Safety of Sports for Athletes With Implantable Cardioverter-Defibrillators
Long-Term Results of a Prospective Multinational Registry
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Until 2015, consensus statements1,2 advised against sports participation more vigorous than golf for patients with implantable cardioverter-defibrillators (ICDs) because of the postulated risks of death caused by failure to defibrillate, injury resulting from arrhythmia-related syncope or shock, or device damage. The multinational, prospective, observational ICD Sports Safety Registry quantified risks associated with sports participation for athletes receiving ICDs on the basis of standard criteria. Initial results (20133) demonstrated no death, failure to defibrillate, or injury resulting from arrhythmia or shock during sports. On the basis of these data, the 2015 eligibility and disqualification recommendations for competitive athletes with cardiovascular disease4 now state that competitive sports may be considered for athletes with ICDs. This report describes 4-year follow-up of the completed registry.3 Methods are as reported previously.3 The Yale University Human Investigation Committee approved the study. All participants gave written informed consent.
Among 440 participants, 393 in organized sports and 47 in high-risk sports, the most common diagnoses were long-QT syndrome (n=87, 20%), hypertrophic cardiomyopathy (n=75, 17%), and arrhythmogenic right ventricular cardiomyopathy (n=55, 13%). Of 201 subjects with a preimplantation history of ventricular fibrillation (VF) or tachycardia (VT), 61 (30%) had VT/VF during sports. At enrollment, median time since implantation was 26 months (interquartile range, 11–59 months), with 126 subjects (29%) enrolled within 1 year of implantation. The most common organized sports were running, basketball, and soccer; the most common dangerous sport was skiing. Seventy-seven subjects (18%) engaged in varsity/junior varsity/traveling team competition, (highly competitive subgroup). Seventy-two postcollege athletes (16%) participated at a national/international level.
Median follow-up was 44 months (interquartile range, 30–48 months), totaling 1446 person-years. Thirty-seven participants did not complete the study: 20 were lost to follow-up (all confirmed alive), 5 withdrew, 6 developed worsening cardiac/medical conditions, 4 had the ICD removed, and 2 died (neither death was sports related, as reported previously3).
There were no tachyarrhythmic deaths or externally resuscitated tachyarrhythmias during or after sports participation or injury resulting from arrhythmia-related syncope or shock during sports. The 95% confidence interval for the occurrence of adverse event based on 376 participants followed up at least 2 years was 0% to 0.9% and based on 167 participants followed up at least 4 years was 0% to 2.2%.
The numbers and rhythms of shocks received for the overall group and the highly competitive subgroup are shown in the Table. Forty-six (10%) received appropriate shocks (for VT/VF) during competition or practice, a rate of 3 per 100 person-years (identical to the initial report3). More participants received shocks during competition/practice or physical activity than rest (20% versus 10%; P<0.0001), but the proportion receiving a shock during competition/practice was similar to the proportion receiving a shock during other physical activity (12% versus 10%; P=0.56). Similarly, the proportion receiving appropriate shocks during competition/practice or other physical activity was greater than the proportion receiving appropriate shocks during rest (11% versus 6%; P=0.005), but there was no difference between competition/practice and other physical activity (7% versus 5%; P=0.08). The only clinical or demographic variable associated with receiving appropriate shocks during competition/practice was presence of arrhythmogenic right ventricular cardiomyopathy. The percentage of individuals in the highly competitive subgroup receiving appropriate shocks during competition/practice (12%) was not different from the percentage of those not in the competitive subgroup (10%). Of 51 subjects receiving shocks during sports (11% of total), 7 stopped all sports, and 13 stopped 1 or several sports; 5 of these 20 returned after 6 to 18 months
Number of Shock Events and of Individuals Receiving Shocks
Sixteen individuals (4% of total) received multiple appropriate shocks for VT/VF because of shock failure (n=2), immediate recurrence within a single device-defined episode (n=6), or electric storm (>1 device-defined episode within 24 hours, n=8). Eight occurred during competition/practice, 4 during other physical activity, and 4 at rest. The rate of arrhythmias requiring multiple shocks for termination was 0.5 per 100 person-years, similar to the previously reported 0.4 per 100 person-years.3 Among all appropriate shock episodes occurring during competition/practice, 23% required multiple shocks for termination versus 15% during other physical activity and 11% during rest (P=NS). Among the 12 participants experiencing multiple shocks during competition/physical activity, 3 (of 45) had coronary artery disease, 3 (of 48) had idiopathic VF, 3 (of 55) had arrhythmogenic right ventricular cardiomyopathy, and 1 each had CPVT (of 12), dilated cardiomyopathy (of 35), and sarcoidosis (of 1).
