Baseline Characteristics and Clinical Insights from the ARTEMIS Registry: A Comprehensive Study of Peripartum

Meral Kayıkçıoğlu1, Murat Biteker2, Ferit Onur Mutluer3

  • 1Department of Cardiology, Ege University Faculty of Medicine, Izmir, Türkiye.

Insights

Peripartum Cardiomyopathy (PPCM) affects women during late pregnancy or postpartum. The ARTEMIS registry in Türkiye found common symptoms, reliance on echocardiography, and a 5.1% mortality rate, emphasizing registry importance for rare disease management.

Area of Science:

  • Cardiology
  • Obstetrics
  • Public Health

Background:

  • Peripartum Cardiomyopathy (PPCM) is a rare, life-threatening heart condition affecting women in late pregnancy or postpartum.
  • Understanding PPCM's characteristics and outcomes in specific populations is crucial for effective management.

Purpose of the Study:

  • To investigate the clinical features, diagnostic approaches, treatment strategies, and outcomes of Peripartum Cardiomyopathy (PPCM) in Turkish patients.
  • To provide insights into PPCM management within Türkiye through the ARTEMIS registry.

Main Methods:

  • Retrospective enrollment of 293 patients diagnosed with PPCM within the last five years across 44 cardiology centers in Türkiye.
  • Data collection included demographics, clinical presentation, diagnostic methods (primarily echocardiography), treatments, and outcomes.
  • Exclusion criteria included age under 18 and pre-existing cardiac conditions.

Main Results:

  • The study population (293 patients) was predominantly aged 25-35, with dyspnea and palpitations as common symptoms, often diagnosed postpartum.
  • Echocardiography was the primary diagnostic tool; advanced imaging use was limited.
  • Common treatments included beta-blockers (97.8%) and ACE inhibitors (71.3%), with bromocriptine used in severe cases (6.9%). A 5.1% mortality rate was observed.

Conclusions:

  • The ARTEMIS registry offers valuable data on PPCM management in Türkiye.
  • Findings highlight the need for enhanced healthcare provider and patient education regarding PPCM.
  • The study underscores the critical role of national registries in advancing the understanding and improving outcomes for rare cardiovascular diseases.
Abstract

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