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. Author manuscript; available in PMC: 2019 Apr 10.
Published in final edited form as: Circulation. 2017 Dec 21;137(15):1561–1570. doi: 10.1161/CIRCULATIONAHA.117.031262

Table 3.

Presumptive Etiology of SCA Among 133 SCA Cases With Autopsy or Clinical Workup Available

All Cases
(n=133)
All Ages
Ages 5–24 Years (n=49) Ages 25–34 Years (n=84)
Sports-Related
Activity
(n = 14)
Non-Sports-
Related Activity
(n = 35)
Sports-Related
Activity
(n = 7)
Non-Sports-
Related Activity
(n = 77)
Sudden arrhythmic death syndrome 41 (31) 5 (36) 14 (40) 1 (14) 21 (27)
Coronary artery disease 29 (22) 1 (7) 4 (14) 2 (29) 21 (27)
Hypertrophic cardiomyopathy 19 (14) 7 (50)* 4 (11)* 0 8 (10)
Isolated left ventricular hypertrophy 9 (7) 0 2 (6) 0 7 (9)
Congenital heart disease 5 (4) 1 (7) 1 (3) 1 (14) 2 (3)
Coronary anomaly 4 (3) 0 3 (9) 0 1 (1)
Long QT syndrome 3 (2) 0 3 (9) 0 0
Acute myocarditis 2 (2) 0 1 (3) 1 (14) 0
Dilated cardiomyopathy 4 (3) 0 0 0 4 (5)
Heart failure 4 (3) 0 0 0 4 (5)
Cardiomyopathy not otherwise specified 2 (2) 0 0 0 2 (3)
Restrictive cardiomyopathy 1 (1) 0 1 (3) 0 0
Mitral valve prolapse 3 (2) 0 0 0 3 (4)
Valvular heart disease 3 (2) 0 0 0 3 (4)
Idiopathic myocardial fibrosis 3 (2) 0 1 (3) 1 (14) 1 (1)
Right ventricular dysplasia 1 (1) 0 0 1 (14) 0

The table includes 133 subjects (108 with autopsy plus 25 without autopsy but with adequate clinical workup to determine cause of arrest). Five sports-related and 48 non-sports-related SCAs had insufficient information to assign a diagnosis. Values displayed are n (%). SCA indicates sudden cardiac arrest.

*

P=0.007.

P=0.08. All other P values >0.10. P values from Fisher exact test.

One of the 4 patients with dilated cardiomyopathy had postpartum dilated cardiomyopathy with heart failure.