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Published on: August 8, 2022
Pregnancy outcome in a case of non-obstructive hypertrophic cardiomyopathy
1Dr Asma Habib, Assistant Professor, Bangladesh Medical College and Hospital, Dhaka, Bangladesh.
Insights
Pregnancy in women with hypertrophic cardiomyopathy (HCM) poses risks due to impaired cardiac function. This case highlights severe complications, including preterm delivery and maternal death, emphasizing careful management for hypertrophic cardiomyopathy patients.
Area of Science:
- Cardiology
- Genetics
- Maternal-Fetal Medicine
Background:
- Hypertrophic cardiomyopathy (HCM) is a common genetic disorder affecting cardiac sarcomere proteins, inherited in an autosomal dominant pattern.
- Pregnancy presents unique physiological challenges for women with HCM, potentially exacerbating cardiac strain and risks.
Observation:
- A case of pregnancy co-existing with non-obstructive hypertrophic cardiomyopathy and nodal bradycardia is presented.
- Physiological changes during pregnancy, including increased cardiac output and vena caval compression, can compromise cardiac function in HCM patients.
- Labor stress may precipitate arrhythmias, further complicating pregnancy management in women with HCM.
Findings:
- The pregnancy resulted in preterm delivery and neonatal death.
- The mother experienced a fatal outcome from overt cardiac failure in the puerperium, despite a relatively uneventful gestation.
- Non-compliant ventricular walls in HCM can impair the physiological increase in cardiac output during pregnancy.
Implications:
- This case underscores the significant risks associated with pregnancy in women with hypertrophic cardiomyopathy and co-existing conditions.
- Careful monitoring and management strategies are crucial for pregnant patients with HCM to mitigate potential life-threatening complications.
- Further research into the management of pregnancy in HCM patients is warranted to improve maternal and neonatal outcomes.
Abstract:
Hypertrophic cardiomyopathy (HCM) is a relatively common genetic disorder (1:500) inherited as an autosomal dominant trait. It is caused by mutations in any one of 10 genes encoding protein components of cardiac sarcomere. Some theoretically calculated risks exist when patients with HCM become pregnant. The physiologic increase of cardiac output and increased stroke volume may be impaired due to the non-compliant ventricular walls. In the first trimester, the physiologic hypervolemia of pregnancy to some extent counteracts the natural decrease in peripheral vascular resistance which would have otherwise provoked an obstruction gradientin systolic flow. As pregnancy advances, the vena caval compression may decrease venous return causing cardiac compromise, whereas the stress of labour may precipitate arrhythmia. We report our experience of a pregnancy with co-existant non-obstructive hypertrophic cardiomyopathy and nodal bradycardia ultimately resulting in pre-term delivery, neonatal death and maternal death in puerperium from overt cardiac failure after a relatively uneventful gestation.
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