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Pathophysiology, diagnosis and management of peripartum cardiomyopathy: a position statement from the Heart Failure Association of the European Society of Cardiology Study Group on peripartum cardiomyopathy

医学 围产期心肌病 心力衰竭 心脏病学 内科学 心脏再同步化治疗 射血分数 心肌病 胺碘酮 怀孕 重症监护医学 心房颤动 遗传学 生物
作者
Johann Bauersachs,Tobias König,Peter van der Meer,Mark C. Petrie,Denise Hilfiker‐Kleiner,Amam Mbakwem,Righab Hamdan,Alice M. Jackson,Paul Forsyth,Rudolf A. de Boer,Christian Mueller,Alexander R. Lyon,Lars H. Lund,Massimo Piepoli,Stéphane Heymans,Ovidiu Chioncel,Stefan D. Anker,Piotr Ponikowski,Petar Seferović,Mark R. Johnson,Alexandre Mebazaa,Karen Sliwa
出处
期刊:European Journal of Heart Failure [Elsevier BV]
卷期号:21 (7): 827-843 被引量:280
标识
DOI:10.1002/ejhf.1493
摘要

Peripartum cardiomyopathy (PPCM) is a potentially life‐threatening condition typically presenting as heart failure with reduced ejection fraction (HFrEF) in the last month of pregnancy or in the months following delivery in women without another known cause of heart failure. This updated position statement summarizes the knowledge about pathophysiological mechanisms, risk factors, clinical presentation, diagnosis and management of PPCM. As shortness of breath, fatigue and leg oedema are common in the peripartum period, a high index of suspicion is required to not miss the diagnosis. Measurement of natriuretic peptides, electrocardiography and echocardiography are recommended to promptly diagnose or exclude heart failure/PPCM. Important differential diagnoses include pulmonary embolism, myocardial infarction, hypertensive heart disease during pregnancy, and pre‐existing heart disease. A genetic contribution is present in up to 20% of PPCM, in particular titin truncating variant. PPCM is associated with high morbidity and mortality, but also with a high probability of partial and often full recovery. Use of guideline‐directed pharmacological therapy for HFrEF is recommended in all patients respecting contraindications during pregnancy/lactation. The oxidative stress‐mediated cleavage of the hormone prolactin into a cardiotoxic fragment has been identified as a driver of PPCM pathophysiology. Pharmacological blockade of prolactin release using bromocriptine as a disease‐specific therapy in addition to standard therapy for heart failure treatment has shown promising results in two clinical trials. Thresholds for devices (implantable cardioverter‐defibrillators, cardiac resynchronization therapy and implanted long‐term ventricular assist devices) are higher in PPCM than in other conditions because of the high rate of recovery. The important role of education and counselling around contraception and future pregnancies is emphasised.
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