Abstract
Idiopathic dilated cardiomyopathy (IDC) is a primary myocardial disease of unknown cause characterized by left ventricular or biventricular dilatation and impaired myocardial contractility1. Depending on the diagnostic criteria used, the reported annual incidence varies between 5 and 8 cases per 100,000 population2–5. However, the true incidence is probably underestimated by those figures, since many asymptomatic cases remain unrecognized. The age-adjusted prevalence of IDC in the United States averages 36 cases per 100,000 population,5 and it accounts for 10,000 deaths annually2. Blacks and males have a 2.5-fold increase in risk, as compared with whites and females, that…
| Original language | English |
|---|---|
| Pages (from-to) | 1564-1575 |
| Number of pages | 12 |
| Journal | New England Journal of Medicine |
| Volume | 331 |
| Issue number | 23 |
| DOIs | |
| State | Published - 8 Dec 1994 |
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