Safety and efficacy of ranolazine in hypertrophic cardiomyopathy: Real-world experience in a National Referral Center.


Journal

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

Informations de publication

Date de publication:
01 Jan 2023
Historique:
received: 03 06 2022
revised: 03 10 2022
accepted: 06 10 2022
pubmed: 14 10 2022
medline: 15 12 2022
entrez: 13 10 2022
Statut: ppublish

Résumé

We assessed the efficacy and safety of ranolazine in real-world patients with hypertrophic cardiomyopathy (HCM). Ranolazine is an anti-anginal drug that inhibits the late phase of the inward sodium current. In a small prospective trial, ranolazine reduced the arrhythmic burden and improved biomarker profile in HCM patients. However, systematic reports reflecting real-world use in this setting are lacking. Changes in clinical and instrumental features, symptoms and arrhythmic burden were evaluated in 119 patients with HCM before and during treatment with ranolazine at a national referral centre for HCM. Patients were treated with ranolazine for 2 [1-4] years; 83 (70%) achieved a dosage ≥1000 mg per day. Treatment interruption was necessary in 24 patients (20%) due to side effects (n = 10, 8%) or disopyramide initiation (n = 8, 7%). Seventy patients (59%) were treated with ranolazine for relief of angina. Among them, 51 (73%) had total symptomatic relief and 47 patients (67%) showed ≥2 Canadian Cardiovascular society (CCS) angina grade improvement. Sixteen patients (13%) were treated for recurrent ventricular arrhythmias, including 4 with a clear ischemic trigger, who experienced no further arrhythmic episodes while on ranolazine. Finally, 33 patients (28%) were treated for heart failure associated with severe diastolic dysfunction: no symptomatic benefit could be observed in this group. Ranolazine was safe and well tolerated in patients with HCM. The use of ranolazine may be considered in patients with HCM and microvascular angina.

Sections du résumé

OBJECTIVES OBJECTIVE
We assessed the efficacy and safety of ranolazine in real-world patients with hypertrophic cardiomyopathy (HCM).
BACKGROUND BACKGROUND
Ranolazine is an anti-anginal drug that inhibits the late phase of the inward sodium current. In a small prospective trial, ranolazine reduced the arrhythmic burden and improved biomarker profile in HCM patients. However, systematic reports reflecting real-world use in this setting are lacking.
METHODS METHODS
Changes in clinical and instrumental features, symptoms and arrhythmic burden were evaluated in 119 patients with HCM before and during treatment with ranolazine at a national referral centre for HCM.
RESULTS RESULTS
Patients were treated with ranolazine for 2 [1-4] years; 83 (70%) achieved a dosage ≥1000 mg per day. Treatment interruption was necessary in 24 patients (20%) due to side effects (n = 10, 8%) or disopyramide initiation (n = 8, 7%). Seventy patients (59%) were treated with ranolazine for relief of angina. Among them, 51 (73%) had total symptomatic relief and 47 patients (67%) showed ≥2 Canadian Cardiovascular society (CCS) angina grade improvement. Sixteen patients (13%) were treated for recurrent ventricular arrhythmias, including 4 with a clear ischemic trigger, who experienced no further arrhythmic episodes while on ranolazine. Finally, 33 patients (28%) were treated for heart failure associated with severe diastolic dysfunction: no symptomatic benefit could be observed in this group.
CONCLUSION CONCLUSIONS
Ranolazine was safe and well tolerated in patients with HCM. The use of ranolazine may be considered in patients with HCM and microvascular angina.

Identifiants

pubmed: 36228766
pii: S0167-5273(22)01523-6
doi: 10.1016/j.ijcard.2022.10.014
pii:
doi:

Substances chimiques

Ranolazine A6IEZ5M406
Acetanilides 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

271-278

Informations de copyright

Copyright © 2022 Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest Prof. Olivotto is in the advisory board and had research grant from BMS-Myokardia, Cytokinetics, Boston Scientific, Sanofi Genzyme, Shire Takeda, Amicus, Menarini International, Bayer, Tenaya.

Auteurs

Alessia Argirò (A)

Cardiomyopathy Unit, Cardiothoracovascular Department, Careggi University Hospital, Florence, Italy.

Mattia Zampieri (M)

Cardiomyopathy Unit, Cardiothoracovascular Department, Careggi University Hospital, Florence, Italy. Electronic address: mattiazampieri29@gmail.com.

Lorenzo-Lupo Dei (LL)

Cardiomyopathy Unit, Cardiothoracovascular Department, Careggi University Hospital, Florence, Italy; Cardiology, Health and Environmental Science|, University of L'Aquila, L'Aquila, Italy.

Cecilia Ferrantini (C)

Department of Experimental and Clinical Medicine, University of Florence, Florence, Italy.

Alberto Marchi (A)

Cardiomyopathy Unit, Cardiothoracovascular Department, Careggi University Hospital, Florence, Italy.

Alessia Tomberli (A)

Cardiomyopathy Unit, Cardiothoracovascular Department, Careggi University Hospital, Florence, Italy.

Katia Baldini (K)

Cardiomyopathy Unit, Cardiothoracovascular Department, Careggi University Hospital, Florence, Italy.

Francesco Cappelli (F)

Cardiomyopathy Unit, Cardiothoracovascular Department, Careggi University Hospital, Florence, Italy.

Silvia Favilli (S)

O.U. of Cardiology, A.O.U. Meyer, Florence, Italy.

Silvia Passantino (S)

O.U. of Cardiology, A.O.U. Meyer, Florence, Italy.

Chiara Zocchi (C)

Cardiomyopathy Unit, Cardiothoracovascular Department, Careggi University Hospital, Florence, Italy.

Luigi Tassetti (L)

Cardiomyopathy Unit, Cardiothoracovascular Department, Careggi University Hospital, Florence, Italy.

Martina Gabriele (M)

Cardiomyopathy Unit, Cardiothoracovascular Department, Careggi University Hospital, Florence, Italy.

Niccolò Maurizi (N)

Cardiomyopathy Unit, Cardiothoracovascular Department, Careggi University Hospital, Florence, Italy; Service of Cardiology, University Hospital of Lausanne, Switzerland.

Niccolò Marchionni (N)

Cardiothoracovascular Department, Careggi University Hospital, Florence, Italy.

Raffaele Coppini (R)

Department NeuroFarBa, University of Florence, Florence, Italy.

Iacopo Olivotto (I)

Cardiomyopathy Unit, Cardiothoracovascular Department, Careggi University Hospital, Florence, Italy.

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Classifications MeSH