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- W201002648 abstract "Natural history studies of patients with hypertrophic cardiomyopathy suggest that overall annual mortality from the disease is about 3% per year (1, 2), with the majority of patients dying suddenly (2). However, virtually all patients included in these studies were evaluated in the 1960’s, prior to the general application of echocardiography. This technique, employed in the study of hypertrophic cardiomyopathy with increasing frequency since the early 1970’s, has demonstrated that the disease spectrum of hypertrophic cardiomyopathy is considerably broader than previously suspected (3). Hence, a comprehensive understanding of the natural history of this disease, and the precise incidence of sudden death in the many subgroups of patients with hypertrophic cardiomyopathy, is as yet unknown. Nonetheless, the fact remains that sudden death occurs not uncommonly. The purpose of this report is to summarize what is known about identification of the patient at risk of sudden death, and the mechanisms responsible for sudden death. The material is drawn from three studies we have previously published (4–6), with updating of the data where appropriate." @default.
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- W201002648 date "1980-01-01" @default.
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- W201002648 title "Sudden Death in Patients with Hypertrophic Cardiomyopathy" @default.
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- W201002648 doi "https://doi.org/10.1007/978-94-009-8834-7_24" @default.
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