578. other treatments, measurements 4 hours with- There have been very few studies assessing the out NIPPV and 4 hours with NIPPV (short study [SS]). NIPPV entailed a correction of Paco; and an increase of Pao.. in LS and SS. Oedema dis- long-term physiological effects of nasal contin- were performed on the fourth day, 474 ± However, Pao. increased in the subgroup of patients with hypoxaemia at to (n = 23), from 7.8 Hgj). res- were included. ESchocardi- ography, cardiac radionuclide assessment, blood salt (PaO:) for stable (9.4 respiratory causes. Asthmatics exhibited greater provides valid information. catecholamines, oxygen tension whole remained with the highest (but nonsignificant) rate ratio for ment of long-term changes and hypoxaemic worsening of a chronic Arterial mm Hg] vs 9.4 ± 1.2 kPa [71 ±9 mm profile of propofol is well established. invasive positive pressure ventilation (NIPPV). piratory insufficiency 1 1 decline), an association adjustment for FEV] level. Eleven patients with oedema and recent hypercapnic 1 and longitudinal lung than nonasthmatics. Independent of dyspnoea, The aim of this study was [71 ± % subsequent 20 years was performed. Subjective Self-evaluation of respiratory deterioration 10(11):2553. < 0.01 ). 1 follow-up evaluation pressure, unlike arterial carbon dioxide tension, An 2 years apart. of Noninvasive Mechanical Ventilation in Res- U, (p kPa second for 5 years with nasal continuous positive airway 1 cline in nard C, Righetti A, Vallotton (tj) the group as a at the 1 76 ± 2 to surements of spirometric values Haemodynamic and Endocrinological Effects M, Rey- of the predicted value in (to) of respiratory health changes and objective mea- which remained JB, Ritz % at baseUne study population. Daytime arterial oxygen tension tudinal It —Thorens 80 ± 2 1 high percentage of smokers and exsmokers in the function changes piratory Failure fixjm A longi- assessment of respiratory health changes. en via a conventional pressurized metered-dose given via Turbuhaler. (FEVi ) volume of a simple estimate of long-term subjective years was significantly related to both cross-sec- is significant, de- crease in forced expiratory significant [NS]) nor did exercising Ppa. In the (95% confidence interval 12-3.2). These studies showed that the same bronchodilating effect can be achieved when half the dose of salbutamol givinhaler baseline assess- ( more potent than 2x 100 /jg salbutamol inhaled via a and Validity of Subjective Assessment of Changes in at the We observed a small, but ± 0.7 kPa (59 + 5 mm Hg) to 8.9 ± 1.2 kPa (67 ± 9 mm Hg). Arterial carbon dioxide tension tricular ejection fraction. cacy and safety variables were measured before was a 4-way crossover study The mean duration of home treatment with Left ventricular ejection fraction did not change. decreased. Natriuretic peptides and catecholamines can occur independently of renin-angiotensin-aldo- and during 6 hours with this syndrome Sixty-five patients were in- Cardiac index was normal on admission and then S, with the aim of estab- administered via Turbuhaler and via CPAP. Bondes- dose inhaler (pMDI). Both studies were of a dou- struction blood gases, and pulmonary in patients Homblad given dose potency arterial haemodynamics J. nin activity, aldosterone, and vasopressin were nor- Two studies are presented, lung function, L. Y, Jemsby P. Kallen A, Ullman A. Werner Svedmyr N. Eur Respir appeared. for uous positive airway pressure (CPAP) for the obstructive sleep apnoea syndrome (OSA). We there- RESPIRATORY CARE • JUNE 1998 VOL 43 NO 6 Individual Independent Study Packages (I Help ISPs) Expand Their Respiratory Care Knowledge Practitioners Clinical Practice Chest Tubes & Tonicity of Solutions & the Respiratory Tract Item CSS Pleural Drainage Temperature adjustment of Blood Qases & pH Item PES Ventilation/Perfusion Relationships in Health & Disease Item CS21 Carbon Monoxide Inha- Item CP3 Measurement of Static Compliances & Dynamic lation: Introduction to Tracheal Intubation I: Upper airway anatomy & Qoals of Intubation Item C9H Tracheal Intubation II: Routes of Intubation Item CPs Tracheal Intubation Physiologic Effects & Respiratory Management Electrical Safety in zation of the Premature Infant in Respiratory Dis- Respiratory Therapy I: for Intubation Identification of Electri- Item CP6 cal muscular Item CP7 II: Hazards Item CSI3 of neuro- Bronchodilators I: Sym- pathomimetic amines Crisis Item CSm Bronchodilators Ihanti- ment of Flail Chest Cholinergics & Xanthines Item CPs Item CS15 ment of Head Trauma Item CPq Cross-Contamination Transpulmonary Pressure Changes Item CSI7 Classification of in Breathing Item CS5 Pulmonary Function ing Item PEll assessment I: Basic Screening Studies Item PE3 Physical assessment Item PEI2 II: Bedside Studies Cessation Pulmonary Function assessment III: Lung Vol- nicotine Classification of Mech- anical Ventilators Practical application Classification of of Qas Laws Item CS7 anical Ventilators II Item CSI4 Item CS20 &. Dependency Bedside Counseling of Item PES the Hospitalized Body Plethysmography Smoker Item PE6 Item SC2 Sources of Error in the Determination of Blood Qas Values & pH Item PE7 m $12 each Order III ($16 nonnienil>ers) All 36 IlSPs itemCPiq Mech- I Evaluation & Treatment Item SCI Individual liSPs: Lung Mechanics Item CS6 N Smoking Item PE4 I Item CSis CM a- Mech- anical Ventilators M 1^ Pulmonary Function ume Determination of Microbial Qrowth & Science Hemodynamic Monitor- Closing Volume Studies Microbiology for Respir- to Patient Evaluation Calculation & atory Therapy: a Review Clinical Interpretation Item PEio Preparation of Respiratory Medications Item CSI6 Pulmonary Edema Item CPio nm assessment Respiratory Manage- Respiratory Manage- Item PE4 an Introduction Respiratory Therapy Management Item tilation arterial Blood Qas tress Electrical Safety in Equipment Procedures Respiratory Characteristics Curves During Mechanical Ven- Recognition & Stabili- Basic Electrical Circuitry Item CS12 III: neonatal Item esq Buy &S $257 ($334 nonmembers) 10 & Save 15%! < < Case Reports Acute Pulmonary Edema following Upper Airway Obstruction: Case Reports and Brief Review M Richard H Kallet MS RRT, Brian Daniel RRT, Michael Cropper MD, and Michael A Matthay MD INTRODUCTION: Postobstructive pulmonary edema is generally characterized by fulminant pulmonary edema that becomes apparent within seconds or minutes after the relief of severe upper airway obstruction. The development of postobstructive pulmonary edema is believed to result from the generation of extremely high negative intrathoracic pressures against an occluded airway. However, the mechanism responsible for the development of acute pulmonary edema in this setting is uncertain. Measurement of the ratio of total protein concentration between pulmonary edema fluid and plasma is an established, accurate method for distinguishing hydrostatic from increased-permeability pulmonary edema. CASE SUMMARIES: We report 3 cases of severe postobstructive pulmonary edema. The pulmonary edema fluid to plasma total protein concentration ratio was measured immediately following relief of the obstruc- The ratio of the pulmonary edema fluid protein concentration to plasma total protein concentration was 0.42(0.10) mean (± standard deviation). Ratios < 0.65 are characteristic of hydrostatic pulmonary edema, whereas patients with increased-permeability pulmonary edema, as seen in acute lung injury, have a ratio between 0.75 and 1.0. Pulmonary edema in all 3 cases resolved within 24 hours. IN CONCLUSION: These data indicate that postobstructive pulmonary edema may result from a primary hydrostatic mechanism. These cases also illustrate the value of measuring the ratio of pulmonary edema fluid to plasma total protein concentration to determine the mechanism of pulmonary edema. [Respir Care 1998;43(6):476-480] Key words: Postobstructive pulmonary edema, pulmonary edema, pulmonary edema tion. fluid, upper airway obstruction. and croup,' airway compression by tumors,'' poststrangula- Introduction and hanging/ laryngospasm,'' foreign body aspiration,* tion Postobstructive pulmonary edema has been described as an infrequent complication following severe upper airway obstruction'- from a variety of causes including epiglottitis and endotracheal tube obstruction.' Postobstructive pulmonary edema is generally edema that becomes characterized by fulminant pulmonary clinically apparent within utes after the obstruction Richard H Kallet eral Hospital; MS RRT; Respiratory Care Services, University of California, San Francisco. Brian tute; San Francisco Gen- Department of Anesthesia; Cardiovascular Research M Daniel RRT; Insti- Car- diovascular Research Institute; University of California, San Francisco. Michael Cropper nia, MD; Department of Anesthesia; University of Califor- San Francisco. Michael A Matthay MD; Departments of Medicine and Anesthesia; Cardiova.scular Research Institute; University of California, arterial relieved.'*"' wedge pressure measurements have been cleared.'''"" In edema in part by the National Institutes of Health, NIH 51856. Correspondence hours.'-'-''-'''"" The development of postobstructive pulmonary edema may result from an acute alteration in lung vascular and interstipressures generated by extremely high negative intratho- theory is that the prolonged mechanical ''•*'' stress An alternative may alter the permeability of the pulmonary microvascular and alveolar & Reprints: Richard H Kallet MS RRT. Respiratory Care Services, San Francisco General Hospital, NH: GA-2, 1001 Potrero Ave, San Francisco 476 reported, most instances, postobstructive pulmonary resolves rapidly within 24 to 48 racic pressures against an occluded airway.' This paper was supported seconds or min- Normal pulmonary but always well after the airway obstruction has been tial San Francisco, San Francisco, California. is CA 941 10; e-mail: Rich_Kallet@quickmail.ucsf.edu. epithelial membrane, thus favoring increased permeability as mechanism in the development of pulmonary edema.''""'- A number of other factors, such as hypoxia,' the primary RESPIRATORY CARE • JUNE 1998 VOL 43 NO 6 ACUTE PULMONARY EDEMA FOLLOWING UPPER AIRWAY OBSTRUCTION massive central nervous system sympathetic discharge,' and ous amounts of frothy pulmonary edema tluid projected from release of vasoactive substances such as histamine, serotonin, the endotracheal tube. and kinins,'* postulated may be contributory. The exact interplay of these mechanisms in the iologic complexity, postobstructive represent pulmonary edema An arterial pathogenesis of postobstruc- pulmonary edema remains uncertain. Because of its phys- tive Samples of this pulmonary edema were obtained as described below. pulmonary edema may primarily caused by increased after a patent 85 torr, PaO: blood gas analysis with F102 a few minutes 1 airway was established revealed 296 torr, with a base deficit ventilated in a volume-control mode 5.1. with fluid pH The PEEP 7. 12, Paco: was patient 10 cm HiO hydrostatic forces, increased permeability, or a combination because of persistent respiratory acidosis (pH 7.23 with Paco: ofboth.'-5»"'- 69 The ratio of the total protein concentration in pulmonary edema fluid to that in plasma is an established, accurate method for distinguishing hydrostatic pulmonary edema."''' from increased-permeability In this article, we report the results of 3 well-documented cases of postobstructive One case is pulmonary edema. reported in detail. torr) and hypoxemia (PaO: 74 torr on Fio: .0). The patient was then given 10 mg of intravenous furosemide. Urine out1 put was 2.2 L over steadily was 3 hours. During this time, oxygenation improved with PaOi 94 edema was successonset of pulmonary edema taken 10 hours after the development of pulmonary revealed mild bibasilar fully extubated Case Summaries on Fio: 0.70. The patient The chest radiograph torr transferred to the intensive care unit. 1 The infiltrates. 7 hours after the patient and was then discharged from the intensive care unit shortly thereafter. Hospital discharge occurred The first patient, a previously healthy 25-year-old Asian American man, was involved in a high speed motor vehicle accident and suffered only facial injuries. A computerized tomography (CT) examination revealed a large orbital floor defect with both zygomatic arch and maxillary fractures. days later, the patient was taken to the operating room Two for repair of his facial fractures. Preoperatively, the chest was clear by auscultation and radiographic exam. The operative course complicated by bleeding. The patient received products and 7.3 of 1 L and .5 L of crystalloid with a urine output of 1 .5 the patient's overall fluid balance 1.3 was L of blood an estimated blood loss At the end of surgery, was -1-5.6 L. Both gas exL. 4 days later. Two subsequent cases of postobstructive pulmonary edema were identified in which pulmonary edema samples were obtained immediately monary edema. The second patient without a history of cardiac disease way after fluid and plasma development of pul- was a 24-year-old who developed man upper air- obstruction from an aspirated foreign body following a drug overdose. Immediately following endotracheal intubation, moderate quantities of pulmonary edema fluid were collected. pulmonary edema resolved within 12 hours. In the third patient, a 1 3-year-old boy developed severe laryngospasm and oxygen desaturation following laser treatment Clinically, the of laryngeal papillomas. There was no history of cardiac dis- change and pulmonary mechanics during surgery were nor- ease or volume overload. After endotracheal intubation, copi- mal with a Pa02^iO: of 470 torr and effective tem compliance of 47 mL/cm H2O. ous quantities of pulmonary edema fluid were suctioned and The respiratory sys- room intubated and breathing spontaneously on a T-piece with an F|o, of 0.40. Shortly thereafter, the patient and bit down on became agitated was attempt- the endotracheal tube while he ing to ventilate, thereby occluding the airway. was not in place because the endotracheal tube had been hypertension (205/95 arterial sure of 132 mm He developed sysHg with a mean pres- mm Hg), tachycardia of 132 beats/min and hypox- emia with a pulse oximeter saturation of 85%. Manual ventilation with an F102 of 1 .0 was attempted with little success because the patient continued to bite patient Pulmonary Edema Fluid Collection down on the endo- The patient intermittently opened his mouth and some ventilation was achieved. However, there The following procedure was tion catheter alleviated. trap Edema tluid was (Sherwood Medical, ples inspi- lasted several minutes. Therefore, the was given 100-mg succinlycholine, 2-mg midazolam, 7.5-mg droperidol. and 5-mg morphine sulfate intravenously to stop him from occluding the endotracheal tube and to make patient it possible to deliver adequate ventilation and oxygenation. Immediately after the patient RESPIRATORY CARE • was sedated and JUNE 1998 VOL 43 relaxed, copi- NO 6 was suctioned with a diately after the obstruction of the endotracheal tube slightly which was cleared. The endowedged 14 French suc(Baxter Health Care Corp, Deerfield ID imme- tracheal tube total protein were 2 episodes of total occlusion and negative pressure carried out in each of the 3 patients just after the obstruction tracheal tube. ratory efforts & Measurement A bite block inserted only for the surgical procedure. temic showed bilateral pulmonary edema. The was extubated the next morning with resolution of the pulmonary edema within 12 hours. the chest radiograph patient arrived in the postanesthetic recovery St Louis MO). Measurement of the on the pulmonary edema was done by was collected in a standard specimen fluid and plasma sam- the biuret and the bromcresol green dye- binding technique.'"' This method provides a good reflection of alveolar edema fluid. '^ Measurement of total protein conedema fluid and plasma correctly charactype of pulmonary edema that results from either centration in the terizes the hydrostatic or increased permeability.'at the same time in '^ Blood was drawn order to measure the corresponding plasma total protein concentration. 477 ACUTE PULMONARY EDEMA FOLLOWING UPPER AIRWAY OBSTRUCTION The mean (± standard deviation) ratio of pulmonary edema plasma total protein concentration was 0.42 (0.10). All 3 patients had ratios of < 0.65 (Table ), which are charfluid to 1 acteristic of hydrostatic pulmonary edema, whereas patients with increased-permeabihty pulmonary edema, as seen in acute lung injury, have ratios between 0.75 and 1.0." Table 1 . Pulmonary Edema Fluid and Plasma Total Protein Concentration Measurements Postobsuiictive Pulmonary Patient in 3 Patients Edema with ACUTE PULMONARY EDEMA FOLLOWING UPPER AIRWAY OBSTRUCTION ing pulmonary venous pressure and Pmv even farther. Hypoxia pulmonary engorgement and hypertension, an can increase both pre- and postcapillary vasomotor tone,-- result in direct which would cause a further increase poxia, hypercapnia, and acidosis tractility, may in Pmv pulmonary venous pressure and Pmv^''^ further raising Therefore, the fact that a patient may be free of cardiac dis- ease or have a normal pulmonary capillary measurement In addition, hy- depress myocardial con- wedge pressure after relief of the obstruction-*'" does not pre- clude the possibility of acute, transient myocardial dysfunction during the relief of is Chest radiographs taken prior to and just after crisis. upper airway obstruction have shown that the heart some slightly enlarged in we In the introduction, patients.'" stated that postobstructive pul- may directly ability.-'' If the pulmonary edema pulmonary edema the ratio of tration would have been studies of re-expansion or minutes after the obstruction al* were the first to was relieved."'" Galvis et recognize that active expiration during acute upper airway obstruction acts as a modified Valsalva maneuver and, therefore, provides functional positive end- expiratory pressure (PEEP). These investigators reasoned that the cardiovascular abnormalities described PEEP be counterbalanced by resulting in a compensated relieved and the PEEP effect above would during the expiratory phase, state." When is lost, pulmonary edema would the obstruction is develop. However, the gross manifestation of pulmonary edema following relief of the obstruction may be mislead- plasma protein concen- comes from pulmonary edema and some of the on neurogenic pulmonary edema."'-" However, application of these theories to account for the mechanism of pulmonary edema formation in postobstruc- early reports tive pulmonary edema is stress case studies described the onset as occurring within seconds fluid to to support the increased permeability hypothesis edema during upper airway uncertain. Early in the first patient resulted higher.-' In general, the evidence cited to the alveolar-capillary is might from both volume overload and increased permeability, then monary edema becomes 'clinically apparent' soon after the obstruction is relieved. The exact time of onset of pulmonary obstruction effect that damage to the pulmonary capillaries,' or hypoxia alter pulmonary capillary endothelial perme- pulmonary edema may when as well as result is from an oxidative injury from change re-expansion suddenly reinflated, reperfusion.-'"''- Shear lung volume. During the obstruc- in tion, functional residual capacity is like effect in both from the application of shear a completely collapsed lung stress requires a damage not convincing. First, the membrane observed supported by the PEEP- caused by active expiration against a partially or fully obstructed relief of the airway."" Chest radiographs taken prior to upper airway obstruction have been reported show marked pulmonary to hyperinflation.'" Therefore, inspi- ratory efforts during the obstruction volumetric pressure swings at most likely occur as iso- an elevated lung volume. This argues against stress-related lung injury as an important factor in postobstructive pulmonary edema. Second, a recent study reported that neurogenic pulmonary edema was associated pulmonary edema with a hydrostatic mechanism in the majority of their cases.'' may form prior to relief of the obstruction, and that the PEEP may prevent alveolar flooding and mask radiographic Therefore, the proposed similarities between postobstructive ing. It has been suggested that interstitial effect Leatherman and Schwartz-'' have documented evidence.'"