Peripartum cardiomyopathy: disease or syndrome?

Heart. 2019 Mar;105(5):357-362. doi: 10.1136/heartjnl-2018-314252. Epub 2019 Feb 12.

Abstract

Peripartum cardiomyopathy (PPCM) is a rare form of pregnancy-associated heart failure and is considered to be a diagnosis of exclusion. There are many hypotheses on the aetiology of PPCM; however, the exact pathophysiological mechanism remains unknown. It shows many resemblances to other conditions, such as familial dilated cardiomyopathy or myocarditis, and therefore it can be hard to make a definite diagnosis. We describe four cases of peripartum-onset heart failure in women who were suspected of having PPCM. We discuss the differential diagnosis, pathophysiological mechanisms and various diagnostic modalities.

Keywords: familial cardiomyopathies; heart failure; idiopathic dilated cardiomyopathy; pregnancy.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Adult
  • Cardiomyopathies / diagnosis*
  • Cardiomyopathies / etiology
  • Cardiomyopathies / physiopathology
  • Cardiomyopathies / therapy
  • Diagnosis, Differential
  • Female
  • Heart Failure / diagnosis*
  • Heart Failure / etiology
  • Heart Failure / physiopathology
  • Heart Failure / therapy
  • Humans
  • Peripartum Period
  • Predictive Value of Tests
  • Pregnancy
  • Prognosis
  • Puerperal Disorders / diagnosis*
  • Puerperal Disorders / etiology
  • Puerperal Disorders / physiopathology
  • Puerperal Disorders / therapy
  • Risk Factors