Pre-Sports Cardiac Evaluation
Transcription
Pre-Sports Cardiac Evaluation
Pre-Sports Cardiac Evaluation Judith Lazol, MD Pediatric Cardiology Feb. 8, 20113 Outline What are the issues? Sports intensity Problematic Pediatric CV diseases Learning from the past: profile of Sudden Death Victims Current customary practice Future practice Objectives Identify the most common cardiac causes of sudden death in young athletes Define an appropriate cardiac evaluation for participation in sports Distinguish the children that require referral to a pediatric cardiologist Pediatric Athletics: What is Sudden Death? An unexpected and non-traumatic event that occurs instantaneously or within minutes of an abrupt change in a person's previous clinical state. Causes of sudden cardiac death in young competitive athletes 1435 athletes (1980-2005) Median age = 17 yrs 85% CARDIAC CAUSE 90% Male 44% African-American 68% Basketball or Football 90% died during training or game Maron, B. J. et al. Circulation 2007 Causes of sudden cardiac death in young competitive athletes HCM + Coronary anomaly 60% < 35 years old CAD 80% > 35 years old Maron, B. J. et al. Circulation 2007 Mar 27. 115 (12): 1643-1655 Incidence of SD in Athletes Causes of sudden cardiac death in young competitive athletes Demographics Most athletes are of high school age at the time of death Majority of the athletes who incur sudden death have been free of cardiovascular symptoms Maron, B. J. et al. Circulation 1996 94:850-856 Sports engaged in at the time of sudden death Maron BJ et al, JAMA 1996;276:199-204 Pediatric Athletics: What’s the Sudden Death Risk? Athletes 500,000 College and Pro Athletes 5 million High school students play sports 25 million children in competitive athletes ~ 30 student athletes die each year from congenital heart malformations ONE in a MILLION?!!!! Cardiovascular Screening for High School Athletes June 10 JAMA 1998;279:1817-1819 Causes of sudden cardiac death in young competitive athletes Here’s the Bad News 158 athletes died 73% (115) had pre-participation physical 4 (3%) were suspected of CV disease CV abnormality responsible for sudden death was correctly identified in only 1 (0.9%) Maron, BJ. et al. JAMA 1996;276;199-204 Pediatric Athletics: What to Do? AMA (1998) assessment: 20 states had no guidelines 40% of High School associations did not properly screen (≤ 4/12 of the AHA recommended elements) Update in 2005 81% of states have adequate questionnaires (≥ 9/12) Circulation (2011) Survey of Pediatricians, family doctors & high school athletic directors in Washington State <6% of PCP follow the national SCD screening guidelines Major Players Athlete Family School/NCAA Lawyers & Courts Physicians Consensus Guidelines Unique Pressures for Primary Care Physicians See many patients, low prevalence of disease First symptom is frequently sudden cardiac death Usually no physical findings Athlete may be stubborn or non-compliant Athlete’s Issues Sahara Marathon Desire to play outweighs almost every concern Spend enormous effort on sport Self worth is wrap in sport Sense of invincibility Problem of Public Health or Perception Athlete is a symbol of health to society High visibility of sudden death events High stakes of sports as business Athlete has celebrity status Cost Effectiveness Issues Not possible to achieve zero-risk Implied acceptance of risk on part of the athlete Testing is expensive Occurrence of HCM 1:500 Echo ~$500 $250,000 to detect 1 previously undiagnosed case Problem of false positives F/U of abnormal results leads to more costly procedures Scope of the Problem 200,000 Competitive athletes screened 150- 200 young athletes per year 1000 with CHD 0.5% 10 with disease capable of causing SCD 1% 10% 1 with sudden death All Sports are not Created Equal Dynamic soccer, long distance running, racquet sports Static weight-lifting, karate, water skiing, gymnastics, field events Combination football, sprint running Sports Classification MVC - Maximum voluntary Contraction Max O2 – Maximum oxygen consumption Mitchell JH, et al. JACC 45: 1364-67. 