Peripartum Cardiomyopathy: A Case Series

Md. Abu Salim, Mohammad Walidur Rahman, D. Adhikary, J. Arzu, Md. Harisul Hoque, A. I. Joarder, M. Mahmood
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Abstract

Peripartum cardiomyopathy (PPCM) is a life threatening entity of peripartum period characterized by left ventricular systolic dysfunction and heart failure in absence of any known cardiac disease. Though its incidence is rising but there is still uncertainty regarding its incidence, pathogenesis, and optimum management protocol. Retrospective analysis of twenty cases of PPCM admitted, within July 20016 to June 2018 in the department of Cardiology, Bangabandhu Sheikh Mujib Medical University (BSMMU), Dhaka is done here. Mean age of study population was 25 (6.3). Majority of the patients were multi-paras 12 (60%). 80% of the patients were diagnosed after delivery. Breathlessness was the most common symptom. Bibasal lung base crepitations was most frequent sign, which was found in 95% cases. Sinus tachycardia was most frequent electrocardiographic change which was found in 80% cases. Mean left ventricular ejection fraction (LVEF) was 35.2(2.8). All the patients had different extent of global hypokinesia of left ventricle (LV) at rest. The patients were treated with bed rest, water and salt restriction, loop diuretic, digitalis, selective Beta-blocker, vitamin B complex and an anticoagulant in relevant cases in antepartum period, Angiotensin converting enzyme inhibitor (ACEI) or Angiotensin receptor blocker (ARB) was added in postpartum period.70% patients were clinically improved and in 45% the left ventricular functional status returned to normal. 30% developed persistent cardiomyopathy beyond six months of presentation. Maternal mortality was 1 (5%). Among all live births three had intra uterine growth retardation. The pathophysiology, emerging investigations modalities, updated management protocol, and prognosis of PPCM are also discussed in this review. University Heart Journal Vol. 17, No. 1, Jan 2021; 71-75
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围产期心肌病:一个病例系列
围产期心肌病(PPCM)是一种以左心室收缩功能障碍和心衰为特征的危及生命的围产期疾病,在没有任何已知的心脏疾病的情况下。虽然其发病率正在上升,但其发病率、发病机制和最佳治疗方案仍不确定。回顾性分析了2006年7月至2018年6月在达卡Bangabandhu Sheikh Mujib医科大学(BSMMU)心内科收治的20例PPCM病例。研究人群平均年龄为25岁(6.3岁)。多数患者为多发病(60%)。80%的患者是在分娩后确诊的。呼吸困难是最常见的症状。双基底肺底搏动是最常见的征象,占95%。窦性心动过速是最常见的心电图改变,占80%。平均左室射血分数(LVEF)为35.2(2.8)。所有患者均有不同程度的静息时左心室整体运动不足。产前给予卧床休息、限水限盐、循环利尿剂、毛地黄、选择性β受体阻滞剂、复合维生素B,相关病例给予抗凝剂治疗,产后给予血管紧张素转换酶抑制剂(ACEI)或血管紧张素受体阻滞剂(ARB)。70%的患者临床改善,45%的患者左心室功能恢复正常。30%的患者在发病6个月后发展为持续性心肌病。产妇死亡率为1(5%)。在所有活产婴儿中,有3例子宫内发育迟缓。本文还讨论了PPCM的病理生理学、新出现的检查方式、最新的治疗方案和预后。《大学心脏杂志》第17卷第1期,2021年1月;71 - 75
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