Machine learning for multidimensional response and survival after cardiac resynchronization therapy using features from cardiac magnetic resonance.

Cardiac resynchronization therapy Heart failure Implantable cardioverter-defibrillator Machine learning Magnetic resonance imaging

Journal

Heart rhythm O2
ISSN: 2666-5018
Titre abrégé: Heart Rhythm O2
Pays: United States
ID NLM: 101768511

Informations de publication

Date de publication:
Oct 2022
Historique:
entrez: 7 11 2022
pubmed: 8 11 2022
medline: 8 11 2022
Statut: epublish

Résumé

Cardiac resynchronization therapy (CRT) response is complex, and better approaches are required to predict survival and need for advanced therapies. The objective was to use machine learning to characterize multidimensional CRT response and its relationship with long-term survival. Associations of 39 baseline features (including cardiac magnetic resonance [CMR] findings and clinical parameters such as glomerular filtration rate [GFR]) with a multidimensional CRT response vector (consisting of post-CRT left ventricular end-systolic volume index [LVESVI] fractional change, post-CRT B-type natriuretic peptide, and change in peak VO Among 200 patients (median age 67.4 years, 27.0% women) with CRT and CMR, associations with more than 1 response parameter were noted for the CMR CURE-SVD dyssynchrony parameter (associated with post-CRT brain natriuretic peptide [BNP] and LVESVI fractional change) and GFR (associated with peak VO Machine learning characterizes distinct CRT response clusters influenced by CMR features, kidney function, and other factors. These clusters have a strong and additive influence on long-term survival relative to baseline features.

Sections du résumé

Background UNASSIGNED
Cardiac resynchronization therapy (CRT) response is complex, and better approaches are required to predict survival and need for advanced therapies.
Objective UNASSIGNED
The objective was to use machine learning to characterize multidimensional CRT response and its relationship with long-term survival.
Methods UNASSIGNED
Associations of 39 baseline features (including cardiac magnetic resonance [CMR] findings and clinical parameters such as glomerular filtration rate [GFR]) with a multidimensional CRT response vector (consisting of post-CRT left ventricular end-systolic volume index [LVESVI] fractional change, post-CRT B-type natriuretic peptide, and change in peak VO
Results UNASSIGNED
Among 200 patients (median age 67.4 years, 27.0% women) with CRT and CMR, associations with more than 1 response parameter were noted for the CMR CURE-SVD dyssynchrony parameter (associated with post-CRT brain natriuretic peptide [BNP] and LVESVI fractional change) and GFR (associated with peak VO
Conclusion UNASSIGNED
Machine learning characterizes distinct CRT response clusters influenced by CMR features, kidney function, and other factors. These clusters have a strong and additive influence on long-term survival relative to baseline features.

Identifiants

pubmed: 36340495
doi: 10.1016/j.hroo.2022.06.005
pii: S2666-5018(22)00148-9
pmc: PMC9626744
doi:

Types de publication

Journal Article

Langues

eng

Pagination

542-552

Subventions

Organisme : NHLBI NIH HHS
ID : R01 HL159945
Pays : United States

Informations de copyright

© 2022 Heart Rhythm Society. Published by Elsevier Inc.

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Auteurs

Derek J Bivona (DJ)

Department of Medicine, University of Virginia Health System, Charlottesville, Virginia.
Department of Biomedical Engineering, University of Virginia Health System, Charlottesville, Virginia.

Srikar Tallavajhala (S)

Department of Medicine, University of Virginia Health System, Charlottesville, Virginia.

Mohamad Abdi (M)

Department of Biomedical Engineering, University of Virginia Health System, Charlottesville, Virginia.

Pim J A Oomen (PJA)

Department of Biomedical Engineering, University of California, Irvine, California.

Xu Gao (X)

Department of Medicine, Northwestern University, Chicago, Illinois.

Rohit Malhotra (R)

Department of Medicine, University of Virginia Health System, Charlottesville, Virginia.

Andrew E Darby (AE)

Department of Medicine, University of Virginia Health System, Charlottesville, Virginia.

Oliver J Monfredi (OJ)

Department of Medicine, University of Virginia Health System, Charlottesville, Virginia.

J Michael Mangrum (JM)

Department of Medicine, University of Virginia Health System, Charlottesville, Virginia.

Pamela K Mason (PK)

Department of Medicine, University of Virginia Health System, Charlottesville, Virginia.

Sula Mazimba (S)

Department of Medicine, University of Virginia Health System, Charlottesville, Virginia.

Michael Salerno (M)

Departments of Medicine and Radiology, Stanford University, Palo Alto, California.

Christopher M Kramer (CM)

Department of Medicine, University of Virginia Health System, Charlottesville, Virginia.
Department of Radiology and Medical Imaging, University of Virginia Health System, Charlottesville, Virginia.

Frederick H Epstein (FH)

Department of Biomedical Engineering, University of Virginia Health System, Charlottesville, Virginia.
Department of Radiology and Medical Imaging, University of Virginia Health System, Charlottesville, Virginia.

Jeffrey W Holmes (JW)

Departments of Medicine, Surgery, and Biomedical Engineering, University of Alabama at Birmingham, Birmingham, Alabama.

Kenneth C Bilchick (KC)

Department of Medicine, University of Virginia Health System, Charlottesville, Virginia.

Classifications MeSH