clinical RefeRence Manual
Transcription
clinical RefeRence Manual
Contact Information iRhythm Technologies, Inc. 650 Townsend Street, Suite 380 San Francisco, CA 94103 www.irhythmtech.com iRhythm National Clinical Center Tel: 1-888-693-2401 Fax: 1-888-693-2402 24 hours / 7 days a week iRhythm Technologies, Inc., the manufacturer and provider of Zio™ products and services, markets Zio™ in collaboration with St. Jude Medical, Inc. ST. JUDE MEDICAL, the nine-squares symbol, and MORE CONTROL. LESS RISK. are registered and unregistered trademarks and service marks of St. Jude Medical, Inc. and its related companies. Zio™ is a trademark of iRhythm Technologies, Inc. ©2010 iRhythm Technologies, Inc. All rights reserved. clinical Reference Manual Table of Contents Zio™ Event Card Package Components 3 Patient Enrollment 4 In-Office Preparation & Device Activation 5 Visual and Audible Indicators 7 Clinician Quick Reference 8 Patient General Usage Guide & Reminders 9 Warnings 10 Contact Information 11 Device Specifications 12 1 Clinical Indications The Zio™ Event Card is a prescription-only, single patient use, ECG looping monitor that can be worn for up to 30 days. It is indicated for use on patients who experience transient symptoms such as syncope, palpitations, shortness of breath, or dizziness. Contraindications There are no known contraindications related to the safety and operation of the Zio™ Event Card. The Zio™ Event Card does not have the ability to automatically detect arrhythmias. CAUTION: Federal (USA) law restricts the sale of this device to or on the order of a physician. Patient Compliance The innovative design of the Zio™ Event Card is intended to improve patient compliance and monitoring outcomes. The device can be worn via a neck lanyard or a belt clip, thereby improving overall patient comfort and diagnostic ECG results. iRhythm Recycling Program iRhythm recycles 100% of each device that is returned to us. No part of the device will end up in a landfill. 2 Zio™ Event Card Package Components 1 Zio™ Event Card Monitor with attached lead wires 32 Lead-Lok® electrodes included The patient should change the electrodes: • Every 2 to 3 days • If the electrode detaches from the skin • If the Zio™ Event Card indicates an error condition 1 Patient Instructions 1 lanyard, plus 1 belt clip 1 pre-paid return envelope addressed to Recycling Program at iRhythm Technologies, Inc. 3 Patient Enrollment You may enroll patients either online, by fax, or by phone. For online enrollment, visit: www.zioreports.com Fax enrollment form to: iRhythm National Clinical Center (iNCC) Fax: 1-888-693-2402 For phone enrollment, call: Tel: 1-888-693-2401 4 In-Office Preparation & Device Activation 1. Connect Zio™ Event Card A. Shave electrode area if hair is present. Clean skin with alcohol. Abrade skin in ‘x’ and ‘+’ motion. B. Remove two of the enclosed Lead-Lok® electrodes from the package; re-seal to keep remaining electrodes fresh. C. Snap wires of the Zio™ Event Card to the electrodes. Lift bottom tab at slit and place the wire underneath through the slit (Fig. 1). Lead-Lok® Electrode D. Position the electrodes on chest (Fig. 2) (white on the right of chest; black on left on lower rib). E. Ensure that the electrodes are securely stuck to chest. 2. Turn on Zio™ Event Card A. To activate Zio™ Event Card, press and hold the ‘RECORD’ button for a few seconds. Electrode Placement • The Zio™ Event Card will flash green, beep and give an upward tone indicating the Zio™ Event Card is now on. Note: Once Zio™ Event Card is activated and connected to a patient, it will continue to run for 30 days. 3. Create Baseline Recording Patient Recording an Event A. After connecting and turning on the Zio™ Event Card, press the ‘RECORD’ button for 1 second and check for a green flashing light. • If light is orange, check to ensure electrodes are securely attached to patient. • If light is green, proceed to next step. Zio™ Event Card Sound Port 5 B. Once Zio™ Event Card is connected to the patient, wait 1 minute for device to warm up. C. After Zio™ Event Card is warmed up, press the ‘RECORD’ button to record the baseline (Fig. 3). • You will hear 3 short beeps and see a flashing green light for 3 seconds. • When completed after 1 minute, the monitor will emit 1 short beep and flash green again for 3 seconds. 