Complete heart block after occlusion and repair for perimembranous ventricular septal defect

Li Lin1, Wanhua Chen1, Hang Chen1

  • 1Department of Cardiology, Heart Center of Fujian Province, Fujian Medical University Union Hospital, Fuzhou, Fujian, P. R. China.

Acta Cardiologica
|March 31, 2025
PubMed

Insights

Device closure of perimembranous ventricular septal defects (pmVSDs) carries a higher risk of complete atrioventricular conduction block (CAVB) compared to surgical repair. Large VSD size and device/defect ratio are key risk factors for CAVB in pmVSD treatment.

Area of Science:

  • Cardiology
  • Pediatric Cardiac Surgery
  • Medical Device Technology

Background:

  • Complete atrioventricular conduction block (CAVB) is a significant complication following interventions for perimembranous ventricular septal defects (pmVSDs).
  • Understanding the incidence and risk factors of CAVB is crucial for improving patient outcomes after pmVSD repair and occlusion.

Purpose of the Study:

  • To analyze the incidence of CAVB after pmVSD occlusion and repair.
  • To identify risk factors associated with CAVB in patients undergoing pmVSD closure.

Main Methods:

  • Retrospective review of patients who underwent pmVSD occlusion or repair between January 2010 and January 2022.
  • Definition of permanent CAVB as requiring pacemaker implantation or occluder extraction.
  • Multivariate regression analysis to identify independent risk factors.

Main Results:

  • The incidence of permanent CAVB was 0.7% for device occlusion and 0.3% for surgical repair.
  • Large pmVSD size and device/defect ratio were independent risk factors for CAVB in respective treatment groups.
  • Device occlusion was associated with a significantly higher risk of permanent CAVB compared to surgical repair (OR, 4.675).

Conclusions:

  • Device occlusion for pmVSDs presents a higher risk of permanent CAVB than surgical repair.
  • Strategies to mitigate CAVB risk in pmVSD closure should consider VSD size and device selection.
Abstract

Related Concept Videos

Chambers of the Heart01:16

Chambers of the Heart

The human heart is a complex organ made up of four chambers: the right and left atria and the right and left ventricles. These internal chambers are separated by partitions known as the interatrial and interventricular septa. The exterior of the heart features a groove known as the coronary sulcus that demarcates the atria from the ventricles, while the anterior and posterior interventricular sulci distinguish between the two ventricles.
Deoxygenated blood from the body is received in the right...
10.0K
Mitral Stenosis I: Introduction01:22

Mitral Stenosis I: Introduction

Mitral Valve Stenosis (MVS) is a heart condition where the mitral valve narrows, impeding blood circulation from the left atrium to the left ventricle. The etiology and pathophysiology of this condition are multifaceted, leading to a cascade of cardiovascular complications.Causes of Mitral Valve StenosisRheumatic Heart Disease: It is the main cause of mitral valve stenosis, particularly in developing nations. This condition arises from rheumatic fever, an inflammatory illness resulting from...
1.8K
Dysrhythmias IV: Characteristics of Bradyarrhythmias01:18

Dysrhythmias IV: Characteristics of Bradyarrhythmias

Bradyarrhythmias are cardiac rhythm disorders characterized by a slower-than-normal heart rate, typically defined as fewer than 60 beats per minute. Some of which are discussed here:Sinus BradycardiaSinus bradycardia presents a heart rate lower than 60 beats per minute, with a regular rhythm originating from the SA node. The ECG typically shows normal P waves preceding each QRS complex, a normal PR interval (0.12 to 0.20 seconds), and a normal QRS duration (0.06 to 0.10 seconds).First-Degree AV...
788
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...
810
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...
461