-''"'^ diffuse alveolar infiltrates on the chest radiograph prior to relief of the obstruction. These cases occurred in young patients without evidence it (-t- 5.6 L) in the possible (although unlikely) that in this case. Stalcup makes development of pul- and Mellins^" observed pulmonary edema development of pulmonary edema pulmonary edema. Only one other case edema has measured total protein ratio to report'"* the mechanism in postobstructive of postobstructive pulmonary pulmonary edema fluid to plasma describe the pathogenesis of pulmonary edema following acute airway obstruction. In that report, a pulmonary edema to plasma total protein ratio of 0.83 was that can occur reported following emergency airway obstruction in the oper- asthma may be potentiated by aggressive fluid ther- ating room.''* that the negative pressure in severe patient volume overload with a rise in left atrial pressure contributed to monary edema first at the and possible cerebral hypoxia) do sive adrenergic discharge not necessarily support an increased-permeabihty for the of cardiac disease. However, the positive fluid balance onset of the obstruction pulmonary edema and neurogenic pulmonary edema (mas- apy, leading to both increased hydrostatic forces and decreased colloid osmotic pressures. tein concentration (6.8 fluid overload However, the normal plasma pro- g/dL) in the first patient argues against because dilution of the plasma protein would have been expected. The hypothesis that that case was complicated by prolonged arterial pressure piratory distress syndrome. It does not appear from that report pulmonary edema fluid to plasma total protein ratio was measured at the time pulmonary edema first occurred, that the postobstructive pulmonary edema may be a form of increased-permeability pulmonary edema on two theories. However, < 50 mm Hg with a pulmonary capillary wedge pressure = 9 mm Hg) and extensive cerebral infarction.''* The patient went on to develop severe acute resshock (mean First, is based subjecting the pulmonary microcir- culation and alveolar epithelium to prolonged mechanical stress from repeated high negative intrathoracic pressure swings disrupt the alveolar-capillary membrane."^" '- Second, the intense adrenergic response to hypoxia and acidosis RESPIRATORY CARE • may may cause JUNE 1998 VOL 43 NO 6 but was measured hours later in the intensive care hydrostatic pulmonary fluid to edema resolves, plasma total protein had 3 confounding factors the unit.'"* As pulmonary edema ratio rises." Therefore, that patient — the timing of the measurement, shock, and the neurologic insult increased ratio of pulmonary — that edema may account fluid to for the plasma protein 479 ... Acute Pulmonary Edema following Upper Airway Obstruction concentration. '* In our review of the literature, 3 individual cases of patients who developed we found relief only 9. syndrome piratory distress edema.''*''* after postobstructive pulmonary interesting that each of those cases It is was com- plicated by the presence of shock (systolic blood pressure 80 10. < measurements of pulmonary edema tein ratio are indicative fluid to plasma 2. total pro- of a primary hydrostatic mechanism. 1 3 pulmonary edema appear to be to upper airway obstruc- Joucken K. Collard E, Mayne A. Pulmonary edema fol- edema occurs by mechanism. fluid to plasma Frank LP, Schreiber GC. Pulmonary edema following acute upper (letter). 16. for determining the mechanism of pulmonary formation. Because of the availability of respiratory care clinicians in the intensive care unit, Am J Med 1 979;67( 1 ):32-38. MA, Eschenbacher WL, Goetzl EJ. Elevated concentrations D4 in pulmonary edema fluid of patients with the adult MA, Matthay Matthay J Immunol 1984:4{6):479-483. Clin Wiener-Kronish JP. Intact epithelial barrier function for the resolution of alveolar MA. 1): edema humans. in Am Rev 1250- 1 257. Pathophysiology of pulmonary edema. Clin Chest Med I985;6(3):301-314. 17. Wise RA. Effect of circulatory mechanics ducing pulmonary edema. emergency depart- ment, and postanesthetic recovery setting, these practition- JF, Staub of leukotriene Matthay RespirDis 1990;l42(6Pt non- Murray Pitts L, value of edema fluid protein measurement in patients with is critical measuring total protein ratio as a Anesthesiology 1986;65(1 ):106. Fein A, Grossman RF, Jones JG, Overland E. respiratory distress syndrome. 15. In addition, this report illustrates the value of pulmonary edema Weissman C. Damask MC, Yang J. Noncardiogenic pulmonary edema pulmonary edema. self-limited with res- hypothesis that postobstructive pulmonary method P, NC. The 14. invasive Randour airway obstruction olution within 12-24 hours"* provides further support to the edema Willms D, Shure D. Pulmonary edema due following laryngeal obstruction. Anesthesiology 1984;60(2):163-165. 1 most reported cases of uncomplicated postob- a hydrostatic Otol Rhinol Laryngol (3):225-231. 1 insight into the pathogenesis of postobstructive pulmonary edema. The results of our early structive Ann 124- 128. lowing acute upper airway obsUuction. Acta Anaesthiol Belg 1986;37 1 fact that 1): tion in adults. Chest 1988;94(5): 1090- 1092. mm Hg).'-"'-* These three case reports provide The of acute upper airway obstruction. 1980;89(2Pt the acute res- 1 8. obstruction. ers are ideally suited to carry out this procedure. 19. J Crit on hydrostatic forces pro- Care 1986:1:247-256. AG. Pulmonary edema complicating Galvis Am J Einerg Med upper airway relief of 1987:5(4):294-297. Brower R. Wise RA, Hassapoyannes C, Bromberger-Bamea B, PerS. Effect of lung inflation on lung blood volume and pulmonary mutt In Conclusion venous flow. in which protein ratio edema the pulmonary edema fluid to plasma Effect of alterations of pleural pressure on cardiac output. Southern Med 2 Lang SA, Duncan PG, Shepard DA, Ha HC. Pulmonary oedema asso- fluid to plasma total protein ratio obstructive pulmonary hydrostatic form of edema 0.42 (0. 10) edema suggest 1 22. and the that post- plasma high altitude: review, patho- Med 1985;6(3):491-507. Barin ES, Stevenson IF, Donnelly GL. Pulmonary oedema follow- (l):54-57. at 25. total protein ratio. Lorch DG. Sahn SA. Post-extubation pulmonary edema following anesthesia induced by upper airway obstruction: are certain patients these case reports also illustrate the clinical value of measuring fluid to Anaesth 1990:37(2):210-218. J at ing acute upper airway obsUuction. Anaesth Intensive Care 1986; 14 to providing mechanism of postobstmctive pulmonary edema, pulmonary edema Can Schoene RB. Pulmonary edema physiology and update. Clin Chest 23. 24. insight into the 1985;78(4):423-428. ciated with airway obstruction. represents a high-pressure or pulmonary edema. In addition J total was measured. The low values of pulmonary rapid resolution of the pulmonary Appl Physiol 1985:58(31:954-963. Wise RA. We report three cases of severe, postobstructive pulmonary edema J 20. increased risk? Chest 1986;90{6):802-805. Sofer S, Bar-Ziv J, Scharf SM. Pulmonary edema following relief of upper airway obstruction. Chest 1984:86(3):401-403. 26. Scherer R, Dreyer P. Jorch G. Pulmonary edema due to partial upper 27. Leatherman JW, Schwartz airway obstruction REFERENCES in a child. Intensive obstruction. Southern Tami TA, Chu F, Wildes TO. Kaplan M. Pulmonary edema and acute KW, Todres Am J ID, MG. Pulmonary edema JAMA 1 977;238( Physiol 1981;51(4):887-894. 30. as a 1 monary edema. Chest 1980;78(6):8I9-821. JJ. Gerblich AA. Upper airway in Galvis 480 AG, Stool SE, Blueslone Theodore J. edema fusion of ischemic 33. Smith Am Rev Am Rev dog lung results in fever, leukopenia, WS, Matthay MA. Evidence for a hydrostatic human neurogenic pulmonary edema. Chest 34. Kollef MH, Pluss and lung Respir Dis 1986;l34(4):752-756. J. 1997;1 1 1 mechanism (5): in 1326- 1333. Noncardiogenic pulmonary edema following up- per airway obstruction: 7 cases and a review of the CD. Pulmonary edema following in rabbits. Robin ED. Pathogenesis of neurogenic pulmonary oedema. Bishop MJ, Boatman ES, Ivey TD, Jordan JP, Cheny FW. Reperedema. Nishizawa M, Chaffee TL, Goto H. Pulmonary edema induced by (5):479-48l. Increased pulmonary vascular Lancet 1975:2(7938): 749-751. 32. obstruction due to inhala- endotracheal tube obstruction: a case report. RespirCare 1993;38 ML, Cheney FW. RespirDis 1981:124(4):422-427. 1 pulmonary edema. Chest 1992; 102 (2):644-645. Pavlin DJ, Nessly permeability as a cause of re-e,\pansion 7): 3 of a tracheal T-tube resulting upper airway 1983:76(8): 1058-1060. J edema in acute asthma. New Engl J Med 1977:297( 1):592-596. Ohkuda K, Nakahara K, Binder A, Staub NC. Venous air emboli in Jackson FN, Rowland V, Corssen G. Laryngospasm-induced pul- tion 1 to sheep: reversible increase in lung microvascular permeability. J Appl 1833-1835. Zulueta 988; 4(6)66 1 -662. 29. Dis Child 1984;138(4):356-358. complication of acute airway obstruction. 1 Stalcup SA, Mellins RB. Mechanical forces producing pulmonary Shannon DC. Pulmonary edema associated with croup and epiglottitis. Pediatrics 1977;59(.5):695-698. Oswalt CE, Gates GA, Holmstrom Med 1 Kanter RK, Watchko JF. Pulmonary edema associated with upper airway obstruction. Med Care Pulmonary edema due 28. airway obstruction. Laryngoscope l986;96(5):506-509. Travis S. literature. Medicine (Baltimore) 1991;70(2):91-98. RESPIRATORY CARE • JUNE 1998 VOL 43 NO 6 & Updates Reviews, Overviews, Leukotriene Modifiers in the Treatment of Asthma David A Stenipel MD Introduction Pathophysiology of Asthma Mechanism of Inflammation & Biopsy Findings Bronchoalveolar Lavage Remodeling Role of Inflammatory Mediators Effects of Leukotrienes Pharmacodynamics of Leukotriene Modifiers Drug-Drug Interactions Adverse Effects Clinical Trials Zaflrlukast Zileuton Leukotriene Modifiers in Exercise-Induced Asthma Leukotriene-Modifying Agents & Aspirin-Induced Asthma Using Leukotriene Modifiers in Asthma Therapy In Summary [RespirCare 1998;43(6):481-489] Key words: Asthma, leukotriene modifiers, pharmacodynamics. Introduction of their high potency for inducing bronchoconstriction in vitro (1,000 times greater than histamine or prostaglandin)."* Asthma is an inflammatory condition, resulting from comamong various inflammatory mediators, cells, plex interactions and other tissues in the airways.' Detailed analyses of bronchial mucosal biopsies of the proximal large airways of asthmatic individuals have revealed a cellular infdtrate typically com- posed of eosinophils and lymphocytes, along with epithelial Several mediators, including histamines, cysteinyl leuko- and kinins, as well as products of eosinophils, such as eosinophilic cationic protein, have also been found in the asthmatic airway.-' These mediators interact with receptor cells in the airways to evoke bronchoconstriction, bronchial hyper- reactivity, mucous obstruction, have been developed process, either first new class of 20 years. These drugs an effort to inhibit the inflammatory by blocking the leukotriene receptor (eg, zafir- by interfering with the binding of arachidonic acid to 5-lipoxygenase (5(eg, zileuton).' Leukotriene-receptor blockers be capable of attenuating the early and late appear to phase bron- choconstriction response and the increase in nonspecific bronchial reactivity following challenge with inhaled allergens;'-^ leukotriene-synthesis inhibitors may be less effec- tive in this regard.^ edema, and microvascular leak- age. Cysteinyl leukotrienes are of particular interest because in in the last lukast) or antagonizing leukotriene synthesis LO) damage and desquamation.trienes, Oral leukotriene modifiers represent the asthma therapy introduced In addition to these drugs, which are currently approved for clinical use, several other leukotriene-modifying drugs are in various stages of development. These include three other leukotriene-receptor antagonists, montelukast.** pranlukast,' and verlukast,'" David A Stempel MD; Mason Medical Department of Allergy and Immunology, Virginia ing sites. all inhibit the binding Correspondence: David Avenue, Seattle A Stempel MD, Virginia Mason Clinic, 11 00 9th WA 98101. RESPIRATORY CARE of which block high affinity LTD4-bind- Two investigational drugs, MK-0591 Center, University of Washington, Seattle, Washington. of 5-LO to JUNE 1998 VOL 43 NO 6 and Bayx-1005, activating protein (FLAP)." Published clinical studies of asthma patients taking leukotriene modifiers are few. • its It appetus that this new class of asthma 481 LEUKOTRIENE MODIFIERS medications As matics. is no marker for these patients. In revised Guidelines for the Diagnosis Institute primary therapy will 11 and Management of of the National Heart, Lung, recommends inhaled in adults corticosteroids as and children age 12 or older with Mediators of acute inflammation produce bronchoconexudation of plasma, edema, and hypersecretion of striction, mucus, of which act to narrow the airway and result in all wheezing, dyspnea, and other symptoms of asthma. Airway inflammation review the mechanisms of action, pharmacology, ical effects, Role of Inflammatory Mediators its mild persistent asthma.' I THE TREATMENT OF ASTHMA effective in only a select population of asth- yet, there is Asthnui, the Expert Panel Repiort and Blood IN clin- and safety of the currently available leukotriene is the primary factor underlying the airway hyper- responsiveness characteristic of asthma. An abundance of in- flammatory mediators have now been associated with asth- matic inflammation. These include histamine, prostaglandins, modifiers. lipid Pathophysiology of Asthma mediators (eg, the cysteinyl leukotrienes), platelet-acti- vating factor (PAF), bradykinin, adenosine, anaphylatoxins, substance P, thromboxane, serotonin, oxygen radicals, com- Mechanism plement fragments, and neurokin A. The wide range of medi- of Inflammation ators involved in the inflammation process It is recognized that individuals who die because of asthma have grossly inflamed airways, marked by edema, mucus plugging, infiltration of the airway wall by eosinophils, mast cells, epithelial cells, fibroblasts, T cells.- By secreting preformed ators that act either directly macrophages, and activated and newly synthesized medi- on the airway or indirectly through neural mechanisms, these cells can adversely affect airway function.' Airway inflammation can be acute, subacute, or chronic. Bronchoalveolar Lavage and Biopsy Findings asthma in all patients.'-'' airway hyperreactivity in is ade of histamine, which has little effect demonstrated by the is assumed fact that block- to play a role in asthma, on asthma symptoms. '* Although PAF has been specifically associated with eosinophilic inflammation, it may not be a major factor in the pathophysiology of asthma because even potent PAF antagonists on bronchial challenges.'^ Bradykinin, however, have failed to have an impact an activator of sensitized sensory nerves producing tightness presence of inflammatory changes even unlikely it The complexity of the inflammatory response underlying tant as Only recently have bronchial biopsies and bronchoalveolar lavage (BAL) in living patients clearly documented the makes one of these will control the symptoms of that altering only in the chest and coughing.'^ many other mediators these and may be is impor- in the airways, The role of a subject of ongoing research. Effects of Leukotrienes those with mild asthma.- Eosinophils, in particular, are thought to contribute to the development of asthma, because they contain several The immediate response by patients with asthma to a spe- may damage the airway epithelium. Sensory nerve endings may then become exposed, leading to activation of cific allergen is neurogenic inflammatory pathways that cause the release of leukotrienes, potent inflammatory mediators, or spasmogens, into the air- gered mast cells in the airways." Leukotrienes have gener- way ated attention because they are far proteins that tissue.'-'-' ators such as prostaglandin D2, histamine, in their Remodeling produced largely through the action of medi- and the cysteinyl which derive from Immunoglobulin E (IgE)-trig- more potent than histamine bronchoconstricting effect.-" Leukotrienes are synthesized from arachidonic acid in the phospholipid bi-layer. Activation of 5-LO converts arachidonic The airway smooth muscle found to with asthma is often acid to an unstable intermediate. 5-hydroxyperoxyeicosate- be hypertrophied. Inflammatory remodeling is char- traenoic acid, acterized by new vessel formation, increased epithelial goblet cells, stitial in patients mucosal edema, and deposition of inter- coUagens beneath the epithelium manent changes numbers of to the airway. shape of the airway and may that may result in per- Inflammation may alter the contribute to the development (LTA4). which LTA4 is the is converted to epoxide leukotriene A4 intermediate product from which all the other leukotrienes are synthesized. Ultimately, the action of 5-LO on arachidonic acid results leukotrienes: in the formation of 5 LTA4. LTB4, LTC4, LTD4. and LTE4 (Fig. 1).^ Leukotrienes C4, D4. and E4 each contain a cysteine residue of persistent bronchial hyperresponsiveness and irreversible and bronchial obstruction. Clinical sUidies have indicated that short- Leukotrienes are rapidly metabolized and eliminated from the term treatment with inhaled corticosteroids can modify the circulation. intensity of inflammatory remodeling and even reverse base- ment membrane that alter 482 thickening.''' '^ There are no data demonstrate leukotriene modifiers have remodeling. at present this ability to are, therefore, referred to as the cysteinyl leukotrienes. LTE4 is a urinary metabolite that can be used to gauge the production of leukotrienes Among the iind in humans.' leukotrienes, the cy.steinyl leukotrienes C4, D4, E4 are the most potent bronchoconstrictors. When injected intradermally, the cysteinyl leukotrienes cause a wheal-and- RESPIRATORY CARE • JUNE 1998 VOL 43 NO 6 LEUKOTRIENE MODIHERS IN THE TREATMENT OF ASTHMA Arachidonic Acid FLAP - I ft 5-HPETE 5-LO Zileuton 5-LO \ LTA4 LTC4 LTB4 i LTD4 Zafirlukast J' LTE4 Fig. 1. Leukotriene production pathway. 5-LO = 5-lipoxygenase; 5-HPETE = 5-hydroxyperoxyeicosatetraenoic acid; FLAP = 5-lipoxygenase activating protein; LTA4 = leukotriene A4; LTB4 = leukotriene B4; LTC4 = leukotriene C4; LTD4 = leukotriene D4; LTE4 = leukotriene E4. flare reaction.^' Cysteinyl leukotrienes constrict both the large and small airways of normal and asthmatic subjects in vivo." ment of asthma in adults and children age 12 years or After oral ingestion, zafirlukast is gastrointestinal tract and reaches peak concentrations tor response to leukotriene challenge.-^ blood roughly 3 hours later. The airways of asthmatic patients are more responsive to LTC4, LTD4, and LTE4 than are the airways of people with- is out asthma, but the degree of hyperresponsiveness apeutic effect of zafirlukast However, individuals vary widely same order as the The reason is in their bronchoconstric- is not of seen with histamine or methacholine." for this finding is unclear and requires more study. In addition to their constricting effects reduced in the Because bioavailability of the drug 40% when taken with food, it is necessary to take zafirlukast ity to older. absorbed rapidly from the 1 hour before or 2 hours after meals.-' The derived primarily from is ther- its abil- attenuate bronchoconstriction mediated by cysteinyl leukotrienes.-* Liver microsomes that metabolize zafirlukast are formed on smooth muscle, the 2C9 (CYP2C9) enzyme pathways. human liver microsomes have demon- cysteinyl leukotrienes inhibit mucociliary function, increase via the cytochrome P450, the production of mucus, and facilitate microvascular per- In vitro studies with -^"^' meability and the formation of edema. strated that zafirlukast inhibits CYP2C9 and cytochrome P450, 3A4 (CYP3A4) isoenzymes at All of these are currently accepted as pathophysiology of asthma. The magnitude of response to blocking or removing only leukotrienes is not clear, because it is matory changes caused by other mediators abated. This fact likely that inflam- may continue un- may have important implications for the effi- plasma concentrations close to those achieved clinically.