4. Transmit Baseline A. Find a quiet location. Loud noise can interfere with transmission of data. • You must send from a landline or portable phone. Do not transmit from a cell phone. • A technician will explain the transmission process. Call iRhythm National Clinical Center at Tel: 1-888-693-2401 B. When instructed, place fingers on electrodes and unsnap the wires from the electrodes. C. Place the Zio™ Event Card face up on a flat stable surface. D. Place the mouthpiece of the phone directly over the sound port located next to the phone icon on the Zio™ Event Card (Fig. 4). E. Press and hold ‘SEND’ button for a few seconds until you hear the Zio™ Event Card beep and see a green light flashing (Fig. 5). F. During transmission, a fax-like warbling tone should be heard. • When tone ends, pick up phone and speak with technician. G. If needed, the technician may instruct you to retransmit your data. 6 Press ‘SEND’ Button Reminders for Patients • Remove Zio™ Event Card from electrodes before bathing or showering. Electrodes can remain on your chest. • Change electrodes every 2 to 3 days or when they start to peel away from the body. • Do not use lotion or moisturizer in the areas of the skin where electrodes will be attached. Lotions prevent electrode contact. • To avoid skin irritation, when changing electrodes move the electrodes slightly from previous position. • As the device is recording or transmitting an event, remain still and refrain from talking. Visual and Audible Indicators • “RECORD” button only works when the device is attached to electrodes • “SEND” button only works when the device is not attached to an electrode NORMAL CONDITIONS Device Action Audible Indicator Visual Indicator Device Activated for First Time 1 upward tone Green flashing light (3 sec) Leads Snapped to Electrodes (any time after initial activation) 1 upward tone Green flashing light (3 sec) Recording Started 3 short beeps Green flashing light (15 sec) Recording Finished 1 short beep Green flashing light stops Leads Unsnapped from Electrodes 1 downward tone Orange flashing light (3 sec) SEND an Event 1 upward tone, pause, continuous warbling transmission tone Green flashing light (3 sec) Sending Complete End of warbling transmission tone None Memory Full none Orange flashing light (every 10 sec) Device Action Audible Indicator Visual Indicator SEND button pressed, but no recordings stored 1 downward tone Orange flashing light (1 sec) SEND button pressed, but leads are attached 1 downward tone Orange flashing light (1 sec) RECORD button pressed, but leads are not attached 1 downward tone Orange flashing light (1 sec) RECORD button pressed while device transmitting none Orange flashing light (1 sec) SEND button pressed again if device transmitting none Orange flashing light (1 sec) Low battery (replace device) none Orange flashing light (continuous) ERROR CONDITIONS 7 Clinician Quick Reference Battery No battery change required. Completion of Monitoring Period When 30-day monitoring with the Zio™ Event Card is completed, the patient will return the monitor to iRhythm for recycling in the pre-paid envelope included in the original packaging. • If the patient should lose the included envelope, s/he should take the monitor to an applicable collection point for the recycling of electrical and electronic equipment, or s/he can mail it to: Attn: Recycling Department iRhythm Technologies, Inc. 650 Townsend Street, Suite 380 San Francisco, CA 94103 Electrodes Each Zio™ Event Card package contains 32 electrodes. The patient should change the electrodes: • Every 2 to 3 days • If the electrode detaches from the chest • If the Zio™ Event Card indicates an error condition The patient can leave electrodes on while showering, bathing or swimming for 2-3 days or until the electrodes peel away from skin method of wear • Lanyard • Belt Clip Patient Enrollment / Initiate Service • Complete the enrollment online, by fax, or by phone: Online: www.zioreports.com Fax: (888) 693-2402 Tel: (888) 693-2401 • Review the “Patient Instructions,” included in the Zio™ Event Card packaging, with the patient. 8 General Usage Guide & Reminders for Patients WARNING: If you experience severe symptoms or you feel the need for immediate medical attention, call 911. The Zio™ Event Card monitor will not provide any medical assistance and cannot contact medical personnel for you. Wearing the Zio™ Event Card You can wear the Zio™ Event Card in one of two ways: belt clip or lanyard. Lanyard: • To adjust the length of the lanyard, use the silver adjustment bead. • Be sure the bead rests on the back of the neck and slide it up or down according to your desired length. • If the lanyard becomes dirty, it can be hand washed. Remove it from the Zio™ Event Card by sliding it through the slit at the top of the device. WASH THE LANYARD ONLY. Changing Electrodes • The electrodes should be changed every 2 to 3 days or when they start to peel away from the body. This will ensure your recordings are clear. • If you experience skin irritation while wearing the electrodes, reposition a new set close to the original position. If you are unsure of where to reposition the electrodes, contact the iRhythm National Clinical Center at 1-888-693-2401. Recording and Transmitting • Press the ‘RECORD’ button if you experience any symptoms. • ECG recordings are very sensitive. When experiencing symptoms, refrain from talking and try to remain as still as possible. • Be sure to transmit your data as soon as possible. The Zio™ Event Card can store up to 2 recordings. • If the memory is full, the Zio™ Event Card will flash orange every 10 seconds, indicating you have to transmit your data. • When transmitting, place the Zio™ Event Card on a flat stable surface and be sure that mouthpiece is placed directly over the sound port (next to the phone icon) on the device. • Once the recordings are transmitted, the memory clears itself when reconnected and is ready for a new recording. Completion of Monitoring • Return the Zio™ Event Card device to iRhythm Technologies, Inc. for recycling. A postage-paid envelope addressed to iRhythm’s Recycling Program is included in the original packaging. 