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Clinical presentation, management, and 6-month outcomes in women with peripartum cardiomyopathy: an ESC EORP registry

  • Karen Sliwa
  • , Mark C. Petrie
  • , Peter van der Meer
  • , Alexandre Mebazaa
  • , Denise Hilfiker-Kleiner
  • , Alice M. Jackson
  • , Aldo P. Maggioni
  • , Cecile Laroche
  • , Vera Regitz-Zagrosek
  • , Maria Schaufelberger
  • , Luigi Tavazzi
  • , Jolien W. Roos-Hesselink
  • , Petar Seferovic
  • , Karin van Spaendonck-Zwarts
  • , Amam Mbakwem
  • , Michael Böhm
  • , Frederic Mouquet
  • , Burkert Pieske
  • , Mark R. Johnson
  • , Righab Hamdan
  • Piotr Ponikowski, Dirk J. van Veldhuisen, John J. V. McMurray, Johann Bauersachs
  • University of Cape Town
  • University of Glasgow
  • University of Groningen, University Medical Center Groningen
  • Department of Anaesthesiology and Critical Care Medicine, Saint Louis and Lariboisière University Hospitals and INSERM UMR-S 942 Paris France
  • Hannover Medical School
  • EURObservational Research Programme, France
  • ANMCO Research Centre, Firenze, Italy
  • Charité – Universitätsmedizin Berlin
  • University of Gothenburg
  • Maria Cecilia Hospital
  • Erasmus MC
  • University of Belgrade
  • University of Amsterdam
  • Lagos State University
  • Saarland University
  • LilleService de Cardiologie, France
  • Department of Obstetrics, London, United Kingdom
  • Department of Cardiology, Beirut, Lebanon
  • Medical University of Warsaw

Research output: Contribution to journalArticleAcademicpeer-review

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Abstract

AIMS : We sought to describe the clinical presentation, management, and 6-month outcomes in women with peripartum cardiomyopathy (PPCM) globally. METHODS AND RESULTS : In 2011, >100 national and affiliated member cardiac societies of the European Society of Cardiology (ESC) were contacted to contribute to a global registry on PPCM, under the auspices of the ESC EURObservational Research Programme. These societies were tasked with identifying centres who could participate in this registry. In low-income countries, e.g. Mozambique or Burkina Faso, where there are no national societies due to a shortage of cardiologists, we identified potential participants through abstracts and publications and encouraged participation into the study. Seven hundred and thirty-nine women were enrolled in 49 countries in Europe (33%), Africa (29%), Asia-Pacific (15%), and the Middle East (22%). Mean age was 31 ± 6 years, mean left ventricular ejection fraction (LVEF) was 31 ± 10%, and 10% had a previous pregnancy complicated by PPCM. Symptom-onset occurred most often within 1 month of delivery (44%). At diagnosis, 67% of patients had severe (NYHA III/IV) symptoms and 67% had a LVEF ≤35%. Fifteen percent received bromocriptine with significant regional variation (Europe 15%, Africa 26%, Asia-Pacific 8%, the Middle East 4%, P < 0.001). Follow-up was available for 598 (81%) women. Six-month mortality was 6% overall, lowest in Europe (4%), and highest in the Middle East (10%). Most deaths were due to heart failure (42%) or sudden (30%). Re-admission for any reason occurred in 10% (with just over half of these for heart failure) and thromboembolic events in 7%. Myocardial recovery (LVEF > 50%) occurred only in 46%, most commonly in Asia-Pacific (62%), and least commonly in the Middle East (25%). Neonatal death occurred in 5% with marked regional variation (Europe 2%, the Middle East 9%). CONCLUSION : Peripartum cardiomyopathy is a global disease, but clinical presentation and outcomes vary by region. Just under half of women experience myocardial recovery. Peripartum cardiomyopathy is a disease with substantial maternal and neonatal morbidity and mortality.
Original languageEnglish
Pages (from-to)3787-3797
Number of pages11
JournalEuropean heart journal
Volume41
Issue number39
DOIs
Publication statusPublished - 14 Oct 2020
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Outcome
  • Peripartum cardiomyopathy
  • Registry

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