-' Because the clearance of zafir- lukast reduced is ble those found in cacy of leukotriene-modifying drugs. Zileuton is maximum compliance AUC) are approximately dou- in elderly patients, its (Cmax) and area under the curve younger ( adults.-' an inhibitor of 5-LO, the enzyme that catalyzes the formation of leukotrienes from arachidonic acid. Like Pharmacodynamics of Leukotriene Modifiers zafirlukast, zileuton it LTD4 antagonists and 5-LO rate inhibitors appear to amelio- asthma symptoms to some degree.-* Zafirlukast is a potent, selective, and long-acting leukotriene LTD4-receptor antag- onist that is indicated for the prophylaxis and chronic treat- RESPIRATORY CARE • JUNE 1998 VOL 43 NO 6 is clinically effective to the degree that limits bronchoconstriction mediated by cysteinyl leuko- trienes.-^' Both zileuton and its N-dehydroxylated metabolite can also be oxidatively metabolized by the cytochrome P450 isoen- zymes CYPl A2, CYP2C9, and CYP3A4. Zileuton is indi- 483 Leukotriene Modifiers in the Treatment of Asthma cated for the prophylaxis and chronic treatment of asthma in Reports of Churg-Strauss syndrome, a sometimes fatal vas- adults and children 12 years of age and older. Unlike zafir- culitis, lukast. zileuton's bioavailability is not significantly affected The syndrome may by the presence of food toms, such as fever, weight loss, and muscle aches and pains. in the stomach.'" have been associated with zafirlukast and zileuton. first appear as generalized flu-like symp- Eosinophilia, vasculitic rash, worsening pulmonary Drug-Drug Interactions symp- toms, cardiac complications, and/or neuropathy have also been reported.-' Due to its inhibition of the The P450 isoenzyme pathways, con- overall annual incidence of Churg-Strauss syndrome current administration of zafirlukast with other drugs metab- in the general olized via these pathways can cause drug-drug interactions; confirmed cases of Churg-Strauss syndrome'- and over a dozen reported cases of hypereosinophilia have been reported these other medications are shown in a Table 36% 1 . Among the most increase in the elim- important of these interactions is ination half-life of S-warfarin, which prolongs prothrombin in the far. population 250,000 patients is 2.4 per million." At least eight who have received zafirlukast thus The incidence of Churg-Strauss syndrome for the eight time by 35%. Patients should have their prothrombin times confirmed cases would, therefore, be 25 per million, a 10- closely monitored and medication dose adjusted accordingly. fold increase Other drugs should be used with caution when co-admin- that above the incidence in the general population. In the majority of these reports, patients were being tapered when istered with zafirlukast include tolbutamide, phenytoin, car- off oral steroids bamazepine. dihyropyridine blockers, cyclosporine, cisapride, one confirmed case of Churg-Strauss syndrome has been and astemizole.-' reported in a patient taking zileuton. This patient Zileuton can interfere with the metabolism of warfarin, fenadine. and propranolol. It is most important 73% a increase in its Cmax- and a who have tak- Liver toxicity has been observed in some subjects receiv- to note that zileu- shown to decrease the clearance of theophylline by approximately 50%. This has resulted in a twofold increase AUC, was not ing oral steroids." ter- ton has been in theophylline's the Churg-Strauss developed. At least ing leukotriene modifiers. In placebo-controlled vations in alanine aminotransferase 24% to 3 times the (ALT) upper limit of normal ( trials, ele- greater than or equal ULN ) occurred in 1 .9% received both of patients treated with zileuton, compared with 0.2% of zileuton and theophylline have experienced an increase in the placebo-treated patients. In patients treated with zileuton for prolongation of its half-life. Patients frequency of theophylline-related adverse events, ie, up compared ton and warfarin resulted in a and a 15% decrease 22% in the clearance increase in the mean AUC months, 4.6% developed elevated these elevations occurred during the of R- warfarin, but no effect risk of elevated prothrombin times.* first then once a month transferase activity first mild headache, and increased amino- However, symptomatic dental injury, dyspepsia, nausea, and myalgia."' had no other attributable cause were diagnosed Effects of Drug-Drug Interactions. Zafirlukast Warfarin Zafirlukast Prolonged Decreased prothrombin time and -- 484 maximum Cn^ AUC of Erythromycin Decrease in mean Theophylline Decrease in mean Increase in that one patient mean plasma levels of plasma levels of plasma levels of zafirlukast zafirlukast zafirlukast Decreased clearance 2 X increase prothrombin time of terfenadine theophylline levels AUC = area under the in Propranolol Aspirin Prolonged compliance; and hyperbilirubinemia hepatitis and Zileuton Terfenadine zafirlukast Zileuton enzyme recommended dosage. headache, unspecified pain, abdominal pain, asthenia, acci- . times the the Hepatic transaminase levels have not been found to be elevated in patients taking zafirlukast at the 1 liver levels return to normal.'" with zafirlukast.-' The most Drug increased year, and peri- frequent adverse effects associated with zileuton have been Table at ALT elevations greater than 5 ULN occur, zileuton should be discontinued until be generally well tolerated. Gas- may occur of months of treatment, every for the first 3 odically thereafter. If trointestinal disuirbances, 61% months of treat- ALTs. The manufacturer recommends 2 to 3 months for the remainder of the to 2 function monitoring prior to the initiation of treatment and Adverse Effects Both drugs appear ALT, compaied ment. Females over the age of 65 years appear to be on S-warfarin. These changes were associated with a clinically significant increase in to 12 with 1.1% of patients receiving only their usual care; with those taking theophylline alone. Co-administration of zileu- in X mcrease m AUC of proprant)lol serum 1 t RESPIRATORY CARE • JUNE 1998 VOL 43 NO 6 3 Leukotriene Modihers who had to received zafirlukast recommended dose) the for at in a dose of 40 mg/day (twice 100 days. Liver enzymes returned normal within 3 months of stopping zafirlukast treatment.-^' the Treatment of asthma 4 weeks, airway function and symptoms were found improved was seen L, in g group, with an increase in FEVj of 0.32 baseline. This response was in the 2.4 1 hour of drug administration. In another study with a similar design, 400 or 600 Most clinical als have trials using zafirlukast have been conducted with mild to moderate asthma. These clinical determined the effects of zafirlukast first protocols with antigens, cold Spector et al-'' air, tri- in challenge mg of zileuton or placebo four times a day for weeks. Eight (6. 1 %) evaluated the efficacy of oral zafirlukast in controlled, dose-ranging study in patients with moderate required concomitant corticosteroid treatment, compared with 21 (15.6%) of the patients receiving placebo. At the time of in those patients receiving zileuton, improvement in the cacy in A total of 276 subjects were ran- may not respond at domized to receive zafirlukast at a dose of either 5, 10, or 20 compared with a 7.7% placebo group."" Although the leukotriene modifiers have demonstrated who had been treated with ^agonists alone or in com- bination with theophylline. in a asthma 2-month patients, all it is also apparent that to these drugs. This clinical trial of zileuton in many effi- patients was demonstrated which half the patients mg twice daily or placebo. Compared with placebo, only the improved, while the other half showed no improvement. 40-mg dose was no improvement awakenings, first significantly effective in reducing nighttime morning asthma symptoms, daytime asthma and /3-agonist score, use. This dose also significantly increased evening peak expiratory flows (PEFR) and forced expiratory volume lukast after 40 1 second (FEV|). Compared with baseline, by 1 1%. zafir- mg twice daily decreased awakenings by 46%, fi- agonist use by 30%, daytime symptoms by 26%, and FEVi A small (n = which 10) double-blind study in received either zafirlukast 40 patients mg or placebo in random order week apart also found a significant increase The onset of action in patients with asthma has been reported to occur within the first week of therapy.''* Zafirlukast was found to be similar in effectiveness to sodium cromolyn in patients with self-assessed mild to modon 2 days in at least FEVi with erate is noted after a 6- to 8-week rent studies suggest continuing therapy.''^ trial, The reasons for this As noted earlier, large difference in response are not clear. leukotriene modifiers are effective against only one of mediators of airway inflammation. In If no cur- many many patients, factors may be dominant. There may also be One recent study, for example, has other than leukotrienes genetic factors at work. suggested that only certain people with a particular genotype respond to inhibition of S-LC" a zafirlukast.^^ asthma." Although the 1 of the patients receiving the 600-mg dose peak drug concentration, the average FEVi improved 15.7% exercise, and aspirin. a 6-week, multicenter, double-blind, randomized, placebo- asthma, 401 patients with mild to moderate asthma were randomized to receive either Zaflrlukast in patients be which was 1 3.4% greater than apparent within Clinical Trials to both zileuton groups. The largest improvement Leukotriene ModiHers in Exercise-Induced Asthma There modifiers is some may early evidence to indicate that leukotriene be useful in ameliorating symptoms in some patients with exercise-induced results of these studies are generally encour- aging, close evaluation often reveals a rather modest effect. 27% decrease from baseline may be involved in the asthma (EIA)." Leukotrienes development of EIA, although this is unclear. Initial studies failed to demonstrate a rise in still in the leukotriene levels in the lavage or urine of asthmatic subjects to only following exercise challenge,''" although such a rise has been 0.24 difference from placebo on a 3-point scale.'" While dif- noted in lavage specimens from patients with asthma after an For example, a reported daytime asthma score at the end of one study amounted ferences between drug-treated and placebo subjects statistically significant, their clinical In this same importance study, the clinical difference is may be questionable. amounted to one moming without asthma symptoms every week, one fewer puffs of ^agonist/day, an FEV| improvement of only 0.23 less L and a moming PEFR improvement of only 1 5 L/min. allergen challenge."' A study using improved methodology, however, has found an increased urinary concentration of LTE4 after an exercise challenge in asthmatic children."* Studies demonstrating the efficacy of leukotriene modifiers in preventing EIA also provided important support for the role of leukotrienes in the etiology of EIA. Improvements have been reported following treatment with orally adminZileuton istered zafirlukasr"^""' and zileuton.'" In another study testing inhaled zafirlukast, 9 patients with been asso- EIA were challenged with exercise on a cycle ergometer." Drug improved peak flows and spirometry (FEVi), administration resulted in significant, though variable, inhibition In controlled clinical trials, oral zileuton has ciated with reduced symptoms, and less need for /3-agonist In rescue.'^""' one multicenter, double-blind, placebo-controlled study,'* of EIA. Three subjects experienced almost complete inhibition; three others showed partial jects experienced to receive either zileuton 1.6 or 2.4 g/day or placebo. After interindividual variation Respiratory Care • June 1998 Vol 43 No 6 little inhibition. or no effect. 139 patients with mild to moderate asthma were randomized The remaining three sub- A considerable degree of was noted in all of these studies. 485 Leukotriene Modifiers in the Treatment of asthma Leukotriene-Modifying Agents zileuton. Identification of responders and Aspirin-Induced Asthma standing of a genetic marker, which may require the is under- yet to be determined. In addition, in three trials comparing the efficacy of leukotriene Aspirin-induced asthma is poody understood. greatest risk appear to be individuals who have asthma and to host rhinosinusitis.'- may be According TTiose at underlying one hypothesis, the overresponsive to products of the lipoxygenase pathway. Alternatively, there may be abnormal cellular re- modifiers to inhaled corticosteroids, the inhaled corticosteroid performed better.^'-^* were compared trial, fluticasone offered significantly greater protection than improvement in PEFR. Another compared pranlukast and inhaled beclometha417 patients with asthma. The increase in FEVj was clinical trial leading to the removal of a helpful substance or to the cre- sone in Patients with aspirin-sensitive some inhaled fluticasone and zafirlukast zafirlukast as well as greater sponses to aspirin and/or different arachidonic metabolites ation of an inflammatory substance of When in a histamine bronchial hyperresponsiveness significantly greater for inhaled kind.-""^ asthma have a dramatic level lukast. Finally, beclomethasone and not pran- when beclomethasone was compared to zafir- 48 1 mild moderate asthmatics, beclomethasone of intolerance to aspirin as well as to other nonsteroidal anti- lukast in inflammatory agents. Patients with aspirin-sensitive asthma demonstrated significanfly superior outcomes (p < 0.01) for morning PEFR and clinical FEV].'' have been shown to release leukotrienes when challenged with acetylsalicylic acid, and these patients also demonstrate a higher basal production of leukotrienes than other asthmatics. Given these findings, it is kotriene modifiers have been -''•'^' perhaps not surprising that leu- shown to have a significant impact on aspirin-sensitive asthma. For example, 8 aspirin-sensitive who participated in In patients to whose asthma is incompletely controlled with inhaled steroids, the question is whether to increase the dose of this medication or add a long-acting bronchodilator or leukotriene modifier. Currently, there is support for the addi- tion of a long-acfing /?-agonist^*' rather than increasing the a double-blind, placebo- dose of inhaled steroids, but there are no data demonstrating showed marked improvement over baseline following administration of MK-0679, an investigational leukotriene antagonist. Bronchodilation was induced for at least 9 hours after oral administration. The average peak improvement in FEVi was 18% above the predrug comparable effect with the addition of zileuton or zafirlukast asthmatic patients controlled, two-period crossover study However, the bronchodilator response varied between baseline. 5% and 34% and was found asthma and aspirin to correlate with the severity of to inhaled steroids. it ticosteroids as first-hne therapy, except in may II' views inhaled corticosteroids effective anti-inflammatory medication recommend currently available and continues to these drugs as first-line therapy for the long-term control of mild persistent to severe asthma Although leukotriene modifiers may some patients, their precise role has not yet defined. The Guidelines for the Diagnosis and be efficacious been clearly (Fig. 2). in Management ofAstlwm^ sible alternatives to This new who have mild in patients persistent 1 2 years asthma (Step 2). class of medication has the limitation of poten- who prescribe these drugs need to follow liver function studies in all patients on zileuton as well as for patients on higher dosages of zafirlukast. should also be aware that these two new agents may They be asso- find that the use of an oral preparation to factor into their decision preliminary 486 a specific instance where appropriate, but comparative studies are necessary to demonstrate whether these drugs are in EIA, but, again, clinical trials do not work indicate that they have greater efficacy than inhaled short-acting /J-2 agonists. For EIA, the use of a short-acting inhaled is still )3-2 agonist probably the best choice. In Summary about half of asthma patients Leukotriene modifiers are a new therapeutic class repre- senting a generation of research about the underlying anism of asthma. They demonstrate that, mech- once researchers understand the pathways of the disease pathogenesis, they can then proceed to develop medications to interfere with these processes. Zafirlukast and zileuton are the first of these new medications; others are certain to follow. Their development suggests that the future holds further advances for the treat- Although inunguing, these new medications do not appear is appealing as an alternative to inhaled steroids, but they need that only is ment of asthma. ciated with Churg-Strauss syndrome. may may be class of medication suggest zafirlukast or zileuton as pos- liver toxicity. Physicians Physicians reduce the risk of hospitalization for asthma.*^*^ truly superior to the other agents. Leukotriene modifiers molyn, nedocromil, or sustained-release theophylline for long- tial to new is low doses of inhaled corticosteroids, cro- term control and prevention of symptoms of age and older who improved patient outcomes, and recently has been Aspirin-induced asthma this most potent and children, corticosteroids in conformity with established guidelines shown The Expert Panel Report young be started on cromolyn or nedocromil. Use of inhaled vital for sensitivity.-''* Using Leukotriene Modifiers in Asthma Therapy as the more experience is gained with leukotriene modiwould seem prudent to continue to use inhaled cor- Until fiers, to be as effective as inhaled corticosteroids or more effective evidence suggesting than cromolyn or nedocromil. may respond drugs at all to may be effective A recent review states that these in aspirin-sensitive asthma,**- but their RESPIRATORY CARE • JUNE 1998 VOL 43 NO 6 Leukotriene Modifiers in the Treatment of Asthma ... . Leukotriene Modifiers 1 1. Negro JM. Miralles JC, Ortiz JL. Funes in the Treatment of asthma E, Garcia A. Biosynthesis Immunopathol inhibitors for leulvotrienes in bronchial asthma. Aliergoi 12. Evans DJ. Coulby LJ, O'Connor BJ. Effect of allergen challenge on 13. 1 996;5 1( 1 2): 1 1 85- 1 1 subjects with bronchial asthma. Donno M. Bertorelli G, Casalini A. Pesci Effect of short-term treatment with low-dose inhaled et al. Am J Med 35 Olivieri D. Chetta A. Del Am J Respir Crit Care Med 5 of inhaled cortico.steroids asthma. in Am J Respir Crit Care Med 1 37, 1 7. 18. 19. Rev Respir Dis 1992: 145(4 PW. The thetic asthma? Respir there adequate informa- is Med role of leukotrienes in asthma and Exp Allergy 1996;26(8):868-879. Lewis RA, Corey EJ, Austen KF. Local leukotrienes (LTC4, LTD4, LTE4, and LTB4) MM, Adelroth E. Morris Russi 24. in human NEnglJMed 41 in Kaliner C4 and D4, increase results Cohn Israel E, J, Dube L, the Zileuton Smdy Group. The trials (abstract). J Israel E, Cohn M. Slow- Am Rev Respir Dis J, Dube L, Allergy Clin Im- Drazen JM. Effect of treatment with zileu- trial. Zileuton Clinical Trial Group. random- JAMA Drazen JM, Yandava C, L and Szczerbak N, Dube A, Pillari 1996:275 treatment in the KH, Swanson In Dydo M, L, the Zileuton Study Group. Relationship between 5-LO gene promoter mutations and lung function response 5-LO 44, Broide inhibition (abstract). DH, Eisman Wasserman 1982:126 SI. S, Airway Am J Respir Crit Care Med Ramsdell JW, Ferguson levels of Schwartz LB, mast cell-derived mediators Am Rev Respir Dis cise-induced asthma. P, 1997:155(4 exer- in 1990;14l(3):563-568. Wenzel SE. Larsen GL, Johnston K, Voelkel NF, Westcott JY. Elevated levels of leukotriene C4 D in vivo and in vitro. activities Proc Natl Acad Sci of leukotrienes USA 46. Kikawa Y, Miyanomae T, Inoue Y, Y, ucts of the 5-lipoxygenase pathway: biochemistry with asthma. diseases. N Engl J Med and relation to path- 1990;323( 10):645-655. bronchoalveolar lavage fluid from in Am Rev Respir Dis 1990:142(l):l 12-1 19. 