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围产期心肌病的管理

Management of peripartum cardiomyopathy.

作者信息

Sliwa Karen, Tibazarwa Kemi, Hilfiker-Kleiner Denise

机构信息

Soweto Cardiovascular Research Unit, Chris Hani Baragwanath Hospital, PO Bertsham 2013, Johannesburg, South Africa.

出版信息

Curr Heart Fail Rep. 2008 Dec;5(4):238-44. doi: 10.1007/s11897-008-0036-7.

Abstract

Peripartum cardiomyopathy (PPCM) is a form of heart failure that occurs in women within 1 month of predelivery and 5 months postdelivery. Echocardiography demonstrates features of cardiomyopathy with impaired ejection fraction; global dilatation and thinned-out walls are sometimes present. The symptoms and signs of PPCM are similar to those in patients with idiopathic dilated cardiomyopathy. The acute form of PPCM is a clinical syndrome, with reduced cardiac output, tissue hypoperfusion, and increase in the pulmonary capillary wedge pressure. Monitoring of the patient with the acute form of PPCM should be initiated as soon as possible. The types and levels of monitoring required for an individual patient vary widely depending on the severity of the cardiac decompensation and response to initial therapy. The syndrome carries a high morbidity and mortality, and diagnosis is often delayed. This review summarizes recent data charting the incidence, recent advances in the understanding of the pathophysiology of PPCM, and outlines the current treatment options available.

摘要

围产期心肌病(PPCM)是一种心力衰竭形式,发生在分娩前1个月内及分娩后5个月内的女性身上。超声心动图显示心肌病伴有射血分数受损的特征;有时会出现全心扩大和心肌变薄。PPCM的症状和体征与特发性扩张型心肌病患者相似。急性PPCM是一种临床综合征,伴有心输出量减少、组织灌注不足以及肺毛细血管楔压升高。一旦确诊急性PPCM,应尽快对患者进行监测。根据心脏失代偿的严重程度和对初始治疗的反应,个体患者所需监测的类型和水平差异很大。该综合征具有较高的发病率和死亡率,诊断往往延迟。本综述总结了近期有关PPCM发病率的数据、对其病理生理学认识的最新进展,并概述了目前可用的治疗选择。

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