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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
Cardiac-resynchronization therapy for mild-to-moderate heart failure
Anthony S L Tang1, George A Wells, Mario Talajic
1Island Medical Program, University of British Columbia, Vancouver, Canada. atang@westerncardiology.ca
Insights
Adding cardiac-resynchronization therapy (CRT) to an implantable cardioverter-defibrillator (ICD) significantly reduces mortality and heart failure hospitalizations in eligible patients. While effective, this combination therapy is associated with a higher incidence of adverse events post-implantation.
Area of Science:
- Cardiology
- Medical Devices
- Heart Failure Management
Background:
- Cardiac-resynchronization therapy (CRT) is beneficial for patients with left ventricular systolic dysfunction and wide QRS complexes.
- Many patients eligible for CRT are also candidates for implantable cardioverter-defibrillators (ICDs).
- The study investigates the added benefit of CRT to ICDs in reducing mortality and morbidity.
Purpose of the Study:
- To evaluate the efficacy of combining CRT with ICD and optimal medical therapy.
- To determine the impact on mortality and heart failure hospitalizations.
- To assess the safety profile of combined ICD and CRT therapy.
Main Methods:
- Randomized assignment of patients with NYHA class II-III heart failure, LVEF ≤30%, and wide QRS (≥120ms intrinsic or ≥200ms paced) to ICD alone or ICD + CRT.
- Primary outcome: all-cause death or heart failure hospitalization.
- Follow-up duration: mean of 40 months for 1798 patients.
Main Results:
- The ICD + CRT group showed a significant reduction in the primary outcome (33.2% vs. 40.3%, HR 0.75, P<0.001).
- Mortality was lower in the ICD + CRT group (HR 0.75, P=0.003).
- Heart failure hospitalizations were reduced (HR 0.68, P<0.001), but adverse events were higher (124 vs. 58, P<0.001).
Conclusions:
- Combining CRT with ICD therapy significantly reduces death and heart failure hospitalizations in selected NYHA class II-III heart failure patients.
- The benefits of ICD + CRT are accompanied by an increased rate of adverse events in the short term post-implantation.
- This strategy offers a valuable treatment option for heart failure patients with specific electrical conduction abnormalities.
Background:
Cardiac-resynchronization therapy (CRT) benefits patients with left ventricular systolic dysfunction and a wide QRS complex. Most of these patients are candidates for an implantable cardioverter-defibrillator (ICD). We evaluated whether adding CRT to an ICD and optimal medical therapy might reduce mortality and morbidity among such patients.
Methods:
We randomly assigned patients with New York Heart Association (NYHA) class II or III heart failure, a left ventricular ejection fraction of 30% or less, and an intrinsic QRS duration of 120 msec or more or a paced QRS duration of 200 msec or more to receive either an ICD alone or an ICD plus CRT. The primary outcome was death from any cause or hospitalization for heart failure.
Results:
We followed 1798 patients for a mean of 40 months. The primary outcome occurred in 297 of 894 patients (33.2%) in the ICD-CRT group and 364 of 904 patients (40.3%) in the ICD group (hazard ratio in the ICD-CRT group, 0.75; 95% confidence interval [CI], 0.64 to 0.87; P<0.001). In the ICD-CRT group, 186 patients died, as compared with 236 in the ICD group (hazard ratio, 0.75; 95% CI, 0.62 to 0.91; P = 0.003), and 174 patients were hospitalized for heart failure, as compared with 236 in the ICD group (hazard ratio, 0.68; 95% CI, 0.56 to 0.83; P<0.001). However, at 30 days after device implantation, adverse events had occurred in 124 patients in the ICD-CRT group, as compared with 58 in the ICD group (P<0.001).
Conclusions:
Among patients with NYHA class II or III heart failure, a wide QRS complex, and left ventricular systolic dysfunction, the addition of CRT to an ICD reduced rates of death and hospitalization for heart failure. This improvement was accompanied by more adverse events. (Funded by the Canadian Institutes of Health Research and Medtronic of Canada; ClinicalTrials.gov number, NCT00251251.).
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