1980:77(7): Lewis RA, Austen KF, Soberman RJ. Leukotrienes and other prod- human mild- of a 6-month dou- atopic asthmatics after endobronchial allergen challenge. in in Eur Respir J 1994;7 (Suppl Drazen JM, Austen KF, Lewis RA, Clark DA, Goto G, Marfat A, 47. et al. M, Nakai A, Shigematsu Saito Urinary leukotriene E4 after exercise challenge Finnerty JP, J Allergy Clin Immunol Wood-Baker R, 1 Thomson in children 992:89(6): 1111-1119. H. Holgate ST. Role of leu- Accolate (zafirlukast) prescribing infonmation. Wilmington DE: Zeneca kotrienes in exercise-induced asthma: inhibitory effect of ICI 2042 9, Pharmaceuticals; 1997. a potent leukotriene 1 Spector SL. Management of asthma with zafirlukast: clinical expe- Wenzel SE, Kamada AK. Zileuton: The treatment of asthma. first Ann Pharmacother Abbott Scott DGl. Epidemiology of systemic vas- changing incidence or definition? Semin Arthritis Rheum AJ, et al. Pulmonary effects of a 5-lipoxygenase inhibitor air. N SR, Kocher O, Wciland DA, Polilo infiltrates, eosinophilia, following corticosteroid withdrawal and cardiomyopathy in patients with asthma receiv- J Med on asthma 1990:323(25): 1740- 1744. PJ, Watson RM, Margolskee DJ, Williams VC, Schwartz O'Byme PM. Inhibition of exercise-induced bronchoconstriction MK-57 a potent leukotriene D4-receptor antagonist. N Engl J Med 1990:323(25): 736- 17.^9. Meltzer SS, Rechsteiner EA, Johns MA, Cohn J, Bleecker ER. Inhi- Manning 1 , bition of e.xercise-induced Flier Engl 1 50 1995:2.5(1 ):28-.34. Wechsler ME, Garpestad E, 1992; JI, by DM, Am Rev Respir Dis receptor antagonist. Dermarkarian R, Rosenberg M, Sperling R, Taylor G, Rubin Drazen JM. The induced by cold, dry 49 Watts RA, Carruthers Israel E, P, 1996:30(7-8): IL: D4 145(4 Part l):746-749. 48. 5-lipoxygenase inhib- Zyflo (zileuton) prescribing information. North Chicago culitis: 488 trial (abstract). 43, Laboratories: 1997. 32. moderate asthma: in O'Byme PM, Israel E, Drazen JM. Antileukotrienes of asthma. Ann Intern Med l997:l27(6):472-480. the release of 858-864. 1 Siegel SC, et 1059-1066. Corey EJ. Comparative airway and vascular itor for the 3 1): 42, respiratory rience and lolerability profile. Drugs 1996;52(Suppl 6):36-46. 30. Drazen JM, Part2):A257. obiology 29. W, by zileuton (12):931-936. re- pa- 4354-4358. 28. Pierson J, 1993:1 19(1 ton, a 5-lipoxygenase inhibitor, in patients with asthma: a skin. Stevenson JS, Codias E, Marom Z, Shelhamer JH. Bach MK, Morton DR, Med Intern the Zileuton Study Group. Effects of zileuton, a 5- J, to C| and 27. M. Cohn function in allergic and nonallergic sheep. J AppI Physiol 1985:59 in vitro. Ann efficacy of zileuton in the u-eatment of asthma: results of combined (3):449-451. 26. Liu (5):1416-1422. mucus from human airways Kemp JP, Grossman double-blind, placebo-controlled 1986:315(8): D4 on mucociliary and Effects of leukotriene P, munol 1995:95:388. effects of syn- Hargreave FE, O' Byrne PM. Airway reacting substances, leukotrienes 25. Allergy Clin Immunol effect of inhibition of 5-lipoxygenase ized controlled EW, Abraham WM, Chapman GA, Wanner A. J 18):282S. 40. 19. with asthma and nonnal controls. The lipoxygenase inhibitor allergic rhini- 480-484. 23. 39, 1996;90( 10):575-586. N A, Dermatol 1983:80(2):1 15-1 Rubin Israel E, to-moderate asthma. ble-blind, placebo-controlled sponsiveness to leukotrienes C4 and D4 and to methacholine tients 1 al. Clin Soter J Invest 22. 38 Part 2):A292. Anti-leukotriene intervention: WW. Busse tis. 21 Allergy Clin J UK 74,505 on allergen-induced early and late response (abstract). tion for clinical use in 20. asthma. in Barnes PJ. Bradykinin and asthma. Thorax 1992:47(1 1):979-983. Ind Immunol 1995:95:844. Nathan RA, Glass M. Snader L. Effects of 3 weeks of treatment with mild to moderate asthma (abstract 990). 994; Immunol 1989:83(2 Part 2):537-547. Kuitert LM. Hui KP. Uthayarkumar S, Burke W, Newland AC, Uden S. Barnes NC. Effect of a platelet activating factor (PAF) antago- Am Onset of action of the leukotriene- 1995:95:388. Holgate ST. Finnerty JP. Antihistamines nist Kemp JP, Glass M, Minkwitz MC. ICI 204,219 (Accolate'") or cromolyn sodium (Intal®) in patients with 150(1): 17-22. 16. asthma with a in receptor antagonist, zafiriukast (Accolate), in patients with asthma Placebo-controlled immunopathologic study of four months et al. 1994:I50(3):61 8-623. Hui KP, Barnes NC. Lung function improvement (abstract). J Allergy Clin ND, Wang J, Calderon MA. Mc Aulay A, Jordan Trigg CJ. Manolilsas SE, Med Respir Crit Care receptor antagonist, in 1062-1063. 36, 1997; 155(6): 1864- 1871. 1 D4 ACCOLATE Asthma Trialists Group. cysleinyl-leukotriene receptor antagonist. Lancet 1991:337(8749): flu- ticasone propionate on airway inflammation and remodeling in mild asthma: a placebo-controlled study. Spector SL, Smith LJ. Glass M. Effects of 6 weeks of therapy with oral doses of ICI 204,2 1 9, a leukotriene 91 Barnes PJ. Anti-inflammatory therapy for asthma. Annu Rev A, 34 in 199.^;44:229-242. 14. 1998:279(6):455-457. Personal communication from Department of Drug Infonmation, Abbott Laboratories: August 1997. airway responsiveness to histamine and sodium metabisulphite mild asthma. Thorax JAMA ing zafiriukast. 33. (Madr) 1997;25(4):209-216. hibitor (absU-act). 51 asthma by zileuton, Am J Respir Crit C;ire Med a 5-lipoxygena.se in- 1994:149(4 P;irt Makker HK. Lau LC. Thomson HW, Sinks SM, Holgate protective effect of inhaled leukotriene RESPIRATORY CARE • D4 2):A215. .ST. The receptor antagonist ICl JUNE 1998 VOL 43 NO 6 . Leukotriene Modifiers 2CW.2 9 against exercise-induced asthma. 1 (6 Part 52. 1): Am Rev RespirDis in the Treatment of Asthma hyperresponsiveness 1993; 147 Bush RK, Asbury D. Aspirin-sensitive asthma. In: Busse W, HolAsthma and rhinitis. Cambridge MA: Blackwell Sci- 58. gate S. editors. Asthma Florida, February 2-4, 1990. J Allergy Clin Immunol 1991:88(3 Part Care 59. 1):303-321. 54. Kumlin M, Dahlen B, Bjorck T, Zetlerstrom O, Granstrom E, Dahlen S-E. Urinary excretion of leukotriene E4 and ane Bi in 1 1 -dehydro-thrombox- 60. Am Rev Respir Dis AW, Charlesson S. Chee P, 6 1 challenge in a.spirin-sensitive asthmatic subjects. 1 Am Rev Respir 62. baseline pulmonary 1205-1210. (FP) 1 J, Am J I. Dubb Respir Crit 1997:155(4 Part 2):A203. LA, Naya Sinks IP, S, Harris zafirlukast and low dose steroids (abstract). Eur Respir J A. Comparative efficacy of in asthmatics on pm /3-2 agonists 1997:10:P2716. Woolcock A, Lundback, effect of inhaled fluticasone propionate 00 /Jg bd compared with • oral zafirlukast Greening AP, Ind B, Ringdal N, Jacques LA. Comparison Am J Respir Crit Care Med 1996; 1 53(5): PW, Northfield M, Shaw G. Added salmeterol ver- symptoms on & Hanburys Limited UK Study 20 mg bd on bronchial JUNE 1998 VOL 43 NO 6 Donahue JG, Weiss ST, Livingston JM. Goetsch MA, Greineder DK, Piatt R. Inhaled steroids JAMA 63. Pasma HR. The RESPIRATORY CARE (abstract). Group. Lancet 1994:.^44(8917):219-224. MK-0679 on function in aspirin sensitive asthmatic subjects. Thorax 1993;48(12): Westbroek Med Laitinen asthma existing inhaled corticosteroid. Allen ):1025-I029. Dahlen B, Margolskee DJ, Zetterstrom O, Dahlen S-E. Effect of the leukotriene receptor antagonist 57. Kerwin E, Silvers W, Faiferman sus higher-dose corticosteroid in asthma patients with Urinary leukotriene E4 concentrations increase after Dis 1991:143(5 Part 56. P, patients with 1481-1488. Christie PE, Tagari P, Ford-Hutchinson a.spirin Chervinsky trial in dose of inhaled steroids. 1992:146(1 ):96-103. Arm JP, Lee TH. S, of addition of salmeterol to inhaled steroids with doubling of the response to bronchial provocations with allergen, aspirin, leu- kotriene D4. and histamine in asthmatics. 55. mild to moderate asthmatics (abstract). Eur Oral pranlukast (Ultair) vs inhaled beclomethasone; results of a 12-week Immunopharmacologic update. Course summary. Naples. '90: Wenzel J. ence 1995:1429-1439. 53. in RespirJ 1997;I0:P1554. 1413-1418. and the risk of hospitalization for asthma. 1997:277(1 1):887-891. Buchner DA, Carlson AM, Stempel DA. Patterns of anti-inflammatory therapy in the post-guidelines era: a retrospective claims analysis of managed care members. Am J Managed Care 1997;3:87-93. 489 1997 Philip Kittredge Memorial Lecture Mechanical Ventilation: The Next 50 Years Neil Mechanical Ventilation in R Maclntyre MD 1997 The outcome of mechanical ventilation dent upon the underlying disease Mechanical ventilators are devices or systems that are designed to provide oxygen to and clear carbon dioxide from pulmonary capillary blood. While positive pressure gas deUv- state. is obviously depen- Generally, patients with rapidly reversing lung diseases and underlying (eg, asthma, good health drug overdose, anesthesia recovery) can expect mortality rates of less than 5%. On the other hand, acute res- mechanical ventilation, sys- syndrome (ARDS) and chronic obstructive pulmonary disease (COPD) may have mortalities approach- tems using positive pressure masks, negative extrathoracic ing 40 to 50%. Moreover, patients on mechanical ventilators pressure, and devices implanted into the vasculature to pro- who have severe multi-organ failure and the sepsis syndrome may have mortality rates approaching 100%. ery to the lungs through an artificial airway common way most to provide is probably the vide either intra- or extracorporeal gas exchange would also meet this definition I will be discussing the issue of positive pressure ventilation applied through an worldwide; approximately half of them are in use in North America. Based on diagnosis-related-group data, it is also estimated that approximately 1 .5 million patients in that are occurring in the use of positive pressure mechanical ventilation in 1997. the number of patients being the Duke is rising. The experience of University Respiratory Care Service shows despite a falling bed census, the has steadily increased over the two reasons last decade. There are at least for this. First, the aging population presents the medical system with more chronic disease and more acute operating rooms and recovery rooms each year. Given these of those chronic diseases. 80% that, number of ventilator hours the United States receive mechanical ventilation outside of numbers and assuming approximately First, intubated and requiring positive pressure mechanical ventilation airway. In 1997, an estimated 100,000 positive pressure ventilators are in use There are two important trends of mechanical ventilation. For the pur- poses of our discussion here, however, artificial piratory distress As we flares take better care of this aging can population, their need for subsequent medical care obviously be calculated that the average length of stay on a ventilator increases. Indeed, every successful extubation and hospital is in the neighborhood of 1 to 1 .5 utilization, it weeks. The average cost of a mechanical ventilator runs anywhere between $10,000 and $30,000 U.S. dollars. Increasing costs are associated with discharge means there will be sion. at least one subsequent admis- A second reason is the delivery of more aggressive med- ical care. Specifically, aggressive surgeries are being carried more increasing capabilities such as graphic displays, sophisticated out on older and more seriously monitors, microprocessor-control systems, and automated aggressive chemotherapies are being given to patients with record keeping. The life span of a mechanical ventilator 10 to 15 years. Using these estimates, is about we can see that the world- wide yearly market for mechanical ventilation the hun- is in ill patients. Similarly, more immunocompromised patients and thus a higher incidence of sepsis and respiratory failure. malignancies resulting in For the same reason, the AIDS (acquired immunodeficiency syndrome) population has also impacted the need dreds of millions of dollars. for mechan- ical ventilation. A second major trend in mechanical is Neil R Maclntyre cal Center; MD; that as patients resolve the acute Department of Medicine; Duke University Medi- tory failure, they often enter a Durham. North Carohna. tilator Dr Maclntyre presented the Phillip Kittredge the 43rd International Respiratory Congress, New Orleans, tory Care Services, Durham 490 NC 27710; P R more Memorial Lecture during them December step-down 6-9. 1997. in Louisiana. Coirespondence: Neil dependence, resulting to O MD. Professor of Medicine, Respira- Box 3111, Duke e-mail: University Medical Center, macin001@mc.duke.edu. more chronic phase of ven- in increasing pressure to cost effective venues of care. This units, subacute hospitals, lator facilities are Maclntyre ventilation in 1997 phase of their respira- growing in move means that and long-term venti- number and in the complexity mean that the need of services provided. Both of these trends for mechanical ventilation will only increase over the fore- seeable future. RESPIRATORY CARE • JUNE 1998 VOL 43 NO 6 . MECHANICAL VENTILATION: THE NEXT 50 YEARS This can lead to a delay in the weaning process and Goals of Mechanical Ventilation withdrawing the patient from the There are both realistic major injury third and unrealistic goals for mechan- ventilator. The and being on that intubation is a ventilator increase the risk of infection. Indeed, Certainly a realistic goal ical ventilation. that is pulmonary ventilation should be able to provide mechanical with appropriate levels of Pq; and Pco:- Moreover, be done without injuring the patient's lungs nosocomial pneumonia capillary blood this is one of the most serious complications that can occur in a patient on mechan- should and ical ventilation in the process. significantly lengthens the it ventilator length of stay. Reducing infections could It is unfortunate that clinicians sometimes also have unreal- be one of the major goals of an improved mechan- istic goals for mechanical ventilation. For instance, a mechan- ical ventilation ical ventilator is that might contribute 3. of lung injury. Certainly, to resolution may may impact for ventilator the duration of respiratory ical ventilator is a part, a mechan- support (not a therapeutic) device that injury. own These consider ICU costs. is Advances on the Immediate Horizon designed to 'buy time" while other therapies, including the patient's This Taken together, the cost per day management can run $ 1 ,000/day or more, a substantial fraction of and mortality. However, for the most failure cost. operational costs. contribute to disease resolution so that a mechanical ventilator Mechanical ventilation carries a high includes not only capital costs but also supply and adequate gas exchange, alveolar recruitment, and minimal atro- genic harm system. sometimes considered a therapeutic device (5 to 10 years) defense system, effect resolution of the lung realistic and unrealistic goals are important when designing There are a number of developments to new mechanical studies looking at to 10 years Lung ventilation technologies. may over the next 5 that address the three limitations noted above. protective ventilator strategies that supply adequate gas exchange while protecting the lung will be a major focus Limitations to Mechanical Ventilation in 1997 of research. Spiecifically, strategies that adequately recruit lung volume but There are three major problems with mechanical ventilation in — 1997 why we three reasons are not attaining our goals. yet do not overdistend more common. To this end, the lung are likely to become pressure-volume plots looking and overdistention will be increas- for alveolar recruitment ingly important in setting ventilator parameters. High-frequency 1 mechanical ventilators In the sickest patients, may not be able to supply adequate gas exchange. Patients dying from gas exchange impairment are cer- tainly in the minority (ie, < 15% of ARDS is maximal alveolar strategy. This seems to show the same thing as new are important adjuncts that future systems. exchange while reducing 2. it is Positive pressure mechanical ventilation can cause The three types of iatrogenic injuries. first is direct is injury can be the result of excessive levels of sup- clinical trials. Surfactant plemental oxygen (oxygen toxicity) or can be the are used as "liquid ticularly important and from the results tissue (particularly the healthier regions fact that lung available. There and Fio, injury. Nitric oxide improves ventilation-perfu- Whether this replacement and fluorocarbons that PEEP" may also help recruit appropriate lung volumes and improve ventilation perfusion matching. Another promising technique of the lungs) flation can be damaged when overdistended by mechan- stretch become also help us improve gas outcome, however, awaits the results of translates into better seems par- may it populations at sion matching and reduces the need for Fio:- lung injury from the mechanical ventilator. This result of stretch injury. Stretch injury in pediatric likely that adult studies will devices certainly promising in that volumes and limited the ultimate lung protection be clear and risk for stretch injury ill a problem that must be addressed with may be stretch deaths), but suboptimal gas exchange in those very patients ventilation with properly recruited lung is the use of tracheal gas insuf- (TGI) to flush the endotracheal tube during exhala- and thereby reduce effective dead space. Because tidal volume can be reduced, TGI may reduce the need for high tion ical ventilation strategies recruit and designed to aggressively ventilate the sicker regions of the lung. This injury seems potentiated recruitment of alveoli is when inadequate also present ventilation pressures. To improve A second major patient-ventilator synchrony, there are a injury from positive pressure mechanical ventila- ber of possible advances on the immediate horizon. tion ventilatory muscle overload from patient- processor technology is in patients and cycling significant criteria receiving partial ven- response. Pressure rise time adjusters and computerized feed- a on the flow deliv- ventilator can cause imposed load and discomfort to the back systems JUNE 1998 VOL 43 NO 6 match ventilator delivery to patient effort are improve synchrony. Placing ventilator sens- ing sites for patient activity closer to the ventilatory muscles is • to likely to further patient that results in substantial needs for sedation. RESPIRATORY CARE getting increasingly better at detect- ing patient activity and producing an appropriate ventilator is tilatory support. Inappropriate triggering, ery, is that ventilator dyssynchrony. This occurs primarily phenomenon num- First, itiicro also likely to occur. Sites such as the distal endotracheal 491 Mechanical Ventilation: The Next 50 Years tube, the pleural space, or that has tilator Better monitors, particularly of the function of cen- may all come even the phrenic nerve tral by the end of the next decade. Another technique to fruition promise gauge its improving synchrony to have the ven- response to a flow signal in a mode known in is nervous system (the most sensitive organ to impairments in gas exchange) and respiratory mus- cle function (critical in determining patient wean- ing capabilities) will be developed. Finally, closely as proportional assist ventilation (PAV). linked ventilator functions and patient Reducing infections may come from a variety of areas. markedly enhance the ventilator's Circuits less prone to contamination, techniques to keep the vide partial support. upper airway free of pharyngeal and gastrointestinal con- practitioners will be critical in ways of sterilizing tamination, and perhaps still may in the future. Ironically, hand washing tech- the simplest and, perhaps, most effective way be useful adjuncts niques are the pharynx compliance with to reduce infections, but this practice is will More advanced nonphysician managing these sophisticated devices. 