Cardiac Magnetic Resonance, Electromechanical Activation, Kidney Function, and Natriuretic Peptides in Cardiac Resynchronization Therapy Upgrades

Author:

Bivona Derek J.1,Oomen Pim J. A.2,Wang Yu3ORCID,Morales Frances L.1,Abdi Mohamad3,Gao Xu4,Malhotra Rohit1,Darby Andrew1,Mehta Nishaki5,Monfredi Oliver J.1,Mangrum J. Michael1,Mason Pamela K.1,Levy Wayne C.6,Mazimba Sula1,Patel Amit R.1ORCID,Epstein Frederick H.37,Bilchick Kenneth C.1

Affiliation:

1. Department of Cardiovascular Medicine, University of Virginia Health System, Charlottesville, VA 22908, USA

2. Department of Biomedical Engineering, University of California Irvine, Irvine, CA 92617, USA

3. Department of Biomedical Engineering, University of Virginia Health System, Charlottesville, VA 22908, USA

4. Department of Medicine, Northwestern University, Chicago, IL 60611, USA

5. Department of Medicine, William Beaumont Oakland University School of Medicine, Royal Oak, MI 48309, USA

6. Department of Medicine, University of Washington, Seattle, WA 98195, USA

7. Department of Radiology and Medical Imaging, University of Virginia Health System, Charlottesville, VA 22908, USA

Abstract

As the mechanism for worse prognosis after cardiac resynchronization therapy (CRT) upgrades in heart failure patients with RVP dependence (RVP-HF) has clinical implications for patient selection and CRT implementation approaches, this study’s objective was to evaluate prognostic implications of cardiac magnetic resonance (CMR) findings and clinical factors in 102 HF patients (23.5% female, median age 66.5 years old, median follow-up 4.8 years) with and without RVP dependence undergoing upgrade and de novo CRT implants. Compared with other CRT groups, RVP-HF patients had decreased survival (p = 0.02), more anterior late-activated LV pacing sites (p = 0.002) by CMR, more atrial fibrillation (p = 0.0006), and higher creatinine (0.002). CMR activation timing at the LV pacing site predicted post-CRT LV functional improvement (p < 0.05), and mechanical activation onset < 34 ms by CMR at the LVP site was associated with decreased post-CRT survival in a model with higher pre-CRT creatinine and B-type natriuretic peptide (AUC 0.89; p < 0.0001); however, only the higher pre-CRT creatinine partially mediated (37%) the decreased survival in RVP-HF patients. In conclusion, RVP-HF had a distinct CMR phenotype, which has important implications for the selection of LV pacing sites in CRT upgrades, and only chronic kidney disease mediated the decreased survival after CRT in RVP-HF.

Funder

NHLBI

Publisher

MDPI AG

Subject

Pharmacology (medical),General Pharmacology, Toxicology and Pharmaceutics

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