There were 31 definite and 13 possible lead malfunctions. The estimated lead survival free of definite malfunction (from implantation date) was 95% at 5 years and 89% at 10 years and free of definite plus possible malfunction was 94% at 5 years and 85% at 10 years. There were no generator malfunctions.
Limitations have been detailed previously.3
In conclusion, in longer-term follow-up of the ICD Sports Registry, athletes with ICDs engaged in vigorous competitive sports without physical injury or failure to terminate arrhythmia, despite the occurrence of inappropriate and appropriate shocks in some. Underlying disease should be considered, in particular arrhythmogenic right ventricular cardiomyopathy, because exercise increases disease progression5 and arrhythmia. These data can guide more informed individualized physician and patient decision making for sports participation for athletes with ICDs and continue to support the recent change in eligibility recommendations.4
Rachel Lampert, MD
Brian Olshansky, MD
Hein Heidbuchel, MD, PhD
Christine Lawless, MD
Elizabeth Saarel, MD
Michael Ackerman, MD
Hugh Calkins, MD
N.A. Mark Estes, MD
Mark S. Link, MD
Barry J. Maron, MD
Frank Marcus, MD
Melvin Scheinman, MD
Bruce L. Wilkoff, MD
Douglas P. Zipes, MD
Charles I. Berul, MD
Alan Cheng, MD
Luc Jordaens, MD, PhD
Ian Law, MD
Michele Loomis, APRN
Rik Willems, MD, PhD
Cheryl Barth, BS
Karin Broos, BA
Cynthia Brandt, MD
James Dziura, PhD
Fangyong Li, MS
Laura Simone, BA
Katleen Vandenberghe, PhD
David Cannom, MD
Acknowledgments
The authors gratefully acknowledge the invaluable assistance of the following organizations in disseminating information about this study to potential participants: Children’s Cardiomyopathy Foundation, Lisa Yue; Hypertrophic Cardiomyopathy Association, Lisa Salberg; Ken Heart Foundation, Linette Derminer; Long QT Syndrome Registry (University of Rochester Medical Center,) Kris Cutter; Parent Heart Watch, Martha Lopez-Anderson; Sudden Arrhythmia Death Syndromes, Alice Lara; Sudden Cardiac Arrest Association, Richard Brown; and Sudden Cardiac Arrest Foundation, Mary M. Newman. Participation of the European sites was approved by the Scientific Committee of the European Heart Rhythm Association and the Sports Cardiology Section of the European Association for Cardiovascular Prevention and Rehabilitation Association of the European Society of Cardiology.
Sources of Funding
This study was supported by investigator-initiated grants from Boston Scientific, Medtronic, and St Jude Medical. These entities had no role in design and conduct of the study; collection, management, analysis, and interpretation of the data; and preparation, review, or approval of the article.