2005 Sudden Cardiac Death: The Young and the Famous Hank Gathers (23, HCM, VT) Reggie Lewis (27, Myocarditis) Jim Fixx (52, Hypercholesterolemia, MI) Sergei Grinkov (28, MI) Krissy Taylor (17, ARVD) River Phoenix (23, Heroin, Cocaine) Jim Morrison (27, HF, drug overdose) Jason Collier (28, Enlarged heart, arrhythmia) Maggie Dixon, (28, Arrhythmia) Andy Gibb (30, Myocarditis, cocaine abuse) Pete Maravich (40, Coronary atresia) Len Bias (22, Arrhythmia, cocaine) Flo Hyman (31, Marfan, aortic dissection) Sudden Cardiac Death: The Young and the Famous Hank Gathers (23, HCM, VT) Reggie Lewis (27, Myocarditis) Jim Fixx (52, Hypercholesterolemia, MI) Sergei Grinkov (28, MI) Krissy Taylor (17, ARVD) River Phoenix (23, Heroin, Cocaine) Jim Morrison (27, HF, drug overdose) Jason Collier (28, Enlarged heart, arrhythmia) Maggie Dixon, (28, Arrhythmia) Andy Gibb (30, Myocarditis, cocaine abuse) Pete Maravich (40, Coronary atresia) Len Bias (22, Arrhythmia, cocaine) Flo Hyman (31, Marfan, aortic dissection) Sudden Cardiac Death (SCD) What Are We Screening For? Structural/Functional 1) Hypertrophic Cardiomyopathy (HCM) 2) Coronary Artery Anomalies 3) Aortic Rupture/Marfan 4) Dilated Cardiomyopathy (DCM) 5) Myocarditis 6) Left Ventricular Outflow Tract Obstruction 7) Mitral Valve Prolapse (MVP) 8) Coronary Artery Atherosclerotic Disease 9) Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC) 10) Post-operative Congenital Heart Disease Electrical 11) Long QT Syndrome (LQTS) 12) Wolff-Parkinson-White Syndrome (WPW) 13) Brugada Syndrome 14) 15) 16) Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT) Short QT Syndrome Complete Heart Block Other 17) Drugs and Stimulants 18) Primary Pulmonary Hypertension (PPH) 19) Commotio Cordis Sudden Cardiac Death (SCD) What Are We Screening For? Structural/Functional 1) Hypertrophic Cardiomyopathy (HCM) 2) Coronary Artery Anomalies 3) Aortic Rupture/Marfan 4) Dilated Cardiomyopathy (DCM) 5) Myocarditis 6) Left Ventricular Outflow Tract Obstruction 7) Mitral Valve Prolapse (MVP) 8) Coronary Artery Atherosclerotic Disease 9) Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC) 10) Post-operative Congenital Heart Disease Electrical 11) Long QT Syndrome (LQTS) 12) Wolff-Parkinson-White Syndrome (WPW) 13) Brugada Syndrome 14) 15) 16) Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT) Short QT Syndrome Complete Heart Block Other 17) Drugs and Stimulants 18) Primary Pulmonary Hypertension (PPH) 19) Commotio Cordis Marc Vivien Foe Cameroon midfielder 28 y.o. Expires in 72nd minute in soccer match in Lyon, France 6/2003 Autopsy: HCM Hypertrophic Cardiomyopathy Relatively common 1:500 Primary disease of cardiac muscle (molecular defect in cardiac sarcomere) LV hypertrophy without dilatation More common in AA M:F 9:1 for sudden cardiac death Autosomal dominant Hypertrophic Cardiomyopathy Most common cause of SCD in young athletes in the U.S. Patients who die suddenly 70% die before 30 y/o 50% show no limitations before death 40% engaged in physical activity Death probably due to arrhythmia HCM Phenotype Cardiac defects Abnormal cellular architecture Hypertrophied LV Intramural coronaries Risks Myocardial ischemia Arrhythmogenic cardiac tissue LVOT obstruction Annual risk of SCD is 1% 1 month 8 months Hypertrophic Cardiomyopathy History ½ pts asymptomatic ½ pts DOE, angina, syncope, palpitations, etc. FHx EKG LVH Abnormal in 75%-95% (most are non-specific) Signs Prominent LV impulse Frequently have no murmur If present, murmur increases with decrease in venous return (supine to standing) Echo LVH and sudden cardiac death Spirito P, et al. NEJM 342: 1778-1785, 2000 Activity level and sudden cardiac death in HCM # of HCM Pts Spirito P, et al. JACC. 15:1521-26, 1990 Hypertrophic Cardiomyopathy Risk Factors for SCD (adult data) Prior arrest or spontaneous sustained VT Family history of premature HCM related death Multiple syncopal episodes Multiple and repetitive non-sustained VT Hypotensive response to exercise Extreme LVH 30mm Early age at diagnosis Limited data in pediatrics Hypertrophic Cardiomyopathy Treatment Medications (e.g. beta-blockers) reduce symptoms but not incidence of sudden death Ventricular septectomy ICD Avoid Competitive sports (except 1A) Digitalis Diuresis/dehydration Screen 1st degree relatives Long QT Syndrome Ion channel mutation Delayed myocardial repolarization Prolonged QTc Risk of Torsades QTc > 470 men, >480 women Annual mortality rate 4.5 % Long QT Syndrome Incidence 1/3000 Exercise/emotion/startle syncope or seizure (occasionally misdiagnosed as neurologic or vasovagal) Drowning/near drowning SIDS Congenital deafness Family history of SCD, seizure, syncope, LQTS Congenital LQTS Limitation of ECG Diagnosis Johnson J N , Ackerman M J Br J Sports Med 2009;43:657-662 Cardiac Events in Long QT Zareba, et al. NEJM. 339:960-965, 1998 Triggers of SCD in Long QT Syndrome particularly swimming Schwartz, P. J. et al. Circulation 2001;103:89-95 Long QT Syndrome Therapy Symptomatic LQTS- Class 1A Asymptomatic LQTS w/ prolonged QTc- Class 1A Genotype positive/phenotype negative- no