Effects of Continuous Accelerated Pacing on Cardiac Structure and Function in Patients With Heart Failure With Preserved Ejection Fraction: Insights From the myPACE Randomized Clinical Trial.

HFpEF pacing ventricular remodeling

Journal

Journal of the American Heart Association
ISSN: 2047-9980
Titre abrégé: J Am Heart Assoc
Pays: England
ID NLM: 101580524

Informations de publication

Date de publication:
29 Dec 2023
Historique:
medline: 29 12 2023
pubmed: 29 12 2023
entrez: 29 12 2023
Statut: aheadofprint

Résumé

Heart failure with preserved ejection fraction ≥50% is prevalent with few evidence-based therapies. In a trial of patients with heart failure with preserved ejection fraction with specialized pacemakers, treatment with accelerated personalized pacing averaging 75 bpm (myPACE) markedly improved quality of life, NT-proBNP (N-terminal pro-brain natriuretic peptide), physical activity, and atrial fibrillation burden compared with the standard lower rate setting of 60 bpm (usual care). In this exploratory study, provider-initiated echocardiographic studies obtained before and after the trial were assessed for changes in left ventricular (LV) structure and function among participants who continued their pacing assignment. The analytic approach aimed to detect differences in standard and advanced echocardiographic parameters within and between study arms. Of the 100 participants, 16 myPACE and 20 usual care arm had a qualifying set of echocardiograms performed a mean (SD) 3 (2.0) years apart. Despite similar baseline echocardiogram measures, sustained exposure to moderately accelerated pacing resulted in reduced septal wall thickness (in cm: myPACE 1.1 [0.2] versus usual care 1.2 [0.2], Exposure to continuous accelerated pacing in heart failure with preserved ejection fraction is associated with a reduced LV wall thickness and a small amount of LV dilation with small reduction in ejection fraction.

Sections du résumé

BACKGROUND BACKGROUND
Heart failure with preserved ejection fraction ≥50% is prevalent with few evidence-based therapies. In a trial of patients with heart failure with preserved ejection fraction with specialized pacemakers, treatment with accelerated personalized pacing averaging 75 bpm (myPACE) markedly improved quality of life, NT-proBNP (N-terminal pro-brain natriuretic peptide), physical activity, and atrial fibrillation burden compared with the standard lower rate setting of 60 bpm (usual care).
METHODS AND RESULTS RESULTS
In this exploratory study, provider-initiated echocardiographic studies obtained before and after the trial were assessed for changes in left ventricular (LV) structure and function among participants who continued their pacing assignment. The analytic approach aimed to detect differences in standard and advanced echocardiographic parameters within and between study arms. Of the 100 participants, 16 myPACE and 20 usual care arm had a qualifying set of echocardiograms performed a mean (SD) 3 (2.0) years apart. Despite similar baseline echocardiogram measures, sustained exposure to moderately accelerated pacing resulted in reduced septal wall thickness (in cm: myPACE 1.1 [0.2] versus usual care 1.2 [0.2],
CONCLUSIONS CONCLUSIONS
Exposure to continuous accelerated pacing in heart failure with preserved ejection fraction is associated with a reduced LV wall thickness and a small amount of LV dilation with small reduction in ejection fraction.

Identifiants

pubmed: 38156545
doi: 10.1161/JAHA.123.032873
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e9139

Auteurs

Kramer J Wahlberg (KJ)

Department of Medicine University of Vermont Larner College of Medicine Burlington VT.

Margaret Infeld (M)

Department of Medicine University of Vermont Larner College of Medicine Burlington VT.

Timothy B Plante (TB)

Department of Medicine University of Vermont Larner College of Medicine Burlington VT.

Alexandra E Novelli (AE)

Department of Medicine University of Vermont Larner College of Medicine Burlington VT.

Nicole Habel (N)

Department of Medicine University of Vermont Larner College of Medicine Burlington VT.

Daniel Burkhoff (D)

Cardiovascular Research Foundation New York NY.

Trace Barrett (T)

Department of Medicine University of Vermont Larner College of Medicine Burlington VT.

Daniel Lustgarten (D)

Department of Medicine University of Vermont Larner College of Medicine Burlington VT.

Markus Meyer (M)

Department of Medicine University of Vermont Larner College of Medicine Burlington VT.
Department of Medicine Lillehei Heart Institute, University of Minnesota College of Medicine Minneapolis MN.

Classifications MeSH