2. It is may finally begin An obvious ap- possible that the ventilator to function as a therapeutic device. no- proach would be to use a ventilator as a system to where near 100%. Reducing the cost of mechanical ventilation deliver drugs into the lung may come from several advances. For instance, increasingly sophisticated but inexpensive microprocessor systems are likely to be devel- oped demands ability to pro- of care. Protocols are likely to come in One could imagine that This ap- the lung could be in various anti-inflammatory, infective, all provide gas ex- change without necessarily providing bulk flow positive pressure ventilation. Will we also develop a 'therapeutic' ventilator pattern? Perhaps high-fre- quency techniques may evolve also reduce the cost two proach. directly. may be an immersion or growth/repair solutions that much simpler mechanical components. Supply cost may also come down as manufacturing techniques improve and nosocomial infections are better controlled. The develered with opment of management protocols should as an aerosol or immersed mechanical ventilation to be deliv- that will allow for parenchyma may be into pressure manip- ulation strategies that enhance recovery. areas. First, ad- vanced-level nonphysician practitioners (eg, advanced res- ventilators without specific physician orders. numbers decrease, the need Technology 3. piratory care practitioners) will be trained to run mechanical to replace positive pressure ventilation delivered through an endotracheal tube As physician develop. is The most obvious approaches likely to are extra- for these 'physician extenders' corporeal systems. Closely related to this are intra- to run these sophisticated systems independently will become vascular systems that provide gas exchange through increasingly important. Similar developments are likely to occur in other ICU management areas such as nutrition, fluid indwelling catheters in the great veins or pulmonary man- artery. agement, antibiotic selection, and sedation. Second, computer protocols will be developed to perform similar functions. Com- ficial puter protocols, however, will be slow to replace practitioners skilled in assessment ers, and subjective sensations will practitioners to make proper arti- lungs or permanently with lungs from cadav- animals, or synthetic engineering laboratories. nario where by require experienced still the use Indeed, one might envision a "Darth Vader" sce- and judgment because important input variables such as patient comfort, respiratory muscle activity, The most dramatic change could be of lung transplantation, either temporarily with all the respiratory function a device that is provided one wraps around the chest. decisions. How Do We Evaluate New Technology? Advances on the Distant Horizon (10 to 50 years) Predicting what will happen over the next 10 to 50 years obviously involves a lot of guesswork. However, these will be the systems that will ventilate you and age, and so come we hope in three it is done right. I me as we enter old think that advances will general areas. As new devices and techniques come along, it is imperwe have a system designed to evaluate them prop- ative that erly. A very important consensus conference was sponsored by the American Association for Respiratory Care and the American Respiratory Care Foundation looking involved in evaluating Care, September 1 . Traditional positive pressure ventilation with oxy- gen supplementation strategies will be greatly im- proved. This will occur for several reasons. Techniques to reduce infection and provide better airway protection are likely to come from improved ven- new technologies at the issues (RESPIRATORY 1995). In essence, this group proposed three levels of evaluation: a simple engineering evaluation, a phys- iologic tion. outcome evaluation, and a clinical outcome evalua- Obviously, the cost of these evaluations rises as they become more complex. that devices with low It risk was felt by this consensus group and low cost needed to be evalu- tilator patient interfaces. Surfactants, vasodilators, and other agents will be developed that enhance ven- tilation perfusion matching and greatly improve the ability of the positive pressure ventilator to supply gas exchange with lower pressures and less harm. 492 ated only on their engineering claims. If the device has moderate cost or more moderate using risk, some meaningful physiologic however, if it more should be evaluated data. Most importantly, a device has significant cost implications or sig- RESPIRATORY CARE • JUNE 1998 VOL 43 NO 6 MECHANICAL VENTILATION: THE NEXT 50 YEARS nificant risks associated with trial to demonstrate must be kept in it, it improved mind should undergo a controlled outcome. This schema clinical we have more and more as gies introduced in an increasingly complex and technolo- cost conscious health care delivery system. Because clinical trials are likely to for expensive be required, especially and risky technologies, it is important that develop evaluation systems to perform them. Clinical networks are going to be extraordinarily important to carry out cost-effective and timely evaluations in clinical trials with As more and more computerized decision-making systems become implemented in ICUs around the country, it is conceivable that these could a randomized, placebo controlled format. be linked to form clinical trials networks. we In Conclusion trials networks would be an important thing for us to begin devel- oping now. An example Health (NIH) might be the National medical centers whose infrastructure Their charge Institutes of ARDS network. This is a consortium of 10 major is to conduct clinical trials is funded by the NIH. on 400 ARDS patients a year. Promising therapies are considered by this group and subject to clinical trials if deemed important enough. Other research networks could include large health care systems (eg, the Veterans Administration, RESPIRATORY CARE • managed care groups). These JUNE 1998 VOL 43 NO 6 It has been an honor and a pleasure to deliver the 1997 Philip Kittredge Memorial LecUire. Phil who contributed was a colleague and a friend an enormous amount to the respiratory care profession. In considering where mechanical ventilation going during the next 50 years, that Phil it, and this I would have invite all of relished. you to I I think there is is an exciting future am excited to be involved with become involved with bringing technology into the 21st century. 493 — Books, Films, Tapes, & Software The Application of Magnetic Resonance Study of Lung, Antonio to the G Cutillo 607 pages. Armonk MD, Editor. Illustrated, NY: Futura Publishing Co; 1996. $98. and Reviews of Books and Other Media. Note Listing films, tapes, and software The editor has achieved he to RESPIRATORY CARE, 600 the stated goals that sets out in the Preface; the material is well Because book this is the combined effort of a group of physicists, biophysicists, bio- Magnetic resonance (MR) imaging of the lung has had its share of problems during its developmental stages. Imaging problems are normal lung anatomy and directly related to ologists, it and pulmonary medicine physicians, should have a wide audience of very spe- cialized readers. of this book and respiratory motion have Umited the wide chapters that lung. MR imaging of the However, continuing research area has developed new in the techniques that are beginning to overcome these inherent ficulties. To this end, this dif- book presents a comprehensive, systematic account of the theoretical and experimental data accumu- lated in both basic and MR research. fundamental MR clinical This book discusses the the I MR in and diagnostic thoracic it is certainly has anything to do be from a basic sci- of pulmonary medicine perspective. This far the most comprehensive book today about the application of the lung because book it rent are apt to is is it MR to the study of includes both a histor- and indications for future While parts of this become outdated fairly rapid- most up-to-date and cur- certainly the comprehensive text available MR on imaging of the lung, with many in-depth, monary vasculature and pulmonary embol- view-style chapters that will transcend time, ism, lung cancer, and obstmctive sleep apnea. for at least a of 57 contributors from all over the re- few years more. The book is 1 legal terms clear, The production reasoning. Despite simpUfication. 1 ter' s 14 chapters, or 438 pages, are dedicated to entists and acknowledges the ambiguity of ethical decision making. He addition to any medical endorses neither today's trendy ethical rel- clinician scientists normal lung and rightly this or bad: first in Part contents. ativism radi- Each of the 7 chapters The author vidual libraries of those dedicated basic sci- The theories of moral relative brevity (163 contains a set of study questions and ap- school library and to the departmental or indi- all. its book provides well-developed pages), the MR imaging, MR physics, ology. There are 18 chapters in in explanadons and generally avoids over- These contributors are well-known authors pulmonary medicine, and pulmonary and ethical theory. Key and concepts are explained two of the primary trasting text as a of its title. does a creditable job of comparing and con- qual- would highly recommend welcome aptly described by understandable language. The author Netherlands, Slovenia, Japan, and Germany. 1 is the reader gains a basic founda- tion in relevant legal ity is superb. , plied exercises that relate closely to the chap- thoroughly referenced and beautifully illustrated. This text In Part world, including countries such as The in the fields ethical Toward this end, Charles Carroll's Legal Issues and Ethical Dilemmas in Respiratory Care is a practical resource. who with the lung, whether This book, edited by Dr Cutillo, has a from simply good sense informed about the ethical and to be well ence perspective or from a clinical practice ly, free life now It is some- thing for everybody imaging, with particular attention to the pul- total for on-the-job behavior, they alone cannot legal issues that affect professional practice. basic clinical research. current use of sense and a professional pulmonary medicine physician who has ical perspective acterization of experimental lung injury, common same fime accountability. remain generally sound guidelines or legal conflicts. recent developments in diagnostic imaging MR char- While attitude guarantee a working not be of any interest to at the demanding more professional many a clinical practice, there by greater participation in health care while there are may too, The public today decision making, while charm is that, WA 98104. Consumerism, effects. its think that part of the properties of normal and diseased lungs, and quantitative lung imaging, has exerted engineers, biochemists, pathologists, radi- physiology. Magnetic susceptibility effects clinical acceptance of to adapt to these factors. demands selected and organized. Send review copies of boolcs, to publishers: Ninth Avenue, Suite 702. Seattle who study the MR imaging of the healthy (ie, "No situation nor yesterday's absolutism one way good to view each (ie, "there situation"). is only The author avoids the 'cookbook approach': he offers and diseased lung. MR properties of normal and diseased lungs, no pat recipes for Eric J Stern quantitative studies of the lung, and lung is in itself depends only on your viewpoint") it ethical success. Instead, MD he presents us with a thoughtful and pragmatic approach to sorting out the relevant to the hard Department of Radiology core pulmonary medicine scientist and physi- Harborview Medical Center would University of Washington ments from each of the dominant ethical Washington viewpoints with elements of pragmatism, These would be of interest injury. cist. Chapter 1 5 is the only chapter that be of particular interest to the clinical pul- Seattle, issues of ethical dilemmas. monologist and radiologist. Chapter 16 scientific would be of interest only roll to those common sense, Car- provides the reader with a helpful At apnea. Chap- Legal Issues and Ethical Dilemmas in Res- method piratory Care, Charles Carroll. 163 Pages. times the process proposed by Carroll seems ter 17 in clinical respiratory MR medicine as it relates imaging, and the potential for imaging in the future. 1 8 is a glos- sary of terms and abbreviations, which actually one of the chapter that has Philadelphia: more useful utility beyond FA Davis Co; 1996. $17.95. MR is chapters, a this textbook. for approaching moral problems. mechanical and somewhat simplistic. But in general his With a 1996 copyright, has the future arrived? Chapter 494 method, and ele- discusses the current state of the art cial interest in obstructive sleep to with a spe- Combining Litigation, risk management, liability, out-of-court settlements, ethical conflicts all of these uncomfortable subjects have had profound influence on the workplace of today. Like all industries, health care has had ful clinician approach provides the thought- with a helpful and effective way of sifting through the myriad factors involved in moral and ethical decision making. Part 2 of the book switches from a heavy emphasis on infomiation RESPIRATORY CARE • to its practical appli- JUNE 1998 VOL 43 NO 6 BOOKS, Films, Tapes, cation. Each of the 8 chapters in Part 2 focuses on a single issue, such as confidentiality or care of the terminally ill. ments of each issue, including relevant legal considerations. The reader is then presented with a variety of hypothetical but highly realistic clinical situations, each of which serves as a departure point for discussion. the several simulated panied by a list dilemmas is • wide array of sion making. dilemmas from The information it contains makes Legal and Ethical Dilemmas in Respiratory Care a worthwhile addition to any Issues clinician's library. However, prove most effective book and this text will when used as a springboard for The as a group dis- cussion. accom- exercises, and discussion points allow the student JUNE 1998 VOL 43 — NO 6 author's well-chosen examples, or the clinician — realistic ethical Whether one chooses reason than to armed," I and moral the safety of a classroom. know to read that it for no other "forewarned is fore- book ranks as impor- Robert Hirnle MS RRT believe this tant reading. work- Each of of questions that form the RESPIRATORY CARE foundation for the readers' analysis and deci- In this section, the author briefly presents key ele- & software to deal with a Respiratory Care Program Highline Community College Des Moines, Washington 495 I* • Interactive Clinical Skills Software Computer- Assisted Hone your clinical skills Clinical Simulations with Interactive Clinical Skills Software. These 13 interactive, computer-assisted clinical & instructional simulations are divided into information-gathering & decision-making sections. Presents users with real-life scenarios that require assessment & treatment decisions. Each simulation is scored, & the user is provided with the coranswers & rationale for the simulation. Available in 31/2" disk format. Computer requirements: Windows 3.1 or higher rect Chest Trauma Simulation Muscular Dystrophy Simulation Item SPio Item 565 SPH $65 Status Asthmaticus Simulation Chest Trauma Item SP12 Item SPiio $65 S65 Drug Overdose Simulation neonate Item SPI3 Item SPiii $65 II Simulation Simulation II $65 Chronic Obstructive Pulmonary Cystic Fibrosis Simulation Disease (COPD) Simulation Item SPn2 S65 Item SPm S65 Pulmonary Rehabilitation Acute Respiratory Distress Simulation Syndrome (ARDS) Simulation Item SPn3 $65 Item SP15 S65 Developed for Daedalus Enlerprises. Inc., bg Hyperactive Soflware. Epiglottitis Simulation O Item SP16 S65 Epiglottitis Simulation • • Drug Overdose Premature neonate Simulation XJ Item SP17 565 L. O Simulation Chest i Simui Head Trauma Simulation Item SP18 S65 -z:::^::- j Test Your Patricia A Dooiley MS RRT and Charles G Postoperative Cough K Kasel MEd Debra Durbin in a Jr MD, Radiologic Skill Section Editors Man Exposed to Tuberculosis RRT, Rhonda L Kasten CRTT, and Neal J Moser Case Summary His social history included 1 20 pack-years of cigarette smok- ing and a history of alcohol abuse. A 66-year-old man presented to the emergency room, complaining of abdominal pain. Subsequent evaluation revealed A post- a perforated duodenal ulcer, requiring surgical repair. operative chest radiograph The was done (Fig. 1 and 2-pillow orthopnea. His current medications at owned several also went to homes of patients with tuberculosis to collect data for clinical active tests. exertion admission included inhaled albuterol and ipratropium bromide for treat- COPD. Twenty-seven years prior to admission, the had a positive tuberculin patient He patient pulmonary (COPD) characterized by extreme dyspnea on ment of his out using a mask. The where he worked with acid fumes with- ). patient's history revealed chronic obstructive disease clinical laboratories MD test. At that time, he was pre- scribed and initially treated with isoniazid and rifampin, iilthough after Debra MD; month 1 K Kasel the patient stopped taking these medications. MEd RRT; Rhonda L Kasten CRTT; and Neal J Moser Respiratory Care Program; Northern Kentucky University, Highland Heights. Kentucky. Rhonda L Kasten CRTT; Children's Hospital Medical Ms Kasten was a stu- Center. Cincinnati. Ohio. At the time of this work, dent at Northern Kentucky University. Highland Heights. Kentucky. Reprints & Correspondence: Ms Debra K Kasel MEd RRT. Respiratory Care Program, Northern Kentucky University. Highland Heights How KY 4 1099. Fig. 1. Postoperative chest radiograph. would you answer these questions? What abnormalities can be seen on the chest radiograph? What is What additional testing the differential diagnosis? would be helpful? Answers RESPIRATORY CARE • JUNE 1998 VOL 43 NO 6 & Discussion on next page 497 Test your Radiologic Skill Answers and fever and symptoms The chest radiograph reveals diffuse, prominent interstitial markings consistent with a chronic process. There hilar enlargement with prominent ating upward. There is is bilateral postsurgical air seen under the right hemidiaphragm. pneumonia. These may reveal loss of breath sounds and vocal but may also be normal. fremi- RML, RML collapse is often difficult to detect on posterior-anteradiographs because the RML is relatively slim and lies markings radi- interstitial increased density of the right middle lobe which suggests partial atelectasis or infiltration. There is examination tus in the chills related to obstructive often persist despite antibiotic therapy. Physical rior obliquely in the superior-inferior plane. It may, however, obscure the right cardiac border and straighten the contour of the heart shadow. Chest radiograph abnormalities are more Differential diagnosis includes granulomatous disease, mon com- and endobronchial lesions. infections, sarcoidosis, Obstruction could be caused by neoplasia, aspirated foreign often seen in the lateral view.' The volume collapse of the right middle lobe is loss resulting from seen as a triangle of increased density between the minor fissure and lower half body, pulmonary secretions, broncholiths, or allergic bron- chopulmonary aspergillosis. Additional beneficial testing to clarify the nature middle lobe process includes a chest 2), lateral chest computed tomographic of the right radiograph (Fig. scan, and bronchoscopy. Discussion For right from fer radiograph demonstrated this patient, a lateral chest middle lobe collapse. This patient right may therefore suf- middle lobe syndrome (RMLS), which is defined as a recurrent or chronic collapse of the middle lobe of the right lung. Graham and colleagues' described a con- dition they attributed to bronchial compression of the right (RML) bronchus from peribronchial lymphadenopathy. Although RMLS commonly presents with middle lobe pulmonary symptoms, such as cough, hemoptysis, and wheezing it can be asymptomatic and detected only by chest roentgenography. sexes and is It occurs in children and adults of both associated with numerous conditions. RMLS can be divided pathophysiologically into obstructive and nonobstructive types. Obstructive RMLS may lesions, extrinsic be caused by endobronchial compression of the right middle lobe bronchus, and granulomatous adenopathy secondary infection.-^ compression of the Additionally, neoplasm common cause of extrin- has been implicated."*^ The most sic "• to sarcoidosis or metastatic RML bronchus is enlargement of peri- choliths, aspirated foreign bodies (particularly in children), and inspissated secretions associated with cystic bronchopulmonary is most susceptible is lateral ventilation present in the right tributes to ful in or the One possible expla- be the relative lack of col- tic to collapse. nation for this propensity to collapse the middle lobe.** This con- poor mucus clearance with peripheral plugging of the small airways. The most common symptoms marked is in patients with RMLS are in Fig. 2. evaluating bronchial patency, lymph node enlargement and calcifications, or other causes of extrinsic compression RML airway.'*'" High-resolution CT scans may also helpfijl in identifying subtle abnormalities.'