Atrial Fibrillation in Hypertrophic Cardiomyopathy.
anti-coagulation
atrial fibrillation
hypertrophic cardiomyopathy
rate control
rhythm control
Journal
JACC. Advances
ISSN: 2772-963X
Titre abrégé: JACC Adv
Pays: United States
ID NLM: 9918419284106676
Informations de publication
Date de publication:
Sep 2024
Sep 2024
Historique:
received:
08
03
2024
revised:
21
06
2024
accepted:
27
06
2024
medline:
9
9
2024
pubmed:
9
9
2024
entrez:
9
9
2024
Statut:
epublish
Résumé
Atrial fibrillation (AF) is common among patients with hypertrophic cardiomyopathy (HCM) with a prevalence greater than 25%. AF in HCM is associated with a high risk of stroke and can be a marker of more advanced cardiomyopathy. Although, it frequently results in cardiac hemodynamic changes which are poorly tolerated, it can be subclinical. Thus, prompt diagnosis and adequate management of AF are essential to minimizing AF-related adverse outcomes in HCM. All HCM patients should be screened for AF regularly, and those with high-risk features should be screened more frequently preferably with extended ambulatory monitoring. Once AF is detected, oral anticoagulation should be initiated. Both general and HCM-specific modifiable risk factors should be addressed and assessment for cardiomyopathy progression should be performed. Although no randomized controlled studies have compared rate versus rhythm control in HCM, early rhythm control could be considered to prevent further LA remodeling.
Identifiants
pubmed: 39247675
doi: 10.1016/j.jacadv.2024.101210
pii: S2772-963X(24)00441-1
pmc: PMC11379995
doi:
Types de publication
Journal Article
Review
Langues
eng
Pagination
101210Informations de copyright
© 2024 The Authors.
Déclaration de conflit d'intérêts
Dr Weissler-Snir has received speaker fees from Bristol Myer Squibb; and fees for publication steering committee participation for Cytokinetics and research grants from 10.13039/100004374Medtronic. Dr Rader has received consultant and speaker fees from Bristol Myer Squibbs, Medtronic, Recor Medical, and Cytokinetics. Dr Saberi has received consultant/advisor fees from Bristol Myers Squibb; and has received research grants from Bristol Myers Squibb, 10.13039/100014941Cytokinetics, 10.13039/100004336Novartis, and 10.13039/100005646Actelion Pharmaceuticals. Dr Wong is the site principal investigator for clinical trials sponsored by Bristol Myers Squibb, Cytokinetics, and Tenaya Therapeutics; and discloses unpaid advisory board participation for Bristol Myers Squibb and Cytokinetics. Dr Owens has received consulting/research support from 10.13039/100014941Cytokinetics, MyoKardia/Bristol Myers Squibb, Pfizer, Lexicon Pharmaceuticals, Tenaya Therapeutics, Stealth BioTherapeutics, Renovacor, Edgewise Therapeutics, BioMarin Pharmaceuticals, and Lexeo Therapeutics.