Related Experiment Video
Updated: Feb 28, 2026

A New Single Chamber Implantable Defibrillator with Atrial Sensing: A Practical Demonstration of Sensing and Ease of Implantation
Published on: February 28, 2012
Incidence and Predictors of Appropriate Implantable Cardioverter-Defibrillator Therapy in Light Chain Cardiac
Thibaut Moulin1, Amira Zaroui2, Khaled Ramoul1
1Department of Cardiology, Assistance Publique-Hôpitaux de Paris, Henri Mondor University Hospital, Créteil, France.
Insights
Sudden cardiac death is common in light chain cardiac amyloidosis (AL CA). Prophylactic ICDs in AL CA patients show high appropriate therapy rates, with impaired LV global longitudinal strain predicting risk.
Area of Science:
- Cardiology
- Electrophysiology
- Cardiac Amyloidosis Research
Background:
- Sudden cardiac death is a significant cause of mortality in light chain cardiac amyloidosis (AL CA).
- Limited data exist on the effectiveness of implantable cardioverter defibrillators (ICDs) in AL CA patients.
- Understanding ICD therapy outcomes is crucial for managing this high-risk population.
Purpose of the Study:
- To determine the incidence of appropriate ICD therapies in AL CA patients.
- To identify predictors of appropriate ICD therapies in this cohort.
- To evaluate the role of ICDs in primary prevention for AL CA.
Main Methods:
- Retrospective study of AL CA patients who received ICDs between November 2014 and May 2024.
- Primary endpoint: first appropriate ICD therapy (shock or antitachycardia pacing).
- Analysis of factors associated with appropriate ICD therapies, including left ventricular (LV) global longitudinal strain.
Main Results:
- 150 AL CA patients with primary prevention ICDs were analyzed.
- 18.0% of patients received at least one appropriate ICD therapy over a median follow-up of 16.8 months.
- Impaired LV global longitudinal strain (cutoff -9.5%) was independently associated with a significantly higher risk of appropriate ICD therapy (aSHR: 5.33).
Conclusions:
- AL CA patients receiving prophylactic ICDs experience frequent appropriate therapies.
- LV global longitudinal strain may aid in risk stratification for ventricular arrhythmias in AL CA.
- Further research is needed to clarify the impact of ICDs on overall survival in AL CA.
Background:
Sudden cardiac death represents a common mode of death in patients with light chain cardiac amyloidosis (AL CA). However, data evaluating the role of implantable cardioverter defibrillator (ICD) in these patients are scarce.
Objectives:
This study aimed to describe the incidence and identify factors associated with appropriate ICD therapies in AL CA patients.
Methods:
This was a retrospective, single referral center study including all AL CA patients implanted with ICDs between November 2014 and May 2024. The primary endpoint was the first appropriate ICD therapy (shock or antitachycardia pacing).
Results:
A total of 150 patients (mean age 63.4 ± 9.2 years, 65.3% male) were included, all with primary prevention ICDs. Over a median follow-up period of 16.8 months (Q1-Q3: 5.4-56.5 months), 27 (18.0%) patients received at least 1 appropriate ICD therapy (1-year cumulative incidence: 11.6%; 95% CI: 7.4%-18.2%; 5-year cumulative incidence: 19.5%; 95% CI: 13.4%-28.4%). In multivariate analysis, impaired left ventricular (LV) global longitudinal strain was independently associated with a higher risk of appropriate ICD therapy (optimal cutoff -9.5%; adjusted subdistribution HR: 5.33; 95% CI: 1.99-14.26; P = 0.0009).
Conclusions:
AL CA patients implanted with prophylactic ICDs experience high rates of appropriate therapies. Assessment of LV involvement with LV global longitudinal strain might improve risk stratification for ventricular arrhythmias. Further studies are needed to assess the impact of ICD on overall survival in this population.
Related Concept Videos
Cardiomyopathy V: Interprofessional Care
Cardiomyopathy II: Dilated Cardiomyopathy
Cardiomyopathy III: Hypertrophic Cardiomyopathy
Cardiomyopathy IV: Restrictive Cardiomyopathy
Heart Failure VI: Adjunct Therapies
Cardiomyopathy I: Introduction and Classification

