A Change of Heart: Case Series of Peripartum Cardiomyopathy
Peripartum cardiomyopathy (PPCM) is an uncommon disease of pregnancy, occurring in about 1 in 2000 live births, and is characterized by the development of heart failure, due to left ventricular systolic dysfunction. It is associated with high rates of maternal and neonatal mortality. Cardiac disease...
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doaj-e5c37a66c97a4f6bb9ed3efe1e68f27d2020-11-24T20:40:22ZengHindawi LimitedCase Reports in Obstetrics and Gynecology2090-66842090-66922013-01-01201310.1155/2013/563158563158A Change of Heart: Case Series of Peripartum CardiomyopathySean Martin0Daniel Short1Chih Mun Wong2Dina McLellan3Maternity Unit, Wishaw General Hospital, 50 Netherton Street, Wishaw, South Lanarkshire ML2 0DP, UKMaternity Unit, Wishaw General Hospital, 50 Netherton Street, Wishaw, South Lanarkshire ML2 0DP, UKScottish Advanced Heart Failure Service, Golden Jubilee National Hospital, Clydebank, Glasgow G42 9TY, UKMaternity Unit, Wishaw General Hospital, 50 Netherton Street, Wishaw, South Lanarkshire ML2 0DP, UKPeripartum cardiomyopathy (PPCM) is an uncommon disease of pregnancy, occurring in about 1 in 2000 live births, and is characterized by the development of heart failure, due to left ventricular systolic dysfunction. It is associated with high rates of maternal and neonatal mortality. Cardiac disease is the leading cause of maternal death in the UK: PPCM accounts for about 17% of these. Clinical findings of decompensated heart failure (HF) are often masked by the normal physiological changes seen in pregnancy making the diagnosis challenging. A high index of suspicion is essential—prompting referral for echocardiogram, which is crucial for diagnosis. Favourable prognosis is dependent on the early initiation of HF medications. Although full recovery occurs in around half of cases, left ventricular systolic dysfunction persists in a significant proportion of patients with PPCM and the risk of recurrence in subsequent pregnancies is high. The pathophysiology of PPCM is under intense research. We present four patients with PPCM and a review of the literature. Owing to the diagnostic challenge of PPCM and decompensated HF in pregnant mothers and its high mortality rate without treatment, prompt investigation and referral are key to improving maternal survival.http://dx.doi.org/10.1155/2013/563158 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Sean Martin Daniel Short Chih Mun Wong Dina McLellan |
spellingShingle |
Sean Martin Daniel Short Chih Mun Wong Dina McLellan A Change of Heart: Case Series of Peripartum Cardiomyopathy Case Reports in Obstetrics and Gynecology |
author_facet |
Sean Martin Daniel Short Chih Mun Wong Dina McLellan |
author_sort |
Sean Martin |
title |
A Change of Heart: Case Series of Peripartum Cardiomyopathy |
title_short |
A Change of Heart: Case Series of Peripartum Cardiomyopathy |
title_full |
A Change of Heart: Case Series of Peripartum Cardiomyopathy |
title_fullStr |
A Change of Heart: Case Series of Peripartum Cardiomyopathy |
title_full_unstemmed |
A Change of Heart: Case Series of Peripartum Cardiomyopathy |
title_sort |
change of heart: case series of peripartum cardiomyopathy |
publisher |
Hindawi Limited |
series |
Case Reports in Obstetrics and Gynecology |
issn |
2090-6684 2090-6692 |
publishDate |
2013-01-01 |
description |
Peripartum cardiomyopathy (PPCM) is an uncommon disease of pregnancy, occurring in about 1 in 2000 live births, and is characterized by the development of heart failure, due to left ventricular systolic dysfunction. It is associated with high rates of maternal and neonatal mortality. Cardiac disease is the leading cause of maternal death in the UK: PPCM accounts for about 17% of these. Clinical findings of decompensated heart failure (HF) are often masked by the normal physiological changes seen in pregnancy making the diagnosis challenging. A high index of suspicion is essential—prompting referral for echocardiogram, which is crucial for diagnosis. Favourable prognosis is dependent on the early initiation of HF medications. Although full recovery occurs in around half of cases, left ventricular systolic dysfunction persists in a significant proportion of patients with PPCM and the risk of recurrence in subsequent pregnancies is high. The pathophysiology of PPCM is under intense research. We present four patients with PPCM and a review of the literature. Owing to the diagnostic challenge of PPCM and decompensated HF in pregnant mothers and its high mortality rate without treatment, prompt investigation and referral are key to improving maternal survival. |
url |
http://dx.doi.org/10.1155/2013/563158 |
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