Clinical outcome of cardiac resynchronization therapy in dilated-phase hypertrophic cardiomyopathy

Min Gu1, Han Jin1, Wei Hua1

  • 1Cardiac Arrhythmia Center, State Key Laboratory of Cardiovascular Disease, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.

Insights

Patients with dilated-phase hypertrophic cardiomyopathy (DHCM) experience worse outcomes after cardiac resynchronization therapy (CRT) compared to those with idiopathic dilated cardiomyopathy (IDCM). DHCM outcomes were similar to or worse than ischemic cardiomyopathy (ICM) patients.

Area of Science:

  • Cardiology
  • Heart Failure Management
  • Cardiac Electrophysiology

Background:

  • Cardiac resynchronization therapy (CRT) is established for non-ischemic cardiomyopathy.
  • Dilated-phase hypertrophic cardiomyopathy (DHCM) patients were excluded from prior CRT trials.
  • Understanding CRT outcomes in DHCM is crucial for patient selection.

Purpose of the Study:

  • To compare the clinical outcomes of CRT in DHCM versus idiopathic dilated cardiomyopathy (IDCM) and ischemic cardiomyopathy (ICM).
  • To evaluate the effectiveness of CRT in a population with DHCM.

Main Methods:

  • Retrospective study of 312 patients undergoing CRT.
  • Patient groups included DHCM (n=16), IDCM (n=231), and ICM (n=65).
  • CRT response defined as ≥15% reduction in left ventricular end-systolic volume at 6 months.

Main Results:

  • DHCM patients had significantly higher total mortality, cardiac mortality, and heart failure hospitalizations compared to IDCM patients.
  • Outcomes for DHCM patients were similar to or worse than ICM patients, though not statistically significant.
  • CRT response rates were numerically lower in DHCM but did not reach statistical significance.

Conclusions:

  • DHCM is associated with worse clinical outcomes following CRT compared to IDCM.
  • DHCM patients demonstrate a distinct response to CRT, warranting further investigation.
  • Current CRT guidelines may need re-evaluation for DHCM patient subgroups.
Abstract

Related Concept Videos

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,...
667
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...
542
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...
568
Heart Failure II: Pathophysiology01:29

Heart Failure II: Pathophysiology

Systolic Heart Failure and Compensatory MechanismsSystolic heart failure (also termed HFrEF, Heart Failure with Reduced Ejection Fraction) is the most prevalent type of heart filure. It results in a decreased volume of blood being pumped from the ventricle. The aortic arch and carotid sinuses have baroreceptors that detect reduced blood pressure, triggering the sympathetic nervous system (SNS) to release epinephrine and norepinephrine. Initially, this response aims to boost heart rate and...
1.1K
Cardiomyopathy IV: Restrictive Cardiomyopathy01:29

Cardiomyopathy IV: Restrictive Cardiomyopathy

Restrictive cardiomyopathy (RCM) is a rare heart muscle disease characterized by impaired ventricular filling due to stiffened ventricular walls, leading to significant diastolic dysfunction.EtiologyRestrictive cardiomyopathy can arise from both inherited and acquired diseases, many of which are systemic. It is categorized into four main types: infiltrative, storage, non-infiltrative, and endomyocardial diseases.Infiltrative diseases, such as amyloidosis, lead to RCM by depositing amyloid...
655
Heart Failure IV: Classification and Diagnostic Evaluation01:30

Heart Failure IV: Classification and Diagnostic Evaluation

Heart failure can be classified in various ways, with the most common classifications based on physical activity limitations, disease progression, severity, and treatment strategies.The Functional Classification of Heart Failure divides patients into four categories based on physical activity limitation due to symptom burden.Class I: Patients in this class have cardiac disease but no physical activity limitations. Ordinary activities like walking, climbing stairs, or routine tasks do not cause...
482