* Flexible fiberop- bronchoscopy is required to evaluate the patency of the RML bronchus. The treatment of RMLS is directed at the underlying cause. was asymptomatic and treat- ment involved bronchodilator therapy, mucous clearance tech- In this particular case, our patient cough, hemoptysis, dyspnea, chest pain, audible wheezing. 498 right Computerized tomographic (CT) scans of the chest are help- RML bronchus However, the RML RMLS, patent with no apparent obstruction. is of the major fissure. This fibrosis or aspergillosis.''-^ In the nonobstructive type of bronchus chest radiograph showing the collapse of the middle lobe. lymph nodes. Less common causes include bron- bronchial allergic Fig. 2. Lateral niques and antibiotic therapy. The RESPIRATORY CARE patient • had previously under- JUNE 1998 VOL 43 NO 6 TEST YOUR Radiologic Skill gone evaluation for RML collapse, which failed to identify 4. Lazarus SC. Disorders of intrathoracic airways. JA, an obstructive source such as endobronchial lesions or extrinsic compression of the for active tuberculosis. RML bronchus. There was no evidence The from the hospital 5 days patient did well Poe RH. Middle-lobe sion. 6. atelectasis NY State J Med due 7. Med lobe syndrome. Post- lobe syndrome. Ann Thorac Surg 9. S, Oda M, Hayashi Y, Ohta Y, Shimizu Treatment of bronchial stricmre due to endobronchial tuberJ Surg 1997;21(5):480-487. RESPIRATORY CARE Eraser sis Wantanabe Y, Murakami World J. Isolated mid- and treatment of the so- Thorax 1980:35(6):449-452. aspergillosis. CR, Terry PB, Traystman aller- Ann Allergy 1980;44<4):217-2I9. Menkes HA. Collateral ven- RJ, and the middle lobe syndrome. Am Rev Respir Dis 1978;1 18(2)305-310. 1983;35(6):679-686. culosis. bronchopulmonary Inners tilation 1948;4:29. Wagner RB. Johnston MR. Middle J, et al. Nadel Eisenberg RS, Valdesuso C. Middle lobe syndrome secondary to gic 8. grad JF, W B Saun- to sarcoidosis with pleural effu- Bertelsen S, Struve-Christensen E, Aasted A, Sparup called middle lobe syndrome. Graham EA, Burford TH, Maver JH. Middle Murray 1978;78(13):2095-2097. dle lobe atelectasis: aetiology, pathogenesis, REFERENCES In: Textbook of respiratory medicine. Philadelphia: ders; 1994:1471-1482. 5. and was discharged after surgery. editors. • JUNE 1998 VOL 43 NO 6 RG, Pare JA, Pare PD, Eraser RS, Genereaux GP. Diagno- of diseases of the chest, 3rd ed. Philadelphia: W B Saunders; 1988:519-529. 10. Gudmundsson G, Gross TJ. Middle lobe syndrome (review). Am Fam Physician 1996;53(8):2547-2550. 499 Nonimmune Hydrops Fetalis Kathy Douglas Case Summary RRT color and was moving all extremities. His blood pressure was within normal limits and he was transferred to the newborn A 37-year-old woman presented to our obstetrics service The estimated fetal gestation was 34-36 weeks by dates. This was the woman's fourth pregnancy; she had three living, healthy children. An ultrasound at 30 weeks of intensive care unit (NICU). Soon in active labor. no gestation revealed fetal The anomalies. had declined patient alpha Fetoprotein screening. All prenatal blood work was nor- mal. Rupture of membranes occurred 9 hours prior to meconium stained. deliv- male infant presented cyanotic and delivery, the admission to the //g/kg/min was added. Morphine sulfate for sedation. Bright red blood therefore, he of age the baby showed increasing orally intubated with a 3.5 endotracheal tube (ETT). Breath sors, the kg infant was given Apgar scores of 2 at utes for a heart rate > 100 beats/min. The 3. 165 1 and 5 min- He had no other spon- both at 0.3 became at 10 mg was given surfactant. edema of his tamine hydrochloride was started furosemide was given bilaterally. again was suctioned from was not given exogenous abdomen were noted to be markedly distended. His extremities were atrophic. He was immediately floppy. His neck and sounds with hand ventilation were equal NICU the infant the By ETT; 10 hours trunk and neck. His urine output was lagging behind his fluid intake, so dobu- ery and the fluid was lightly Upon after hypotensive and a dopamine hydrochloride drip at 10 jUg/kg/min and to increase renal perfusion 3-mg and urine output. In addition to complete parenteral support with pres- baby was maintained on mechanical ventilation with an Fdo: between 0.75 and 1.00. His second chest radiograph, taken at 12 hours of age, is shown in Fig. 1. taneous activity or breathing. Cord blood gases were significant: Pa02 10 mm Hg (1.3 kPa), Paco: 89 mm Hg (1 1.9 kPa). pH of 7.08, bicarbonate level of 25.3 mEq/L, and a base deficit of -7.9. The venous cord blood values were: Pq: 28 (3.7 kPa), Pco: mEq/L, and By 46 mm Hg (6.1 kPa), pH 7.3, mm Hg HCOj 10 minutes of age the infant had slowly improved color while receiving positive pressure ventilation by ual resuscitation at an Fdo: of ities 1 .(X). He was moving and showed some respiratory and venous lines were inserted. effort. and glucose. The baby's mg%, initial Coombs test, arterial for blood blood cul- blood glucose screen was necessitating a push of 8-cc DiqW. A 300-mg dose of ampicillin was given. The infant's heart rate remained ble in the 1 in man- his extrem- Umbilical Blood was drawn gases, complete blood count, type. ture, 21.7 a base deficit of -4.2. sta- 50 beats/min range, and effective ventilation was provided with a time-cycled, pressure-limited infant ventilator. SpO: remained above manate was given of 32. for a 90%. A bolus of 30 mL of plas- blood pressure of 40/22 with a mean By 30 minutes of age the infant continued to have good Kathy Douglas RRT, Departmenl of Respiratory Care. The Toledo Hos pital, Toledo. Ohio Correspondence: Kathy Douglas RRT. Department of Respiratory Care. The Toledo 500 Hospital, 2142 N Cove Blvd. Toledo OH 4.^606. Fig. 1 . The infant's chest radiograph taken at 12 hours of age. RESPIRATORY CARE • JUNE 1998 VOL 43 NO 6 TEST YOUR Radiologic Skill How What is shown on Based on this chest this radiograph, What procedure is would you answer these questions? radiograph? what might be included in the differential diagnosis? indicated? Answers RESPIRATORY CARE • JUNE 1998 VOL 43 NO 6 & Discussion on next page 501 Test Your Radiologic Skill Answers The chest radiograph revealed that the ETT is in good posi- tion at the third thoracic vertebrae. Tips of the umbilical and arterial catheters tions. can be seen and are venous acceptable posi- There are monitoring devices (electrocardiogram leads) over the left lower quadrant and are diffuse bilateral pulmonary are visible, particularly in the ble can be seen in the is in left in the right upper chest. There infiltrates. Air bronchograms left chest. The stomach bub- upper abdominal quadrant. There a large pleural effusion on the right. (Fig. 2) Included in the difTerential diagnosis for this patient would be the causative or associated factor(s) for the pleural effusion, which are respiratory distress syndrome, hypoplastic lung, or pneumonia. The indicated procedure the compressed right lung. is to insert a chest tube to expand . Test Your Radiologic Skill REFERENCES of acceptable blood gases and acid-base balance. The baby's initial hypoglycemia was immediately corrected. Coagulopathy and hyperbilirubinemia were managed and corrected within the baby's first days of life. He was extubated and 1 (CPAP) on his fifth hospital day. On his tenth day of life the baby was weaned from CPAP. He was given low flow oxygen via nasal cannula. Chest tubes were clamped and then removed at 8 and 1 days of life. He was placed in an open crib on his twelfth hospital day and discharged by 4 weeks of age. 2. AE, Bain AD. 3. 4. pected prior to delivery. Survival ability fetalis may depend on of a highly skilled resuscitation team delivery. Although the can be sus- infant's survival the avail- is enhanced by the ability to 5. at the infant's good out- setting and editors. Diseases in the fetus P. Gastrointestinal disorders. In: Core curriculum phia; In: and neonatal physi- Reed GB, Claireaux and newborn. St Louis: WB Saunders; Beachy P, Deacon J, edi- for neonatal intensive care nursing. Philadel- 1993. Apkon M. Pathophysiology of hydrops Rejjal natal ARA, Rahbeeni Z, al-Zahrani AF. management J Perinat 6. provide expert manage- ment and intensive support in both the delivery in the immediate postnatal period. Fetal 1992. Blood disorders. 1989. tors. fetalis. Semin Perinatol Med in Prognostic factors and pre- non immune hydrops fetalis are still a dilemma. 1996;24(5):461-466. human parvovirus B 19 infection in idiononimmune hydrops fetalis. Am J Obstet Gynecol Jordan JA. Identification of pathic come Z. 1995;19(6):437-446. may be determined primarily by prenatal factors, the likelihood of a Beachy and other causes of neonatal edema and WW, editors. WB Saunders; Mahnovski V, Pavlova CVMosby; 1 most cases, the presence of hydrops fetali.s RA, Fox ology. Philadelphia: nasal continuous positive airway pressure In Phibbs RH. Hydrops ascites. In: Polin placed on 1996;174(l):37-42. 7. Gallagher 8. Jones DC. PG. Seminars in perinatology. Semin Perinatol I995;19(6):435-436. Nonimmune fetal hydrops: diagnosis and obstetrical man- agement. Semin Perinatol 1995;19(6):447-461. 9. ACKNOWLEDGMENT I thank Brian Bradley RESPIRATORY CARE MD for reviewing this manuscript. • JUNE 1998 VOL 43 NO 6 Maisels MJ. Jaundice. editors. In: Avery GB, Fletcher MA, MacDonald MG, Neonatology: pathophysiology and management of the new- bom, 4th ed. JB Lippincott; 1994. 503 Distinguished Lectures in Respiratory Care'' Audiotape Series Assessment-Based Respiratory Care nEW! Watch Learned about Mechanical Ventilation Five Things It!- Practical Aspects of nitric Oxide By John By John Thompson, RRT, MO minutes. E. Item 0174 Item C725 HEW! Metabolic Testing-Does It Change the Exercise Prescription? W By Mark MD Millard. "JO Ventilator Weaning Sleep Medicine from A to Z-Part minutes. BiPAP '-CPAP Evaluation of Bronchodilator Therapy By Thomas A. Barnes. EcJD. RRT. 30 minutes. Item CM20 in Obstructive Sleep Apnea By Paul A. Selecky. M5 minutes. Ventilator Weaning from A to Z-Part 2 Item C48I Use & Titration of nasal CPAP & BiPAP* 60 minutes. By Timothy By Pamela Ventilator Weaning from A to Z-Part 3 B. Op'l Holt. EdD, RRT. 30 minutes. Item C^(o By James Item 0424 Minkley. RRT, CPFT. RPSGT. MO minutes. L. Item C7I2 Oxygen Therapy Burchfield. RRT. 30 minutes. E. 60 minutes. Subacute Care Item 0454 Item CMSO What Should the Management riEW! Care Plan Development By John Item Sabo, MS, RRT. ^0 minutes. S. CH5 By Emmett C. Murphy. PhD. 50 minutes. Item CiSM By Kathleen M. Item 0740 Griffin, PhD. mo minutes. By Dianne Item CI085 By Kevin Stewart, BS, RRT. 20 minutes. J. Item C55^ A. Cornish. RRT. mo The RCP Inspection By Dianne Ehrmeyer, PhD, MT (ASCP). S. 30 minutes. A. Souza, RD. mo minutes. Item 0445 to Measure & How By Vianna Zimbel. BS, CRTT. MO minutes. in L. By Jeffrey What Outcomes minutes. Item Cioqs Preparing the Laboratory for Item 0455 Subacute Care Lewis, MS. RRT. 20 minutes. Outcomes MeasurementWhat Lies Ahead Item 0714 Item CiiOM By Jeffrey A Souza, Rn. mo minutes. Pulmonary Rehabilitation Item 0465 Traveling with Oxygen Pulmonary Rehabilitation, Outcome Measurements: nEW! Building your Outcome Management Goals By James Guidelines for Evaluating Efficacy By Michael Boroch. MBA. RRT. 30 minutes. Home Care K. Stoller. MD. 25 minutes. Oil 54 By Barry M. Make, MD. M5 minutes. Home Care RCPs & the Law Item 0343 By Thomas M. Antone Developing a Marketing Plan for mo minutes. IV. Item Ci72 By Ellen nelson, MBA, Rn, RRT. 30 minutes. & Health Care Reform Shrake, MA, RRT, FACHE. MO minutes. L. Individual Tapes^ Item 0570 Ventilation Overview of Managed Care Models By Patrick j. Dunne, MEd, RRT. 20 minutes. Item cs^^ Respiratory Muscle RetrainingDoes It Improve Function? nitric Appropriate Is Ventilator Oxide neil R. Management Today? Order Maclntyre. MD. 35 minutes. Scientific Rationale for Clinical Use of nitric Oxide Thompson, RRT. mo minutes. of Acute Respiratory Failure Without Intubation By Robert M. Kacmarek. PhD. RRT. Item 0315 HEW! Current & Future Applications of nitric Oxide Ventilator M Kacmarek. Item C7I5 PhD. RRT. MO minutes. 36 8, David J. Audiotapes & Save! Pierson, MD. 50 minutes. Item C705 By Robert All Item 0225 Management HEW! [ $15 each nonmembers) Item 0815 What By • • ($20 By Barry M. Make, MD. MO minutes. Item C62<( By John Item 0545 Pulmonary Rehabilitation Programs Hospital Restructuring By Kevin o Tobin. MD. M5 minutes. What Are Outcomes & Why Are They needed? Lewis, MS. RRT. mo minutes. L. By Karen strating Value, Creating Opportunity o J. Outcomes nEW! Using Outcome Data RCPs & Health Care Reform: Demon- o By Martin Item CI075 nEW! Providing Subacute Services in a Managed Care Environment Item OS Do When a Patient "Fights the Ventilator?" The RCP's Value as a Case Manager By Sharon Clinician nEW! Defining Subacute Care Services: Patients, Settings, & Outcomes to Justify Subacute Care Services The Work Redesign Challenge O < < Item 0384 Evaluation for Chest Physical Therapy Evaluation for N* i 60 minutes. Item C825 M M CM A M I Marini. MD. 30 minutes. J. to Management Avoid Barotrauma By David J Item 0405 Pierson, MD. mo minutes. itemcqqq ($468 $351 nonmembers) News There to is releases about no charge new products and services will be considered for publication tor these listings. RESPIRATORY CARE, New Send descriptive Products & Services Depl. The Reader Service Card immediately follows New Products in this section. release and glossy black and white photographs & the authors 1 1030 Abies Lane, Dallas TX & Services 75229-4593, advertisers index at the back of the Journal. Measurement System. The system consists of a patented fiber optic sensor which attaches directly to the patient's arterial line. Arterial blood gases are obtained by draw- ing a blood sample into the sensor. After a 60-s measurement time, the blood to the patient. is returned Blood gases can be obtained without any blood loss or contact with the sample by the clinician. According to system Instru- mentation Laboratory, this Test Strips for Disinfectant suited for critically patients, including Solution. neonates, pediatrics, and adults. For Control III Designed Maril Products Inc reports that now Test Strips are available. to verify proper solution prepa- ration of Control III disinfectant, the strips change color to confirm proper mixing. Control III disinfectant remains active up to 14 ill is well more information from Instrumentation Labora- number 161 on tory circle vice Card in this issue, or the Reader Ser- send your request and control bacterial, viral, it has received 510(k) marketing clearance FDA for its Portable BioZ^^' non- from http://www.aarc.org/buyers_guide/ invasive cardiac function monitoring sys- the tem. CardioDynamics International says the BioZ System noninvasively monitors up commonly used to disinfect is Corporation reports that ics International electronically via "Advertisers Online" at days after mixing when stored in a covered container and NONINVASIVE Cardiac function Monitoring System. CardioDynam- and fungal hemodynamic parameters within 12 to minute 1 pathogens on hard surfaces and equipment. and has been used as an alternative For more information from Maril Products invasive monitoring methods for critically Inc. circle vice Card number 160 on in this issue, the Reader Ser- ill patients. For more information from Car- dioDynamics or send your request International Corporation cir- number 163 on electronically via "Advertisers Online" at cle http://www.aarc.org/buyers_guide/ in this issue, or tronically to the via the Reader Service Card send your request elec- Online" "Advertisers at http://www.aarc.org/buyers_guide/ Patient central monitor. MarInhaled Corticosteriod Powder. quette introduces the Prism suite of network GlaxoWellcome announces products and applications designed to powder form of flu- Rotadisk®, an inhalation ticasome propionate, is scription in the U. S. the drug ment for young is as is that Flovent* now available indicated as a preventive treat- asthma in adults and children as 4 years of age. Flovent Rotadisk a foil-covered disk containing 4 blisters, imum at a variety to the infor- of locations with a min- of hardware. The client server PC- Windows based system has a 32-bit NT mation Center application. The company says when and a dose of medthe patient inhales For more it can monitor up to 16 patients simultane- up ously, continuously displaying iological waveforms/patient on its to 4 phys- main dis- information from GlaxoWellcome circle play screen. For more information from number 162 on Marquette, circle number 164 on the Reader Blood Gas measurement System. in this issue, or Instrumentation Laboratory announces the tronically • mation tem. Marquette offers the Clinical Infor- through the mouthpiece. RESPIRATORY CARE applicadons on a single system while providing access into a specially designed plas- ication dispensed SensiCath Blood Gas pitals to consolidate inhalation device called the Diskhaler®, a blister can be pierced GEM resentative says that the system allows hos- operating system. Designed for the Prism sys- Once loaded tic in- A company rep- powder medication. or compartments, of launch of the by pre- GlaxoWellcome says crease caregiver efficiency. the Reader Service Card send your request elec- via "Advertisers Online" at http://www.aarc.org/buyers_guide/ JUNE 1998 VOL 43 NO 6 Service Card in this issue, or send your request Online" electronically at via "Advertisers http://www.aarc.org/buyers_guide/ 505 Sound Images, A ARC American Association New Orleans, Any 12 Any 12 Any 12 Any 12 Louisiana Audio Tape Order Form Post- Conference Care for Respiratory 43rd International Respiratory Congress December 6-9, 1997 Inc. Audio Tape Specials Price per Audio Tape-$ 9.00 in FREE Albums $ 99.00 (Save tapes in FREE Albums $ 198.00 (Save tapes in FREE Albums $ 297.00 (Save tapes in FREE Albums $ 396.00 (Save tapes 1 1 1 1 Missed the 43rd International Respiratory Congress held December 6-9, 1997 in New Orleans, Louisiana? is your chance to acquire the valuable information that was presented by purcahseing audio tapes of the presentations. You can order directly from Sound Images, Inc. by phone (303) 649-1811, by fax (303) 790-4230, by mail to 7388 S. Revere Pkwy., Suite 806, Englewood. CO 801 12, or by email to SoundImages@compuserve.com. Please allow 21 days for delivery. Here Q Q Q AARC97-00 AARC97-01 AARC97-03 AARC97-04 AARC97-05 AARC97-06 AARC97-07 AARC97-08 AARC97-09 50 Years of Respiratory Care, Robert R. Weilacher Keynote Address, Richard M. Scrushy Long-Term Acute Care Hospitals, David E. Moseley Part 1-Meehanics: How the Lungs Work and How Diseases Affect Them, Kenneth P. Steinberg How To Implement a Program, Julien M. Roy How To Write a Business Plan and Market Your Program, Trina M. Limberg More Reimbursement, Julien M. Roy Outcomes, Outcomes, Outcomes, Trina M. Limberg Competency Assessment - Who Needs It?, Robert Hospital Environment, Richard Sheldon AARC97-36B Ask the Experts!, James Q Development of Age-Specific Education Material, Melva Proudlock PeerAssessmentCanTakethe"YUK!"Outof Performance Appraisals, AARC97-38 Q Scott Reistad Assessing the Aging Adult, John E. Carlson I've Fallen and I Can't Get Up!: Promoting Q 1 5 Nobody is "Moving" Time?, Jerry AARC97-16 Ventilation 17 AARC97-47 AARC97-48 "Moves" - (Oscillation, Nitric Oxide, Their Uses in Transport, Adams Kathleen S. Difficult "Moves": Places, Kathleen AARC97-18 Workshop: AARC97-46 What Do We Do With Our A. Focht Conventional) AARC97 - S. Disease AARC97-45 Home Safety for the Older Patient, Melaine Giordano AARC97- AARC97-42 AARC97-43 AARC97-44 AARC97- 2 Telemedicine in Home Care, Nicholas J. Macmillan AARC97-13 The Go-Goes, the Slow-Goes, and the Can't-Goes: AARC97-14 AARC97-49 Difficult Airways and Difficult George G. Burton. Jeanne Pollock. Judy Tietsort of Measuring Outcomes in Respiratory Critical Care, William J. Sibbald AARC97-22 Star Trek Respiratory Care: Going Where No One Has Gone Before with Telemedicine, Michael W. Runge AARC97-23 Use of Invasive Monitoring in a Patient in Acute AARC97-21 The "Whys" and "Wherefores" Q Respiratory Failure, Jolm W. Hint. Charles G. Durhin, Jr AARC97-24 Experiences in Developing, Selling, and Managing DME Company-Based Asthma Education and Intervention Program, Joseph AARC97-25 Competency Documentation S. for AARC97-52 Mechanical P. L. CO2 Steinberg Post AARC97-30 Q a AARC97-3 Financial Tools for Today's Manager, Kevin L Shrake AARC97-32 "Partnering" in Health Care, Karen J. Stewart AARC97-33 Program Overview; Medical Direction of Patient-Driven Protocols To Help Control Utilization, Kevin L. Shrake 1 & G AARC97-35 Inactive Medical Director: What Can Anyone Do?, George G. Burton RCP/Medical Director Team, David M. Burns 7388 S. Revere Pkwy, #806 Englewood, CO for Inclusion of Respiratory Services as Part of AARC97-59 AARC97-60 AARC97-61 AARC97-62 Managed Care Care Contracts, Colleen Bittner. Jeanne M. Pollock in a Pulmonary Function Lab: How To Get to the Bottom of Unexplained Dyspnea, Fernando Martinez. John Wald Neurologic and Cellular Causes for Dyspnea: A Neurologist's Viewpoint, John Wald Case Studies for Unexplained Dyspnea Connected with Neurologic Disorders, Fernando Martinez An Approach to Technology Assessment, David H. Walker Critical Care is Expensive, ye/f//«vrfH Standardization of Technology - A Case Study, AARC97-63 Part 3-Acid-Base Balance: How It Works and What Can Go Wrong, Robert B. Schoene AARC97-64 Home Care in Europe; Socialized Medicine; 65 66 2 tapes Epidemiology of Home Mechanical Ventilation in Europe; The Providers of Respiratory Home Care Services in Europe, Patrick U'gcr Susan Sortor Leger AARC97-69 How Did the Dinosaurs Breathe?, David J. Pierson AARC97-70 Pulmonary Negligence - A Mock Trial, A. L. DeWitt. 