Disclosures
Dr Lampert reports consulting fees/honoraria from Medtronic, Inc, and research grants from Boston Scientific Corp, Medtronic, Inc, and St. Jude Medical. Dr Olshansky reports consulting fees from Lundbeck, Amarin, and Boehringer Ingelheim. Dr Heidbuchel reports consulting fees/honoraria from Boehringer Ingelheim, Daiichi-Sankyo, Pfizer Inc, Merck Pharmaceuticals, and Bayer HealthCare, as well as research grants from Biotronik and Boston Scientific Corp. Dr Ackerman reports consulting fees from Boston Scientific Corp, Gilead Sciences, Invitae, Medtronic, Inc, MyoKardia, and St. Jude Medical, as well as royalty income from AliveCor and Transgenomic. Dr Calkins reports consulting fees/honoraria from Medtronic, Inc and Boston Scientific and research grants from St. Jude Medical and Boston Scientific Corp. Dr Estes reports consulting fees/honoraria and fellowship support from Medtronic, Inc, Boston Scientific Corp, and St. Jude Medical. Dr Maron reports consulting fees/honoraria from GeneDX and research grants from Medtronic, Inc. Dr Scheinman reports consulting fees/honoraria from Gilead, Medtronic, Inc, Boston Scientific Corp, Biosense Webster, Inc, St. Jude Medical, and Biotronik. Dr Wilkoff reports consulting/honoraria from Medtronic, Inc, St. Jude Medical, Spectranetics, Boston Scientific Corp, and ConvaTec. Dr Cheng is an employee of Medtronic. Dr Jordaens reports consulting fees/honoraria from Biotronik. Dr Willems reports research grants from Fund for Scientific Research Flanders, Biotronik, Boston Scientific Belgium, and Medtronic Belgium, as well as consulting fees/honoraria from Medtronic, Boston Scientific, Biotronik, St. Jude Medical, and Sorin. Dr Cannom reports consulting fees/honoraria from Medtronic, Inc and Boston Scientific Corp, as well as being on the Speakers’ Bureau for Medtronic, Inc, Boston Scientific Corp, Sanofi Aventis, and St. Jude Medical. The other authors report no conflicts.
Footnotes
This article was handled independently by William G. Stevenson, MD.
The online-only Data Supplement is available with this article at http://circ.ahajournals.org/lookup/suppl/doi:10.1161/CIRCULATIONAHA.117.027828/-/DC1.
Circulation is available at http://circ.ahajournals.org.
- © 2017 American Heart Association, Inc.
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- Safety of Sports for Athletes With Implantable Cardioverter-DefibrillatorsRachel Lampert, Brian Olshansky, Hein Heidbuchel, Christine Lawless, Elizabeth Saarel, Michael Ackerman, Hugh Calkins, N.A. Mark Estes, Mark S. Link, Barry J. Maron, Frank Marcus, Melvin Scheinman, Bruce L. Wilkoff, Douglas P. Zipes, Charles I. Berul, Alan Cheng, Luc Jordaens, Ian Law, Michele Loomis, Rik Willems, Cheryl Barth, Karin Broos, Cynthia Brandt, James Dziura, Fangyong Li, Laura Simone, Katleen Vandenberghe and David CannomCirculation. 2017;135:2310-2312, originally published June 5, 2017https://doi.org/10.1161/CIRCULATIONAHA.117.027828
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- Safety of Sports for Athletes With Implantable Cardioverter-DefibrillatorsRachel Lampert, Brian Olshansky, Hein Heidbuchel, Christine Lawless, Elizabeth Saarel, Michael Ackerman, Hugh Calkins, N.A. Mark Estes, Mark S. Link, Barry J. Maron, Frank Marcus, Melvin Scheinman, Bruce L. Wilkoff, Douglas P. Zipes, Charles I. Berul, Alan Cheng, Luc Jordaens, Ian Law, Michele Loomis, Rik Willems, Cheryl Barth, Karin Broos, Cynthia Brandt, James Dziura, Fangyong Li, Laura Simone, Katleen Vandenberghe and David CannomCirculation. 2017;135:2310-2312, originally published June 5, 2017https://doi.org/10.1161/CIRCULATIONAHA.117.027828







