Left bundle branch area pacing prevents pacing induced cardiomyopathy in long-term observation

Agnieszka Bednarek1, Grzegorz Kiełbasa1, Paweł Moskal1

  • 1First Department of Cardiology, Interventional Electrocardiology and Hypertension, Jagiellonian University, Medical College, Krakow, Poland.

Insights

Left bundle branch area pacing (LBBAP) avoids pacing-induced cardiomyopathy and improves heart function in bradyarrhythmia patients. This study suggests LBBAP may be a preferred pacing method for these conditions.

Area of Science:

  • Cardiology
  • Electrophysiology
  • Cardiac Pacing

Background:

  • Conventional right ventricular pacing can have negative impacts.
  • Left bundle branch area pacing (LBBAP) is an alternative conduction system pacing method.
  • LBBAP aims to mitigate adverse effects associated with traditional pacing.

Purpose of the Study:

  • To evaluate long-term echocardiographic outcomes in patients receiving LBBAP for bradyarrhythmia.
  • To assess the impact of LBBAP on cardiac function and strain.
  • To determine if LBBAP prevents pacing-induced cardiomyopathy (PICM).

Main Methods:

  • Prospective study of 151 patients with symptomatic bradycardia and LBBAP.
  • Exclusion criteria included left bundle branch block with CRT indications, low ventricular pacing burden, and LBBAP loss.
  • Echocardiography with GLS, ECG, pacemaker interrogation, and NT-proBNP levels were assessed at baseline and follow-up (median 23 months).

Main Results:

  • No patients developed PICM.
  • In patients with baseline LVEF <50% (n=39), LVEF improved from 41.4% to 45.6% and GLS from 12.9% to 15.5%.
  • In patients with preserved LVEF (n=62), LVEF and GLS remained stable.

Conclusions:

  • LBBAP effectively prevents PICM in patients with preserved LVEF.
  • LBBAP improves left ventricular function in patients with depressed LVEF.
  • LBBAP is a potentially superior pacing modality for bradyarrhythmia indications.
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,...
13
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...
18
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...
13
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...
20
Cardiomyopathy I: Introduction and Classification01:25

Cardiomyopathy I: Introduction and Classification

Cardiomyopathy, or CMP, is a group of diseases affecting the myocardial structure, impairing its ability to pump blood effectively. This condition can lead to arrhythmias, heart failure, or sudden cardiac death.Cardiomyopathies are classified into primary and secondary categories:Primary Cardiomyopathy refers to conditions involving only the heart muscle that are often idiopathic (of unknown cause) or genetic. They primarily affect the myocardium without the involvement of other systemic...
26
Cardiomyopathy VI: Nursing Management01:29

Cardiomyopathy VI: Nursing Management

Assessment: Nursing management of patients with cardiomyopathy begins with a thorough assessment of the patient's history, including a family history of cardiomyopathy or sudden cardiac death, personal history of heart disease, hypertension, diabetes, and any alcohol consumption or drug use.During the physical examination, assess vital signs, look for signs of heart failure (such as edema, jugular venous distention, and cyanosis), auscultate for abnormal heart sounds (like murmurs and gallops),...
20