Peripartum cardiomyopathy: a comprehensive and contemporary review
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Published on: October 24, 2020
Farai Russell Sigauke1, Hopewell Ntsinjana2, Nqoba Tsabedze3
1Division of Cardiology, Department of Internal Medicine, School of Clinical Medicine, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, 2193, South Africa. frsigauke@yahoo.co.uk.
Insights
Peripartum cardiomyopathy, a form of heart failure in pregnant women, presents significant health risks. Recent advancements offer new hope for improved diagnosis and management of this condition.
Area of Science:
- Cardiology
- Obstetrics
- Public Health
Background:
- Cardiovascular disease is a leading global non-communicable disease.
- It is a major cause of death in pregnant individuals, often without prior heart conditions.
- Peripartum cardiomyopathy (PPCM) is a specific type of heart failure developing during late pregnancy or postpartum.
Purpose of the Study:
- To provide a comprehensive overview of peripartum cardiomyopathy.
- To discuss recent advancements in understanding and managing PPCM.
- To highlight future research directions in PPCM.
Main Methods:
- This narrative review synthesizes current knowledge on PPCM.
- It covers epidemiology, pathophysiology, diagnosis, and management.
- It incorporates recent findings on biomarkers, genetics, therapies, and patient care.
Main Results:
- Diagnosing and managing PPCM remains challenging, leading to high morbidity and mortality.
- Novel approaches include molecular/non-molecular biomarkers, genetic risk prediction, and targeted therapies.
- Multidisciplinary care and patient education are crucial for improved outcomes.
Conclusions:
- Peripartum cardiomyopathy requires continued research and enhanced clinical strategies.
- Early detection and tailored management are key to reducing adverse outcomes.
- Future efforts should focus on refining predictive models and therapeutic interventions for PPCM.
Abstract:
Cardiovascular disease is a major non-communicable disease globally, with increasing prevalence, posing a significant public health challenge. It is the leading non-obstetric cause of perinatal morbidity and mortality, with a substantial number of cardiac fatalities occurring in individuals without any known pre-existing cardiovascular disease. Peripartum cardiomyopathy is a type of de novo heart failure that occurs in pregnant women in the late stages of pregnancy or following delivery. Despite extensive research, diagnosing and managing peripartum cardiomyopathy remains challenging, resulting in significant morbidity and mortality. Recent advancements and novel approaches have been made to better understand and manage peripartum cardiomyopathy, including molecular and non-molecular biomarkers, genetic predisposition and risk prediction, targeted therapies, multidisciplinary care, and improved patient education. This narrative review provides a comprehensive overview and new perspectives on peripartum cardiomyopathy, covering its epidemiology, updated pathophysiological mechanisms, diagnosis, management, and future research directions for healthcare professionals, researchers, and clinicians.
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