Hemodynamics and prognosis after primary cardiac resynchronization system implantation compared to "upgrade"

Herbert Nägele1, Julia Dodeck, Stefan Behrens

  • 1St. Adolfstift, Reinbek, Medical Department, Reinbek, Germany. herbert_naegele@yahoo.de

Insights

Cardiac resynchronization therapy (CRT) benefits patients with left bundle branch block (LBBB) and right ventricular stimulation (RVS) similarly. Both groups showed comparable improvements in heart failure symptoms and long-term prognosis after CRT implantation.

Area of Science:

  • Cardiology
  • Electrophysiology
  • Heart Failure Management

Background:

  • Left bundle branch block (LBBB) and right ventricular stimulation (RVS) can cause cardiac dyssynchrony and heart failure.
  • The comparative effectiveness of cardiac resynchronization therapy (CRT) for LBBB versus RVS is not well-established.

Purpose of the Study:

  • To compare the response to CRT in patients with primary LBBB implants versus those upgraded from RVS.
  • To evaluate long-term cardiac events and prognosis in these two patient groups.

Main Methods:

  • Retrospective analysis of 328 patients receiving CRT (1999-2006), comparing primary LBBB implants (n=221) with RVS upgrades (n=107).
  • Detailed subgroup analysis (n=105) assessed New York Heart Association class, quality of life, LVEF, and hemodynamic parameters at baseline and 1-year follow-up.

Main Results:

  • Baseline characteristics, including NYHA class and LVEF, were similar between LBBB and RVS groups, though RVS had more atrial fibrillation.
  • After 1 year, both groups showed comparable improvements in NYHA class, LVEF, and clinical parameters.
  • Median follow-up of ~2.4 years revealed no significant difference in long-term prognosis or cardiac event rates (5-year event rate: 53% vs 55%).

Conclusions:

  • Patients upgraded to CRT from RVS demonstrate similar baseline profiles and CRT response compared to primary LBBB implants.
  • CRT offers comparable long-term benefits and prognosis for both LBBB and RVS patient populations.
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 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...
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...
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 VII: Pre and Post Operative Nursing Management01:28

Cardiomyopathy VII: Pre and Post Operative Nursing Management

Patients with hypertrophic cardiomyopathy (HCM) and left ventricular outflow tract (LVOT) obstruction who remain symptomatic despite optimal medical therapy may undergo a septal myectomy (Morrow procedure). This procedure involves excising a portion of the hypertrophied septum below the aortic valve using a heart-lung machine to improve blood flow through the LVOT. Effective preoperative and postoperative nursing management ensures successful patient outcomes, minimizes complications, and...
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...