Biventricular pacemaker therapy improves exercise capacity in patients with non-obstructive hypertrophic

Ibrar Ahmed1, Brodie L Loudon2, Khalid Abozguia1,3

  • 1Department of Cardiovascular Medicine, University of Birmingham, Birmingham, UK.

Insights

Biventricular pacing improves exercise capacity in non-obstructive hypertrophic cardiomyopathy (HCM) patients by enhancing diastolic filling, particularly in those with reduced exercise-induced volume changes. This offers a new treatment avenue for symptomatic HCM.

Area of Science:

  • Cardiology
  • Medical Devices
  • Exercise Physiology

Background:

  • Limited treatment options exist for non-obstructive hypertrophic cardiomyopathy (HCM).
  • Biventricular (BiV) pacing is a potential intervention, but its efficacy and mechanism in HCM require clarification.

Purpose of the Study:

  • To determine if BiV pacing improves exercise capacity in symptomatic non-obstructive HCM patients.
  • To investigate whether improvements are mediated by augmented diastolic filling during exercise.

Main Methods:

  • Thirty-one symptomatic non-obstructive HCM patients underwent BiV and sham pacing in a crossover study.
  • Exercise diastolic filling was assessed using radionuclide ventriculography.
  • Exercise capacity (peak oxygen consumption) and quality of life were evaluated over 8 months.

Main Results:

  • BiV pacing significantly increased exercise-induced left ventricular end-diastolic volume and stroke volume in patients with baseline reduced filling (-LVEDV group).
  • The -LVEDV group showed significant improvements in peak oxygen consumption and quality of life scores with BiV pacing.
  • No significant improvements in ejection fraction or end-systolic elastance were observed; no effect on mechanical dyssynchrony.

Conclusions:

  • Symptomatic non-obstructive HCM patients may benefit from BiV pacing through enhanced diastolic filling during exercise.
  • The mechanism appears to involve improved diastolic function rather than contractile enhancement.
  • Relief of diastolic ventricular interaction may contribute to observed benefits.
Abstract

Related Concept Videos

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...
255
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...
310
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,...
383
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...
607
Heart Failure VI: Adjunct Therapies01:22

Heart Failure VI: Adjunct Therapies

Additional therapies for treating patients with heart failure (HF) may include procedural interventions, supplemental oxygen, the management of sleep disorders, and nutritional therapy.Procedural InterventionsImplantable Cardioverter-Defibrillator: For patients at risk of life-threatening arrhythmias due to severe left ventricular dysfunction, an Implantable Cardioverter-Defibrillator (ICD) can detect and terminate these arrhythmias, preventing sudden cardiac death and improving survival rates.
203
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...
393