Markers of responsiveness to disopyramide in patients with hypertrophic cardiomyopathy.


Journal

International journal of cardiology
ISSN: 1874-1754
Titre abrégé: Int J Cardiol
Pays: Netherlands
ID NLM: 8200291

Informations de publication

Date de publication:
15 12 2019
Historique:
received: 09 05 2019
revised: 11 09 2019
accepted: 23 09 2019
pubmed: 17 10 2019
medline: 11 7 2020
entrez: 17 10 2019
Statut: ppublish

Résumé

Significant left-ventricular outflow tract obstruction (LVOTO) in hypertrophic cardiomyopathy (HCM) may result in symptoms and is associated with adverse outcomes. Although disopyramide can reduce resting gradients, nearly 30% of HCM patients do not respond. We sought to study the clinical and echocardiographic variables associated with disopyramide-induced LVOT-gradient reduction. Forty-one disopyramide-treated HCM patients (average daily-dose 305 mg) were subdivided into two groups: (1) nineteen responders, with a reduction of LVOT-gradients of at least 30% from baseline, and (2) twenty-two non-responders, in whom LVOT-gradients did not change or increased following treatment. All patients had a thorough clinical and echocardiographic assessment pre- and post-treatment initiation. Patients who responded to disopyramide had better pretreatment left ventricular (LV) systolic function (LV ejection fraction of 67.9 ± 5.6% vs. 59.7 ± 5.8%, p = 0.0001), better LV global longitudinal strain (-17.9 ± 2.3% vs. -16.1 ± 2.5%, p = 0.048), less mitral regurgitation, smaller LV size (indexed LV end-systolic volume of 16.2 ± 5.1 ml/m Obstructive HCM patients with more severe disease at baseline tend to respond less to disopyramide treatment. In those patients, early referral for alcohol septal ablation or myectomy surgery should be considered.

Sections du résumé

BACKGROUND
Significant left-ventricular outflow tract obstruction (LVOTO) in hypertrophic cardiomyopathy (HCM) may result in symptoms and is associated with adverse outcomes. Although disopyramide can reduce resting gradients, nearly 30% of HCM patients do not respond. We sought to study the clinical and echocardiographic variables associated with disopyramide-induced LVOT-gradient reduction.
METHODS
Forty-one disopyramide-treated HCM patients (average daily-dose 305 mg) were subdivided into two groups: (1) nineteen responders, with a reduction of LVOT-gradients of at least 30% from baseline, and (2) twenty-two non-responders, in whom LVOT-gradients did not change or increased following treatment. All patients had a thorough clinical and echocardiographic assessment pre- and post-treatment initiation.
RESULTS
Patients who responded to disopyramide had better pretreatment left ventricular (LV) systolic function (LV ejection fraction of 67.9 ± 5.6% vs. 59.7 ± 5.8%, p = 0.0001), better LV global longitudinal strain (-17.9 ± 2.3% vs. -16.1 ± 2.5%, p = 0.048), less mitral regurgitation, smaller LV size (indexed LV end-systolic volume of 16.2 ± 5.1 ml/m
CONCLUSIONS
Obstructive HCM patients with more severe disease at baseline tend to respond less to disopyramide treatment. In those patients, early referral for alcohol septal ablation or myectomy surgery should be considered.

Identifiants

pubmed: 31615649
pii: S0167-5273(19)32410-6
doi: 10.1016/j.ijcard.2019.09.066
pii:
doi:

Substances chimiques

Voltage-Gated Sodium Channel Blockers 0
Disopyramide GFO928U8MQ

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

75-82

Informations de copyright

Copyright © 2019 Elsevier B.V. All rights reserved.

Auteurs

Manhal Habib (M)

Department of Cardiology, Toronto General Hospital, Toronto, Canada.

Sara Hoss (S)

Department of Cardiology, Toronto General Hospital, Toronto, Canada.

Beata Bruchal-Garbicz (B)

Department of Cardiology, Toronto General Hospital, Toronto, Canada.

Raymond H Chan (RH)

Department of Cardiology, Toronto General Hospital, Toronto, Canada.

Harry Rakowski (H)

Department of Cardiology, Toronto General Hospital, Toronto, Canada.

Lynne Williams (L)

Department of Cardiology, Royal Papworth Hospital, Cambridge, UK.

Arnon Adler (A)

Department of Cardiology, Toronto General Hospital, Toronto, Canada. Electronic address: Arnon.Adler@uhn.ca.

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Classifications MeSH