Pregnancy outcome in a case of non-obstructive hypertrophic cardiomyopathy

A Habib1, T Haque

  • 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.

Related Concept Videos

Cardiomyopathy III: Hypertrophic Cardiomyopathy01:29

Cardiomyopathy III: Hypertrophic Cardiomyopathy

Hypertrophic cardiomyopathy, or HCM, is an autosomal dominant genetic disorder characterized by asymmetric left ventricular hypertrophy without ventricular dilation. It is more common in men and is typically diagnosed in young, athletic adults.EtiologyHCM is primarily genetic and is caused by mutations in genes encoding sarcomeric proteins. Researchers have identified over 1400 mutations across at least 11 different genes. Among these, the most frequently occurring mutations are found in the...
Cardiomyopathy V: Interprofessional Care01:29

Cardiomyopathy V: Interprofessional Care

Managing cardiomyopathy involves addressing underlying or precipitating causes, treating heart failure with medications, and implementing dietary changes and a balanced exercise and rest regimen.Lifestyle ModificationsCardiomyopathy patients should adopt a low-sodium diet to reduce fluid retention and manage heart failure. A personalized exercise and rest plan helps maintain physical fitness without overstraining the heart. Avoiding alcohol and tobacco is essential to prevent further damage to...
Cardiomyopathy VII: Pre and Post Operative Nursing Management01:28

Cardiomyopathy VII: Pre and Post Operative Nursing Management

Patients with hypertrophic cardiomyopathy (HCM) and left ventricular outflow tract (LVOT) obstruction who remain symptomatic despite optimal medical therapy may undergo a septal myectomy (Morrow procedure). This procedure involves excising a portion of the hypertrophied septum below the aortic valve using a heart-lung machine to improve blood flow through the LVOT. Effective preoperative and postoperative nursing management ensures successful patient outcomes, minimizes complications, and...
Mitral Valve Prolapse III: Nursing Management01:19

Mitral Valve Prolapse III: Nursing Management

The nursing management of Mitral Valve Prolapse, or MVP, centers around patient education, symptom monitoring, and lifestyle modifications.Patient Education on MVP Diagnosis and Heredity: Nurses should provide comprehensive education about MVP, a condition where the mitral valve does not close appropriately during heartbeats. This education often includes the condition's pathophysiology, symptoms, and potential complications, like arrhythmias or mitral regurgitation. Though not fully...
Cardiomyopathy II: Dilated Cardiomyopathy01:30

Cardiomyopathy II: Dilated Cardiomyopathy

Dilated cardiomyopathy, or DCM, is a progressive myocardial disorder characterized by ventricular chamber dilation and contractile dysfunction.EtiologyVarious factors can cause DCM, including hypertension and heavy alcohol intake, which contribute to the weakening and enlargement of the heart muscle. Viral infections, such as Coxsackievirus B, adenoviruses, and influenza, can lead to DCM by causing inflammation and damage to heart tissue. Certain chemotherapeutic agents, including daunorubicin,...
Cardiomyopathy I: Introduction and Classification01:25

Cardiomyopathy I: Introduction and Classification

Cardiomyopathy, or CMP, is a group of diseases affecting the myocardial structure, impairing its ability to pump blood effectively. This condition can lead to arrhythmias, heart failure, or sudden cardiac death.Cardiomyopathies are classified into primary and secondary categories:Primary Cardiomyopathy refers to conditions involving only the heart muscle that are often idiopathic (of unknown cause) or genetic. They primarily affect the myocardium without the involvement of other systemic...