restrictions * Beta blocker Pacemaker, ICD or AED Avoidance of QT prolonging medications * No water sports for LQT1 patients Implantable Cardiac Defibrillator Risk of ICD damage/displacement Recommendations Class 1A sports only Congenital Coronary Abnormalities Coronary arises from wrong sinus Passes between great vessels Can be compressed when CO increased Can be surgically corrected EKG is usually normal Found in 1 % of population Cause up to 20% of deaths on the athletic field Normal LCA from Rt sinus RCA from Lt sinus Single Coronary Artery Pete Maravich 1947-1988 Played for 3 NBA teams Died suddenly at age 40 during a pick up game Congenital Coronary Artery Anomalies Incidence 1/1,100 Sudden death can be initial presentation Signs and Symptoms No Symptoms Syncope with exercise (most common) Chest pain with exercise (much less common) Variety of abnormalities can predispose to SCD (especially if origin from the wrong sinus) Congenital Coronary Artery Anomalies Usually have normal EKG, and stress test High index of suspicion Majority are amenable to surgical correction Anomalous Coronary Artery Possible consequences Myocardial ischemia during exercise Ventricular tachyarrhythmia from scarred myocardium Recommendations No competitive sports May participate in all sports after surgery with normal maximal stress testing Kawasaki Disease Acquired coronary artery aneurysm Sports participation depends on presence and size of aneurysm Coronary Complications Coronary stenosis Saccular Aneurysms Reggie Lewis 1965-1993 Died @ 27 during an off season practice Collapse during a play-off in the preceding mos Cardiomyopathy 2* adenovirus Myocarditis Myocarditis Myocarditis Inflammatory disease of the myocardium Etiology Viral (enterovirus, parvovirus, adenovirus) Drugs Symptoms Chest pain, DOE, fatigue, syncope, arrhythmias, CHF Non-specific Myocarditis Frequent cause of non-structural SCD Pathogenesis Myocardial inflammatory infiltrates, myocyte necrosis, replacement fibrosis Arrhythmogenic substrate Recommendations 6 month off period Re-evaluation by cardiologist EKG, Echo Stress test Holter monitor Serum markers of inflammation, heart failure Flo Hyman American volleyball player, 6’5’’ Gold medal in 1982 World Championship Silver medal in 1984 Olympic games Collapsed while sitting on a sideline Died at the age of 31 Aortic dissection due to Marfan Marfan Syndrome CT disease 1 in 5,000 to 10,000 AD w/ highly variable clinical presentation 1/3 of cases represent new mutations CV Dilatation of Ascending aorta/Aortic dissection MVP, MR Dilatation of MPA Recommendations Aortic root involvement Moderate/severe MV regurgitation FH of Marfan related death or aortic dissection ARRYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA 3rd leading cause of SCD in young athletes Prevalence 1 in 5000 in general population Pathology Fatty-fibrous replacement of myocytes in the right ventricular free wall Etiology- unclear Familial occurrence Recurrent or intractable ventricular arrhythmias ARRYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA Diagnosis ECG: T- wave inversions in V1 and V2 and isolated PVC s are common as well as LBBB morphology MRI: more reliable than echo in noninvasive diagnosis ARRYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA Prognosis 3% mortality rate without treatment 1% mortality rate with pharmacotherapy Treatment Beta blockers RFA ICD No athletic competition except maybe class 1A Commotio Cordis Maron: N Engl J Med, Volume 349(11).September 11, 2003.1064-1075 Commotio Cordis “Blunt, non-penetrating, and innocent blows to the chest that produce ventricular fibrillation, unassociated with structural injury to the ribs, sternum, or heart.” Most common in children and adolescents Survival rare (15%) of reported cases Maron: JAMA, Volume 287(9).March 6, 2002.1142-1146 Pathophysiology No underlying heart disease No major damage to the heart or great vessels Unimpressive force of impact Age & Type of Activity 224 cases National Commotio Registry (15 years) Maron: NEJM, Volume 362(10).March 11, 2010. 917-927 Sports Participated in at the Time of Commotio Cordis Events Maron: NEJM, Volume 362(10).March 11, 2010. 917-927 Commotio Cordis AED’s can reduce mortality Prevention education soft balls yes chest protectors inadequate Maron: NEJM, Volume 362(10). March 11, 2010. 