2 tapes SOUND IMAGES, INC. Maclntyre John W. Salyer Present, James K. Stoller AARC97-34 The Apnea Monitoring The Next 50 Years, Celeste Beal Q Respiratory Care: Past Infant Lewarski Practice of Routine Ventilator Checks, AARC97-54 Techniques AARC97-58 AARC97-27 Pulmonary Rehabilitation and the Non-obstructive Lung Disease Patient, John E. Hodgkin AARC97-29 Pressure-Controlled Ventilation (PCV): What's with the Pressure?, Marshall R. Home S. Ventilation: AARC97-57 The "Shocking Truth" Lewarski Out-Practical Applications, Kenneth Neal AARC97-53 The a JCAHO and Performance Improvement, Daniel J. Grady AARC97-26 Part 2-Gas Exchange: Getting Oxygen In and Q of a Program, Joseph Management Across the Continuum, Studies and How To Decannulate, Mike Harrell Communication Alternatives for the T^acheostomized Patient, Mary Spremulli Monitoring and Delivery of Inhaled Nitric Oxide, Robert M. Kacmarek Use in Adults, Richard D. Branson Use in Pediatrics, Cardiac Surgery and Sickle Cell Anemia, Peter Betit Use in Neonatal Hypoxemic Respiratory Failure, John E. Thompson Financial Analysis of Home Care Business Operations, Patrick J. Duime Merging Sales and Clinical Skills, Robert W. King Clinical Products' Development and Marketing, Patrick J. Dimne A Success Story in Home Care: Development and Management Adams 2 tapes Q Blockade: Etiology and Prevention, John W. Hoyt Introduction: Why, How, When, Types of TXibes, and Problems, Mike Harrell Impact IVacheostomy on Quality of Life, Mary Spremulli AARC97-39 AARC97-40 Weaning and Decannulation: Swallowing 1 Q George G. Burton. AARC97-37 Prolonged Weakness Following Neuromuscular AARC97-41 Q K. Stoller. Richard Sheldon, David M. Burns R. Fhick. Jr. Q AARC97-10 AARC97-11 AARC97-36A RCP/Medical Director Interactions OuUide the Edward Richards 80112 Phone: (303)649-1811 Fax: (.303) 790-4230 e-mail: Soundlmages@compuserve.com AARC97-71 Q New Understanding All That Jazz... The AARC97-92 Successful Strategies for Blood Infant/Pediatric Ventilators, Charles B. Speunnan AARC97-72 A Nightingale's Song: Mechanical Ventilation, John AARC97-73 Liquid Ventilation: From Q Q a Q AARC97-95 How Can My AARC97-79 Medicare Denials: The Provider's Joseph Skilled Nursing Facihties, AARC97-81 Fraud and Abuse Gary A. Gruver Activities in Post-acute Q AARC97-87 Your Profession: Agency Updates - a ATS What They Say Improves Outcomes, Karen a Q Q Is True?. J. Stewart. Robert M. Kacmurek, Sharon S. Ehrmeyer Susan B. Blonshine AARC97-103 The 6-Minute Walk Is Nothing When Compared to a and 104 Complete Exercise Evaluation/Charting Should Be Done by Exception Instead of by Conventional Means, Carl Mottram. Gretchen Lawrence. Patricia Ann Doorley. Gary W. Kaujfman AARC97-105 Managed Care Curricula, Shelley C. Mishoe AARC97-106 Wellness and Disease-Prevention Curricula, William Q Q Q F. Galvin AARC97-107 Disease Management Curricula, Joseph L. Rau AARC97-108 Gerontology Curricula, Helen M. Sorenson AARC97-I09 Smoking Cessation Curricula, Crystal L Dunlevy Guidelines for the Diagnosis and Management of Asthma: AARC97The Expert Panel Report II, Allan T. Luskin Impact on Quality of Life: Recent Advances in AARC97-1 Asthma Management, Andrew P. Greening AARC97- 2 Safety and Efficacy of Steroids in Asthma, 1 1 Q a 1 1 1 1 Allan AARC97-113A JRCRTE-NBRC, a Tell If Respiratory Practitioners/Point-of-Care Testing and 102 AARC- Kerry E. George. Carole J. Miller. Benjamin F. George AARC97-89 Part 1 -Ventilator-Associated Pneumonia: Pathogenesis and Risk Factors, Marin H. Kollef AARC97-90 Part 2-The Prevention of VAP in the Year 2000, Marin H. Kollef AARC97-9I The Bronchial Provocation Challenge: Meeting the I Rau AARC97-1(X) What Do I Need To Know about the Lung Transplant Patient?, Patricia Ann Doorley AARC97-101 Ventilator Care Should Be Done by Credentialed Care and Their Effect on Respiratory Care; Panel Discussion, Panelists: K. Cornish, T. Carter, G. Gruver M. Welch AARC97-82 Five Things I Learned This Year about Lung-Voliuneand 83 Reduction Sm^gery/Five Things I Learned This Year About Creating Credibility Outside Respiratory Care, Catherine M. Foss/Barbara L. Butler AARC97-84 Five Things I Learned This Year about the TVeatment and 85 of COPD/Five Things I Learned This Year About Point-of-Care Testing, Dm '«// Pierson/Catherine M. Foss AARC97-86 Five Things I Learned This Year about Patient Compliance through Education, Gretchen Lawrence Settings L. Neil R. Maclnryre Perspective, of Respiratory Care Services in Ehrmeyer AARC97-96 What Do The Numbers Mean?, Cr\stal L. Dunlevy AARC97-97 Part 4-Exercise: Normal and Abnormal Responses and How To Use Them, Robert B. Schoene AARC97-99 Report from the 1996 Consensus Conference, Tami Carter AARC97-80 Reimbursement Pass Shelley C. Mishoe McPeck Baby's Singing the Blues... Jazz Him Up with Waveforms!, Katie Sabato AARC97-76 Invasive Bi-Level Pressure Ventilation in Neonates, Infants, and Children: A Retrospective on Three Years of Utilization, Curtis J. Bauer AARC97-77A International Respiratory Care: Around the World in Four Hours, Jerome M. Sullivan. Suhharee Suwanjutha, Alan C. Biggs AARC97-77B international Respiratory Care: Around the World in Four Hours, Toshihiko Koga, R. Vijai Kumar. Hector L^on Garza AARC97-77C International Respiratory Care: Around the World in Four Hours, Pierre Emery. Tamotsu Sugimoto, Airton Stinglein Crespo. Kamarudin Jaulam AARC97-78 Medicare Denials: The Payer's Perspective, Melvin A. Welch, Jr AARC97-75 S. Meet to AARC97-93 Pulmonary Function Testing: What Do You Need and When Do You Need It?, Charles G. Ir\-in AARC97-94 How Can I Manage the Information Explosion?, Delivery Challenges during Pediatric Mechanical Ventilation, Michael Gas Labs (JCAHO, CAP, CLIA) and Inspections, Sharon a W. Salver the Abyss to the Bedside, Jeanette Asselin AARC97-74 Meeting Aerosol the Regulations Outcomes of Pediatric T. Luskin A Cost-Effective Program for Children Hospitalized with Asthma, Timothy R. Myers AARC97-113B Panel Discussion: Drugs and Medications - What's Right and What's Wrong, Andrew P. Greening. Allan T. Luskin. Timothy R. Myers AARC97- 1 4 Pre-hospital and Inter-hospital Ti'ansport, Jerry A. Focht AARC97-1 15 Ventilation during Transport and Diagnostic Studies in Acute Care Hospital, Robert S. Campbell AARC97- 6 Ventilatory Support in the Operating Room, 1 a 1 Charles G. Durbin. Jr AARC97- Guidelines, Charles G. liTin 1 1 1 7 Use of Ventilators in the Home, Robert M. Kacmarek Optional Overnight Shipping Service: Please supply us with your FedEx account number or FedEx can charge your credit card. (This to the First Name Last/Family Mailing Address {include business City, State/Country L name Name if mailing to Zip/Postal Code Q Purchase Order business address) I Daytime Telephone i ) Fax G Cash QTravelers Checks Check (Payable to (Add Sound Images. 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VOLUNTARY MEcJJfccH THE FDA MFIJK AL F R U () 1) T S I REFORTINt. PRIK.RA 2 Age at FOA Use Only (Resp No. 0910-0291 Expires: 4/30/91 Cai Page C. A. Patient information Patient identifier i reporting For by health professionals of adverse events and product probletns 3 Sex time 4 Weigtit Suspect medication(s) Name 1 (give labeled strength S mfr/labeler, if known) of event: female I I I I Date In of confidence birtti: male Adverse event or product problem B. Adverse event 1 lJ 2 Outcomes (cfieck all and/or QJ Product problem (eg , I I Diagnosis for use 6 Lot # Therapy dates (if unknown, give duration) defects/malfunctions) I I I I congenital anomaly I 4 3. disability I life-ttireatening I Dose, frequency & route used attributed to adverse event that apply) deatfi I 2 hospitalization 5 (indication) - initial or prolonged event #1 Dyes #2 Dyes \_\ othe (If known) Exp. date (if 4 Date of ttiis report 3 Date of Event abated after use stopped or dose reduced required intervention to prevent permanent impairmenfdamage known) 8 D D no Dfe"'' no DgggPy"'' Event reappeared after reintroduction 5 Describe event or problem NDC 9 10. 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Title Page, Text, References, Tables, Respiratory Care welcomes original manuscripts related to the and Illustrations may be included. science and technology of respiratory care and prepared accordthese Instructions and the Uniform Requirements for ing to Special Article: A pertinent paper not fitting one of the foregoing Manuscripts Submitted to Biomedical Journals [Respir Care 1997; categories 42(6):623-634]. Manuscripts are blinded and reviewed by pro- Editor before writing or submitting such a paper. fessionals who are for all aspects of the manuscript message is and receive galleys clear and it is to proofread copyedited so that conforms to the Journal's papers are copyrighted by Daedalus Inc and may style. Published Editorial consultation On request, is is provided for it may present an opposing opinion, clarify a position, or bring a problem into focus. A Letter: available at any stage of planning or writ- specific guidance A paper drawing attention to a pertinent concern; Editorial: not be published elsewhere without permission. ing. be acceptable as a Special Article. Consult with the experts in their fields. Authors are responsible before publication. Each accepted manuscript its may all publication cat- To receive these Instructions and related materials, write RESPIRATORY CARE, 600 Ninth Avenue, Suite 702, Seanle WA signed communication, marked "For publication," about prior publications ics. in this Tables and illustrations Journal or about other pertinent top- may be included. egories. to 98104, call Publication Categories Blood Gas Comer: gas values (206) 223-0558, or fax (206) 223-0563. A brief, instructive case report involving blood — with Questions, Answers, and Discussion. Drug Capsule: A mini-review paper about & Structure that includes discussions of Research Article: It A a drug or class of drugs pharmacology, pharmacokinetics, and pharmacotherapy. report of an original investigation (a study). includes a Title Page, Abstract, Introduction, Methods, Results, Discussion, Conclusions, Product Sources, Acknowledgments, Ref- Graphics Comer: A brief case report incorporating waveforms for monitoring or diagnosis — with Questions, Answers, and Discussion. erences, Tables, Appendices, Figures, and Figure Captions. Evaluation of Device/Method/Technique: uation of an old It or new A description and eval- Kittredge's Comer: care equipment device, method, technique, or modification. rial A brief description of the operation of respiratory — with information from manufacturers and comments and edito- suggestions. has a Title Page, Abstract, Introduction, Description of De- vice/Method/Technique, Evaluation Methods, Evaluation Results, PFT Discussion, Conclusions, Product Sources, Acknowledgments, Ref- function erences, Tables, Appendices, Figures, and Figure Captions. Corner: Like Blood Gas Comer, but involving pulmonary tests. Com- parative cost data should be included wherever possible. Cardiorespiratory Interactions. interaction A report of a clinical case that is uncommon, or was Case Report: managed in a new way, must be associated with or is exceptionally instructive. All authors the case. A case-managing physician must either be an author or furnish a letter approving the manuscript. Its components ry, are Title Page, Abstract, Introduction, A case report demonstrating the between the cardiovascular and respiratory systems. should be a patient-care scenario; however, the case theme — is the systems interaction. equations, and a glossary. See the TORY Care for more — CRI is characterized by figures, March 1996 Issue of RESPIRA- detail. Case Summa- Discussion, References, Tables, Figures, and Figure Captions. Test Your Radiologic Skill: Like Blood Gas Comer, but involv- ing pulmonary medicine radiography and including one or Review Article: A comprehensive, critical review of the literature and state-of-the-art summary of a pertinent topic subject of at least line, Introduction, 40 published research Review of the that has articles. Title Literature, been the may graphs; may more radio- involve imaging techniques other than conventional chest radiography. Page, Out- Summary, Acknowl- edgments, References. Tables, Appendices, and Figures and Captions It the central Review of Book, Film, Tape, or Software: A balanced, critical review of a recent release. be included. Preparing the Manuscript Overview: A critical review of a pertinent topic that has fewer than 40 published research articles. Print Update: been A report of subsequent developments in a topic that has critically reviewed in this Journal or elsewhere. RESPIRATORY CARE Manuscript in. x in. (216 x 279 mm) mm) on all sides of the page. Use on one side of white bond paper, 8.5 with margins of at least 1 in. (25 1 1 double-spacing throughout the entire manuscript. Use a standard font (eg, Times, Helvetica, or Courier) at least 10 points in size, Preparation Guide, Revised 2/98 and Manuscript preparation Guide do not use italics Number all pages in Do not justify. Do except for special emphasis. Paper accepted but not yet published: upper-right comers. Indent paragraphs 5 spaces. Hess D. New therapies for asthma. Respir Care (year, in press). not put authors' names, institutional affiliations or allusions to institutional affiliations in the text, or other identification any- Personal author book: (For any book, specific pages should be cited where except on the whenever the abstract page. page. Repeat title only (no authors) on title Begin each of the following on a new page: Title Page, Abstract, Text. Product Sources List, Acknowledgments, References, each Table, and each Appendix. the first Use standard English and small sion). ital and small at the left letters (eg, Patients, New in cap- margin and type them Equipment, uations, 3rd ed. Littleton Statistical Analysis). may be reviewer inspection. Cite references text with superscript numerals. erences are in On first cited. Assign numbers the reference page, in the order that ref- the cited list in the works numerical order. Follow the Journal's style for references. Abbre- viate journal names Chapter book with in AK. Acute respiratory failure. In: Guenter Harwood RJ. CA. Welch MH, edi- Pulmonary medicine. Philadelphia: JB Lippincott; 1977:26-42. tors. Tables. Use consecutively numbered tables to display information. each table on a separate page. Start Number and including all nonstandard abbreviations and symbols. notes with conventional designations (*, them superscript t, |, §, \\.%, and Key the foot- **, tt) in con- in the table body. Do not use Do not submit tables as pho- tographs, reduced in size, or on oversize paper. Comparison of nebulizer delivery methods the table title give each column a brief heading. Place explanations in footnotes, sistent order, placing as in Index Medicus. List all authors. Article in a journal carrying pagination throughout volume: JL. 1977. editor(s): horizontal or vertical rules or borders. Rau AMA drag eval- CO: Publishing Sciences Group; cited as references: desig- nate the accepting journal, followed by (in press), and provide 3 copies article for dis- in cap- Pierce of the in-press pulmonary 76-85. p. American Medical Association Department of Drugs. Methods, Results, Discus- References. Cite only published works as references. Manuscripts accepted but not yet published Clinical profiles of diffuse interstitial York: Futura; 1990. Corporate author book: letters (eg. Introduction, Begin subheadings ease. in person and active voice. Center main section headings on the page and type them ital possible.) DeRemee RA. Use the same type- face as in the text. through a neonatal endotracheal tube: a bench study. Respir Care 1992:37(1 1): 1 Illustrations. Graphs, line drawings, photographs, 233- 1 240. are figures. Article in a publication that Page numbers each issue beginning with Use only Number them illustrations that clarify consecutively as Fig. 1 , and radiographs and augment the Fig. 2, ing to the order by which they are mentioned in the text. 1: Bunch D. Establishing a national database for home care. AARC Times all figures are cited. If any figure text. and so forth accord- Be sure was previously published, include copyright holder's written permission to reproduce. Figures for l99l;l5(Mar):6l,62,64. publication must be of professional quality. Data for the original Corporate author journal article: American Association graphs should be available to the Editor upon request. for Respiratory Care. Criteria for establish- consult the Editor for more information. If color is essen- In reports of ing units for chronic ventilator-dependent patients in hospitals. Respir experiments, use schematic drawings, not photographs. Care I988;33(l I):I044-I046. consent must accompany any photograph of a person. Article in journal supplement: (Journals differ in their numbering and identifying supplements. Supply to tial, promote methods of and detailed explanations on figures; put titles this animal A letter of Do not place information in figure captions. If possible, submit radiographs as prints and fullsufficient information size copies of film. retrieval.) Reynolds HY. Idiopathic interstitial pulmonary fibrosis. Chest 1986; 89(3Suppl):l39S-l43S. ic Abstract in journal: (Abstracts citations are to be avoided. Those more Stevens DP. Scavenging ribavirin from an oxygen hood to reduce envi- ronmental exposure (abstract). Respir Care 1990:35(11): 1087-1088. may Can we be given relax during spirometry? (editorial). Am Rev Respir drugs and chemicals used, giving gener- on the product-sources page. In parentheses in the text, identify mercial product (including model is country. If four or bers Negative-pressure ventilation for chronic obstructive pulmonary dis- number if applicable) the mentioned, giving the manufacturer's name, at the no author given: brand names If desired, parentheses after generic names. Drugs should be more products ufacturers in the text; instead, Dis 1993;I48(2):274. Editorial with in Commercial Products. it Editorial in journal: all names, doses, and routes of administration. listed than 3 years old should not be cited.) Enright P. Drugs. Identify precisely end of the when text, are mentioned, list do city, not any comfirst and list time state or any man- them on a Product Sources page before the References. Provide model available and manufacturer's suggested price, if num- the study has cost implications. ease (editorial). Lancet 1992;340(8833):I440-I441. Ethics. Letter in journal: Aelony Y. Ethnic norms 1 When reporting experiments on that procedures 99 1:99(4): 05 1 for pulmonary function tests (letter). Chest were conducted in human subjects, indicate accordance with the ethical stan- dards of the World Medical Associatiim Declaration of Helsinki [Respir Care 1997;42(6):635-636] or of the institution's committee 1. RESPIRATORY CARE Manuscript Preparation Guide, Revised 2/98 Manuscript preparation Guide on human experimentation. State Do obtained. that informed consent was not use patient's names, initials, or hospital numbers will be acknowledged. Computer