Sudden Cardiac Death in College Athletes
abstract
This abstract is available on the publisher's site.
Access this abstract nowBACKGROUND
The etiology of sudden cardiac death (SCD) in college athletes has not been defined by systematic case identification.
METHODS AND RESULTS
45 cases of SCD were identified in National Collegiate Athletic Association (NCAA) athletes from 2004 - 2008 based on an internal reporting system and review of media reports. Autopsy reports were reviewed and adjudicated by a multi-disciplinary panel. Cause of death could be reasonably determined in 36 cases. 3 athletes had no autopsy, 5 autopsy reports could not be obtained, and 1 autopsy had insufficient information to determine cause of death. The most common finding at death was a structurally normal heart or autopsy-negative sudden unexplained death (11, 31%), followed by coronary artery abnormalities (5, 14%), dilated cardiomyopathy (3, 8%), myocarditis related (3, 8%), aortic dissection (3, 8%), and idiopathic left ventricular hypertrophy (LVH)/possible hypertrophic cardiomyopathy (HCM) (3, 8%). There was one case each (3%) of HCM, arrhythmogenic right ventricular cardiomyopathy, long QT syndrome, commotio cordis, and Kawasaki's disease. There was one case of death in a sickle cell positive athlete who also had LVH. The adjudicated diagnosis agreed with the official pathology report in only 59% of cases.
CONCLUSIONS
Unexplained death with a structurally normal heart is the most common finding after suspected SCD in NCAA athletes. HCM is infrequently seen, and conclusions in autopsy reports may not accurately reflect the pathologic findings. Standardized protocols for cardiovascular autopsies in athletes are needed, including post-mortem genetic testing, particularly in autopsy-negative cases.
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Additional Info
Etiologies of Sudden Cardiac Death in National Collegiate Athletic Association Athletes
Circ Arrhythm Electrophysiol 2014 Mar 01;[EPub Ahead of Print], KG Harmon, JA Drezner, JJ Maleszewski, M Lopez-Anderson, D Owens, JM Prutkin, IM Asif, D Klossner, MJ AckermanFrom MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.
Preparticipation screening for cardiovascular disease with history and physical examination has been customary practice in the US for high-school and college-aged competitive athletes probably for at least 50 years, and this responsibility has fallen largely to the primary care (family practice) community. Although the process is not perfect, it has improved measurably, with increasing numbers of athletes identified as having cardiac disease. A careful family history is potentially very powerful, given that most of the deaths occur due to genetic heart diseases such as hypertrophic cardiomyopathy.
In recent years, public health issues surrounding sudden deaths in young athletes and strategies for identification of at-risk individuals have emerged and triggered a highly visible and sometimes contentious debate. There have been proponents for nationwide routine ECGs for all athletes in the US, although no conclusive evidence exists that adding a 12-lead ECG to the screening process would necessarily improve its overall efficacy, not to mention practicality. An occasional athlete with heart disease will be detected via ECG, but there will also be thousands of false positives, sometimes leading to over-diagnosis and unnecessary disqualification, as well as numerous false negatives, which can result in an unintended consequence of screening—sudden death.
Unfortunately, over-estimating the incidence of cardiovascular sudden death in athletes, media-based hyperbole, personal investigator bias, and misunderstanding of the complications incurred by applying the 12-lead ECG to general healthy populations has left the primary care community feeling unnecessarily vulnerable to attack and liability if not engaging in the practice of routine ECG screening. This should be resisted.
Fortunately, however, a large measure of clarification regarding the screening discussion comes from three recent and timely publications in the cardiovascular literature. In one study, by Maron and colleagues in the Journal of the American College of Cardiology (JACC),1 an expansive study of more than 4 million college (NCAA) athletes over 10 years shows that risk for sudden death due to forensically proven cardiovascular diseases such as hypertrophic cardiomyopathy is relatively low—about 1/100,000 athlete-participation years, with 4 deaths occurring annually. These data are consistent with a vast and accumulating literature from cardiology investigators, which accurately characterize these tragic occurrences in young people as a low–event rate phenomenon.
The new NCAA data are important for three additional reasons:
Particularly relevant to the issue of cardiovascular screening in general populations of young people is the robust paper from the UK by Chandra and colleagues, also published in JACC,2 reporting on ECG screening in almost 12,000 young athletes and non-athletes. The authors found that fully 20% of non-athletes in a general population (and only one-third of athletes) had, in fact, ECG patterns judged to be pathologic by established European Society of Cardiology criteria. As the authors underscore, their data offer a paradigm shift in our perceptions of the practicality and effectiveness of ECG screening in general populations of healthy young people. There are significant limitations to the feasibility and cost-effectiveness of any nationwide screening program to detect cardiovascular disease in athletes and non-athletes alike.
The third paper by Harmon and colleagues in Circulation Arrhythmia and Electrophysiology3 appears to be an addendum (with forensic data) to a prior survey of sudden deaths in college athletes from a family practice group involved in preparticipation screening, arguing that standardized protocols for cardiovascular autopsies would be advantageous. This is a proposal about which we can certainly all agree.
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