Related Experiment Video
Updated: Oct 17, 2026

Implantation of Total Artificial Heart in Congenital Heart Disease
Published on: July 18, 2014
Sudden death in patients after transcatheter device implantation for congenital heart disease
Y Y Perry1, J K Triedman, K Gauvreau
1Department of Cardiology, Children's Hospital, and Department of Pediatrics, Harvard Medical School, Boston, Massachusetts, USA.
Insights
Transcatheter intracardiac devices did not increase sudden death risk. Patients with severe heart disease or multiple devices were more likely to experience sudden death after implantation.
Area of Science:
- Cardiology
- Medical Devices
- Sudden Cardiac Death
Background:
- Transcatheter intracardiac devices are used for various cardiac defect closures.
- Understanding risks associated with these devices is crucial for patient safety.
Purpose of the Study:
- To investigate the association between transcatheter intracardiac device implantation and the risk of sudden death.
- To identify patient and device-related factors influencing sudden death post-implantation.
Main Methods:
- A case-control study design was employed.
- Cases were patients who died suddenly after device closure; controls were matched patients.
- Data were collected via medical record review from three large databases.
Main Results:
- Of 777 patients, 9 (1.2%) died suddenly.
- Sudden death was associated with a history of serious arrhythmias, severe valve regurgitation, prior cardiac surgery, and multiple devices.
- Device arm fractures were less common in sudden death cases.
Conclusions:
- Sudden death after intracardiac device implantation is not linked to device-specific factors like size or malposition.
- Severe underlying cardiac disease and the use of multiple devices are associated with increased sudden death risk.
Abstract:
To explore whether transcatheter intracardiac devices increase risk for sudden death, we analyzed patient and device-related variables with a case-control design. Sudden death was defined as unexpected death with abrupt onset and rapid deterioration. Cases included all patients known to have died suddenly after device closure at our institution, using 3 large databases. Controls (2:1), matched on year of procedure, were chosen randomly from the same databases. Data were obtained from medical record review. Of 777 patients who received implants between February 1989 and February 1999, 9 were known to have died suddenly (1.2%). In 27 cases and controls, diverse defects were occluded: atrial (n = 16), ventricular (n = 4), Fontan fenestration (n = 4), or other (n = 3). Cases were more likely to have had a history of serious arrhythmias (p = 0.008), severe valve regurgitation (p = 0.03), > or =1 cardiac surgery (p = 0.009), and multiple devices (p = 0.03). Cases were somewhat more likely to have pulmonary hypertension (p = 0.09), ventricular dysfunction (p = 0.09), and nonatrial septal defects (p = 0.10). Patients were less likely to have device arm fractures (p = 0.05). The following were not related to sudden death: age, weight, gender, low systemic cardiac index, end-diastolic pressure, major noncardiac disease, serious adverse events, maximum device size, malposition, and residual leak. This study suggests that sudden death was more likely to occur in device-implanted patients who had severe underlying cardiac disease and/or multiple devices. No other device-related variables were associated with sudden death.
Related Concept Videos
Cardiac Catheterization II: Right Heart Catheterization
Cardiac Catheterization I: Pre-Procedure Overview
Cardiomyopathy III: Hypertrophic Cardiomyopathy
Coronary Artery Disease III: Clinical Manifestations
Introduction Cardiac Emergencies

