Study characteristic | n (%) |
Setting | |
North America | 7 (58) |
Europe | 2 (17) |
Asia | 2 (17) |
Not specified | 1 (8) |
Year of publication | |
2000–2004 | 1 (8) |
2005–2008 | 2 (17) |
2009–2012 | 1 (8) |
2013-October 2016 | 8 (67) |
Publication lag | |
1–2 years | 2 (17) |
3–5 years | 8 (67) |
6–9 years | 1 (8) |
Not specified | 1 (8) |
Inherited heart disease(s) of interest* | |
Marfan syndrome | 7 (41) |
Hypertrophic cardiomyopathy | 5 (29) |
Arrhythmogenic right ventricular cardiomyopathy | 1 (6) |
Brugada syndrome | 1 (6) |
Catecholaminergic polymorphic ventricular tachycardia | 1 (6) |
Left ventricular non-compaction | 1 (6) |
Long QT syndrome | 1 (6) |
Data source(s)† | |
Hospitalisation data | 8 (62) |
Health insurance | 3 (23) |
Medical records | 2 (15) |
Data coverage | |
National | 9 (75) |
Single jurisdiction | 2 (17) |
Not specified | 1 (8) |
*One paper defined six inherited heart diseases (denominator=17).
†One paper used two data sources (denominator=13).