Peripartum cardiomyopathy.

S. Goland, U. Elkayam
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Abstract

—Peripartum cardiomyopathy is a potentially life-threatening pregnancy-associated disease that typically arises in the peripartum period and is marked by left ventricular dysfunction and heart failure. The disease is relatively uncommon, but its incidence is rising. Women often recover cardiac function, but long-lasting morbidity and mortality are not infrequent. Management of peripartum cardiomyopathy is largely limited to the same neurohormonal antagonists used in other forms of cardiomyopathy, and no proven disease-specific therapies exist yet. Research in the past decade has suggested that peripartum cardiomyopathy is caused by vascular dysfunction, triggered by late-gestational maternal hormones. Most recently, information has also indicated that many cases of peripartum cardiomyopathy have genetic underpinnings. We review here the known epidemiology, clinical presentation, and management of peripartum cardiomyopathy, as well as the current knowledge of the pathophysiology of the disease. ( Circulation . 2016;133:1397-1409. DOI: 10.1161/ CIRCULATIONAHA.115.020491.) peripartum
围产期心肌病是一种潜在危及生命的妊娠相关疾病,通常发生在围产期,以左心室功能障碍和心力衰竭为特征。这种疾病相对不常见,但发病率正在上升。妇女通常恢复心脏功能,但长期的发病率和死亡率并不罕见。围产期心肌病的治疗在很大程度上局限于与其他形式的心肌病相同的神经激素拮抗剂,目前还没有证实的疾病特异性治疗方法。过去十年的研究表明,围产期心肌病是由妊娠晚期母体激素引发的血管功能障碍引起的。最近,信息也表明,许多围生期心肌病的病例有遗传基础。我们在这里回顾了已知的流行病学,临床表现,围产期心肌病的管理,以及当前的疾病病理生理学知识。(循环。2016; 133:1397 - 1409。DOI: 10.1161/ CIRCULATIONAHA.115.020491)围产期
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