Epicardial versus endocardial permanent pacing in adults with congenital heart disease

Christopher John McLeod1, Christine H Attenhofer Jost, Carole A Warnes

  • 1Division of Cardiovascular Diseases, Mayo Clinic, 200 First Street SW, Rochester, MN 55905, USA.

Insights

Permanent pacing in congenital heart disease (CHD) patients often requires repeat interventions, particularly due to lead failure. Epicardial systems show higher lead failure rates and lower durability compared to endocardial systems in this population.

Area of Science:

  • Cardiology
  • Pediatric Cardiology
  • Cardiac Electrophysiology

Background:

  • Permanent pacing (PM) in congenital heart disease (CHD) presents unique challenges.
  • Long-term outcomes of PM in CHD patients are not well-established.

Purpose of the Study:

  • To evaluate long-term outcomes and complications of permanent pacing in patients with congenital heart disease.
  • To compare the durability and complication rates of epicardial versus endocardial pacing systems in CHD.

Main Methods:

  • A retrospective review of pacemaker complications and reinterventions over a 38-year period.
  • Data grouped by epicardial or endocardial pacing approaches.
  • Analysis of 106 patients and 259 PM procedures.

Main Results:

  • Lead failure was the primary driver for reintervention (49%).
  • Epicardial pacing was more common in patients with complex CHD, cyanosis, residual shunts, or Ebstein's anomaly.
  • Epicardial systems demonstrated significantly higher lead failure rates and lower durability compared to endocardial systems.

Conclusions:

  • Permanent pacing in CHD is associated with significant morbidity and a high need for repeat interventions.
  • Patients with Ebstein's anomaly and those with epicardial pacing systems face a higher risk of lead failure.
  • Endocardial pacing systems offer greater durability in the long term for CHD patients.
Abstract

Related Concept Videos

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 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,...
Conduction System of the Heart01:19

Conduction System of the Heart

Autorhythmicity is a term that refers to the heart's inherent ability to generate electrical signals and instigate muscle contractions. This self-regulating conduction system within the heart consists of two key components: the pacemaker cells and specialized conducting cells.
The pacemaker cells are located in two primary nodes: the sinoatrial (SA) node and the atrioventricular (AV) node. The SA node pacemaker cells can autonomously depolarize, triggering an action potential that leads to 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...
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...
Electrophysiology of Normal Cardiac Rhythm01:19

Electrophysiology of Normal Cardiac Rhythm

The normal cardiac rhythm is a synchronized electrical activity that facilitates the regular and coordinated contraction of the heart muscle. This process is essential for efficient blood circulation throughout the body. The fundamental elements involved in establishing and maintaining this rhythm include the unique electrical properties of cardiac muscle cells, the sinoatrial (SA) node's pacemaker function, the specialized conducting system, and the ionic mechanisms underlying each phase of...