917-927 Profile of the Athlete with Sudden Death Median age= 17 y/o Male (90%) No obvious race predilection High school level of competition Asymptomatic (82%) Sports Cross-country, track, basketball Purpose of Pre-participation Evaluation Identify individuals known to have risk factors Not known to be at risk Make recommendations regarding participation Can We Really “Clear” Someone to Play Sports? “Medical Clearance is not a promise that the athlete is free from potentially fatal cardiovascular disease. Thus, we need to acknowledge that, albeit potentially reduced, small risks remain for potentially fatal disease, even after a normal screening examination” Maron, B.J. Cardiovascular risks to young athletes on the athletic field. Ann Intern Med 1998;129:379-86 Legal Considerations Must use reasonable care No clear legal precedent Malpractice liability for failure to discover a latent condition requires proof that the physician deviated from customary medical practice Medical profession allowed to establish the nature and scope of pre-participation screening Pediatric Athletic Screening: AHA 12 element preparticipation cardiovascular screening History (parental verification) Personal 1. Exertional chest pain/discomfort 2. Unexplained syncope/near syncope (not neurocardiogenic/vasovagal) 3. Excessive exercise dyspnea or fatigue 4. Prior recognition of a heart murmur 5. Hypertension Circulation 2007;115:000-000 Pediatric Athletic Screening: AHA 12 element preparticipation cardiovascular screening History (parental verification) Family 6. Premature death (sudden, unexpected or otherwise) < 50 y/o in ≥ 1 degree relative 7. Disability from heart disease <50 in close relative 8. Specific knowledge of an inherited cardiac condition (HCM, DCM, LQTS, channelopathies, Marfan Syndrome, clinically impt arrhythmias) Pediatric Athletic Screening: AHA 12 element preparticipation cardiovascular screening Physical Examination 9. 10. 11. 12. Heart murmur (supine and standing or w/ valsalva) Femoral pulses to exclude aortic coarctation Evaluate for physical stigmata of Marfan Syndrome Brachial BP in seated position (preferably both arms) Circulation 2007;115:1643-1655 AHA Cardiovascular PPE Recommendations 1st yr at institution/high school: Comprehensive personal and family history Physical examination by qualified examiner CV PPE every 2 years after initial screening During intervening years: history Refer when abnormal Pediatric Athletic Screening: Common Red Flags Exertional Syncope Chest Pain Dyspnea Palpitations Pediatric Athletic Screening: Common Red Flags Exertional Symptoms ECG, Echo, Stress Test ± TEE, coronary angiogram ± Nuclear test ± Electrophysiology study Non invasive Screening Test Echo will enhance detection of abnormalities CM AS Aortic dilatation Coronary artery abnormalities But no guarantee Some coronary anomalies ARVD Limitations in Screening False negatives False positives Athlete disqualification Cost efficiency Screening volume The current US approach to PPE The Italian approach to PPE Cost Effectiveness of Screening Modalities EKG is most cost-effective To be equally cost- Effective: Hx/PE need 2x inc in sensitivity Echo needs 4x decrease in cost FULLER: Med Sci Sports Exerc, Volume 32(5).May 2000.887-890 Barriers to routine ECG-based screening Large number of athletes for the size of appropriate physician work force Lack of standardization for interpretation of ECGs in athletes Lack of normative data in certain demographic and ethnic group Mandatory ECG Screening (?) reduce the risk of SCD Israel Sport Authority Results compared 12 yrs before & after 1997 legislation Mandatory screening with resting ECG & exercise testing Mandatory ECG screening of athletes had no apparent effect on the risk of cardiac death 1985-2009 Before 1997 After 1997 11 13 2.54 events 2.66 events p=0.88 Steinvil, et.al. JACC. 2011; 57: 1291-1296 Annual Incidence of Sudden Cardiac Death Expressed per 100,000 PersonYears in the 3 Studies Evaluating the Effects of Screening on the Mortality of Athletes Over Time Steinvil, et.al. JACC. 2011; 57: 1291-1296 NBA Mandatory Screening 2006 Season Consists of Personal & Family Hx PE Blood work EKG Resting echo Stress echo Administered annually No training camp until complete Other League Policies MLB and NHL No uniform league wide screening program NFL Mandates CV exam & EKG Partnered w/ Living Heart Foundation Active & retired players esp those at risk- e.g. large BMI NCAA Left to individual athletic departments Take Home Message Sudden Death is rare Issue of public perception (not necessarily public health) Most common cause HCM Coronary abnormalities No legal precedent of malpractice Follow AHA recommendations Refer to Cardiology for any (+) Hx, FHx, or PE THANK YOU
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