Cardiac resynchronization therapy in patients with right bundle branch block: analysis of pooled data from the

Cesar A Egoavil1, Reginald T Ho, Arnold J Greenspon

  • 1Thomas Jefferson University and Jefferson Heart Institute, Philadelphia, Pennsylvania 19107, USA.

Heart Rhythm
|June 1, 2005
PubMed

Insights

Cardiac resynchronization therapy (CRT) showed limited benefits for patients with right bundle branch block (RBBB), with only New York Heart Association class improving. Further studies are needed to confirm if CRT benefits RBBB patients.

Area of Science:

  • Cardiology
  • Electrophysiology

Background:

  • Limited inclusion of right bundle branch block (RBBB) patients in cardiac resynchronization therapy (CRT) clinical trials.
  • RBBB is a specific conduction abnormality affecting ventricular depolarization.

Purpose of the Study:

  • To assess the outcomes of patients with RBBB who received CRT.
  • To pool data from two randomized controlled trials (MIRACLE and Contak CD) for RBBB patient analysis.

Main Methods:

  • Identified 61 patients with RBBB, randomized to CRT (34) or control (27) groups.
  • Analyzed baseline demographics, QRS duration, and various outcome variables at 3 and 6 months.

Main Results:

  • No significant differences in baseline demographics between CRT and control groups.
  • CRT patients showed improvements in NYHA class, with trends in walk distance and quality of life.
  • Control group also improved in NYHA class, suggesting a potential placebo effect for objective measures.

Conclusions:

  • Patients with RBBB as the qualifying wide QRS did not derive significant benefit from CRT, except for NYHA class.
  • Current analysis does not support CRT use in RBBB patients, pending larger cohort studies.
  • Observed improvements in control group suggest a placebo effect, complicating interpretation of CRT benefits in RBBB.
Abstract

Related Concept Videos

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...
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...
Acute Coronary Syndrome III: Diagnostic Studies01:30

Acute Coronary Syndrome III: Diagnostic Studies

Diagnosing acute coronary syndrome or ACS begins with a thorough patient history. Notable symptoms include central, crushing chest pain radiating to the left arm, neck, jaw, or back, along with shortness of breath, sweating (diaphoresis), nausea, vomiting, dizziness, and palpitations.It is crucial to note any history of cardiac illnesses and assess risk factors, including age, gender, smoking, hypertension, diabetes, hyperlipidemia, and a sedentary lifestyle.During physical examination, vital...
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 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...
Pulse rhythm01:30

Pulse rhythm

Pulse rhythm refers to the pattern of pulsations within specific intervals, offering valuable insights into the regularity or irregularity of the heart's beats as observed through the pattern of pulsation within specific intervals. A regular pulse exhibits a consistent heart rate with uniform waveforms and pulsation force, variations of which can be classified as normal, weak, or bounding.
Conversely, an irregular pulse pattern is termed dysrhythmia, stemming from disruptions in cardiac muscle...