9 Warnings • Do not use the Zio™ Event Card in combination with external cardiac defibrillators or high frequency surgical equipment. • Unless otherwise instructed, you are to wear the Zio™ Event Card monitor continuously during your normal daily activities. • Heavy exercise or other activities that expose the Zio™ Event Card to moisture can cause temporary failure. It is recommended to wear the device away from the body during these activities, such as in a shirt pocket or on the belt clip. • Avoid contact with water. • Remove the Zio™ Event Card before showering, bathing or swimming. The recorder is not waterproof. • You may leave the electrodes on if they are still firmly attached to the skin. Showering • CAUTION: The Zio™ Event Card is NOT waterproof. Do not shower or bathe with the monitor attached to the electrodes. • Before taking a shower or bath, unsnap the lead wires from the electrodes (that are attached to chest) and place the recorder in a dry place. • Water will not affect the electrodes, so you do not need to remove them before showering if they are still firmly attached to the skin. • If you shower with your electrodes, gently pat them dry with a towel before reconnecting the lead wires to the electrodes. General Device Precautions CAUTION: Portable and mobile RF communications equipment can affect medical electrical equipment. This device should not be used adjacent to or stacked with other equipment in accordance with the directions described in the Practice Reference Manual. Warning: Lead wires should not contact other conductive equipment or electric ground including earth. • This is an EC 38 Type 3 AECG device. • Lead failures are detected by a 10 mV peak, 50% duty cycle rectangular pulse, which is applied to each patient electrode connection through a 4.9Mohm resistor at a rate of 15 Hz with respect to the system ground. • This is a prescribed medical device, not a toy; keep away from small children. • In the event of exposed electronics, discontinue use and call iRhythm National Clinical Center (1-888-693-2401) for return and replacement. 10 This product shall not be treated as household waste. It should be taken to an applicable collection point for the recycling of electrical and electronic equipment. Please return Zio™ Event Card to iRhythm Technologies, Inc. in the included postagepaid envelope for recycling. iRhythm recycles 100% of each device that is returned to us. No part of the device will end up in a landfill. Contact Information iRhythm National Clinical Center (iNCC) 2 Marriott Drive Lincolnshire, IL 60069 Tel: 1-888-693-2401 Fax: 1-888-693-2402 www.zioreports.com iRhythm Technologies, Inc. Corporate Headquarters 650 Townsend Street, Suite 380 San Francisco, CA 94103 www.irhythmtech.com iRhythm Technologies, Inc. Orange County 14462 Astronautics Lane Huntington Beach, CA 92647 11 Device Specifications technical Features Simple 1-button operation to record ECG Memory Characteristics ECG Channels Maximum Capacity 1 channel 2 recordings, 60s each Electrical Characteristics Frequency Response Input Impedance Differential Range A/D Sampling Rate Resolution 0.5Hz to 30 Hz ≥ 2.0 Mohm +/- 2.0mV 120 samples/second 8 bits Physical Characteristics Dimensions Weight 82 x 48 x 7.5mm < 2 ounces (lanyard and cables included) Power Requirements Battery type Battery Life 2 Lithium coin cells 30 days (no changes required), typical usage Standards Compliance AAMI/ANSI EC38 IEC 60601-1 E100A4010.06 | Nov. 2010 12 Contact Information iRhythm Technologies, Inc. 650 Townsend Street, Suite 380 San Francisco, CA 94103 www.irhythmtech.com iRhythm National Clinical Center Tel: 1-888-693-2401 Fax: 1-888-693-2402 24 hours / 7 days a week iRhythm Technologies, Inc., the manufacturer and provider of Zio™ products and services, markets Zio™ in collaboration with St. Jude Medical, Inc. ST. JUDE MEDICAL, the nine-squares symbol, and MORE CONTROL. LESS RISK. are registered and unregistered trademarks and service marks of St. Jude Medical, Inc. and its related companies. Zio™ is a trademark of iRhythm Technologies, Inc. ©2010 iRhythm Technologies, Inc. All rights reserved. clinical Reference Manual
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