Cardiac Resynchronization Therapy Improves Outcomes in Patients With Intraventricular Conduction Delay But Not Right Bundle Branch Block: A Patient-Level Meta-Analysis of Randomized Controlled Trials

Author:

Friedman Daniel J.12ORCID,Al-Khatib Sana M.12ORCID,Dalgaard Frederik23ORCID,Fudim Marat12ORCID,Abraham William T.4ORCID,Cleland John G.F.56ORCID,Curtis Anne B.7ORCID,Gold Michael R.8ORCID,Kutyifa Valentina9ORCID,Linde Cecilia10,Tang Anthony S.11ORCID,Ali-Ahmed Fatima2,Olivas-Martinez Antonio12,Inoue Lurdes Y.T.12,Sanders Gillian D.1321415

Affiliation:

1. Division of Cardiology (D.J.F., S.M.A-K., M.F.), Duke University School of Medicine, Durham, NC.

2. Duke Clinical Research Institute (D.J.F, S.M.A-K., F.D., M.F, G.D.S., F.A-A.), Duke University School of Medicine, Durham, NC.

3. Department of Medicine, Nykøbing Falster Sygehus, Nykøbing, Denmark (F.D.).

4. Division of Cardiovascular Medicine, The Ohio State University, Columbus (W.T.A.).

5. National Heart and Lung Institute, Royal Brompton & Harefield Hospitals, Imperial College, London, United Kingdom (J.G.F.C.).

6. British Heart Foundation Centre of Research Excellence, School of Cardiovascular and Metabolic Health, University of Glasgow, United Kingdom (J.G.F.C.).

7. Department of Medicine, University at Buffalo, NY (A.B.C.).

8. Medical University of South Carolina, Charleston (M.R.G.).

9. Division of Cardiology, Department of Medicine, University of Rochester Medical Center, NY (V.K.).

10. Karolinska Institutet and Department of Cardiology, Karolinska University, Stockholm, Sweden (C.L.).

11. Department of Medicine, Western University, Ontario, Canada (A.S.T.).

12. Department of Biostatistics, University of Washington, Seattle (A.O-M., L.Y.T.I.).

13. Evidence Synthesis Group (G.D.S), Duke University School of Medicine, Durham, NC.

14. Department of Population Health Sciences (G.D.S), Duke University School of Medicine, Durham, NC.

15. Duke-Margolis Center for Health Policy, Duke University, Durham, NC (G.D.S.).

Abstract

Background: Benefit from cardiac resynchronization therapy (CRT) varies by QRS characteristics; individual randomized trials are underpowered to assess benefit for relatively small subgroups. Methods: The authors analyzed patient-level data from pivotal CRT trials (MIRACLE [Multicenter InSync Randomized Clinical Evaluation], MIRACLE-ICD [Multicenter InSync ICD Randomized Clinical Evaluation], MIRACLE-ICD II [Multicenter InSync ICD Randomized Clinical Evaluation II], REVERSE [Resynchronization Reverses Remodeling in Systolic Left Ventricular Dysfunction], RAFT [Resynchronization-Defibrillation for Ambulatory Heart Failure], BLOCK-HF [Biventricular Versus Right Ventricular Pacing in Heart Failure Patients with Atrioventricular Block], COMPANION [Comparison of Medical Therapy, Pacing and Defibrillation in Heart Failure], and MADIT-CRT [Multicenter Automatic Defibrillator Implantation Trial – Cardiac Resynchronization Therapy]) using Bayesian Hierarchical Weibull survival regression models to assess CRT benefit by QRS morphology (left bundle branch block [LBBB], n=4549; right bundle branch block [RBBB], n=691; and intraventricular conduction delay [IVCD], n=1024) and duration (with 150-ms partition). The continuous relationship between QRS duration and CRT benefit was also examined within subgroups defined by QRS morphology. The primary end point was time to heart failure hospitalization (HFH) or death; a secondary end point was time to all-cause death. Results: Of 6264 patients included, 25% were women, the median age was 66 [interquartile range, 58 to 73] years, and 61% received CRT (with or without an implantable cardioverter defibrillator). CRT was associated with an overall lower risk of HFH or death (hazard ratio [HR], 0.73 [credible interval (CrI), 0.65 to 0.84]), and in subgroups of patients with QRS ≥150 ms and either LBBB (HR, 0.56 [CrI, 0.48 to 0.66]) or IVCD (HR, 0.59 [CrI, 0.39 to 0.89]), but not RBBB (HR 0.97 [CrI, 0.68 to 1.34]; P interaction <0.001). No significant association for CRT with HFH or death was observed when QRS was <150 ms (regardless of QRS morphology) or in the presence of RBBB. Similar relationships were observed for all-cause death. Conclusions: CRT is associated with reduced HFH or death in patients with QRS ≥150 ms and LBBB or IVCD, but not for those with RBBB. Aggregating RBBB and IVCD into a single “non-LBBB” category when selecting patients for CRT should be reconsidered. Registration: URL: https://www.clinicaltrials.gov ; Unique identifiers: NCT00271154, NCT00251251, NCT00267098, and NCT00180271.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

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