Peripartum Cardiomyopathy

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چکیده

PERIPARTUM CARDIOMYOPATHY, a disorder of heart muscle, presents clinically with the onset of cardiac failure in the last month of pregnancy or in the first 5 postpartum months. The first description of idiopathic myocardial failure with onset in the puerperium has been attributed to Ritchie in 1849.1 Postpartum cardiomyopathy was again recognized in 1937 by Hull and Hafkesbring and by Gouley et al.2 Since some of the reported patients developed cardiac failure in the last month of pregnancy it is probably more appropriate to use the term "peripartum cardiomyopathy" (PPCM)4 rather than postpartum cardiomyopathy. The criteria for the diagnosis of PPCM are: (1) development of heart failure in the last month of pregnancy or within the first 5 postpartum months, (2) absence of a determinable etiology for the cardiac failure, and (3) absence of demonstrable heart disease prior to the last month of pregnancy. Thus, congenital, or acquired heart disease or myocardial disease due to determinable causes are presumed to be absent.

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Peripartum Cardiomyopathy (PPCM) is a rare and specific form of dilated and fatal cardiomyopathy which leads to systolic complication of the left ventricle. The disease usually begins slowly but its progression is fatal. Thus, the prognosis of the disease is often poor. Because of the low prevalence of the disease, extensive epidemiologic and clinical studies are not available. Few papers, most...

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Clinical characteristics of peripartum cardiomyopathy in the United States: diagnosis, prognosis, and management.

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[Peripartum cardiomyopathy].

Peripartum cardiomyopathy is a rare and under recognized form of dilated cardiomyopathy, defined as a heart failure in the last month of pregnancy or in the first five months post-partum with absence of determinable cause for cardiac failure and absence of demonstrable heart disease. The incidence of peripartum cardiomyopathy ranges from 1 in 1300 to 1 in 15,000 pregnancy. Advanced maternal age...

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تاریخ انتشار 2005