Cardiac resynchronization therapy outcomes in patients with chronic heart failure: cardiac resynchronization therapy

Michael Drozd1, John Gierula, Judith E Lowry

  • 1aLeeds Institute of Cardiovascular and Metabolic Medicine, University of LeedsbLeeds Teaching Hospitals NHS TrustcClinical Trials Research Unit, Leeds Institute of Clinical Trials Research, Leeds, UK.

Insights

Cardiac resynchronization therapy with a defibrillator (CRT-D) did not show a survival benefit over a pacemaker (CRT-P) in heart failure patients. Patients needing CRT may not gain additional survival advantages from a defibrillator.

Area of Science:

  • Cardiology
  • Electrophysiology
  • Heart Failure Management

Background:

  • Cardiac resynchronization therapy (CRT) improves survival in chronic heart failure with left ventricular systolic dysfunction (LVSD).
  • Limited comparative data exist for CRT with a pacemaker (CRT-P) versus CRT with a defibrillator (CRT-D).

Purpose of the Study:

  • To compare the long-term prognosis of patients receiving CRT-P versus CRT-D.
  • To investigate survival outcomes between CRT-P and CRT-D in a large patient cohort.

Main Methods:

  • Prospective data collection from 795 patients implanted with CRT devices between 2008 and 2012.
  • Comparison of all-cause mortality between CRT-P and CRT-D groups.
  • Subgroup analysis for patients with ischaemic cardiomyopathy.

Main Results:

  • No significant survival benefit was observed for CRT-D compared to CRT-P (HR 1.09, P=0.51).
  • A non-significant trend for improved survival with CRT-D was noted in ischaemic heart failure patients.
  • No differences in mode-specific mortality were found between CRT-D and CRT-P.

Conclusions:

  • CRT-D did not confer a survival advantage over CRT-P in this patient cohort.
  • The addition of a defibrillator to CRT may not reliably improve survival for all indicated patients.
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,...
622
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...
501
Cardiopulmonary Resuscitation III: AED Use01:23

Cardiopulmonary Resuscitation III: AED Use

Introduction to AEDAn Automated External Defibrillator (AED) is a portable medical device that analyzes the heart's rhythm and, if necessary, delivers an electrical shock to help the heart re-establish an effective rhythm during sudden cardiac arrest (SCA). SCA occurs when the heart suddenly and unexpectedly stops beating, leading to a loss of blood flow to the brain and other vital organs. In such emergencies, time is of the essence, and using an AED, combined with Cardiopulmonary...
824
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.
428
Dysrhythmias VI: Management of Dysrhythmias01:25

Dysrhythmias VI: Management of Dysrhythmias

Dysrhythmia management involves a multifaceted approach, incorporating pharmacological treatments, medical procedures, surgical interventions, lifestyle modifications, and patient education.Pharmacological ManagementAntiarrhythmic Drugs:Class I (Sodium Channel Blockers): This class includes quinidine and procainamide, which reduce the speed of impulse conduction in the heart, stabilize the cardiac membrane, and control arrhythmias. Quinidine and procainamide are Class IA agents that prolong the...
514
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...
545