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Updated: May 7, 2026

Benefits of Cardiac Resynchronization Therapy in an Asynchronous Heart Failure Model Induced by Left Bundle Branch Ablation and Rapid Pacing
Published on: December 11, 2017
Response to preventive cardiac resynchronization therapy in patients with ischaemic and nonischaemic cardiomyopathy
Alon Barsheshet1, Ilan Goldenberg, Arthur J Moss
1Cardiology Division, Heart Research Follow-up Program, University of Rochester Medical Center, Rochester, NY, USA. alon.barsheshet@heart.rochester.edu
Mildly symptomatic patients with heart failure responded differently to cardiac resynchronization therapy with defibrillator (CRT-D) based on their cardiomyopathy aetiology. Echocardiographic and clinical benefits varied, indicating a need for aetiology-specific risk assessment for CRT-D.
Area of Science:
- Cardiology
- Electrophysiology
- Heart Failure Management
Background:
- Cardiac resynchronization therapy with a defibrillator (CRT-D) is a key treatment for heart failure.
- Limited data exist on how cardiomyopathy aetiology affects CRT-D response in mildly symptomatic patients.
Purpose of the Study:
- To evaluate the differential outcomes of CRT-D based on ischaemic (ICM) versus non-ischaemic (non-ICM) cardiomyopathy aetiology.
- To identify specific patient subsets within each aetiology that benefit most from CRT-D.
Main Methods:
- Analysis of patients from the MADIT-CRT trial with ICM (n=1046) and non-ICM (n=774) aetiologies.
- Assessment of clinical response (heart failure/death) and echocardiographic response (ventricular volumes) over 2.4 years and 1 year, respectively.
Main Results:
- Both ICM and non-ICM groups showed significant risk reduction for heart failure/death with CRT-D.
- Non-ICM patients exhibited greater reductions in left ventricular volumes compared to ICM patients.
- Favorable clinical response subsets differed, including QRS duration and LBBB in ICM, and female sex and diabetes in non-ICM.
Conclusions:
- Mildly symptomatic patients with ICM and non-ICM cardiomyopathies demonstrate distinct echocardiographic and clinical responses to CRT-D.
- Risk stratification for CRT-D therapy in this population should consider the specific aetiology of cardiomyopathy.
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