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Published on: August 8, 2022
Pregnancy Management and Outcomes with Hypertrophic Cardiomyopathy
Adhya Mehta1, Sarah Schumacher2, Rebekah Alison Bhansali3
1Inova Health System, Falls Church, Virginia, USA.
Insights
Pregnancy in women with hypertrophic cardiomyopathy (HCM) requires careful management due to potential cardiovascular risks. Standardized care and further research are crucial for optimizing outcomes for both mother and fetus.
Area of Science:
- Cardiology
- Genetics
- Maternal-Fetal Medicine
Background:
- Hypertrophic cardiomyopathy (HCM) is a prevalent inherited cardiac condition.
- Increasing diagnosis in women of childbearing age due to genetic testing and screening.
- Pregnancy can present unique challenges and risks for women with HCM.
Purpose of the Study:
- To review the specific challenges of managing hypertrophic cardiomyopathy during pregnancy.
- To highlight the need for standardized protocols and multicentric studies.
- To improve maternal and fetal outcomes in pregnant women with HCM.
Main Methods:
- Literature review focusing on hypertrophic cardiomyopathy in pregnancy.
- Analysis of current management practices and existing research.
- Identification of knowledge gaps and areas for future research.
Main Results:
- Most women with HCM tolerate pregnancy, but risks of heart failure and arrhythmias exist.
- Adverse maternal and fetal outcomes are possible, especially with suboptimal health.
- Medical therapy is the primary treatment; invasive procedures have limited data in pregnancy.
Conclusions:
- Management of HCM in pregnancy is complex and varies across centers.
- There is a significant need for large-scale, multicentric studies.
- Standardized care protocols are essential to optimize outcomes for pregnant women with HCM and their infants.
Abstract:
Hypertrophic cardiomyopathy (HCM) is a common inherited genetic cardiac disorder that increasingly is being diagnosed in people of childbearing age, due to advancements in genetic testing and the evolution of screening guidelines. Many women may first present with HCM during pregnancy, which can lead to adverse maternal and fetal outcomes if not appropriately managed. Although most women with HCM tolerate pregnancy well, it can be associated with increased cardiovascular risks, including heart failure, arrhythmias, and adverse fetal outcomes, particularly among those with suboptimal baseline functional status. Medical therapy remains the mainstay of management of HCM in pregnancy, as only a limited number of studies have been done on the safety and effectiveness of invasive procedures, such as alcohol septal ablation and cardiac myomectomy, in pregnant women. Large cohort studies of women with HCM are very limited, and management practices vary within centres, with no protocolized care. This review aims to summarize the unique challenges faced by pregnant women with HCM, highlighting the need for large multicentric studies and more standardized care protocols to optimize maternal and fetal outcomes.
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