Disltettes. Authors encouraged are to submit electron- animals, indi- ic versions of manuscripts as well as printed copies (3.5 cate that the institution's policy, a national guideline, or a law on in Macintosh or or illustrations. in text When reporting experiments on the care and use of laboratory animals author's name; was followed. IBM-DOS name and used in analyzing the data, and give the prospectively determined level of significance Methods book and published tify in the section. Report actual p values in Results. Cite only textarticle references to support choices of tests. Iden- Do to produce graphics and tables should not write on diskette labels except with felt-tipped pen. If revision of a manuscript tion of acceptance for publication, we is required as a condi- ask that an electronic version of revision be supplied to facilitate copyediting and production. any general-use or commercial computer programs used, nam- ing manufacturers and their locations. These should be listed on the Units of Measurement. Express measurements of length, height, weight, and volume in metric units appropriately abbreviated; temperatures in degrees Celsius; and blood pressures in millimeters of mercury (mm surements units. in Show Hg). Report hematologic and clinical-chemistry mea- conventional metric and in SI (Systeme Internationale) gas pressures (including blood gas tensions) in List SI equivalent values, Prior and Duplicate Publication. when that has been published the Editor may publish is given by the author and original publisher. Please con- sult the Editor before submitting such work. Authorship. All persons ed in the reported listed as authors work and in the should have participat- shaping of the manuscript; have proofread the submitted manuscript; and 1988;33( 10):861-873 (Oct 1988), 1989;34(2):145(Feb 1989). and 1997;42(6):639-640(June all must should be able to all publicly discuss and defend the paper's content. A paper with cor- porate authorship must specify the key persons responsible for the [0.981 kPa]." For conarticle. RESPIRATORY CARE consider such material, provided that permission to torr. possible, in brackets following non- values— for example. "PEEP. 10 cm H2O version to SI. see Work or accepted elsewhere should not be submitted. In special instances. product-sources page. Si be similarly identified. diskettes version of word-processing program used; and filename(s). Software used Statistics. Identify the statistical tests in. format). Label each diskette with date; Authorship is not justified solely on the basis of solicitation of funding, collection or analysis of data, provision of advice, or similar services. Persons who provide such ancillary services exclusively 1997). may Conflict of Interest Authors are asked to disclose any liaison or finan- Permissions. The manuscript must be accompanied by copies of arrangement they have with a manufacturer or distributor whose permissions to reproduce previously published material (figures or cial product is part of the submitted manuscript or with the manufacturer or distributor of a competing product. (Such arrangements do not disqualify a paper ers.) from consideration and A statement to this effect is are not disclosed to review- tables); to use illustrations edgments Abbreviations and Symbols. Use standard abbreviations and sym- Avoid creating new abbreviations. Avoid and unusual abbreviations viation only if name persons it parentheses. Thereafter, all abbreviations in the abstract. Use an abbre- sider expert to the abbreviation alone. it. Never Standard units of mea- 15 torr. 2.3 kPa). Please use the following forms; cm HiO (not cmH20). f (not bpm), L (not 1), L/min (not LPM, l/min, or 1pm), mL (not ml), mm Hg (not mmHg), pH (not Ph or PH), p > 0.001 (not p>0.001), s (not sec), SpO; (pulse-oximetry saturation). See RESPIRATORY CARE: Standard Abbreviations and Symbols [Respir Care 1997;42(6):637- Editorial Office: 642). RESPIRATORY CARE Submitting the Manuscript 600 Ninth Avenue, Suite 702 Seattle A 98104 W copy with author(s) name(s), affiliation(s), 2 copies without name(s) and affiliation(s) for reviewers] of the script, figures, and 1 diskette, and the Cover Letter manu- & Checklist to RESPIRATORY CARE. 600 Ninth Avenue. Suite 702. Seattle WA 98104. Do not fax manuscripts. Protect figures with cardboard. Keep a copy of the manuscript and figures. Receipt of your manuscript RESPIRATORY CARE Manuscript whom address- you con- on the topic of your paper. Your manuscript may be one or more of them for blind peer review. surement can be abbreviated without explanation (eg, 10 L/min. [I Acknowl- affiliations, and phone/fax numbers of three professionals appears, followed by the abbreviation employ use an abbreviation without defining Mail three copies in the section. the term occurs several times in the paper. Write out the full term the first time in report sensitive personal infonnation Reviewers. 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Please print and include credentials, title, institution, academic appointments, city and state. than 4 authors, please use another copy of this form.* •First its If sub- more Author: Author Signature/Date. *Second Author: Author Signature/Date, •Third Author: Author Signature/Date. •Fourth Author: Author Signature/Date. Has If this in any this Yes forum? No when and by whom? No Yes research received any awards? research received any grants or other support, financial or material? Yes No yes, please describe. Do any of the authors of this manuscript have a financial interest products or manufacturers mentioned If public yes, please describe. Has If research been presented yes, where, Has If this in this in (or a commercial or consulting relationship paper or any competing products or manufacturers? Yes of the manuscript on diskette? yes, please describe. Have you enclosed a copy Is § Q double-spacing used throughout entire manuscript? Are all pages numbered Are all references, figures, and tables cited in upper-right corners? in the text? Has the accuracy of the references been checked, and are they correctly formatted? Have SI values been provided? Has all arithmetic been checked? Have generic names of drugs been provided? Have necessary written permissions been provided? Have authors' names been omitted from text and figure labels? Have copies of 'in press' references been provided? Has the manuscript been proofread by all the authors? Have the manufacturers and their locations been provided for all devices and equipment used? Rl-:.SPIRATORY Care Manuscript Preparation Guide. Revised 2/98 to) any No of the American Association for Respiratory Care I JV_ Please read the eligibility requirements far each of the classifications in the right-hand column, then complete the applicable section. All information requested below must be provided, except where indicated as optional. See other side for more information and fee schedule. Please sign and date application on reverse side tion takes approximately D 1 and type or print clearly. Processing of applica- 5 days. Active Associate ID n D D n Foreign Physician Industrial FOR ACTIVE MEMBER US Special or its territories or was on Active Member if he/she lives in the borders or territories, and meets ONE of the following criteria M is o respirotory core professional if employed in a state that mandates uch, OR |21 is a groduole of an accredited educational program m_ respiratory care, OR (3] holds o credential Tssued by the NBRC An individual who is on AARC Active Membei in go standing on December 8, 1994, will continue as such provided his/her membership r( An Student individual prior to eligible is moving outside its ) legally credentioled as Last Nome First Nome _ good standing. Place of Employment Social Security No. _ Address Home Address City_ .Zip State City Phone No. .Zip State ) ( Medical Director/Medical Sponsor Phone No. FOR ASSOCIATE OR SPECIAL MEMBER Individuols who hold a position related to respiratory care but do not meet the requirements of Member shall be Associate Members They hove oil the rights ond benefits of the Association except to hold office, vote, or serve as choir of a standing committee The following subclosses of Associate Membership ore available Foreign, Physicion, and Industrial (individuals whose primary occupation is directly or indirectly devoted to the manufacture, sale, or distribution of respirotory care eciuipment or supplies) Special Members ore those not workmg in a Primary Job Responsibility fcheck one only) D Technical Director D D n n n n D D D n D Active Assistant Technical Director respirotory core-related field Pulmonary Function Specialist Instructor/Educator Supervisor Place of Employment Staff Therapist Staff Address Technician Rehabilitation/Home Care City Medical Director .Zip State Sales Phone No. Student Other, specify Type of Business a Hospital D Skilled Nursing n DME/HME FOR STUDENT MEMBER Members Individuals will in enrolled — n Other, specify Agency School/RC Program Institution Address City .Zip State Dote of Sex Birth |optional) U.S. Citizen? in credits Manufacturer or supplier Health Educational if they meet oil the requirements for Associate on educational program in respiratory care accredited by, or on AARC-recognized agency, classified as Student the process of seeking accreditation from, Student Members do not receive Continuing Respiratory Core Education SPECIAL NOTICE (CRCE) transcripts Upon completion of your respiratory core education, continuing education may be pursued upon your reclossification to Active or Associate Member Facility n n n Home be Membership and ore Yes Have you ever been a member (optional] Phone No. Length of program No of the ) ( AARC? D n 1 d D year 2 years 4 years Other, specify , Expeeted Date of Graduation If so, when? From 4f (REQUIRED INFORMATION) Preferred mailing address: H Home G American Association for Respiratory Care Year Month B . 1 1030 Abies Lane • Dallas, TX 75229-4593 • [972] 243-2272 . Fax [972] 484-2720 American Association for Respiratory Care DemograpMt Questions We request that you answer these questions design services and programs to in order to help us meet your needs. Check the Highest Degree Earned D n D D D n High School RC Graduate Bachelor's Degree Master's Degree Doctorate Degree Number a n n Technician Associate Degree of Years in Respiratory Care 0-2 years 3-5 years 6-10 years Job Status D Q 11-15 Years 16 years or more — — — . Calendar of Events Not-for-profit organizations are offered a free advertisement ol up to eight lines to appear, on a space-available Calendar of Events basis, in an insertion order. Deadline Submit copy and insertion orders is to in RESPIRAORY CARE. Ads the 20th of the RESPIRATORY CARE. Calendar of Events. AARC & AFFILIATES for other meetings are priced at $5.50 per month two months preceding the I month 1030 hnc and require which you wish the ad in Lane. Dallas .-Xbles TX to run. 75224-4593. — AARC Patient September 11-13 OTHER MEETINGS Assessment Course June 12-14 — AARC Palient Clarion International Quality Inn Assessment Course O'Hare. Chicago, is Georgia. Preregistration CRCE: required. is Contact: For more information and an application, call (972) 243-2272. & (972) 243-2272. participate in a live telephone 1 8"^ Jefferson University Hospital's Management Seminar, CRCE: Credit has been requested Contact: (888) Annual Conference by the Sea, Sher- Two certification vanced Respiratoiy Ad- programs Skills for Skilled & — JEFF-CME or fax (215) 923-3212. aton in Ocean City, Ocean City, Maryland. Philadelphia, Pennsylvania. — Marylaml/ District of Columbia Society — Videotape Teleconference June 16 View Protocols Revisited: 1998. Part 4 of the AARC's 1998 Professor's Rounds Series. AARC at September 16-18 Thomas Department of Patient Care SeiTices 2nd Annual Jefferson Ventilator 16 hours are available. Contact: The 16 hours. Illinois. Preregistration required. Atlanta Airport Marriott Hotel. Atlanta. CRCE: June 5 — Jefferson Medical College & at June 5-6 — Joint Commission on Accreditation of Healthcare Organizations question-and-answer session. Subacute Care and Patient Assessment CRCE: will also be offered. for Contact: Jeanette Ledbetter City Centre, 'Washington credit hour. 1 Contact: The to receive the AARC at (972) 243-2272 & register 90-minute video for the teleconference. October 8 June 17-19 SO"" — Illinois Society Annual Convention and Exhibition Oakbrook Terrace, Center. CRCE: Illinois. Credit has been requested. Contact: Larry Dastych— (847)618-3190. July 7 — Videotape Teleconference View Outcomes Measurement: Part 5 of the AARC's 1998 Professor's Rounds Series, & CRCE: Contact: The AARC at (972) to receive the 90-minute video 243-2272 & ~ AARC s November 18-21 AARC Sam Giordano MBA "The RCP: Practice NYSSRC will and SUNY in and a assessment workshop Oct 9-10 in — Atlanta. Georgia The 1998 Medtrade' Exhibition Conference will be held & Georgia 1 .200 exhibitors representing 2,500 manufacturers, showcasing more than 250,000 products and services, including FDA approvals. the latest in at the Contact:(770)641-8181; fax (770) 641-1499; web: http://www.semcopro.com. Manhattan. register Contact:(5l6)444-3181 www.nyssrc.org. 1998 December 9-11 An — Grenoble. France international conference on the Diagnosis and Treatment of Sleep speakers from for facility July AARC at (972) Oct 1 Contact: Congress Secretariat CRCE. ADTSAS, 243-2272 Hopital de la Service de Reanimation for registry information. — Nevada Society 93 Grande Rue de la Atlantis Hotel Casino, Reno, Nevada. 76 55 CRCE: Patrick. levy @imag.fr.= 10 credits have been requested. 8943L et d' Assistance Croix Rousse, 69317 Lyon Cedex NV at Croix Rousse, Respiratoire. Hopital de la Croix Rousse. Annual Conference and Business Meeting, Contact: John Steinmetz all French. Abstracts for presentation are due 19-20; participants can earn 7 hours of over the world with all sessions translated into either English or Spirometry Workshop will be conducted Circle. Sparks at the World Congress Center. Featuring nearly Stony be hosting a clinical Cornell Club will Capital Hilton. Contact: (630) 792-5800. New workshop on hemodynamic monitoring. up to 20 hours. Following the Summer Forum, a July 20-21 is York, Care and Hospice, at the Breathing Disorders will feature 50 CRCE: Approved Contact: The New rehabilitation, sleep diagnostics, Registry Resort, Naples. Florida. same Manhattan, asthma case management, pulmonary Summer Forum at the be held June 4 the 21st Century." Other topics include for the teleconference. July 17-19 in RRT speaking on Brook credit hour. 1 ORYX for Home York. Featured speaker Also, the A DC. — New York Societ}- Executive Director participate in a live telephone question-and-answer session. Care and Hospice, Sheraton preconference program. All About 30th Annual Symposium, Marriott Marquis Home (202) 574-6348. Southeastern Chapter Drury Lane Theater and Conference 4th National Conference and Exhibition at 181 Brooks i 6, 04, France. June 12-16, 1999 (702) 331-0721 for Aerosols for information or a registration brochure. 1 — August 21 Ohio Society The Critical Care Committee's annual Phone 33 (0)4 76 fax 33 (0)4 76 76 56 in in 7, e-mail: — Intenuilional Societ}' Medicine 2th International Congress Center 1 at the Austria Vienna. Austria. Contact: The Vienna Academy of seminar. Holiday Inn Rockside Road, Postgraduate Medical Education and Independence, Ohio. Research, Alser Strasse 4, A- 1090 CRCE: Vienna, Austria. Phone (-h43/l) 405 13 6 credits are available. 83-22, fax (+43/1) 405 13 83-23, e-mail: Contact: Nancy Johnson~(330) 929-7166 e-mail: medacad@via.at. abbyru@aol.com. RESPIRATORY CARE • JUNE 1998 "VOL 43 NO 6 517 Notices of competitions, scholarships, fellowships, examination dates, and the before the desired month of publication (January Notices pertinent information and mail notices to 1 for the March RESPIRATORY CARE issue, Send New Manuscripts the Seattle Editorial J Pierson MD, to Oice Editor E-mail: pierson@aarc.org Katherine Kreiiitamp, Editorial Assistant E-mail: kreilkamp@aarc.org RESPIRATORY CARE Seattle Editorial Office 600 Ninth Avenue Suite 702 Seattle WA 981 04 VOICE: (206) 223-0558 FAX: (206) 223-0563 educational programs, must reach the Journal 60 days February Notices Dept, i David new like will be listed here free of charge. Items for the Notices section 1 I for the April issue, etc). Include all 1030 Abies Lane, Dallas TX 75229-4593. Notices New Federal Register Notices Now Available The Center for Devices and Radiological Health announces the new Facts-on-Demand FOD notices Federal Register. The new publications: FOD#774 publication of it [/l/i/(/ly/l^iy(y in the — Medical Devices; Preemption of State Product Liability Claims; Proposed Rule: FOD#607 — Rebuilders, Reconditioners, Services, and "As Is" Remarketers of Medical Devices; Review A^A-^" I NTERN ATIDN AU RESPIRATORY CONGRESS N O VEMBER '7 \ ^ ti , J^ 9 B Atlanta, Georgia and Revision of Compliance Policy Guides and Regulatory Requirements; Request for Comments and Information: Proposed Rule; and FOD#513 Medical Devices; Reports of Corrections and Removals; Stay of Effective Date of Information Collection Requirements; Stay of Effective Date — of Final Regulation. For more information about Facts-on-Demand call (800) 8990381 or (301) 826-0111. The FOD system is also on the Internet at www.fda.gov/ cdrh/fedregin.html. NAMES 1998 Education, Conference C) C) ^> WATC H FOR CRCE THROUGH Schedule Set The National Association for Medical Equipment Services (NAMES) announces its 1998 national conferences and regional education seminars. For information about upcoming events, call the NAMES Education & Meeting Department at (703) 836-6263, or visit the web site: www.names.org. Summer Fonim Hapies, Florida THE JOURNAL RESPIRATORY CARE Juig 17. 18, & 19 AUGUST 1998 fufJJJUfy]JJJufJJrJlluJJ.J^!JJJrHiMri RESPIRATORY CARE • JUNE 1998 VOL 43 NO 6 519 Authors in This Issue M Rhonda L 476 Kasten, Douglas. Kathy 500 Maclntyre. Neil Gropper, Michael 476 Matthay, Michael Himle. Robert 494 Moser, Neal 476 Stempel, David 497 Stem, Eric Daniel, Brian Kallet. Richard Kasei. Debra H K To advenise Advertisers in RESPIRATORY CARE, classified advertising contact Call (800) 847-8000 Circle Reader Service No. 104 Call (800) 456-6695 Marketing Director for & Helen Ziegler 442 IngMar Medical rale.s Circle. 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Copyright © RESPIRATORY CARE 1 998, by • Daedalus Enterprises Inc. JUNE 1998 VOL 43 NO 6 RE/PIRATORU QVRE June 1998 Reader Service Reply Card Expires 9/30/98 Institution Street Cify/State/Zip _ For faster service, FAX to (609) 786-4415 NO POSTAGE NECESSARY IF Authors MAILED IN THE UNITED STATES in This Ise M. Daniel. Brian Douglas, Kathy . BUSINESS REPLY MAIL . . FIRST-CLASS MAIL Gropper, Michael Himle. Robert Kallet, . Richard K Kasel, Debra . POSTAGE WILL BE . PERMIT PAID RIVERTON, NJ NO. 881 BY ADDRESSEE H . . AARC Publications PO BOX 11605 RIVERTON NJ 08076-7205 I...I..I.II...I...I.II..I...I..I.III....I.I.. I.I.I Advertis in This Ise NO POSTAGE NECESSARY IF Cardiopulmonary Corp Circle Reader Service No. DEY MAILED IN THE UNITED STATES Laboratories .... Circle Reader Service No. DHD Diemolding Heall Circle Reader Senice No. BUSINESS REPLY MAIL Hans Rudolph Circle Reader Service No. FIRST-CLASS MAIL PERMIT NO. 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Manuscripts PIRATORY CARE, 600 may be submitted to the Editorial Office, the Instructions is RES- WA 98104. In- An expanded version of Ninth Avenue, Suite 702. Seattle structions for authors are printed in every issue. med- available from the editorial office. Copyright © RE.SPIRATORY CARE IWS. h\ Daeihihis Enterprises • JUNF. 1998 VOL 43 Inc. NO 6 V)e To our way of thinking, other ventilators only solve half the problem. Exhalation Assist. Today's ventilators only address the inspiratory is phase just half the battle. Ventilator from rapid The Venturi™ Cardiopulmonary Corp. to your It's and expiratory phases The critical the Ventilator ventilator is intended to help the patient overcome Call airway resistance and achieve a more care ventilatory needs. one more reason the Venturi™ of breathing. Venturi's Exhalation Assist makes Venturi™ Ventilator a unique solution provides control of both the inspiratory N:li and complete exhalation. 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