Sustained benefit of cardiac resynchronization therapy

Peter Paul H M Delnoy1, Jan Paul Ottervanger, Henk Oude Luttikhuis

  • 1Department of Cardiology, Isala Klinieken, Zwolle, The Netherlands. v.r.c.derks@isala.nl

Insights

Cardiac resynchronization therapy (CRT) shows sustained echocardiographic improvements in heart failure patients over two years. Early CRT response, indicated by LVEF increase, predicts better long-term survival.

Area of Science:

  • Cardiology
  • Medical Devices
  • Heart Failure Management

Background:

  • Limited long-term echocardiographic data exists for cardiac resynchronization therapy (CRT) from real-world patient populations.
  • Most existing CRT data comes from highly selected patient cohorts in clinical trials.

Purpose of the Study:

  • To assess long-term echocardiographic remodeling following CRT in a general patient population.
  • To evaluate the sustained effects of CRT on heart function and structure over two years.

Main Methods:

  • A biventricular pacemaker was implanted in 130 advanced heart failure patients.
  • Two-year echocardiographic follow-up was conducted.
  • Patient data included baseline characteristics, echocardiographic parameters, and mortality.

Main Results:

  • Echocardiographic response (≥5% LVEF improvement) was observed in 69% at 3 months, increasing to 91% by 2 years in survivors.
  • Left ventricular ejection fraction (LVEF) improved significantly from 22% at baseline to 39.7% at 2 years.
  • Reverse remodeling (≥10% reduction in LV end-systolic volume) was sustained, reaching 91.7% by 2 years.
  • Early LVEF improvement after 3 months correlated with better long-term survival (P=0.04).
  • Mortality was higher in males, patients with elevated NT-proBNP, renal dysfunction, or left atrial dilatation.

Conclusions:

  • Cardiac resynchronization therapy leads to sustained left ventricular reverse remodeling and improved echocardiographic measures over two years.
  • An increase in LVEF of 5% or more within 3 months of CRT implantation is associated with improved long-term survival.
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,...
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...
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.
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...
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...