Centre de Référence des Maladies Neuromusculaires Nord/Est/Île-de-France, Cardiology Department, Cochin Hospital, AP-HP, Paris Cité University, 75014 Paris, France; Paris Cardiovascular Research Centre (PARCC), Inserm Unit 970, Georges-Pompidou European Hospital, 75015 Paris, France.
Constitutive Reference Centre for Neuromuscular Diseases, Neuro-Myology Department, Pitié-Salpêtrière University Hospital, AP-HP, 75013 Paris, France.
Arch Cardiovasc Dis. 2024 Jun-Jul;117(6-7):450-456. doi: 10.1016/j.acvd.2024.03.001. Epub 2024 Apr 15.
In France, mexiletine - a class I antiarrhythmic drug - can be prescribed for the symptomatic treatment of myotonia of the skeletal muscles in adult patients with myotonic dystrophy under a compassionate use programme. Mexiletine is used according to its summary of product characteristics, which describes its use for myotonia treatment in adult patients with non-dystrophic myotonia, a different neuromuscular condition without cardiac involvement. A cardiac assessment is required prior to initiation and throughout treatment due to potential proarrhythmic effects. The presence of conduction system disease, the most common cardiac manifestation of myotonic dystrophy, mandates repeated cardiac evaluations in patients with this condition, and becomes even more important when they are given mexiletine. A group of experts, including three neurologists and five cardiologists from French neuromuscular reference centres, were involved in a task force to develop a treatment algorithm to guide mexiletine use in myotonic dystrophy. The recommendations are based on data from a literature review of the safety of mexiletine-treated patients with myotonic dystrophy, the compassionate use protocol for mexiletine and the personal clinical experience of the experts. The main conclusion of the expert group is that, although existing safety data in mexiletine-treated patients with myotonic dystrophy are reassuring, cardiac assessments should be reinforced in such patients compared with mexiletine-treated patients with non-dystrophic myotonia. This expert opinion to guide mexiletine treatment in patients with myotonic dystrophy should help to reduce the risk of severe adverse events and facilitate interactions between specialists involved in the routine care of patients with myotonic dystrophy.
在法国,根据同情用药方案,米贝地尔(一种 I 类抗心律失常药物)可用于治疗成年肌强直性营养不良患者骨骼肌肌强直的症状。米贝地尔的使用依据其产品特性摘要,其中描述了其在非营养不良性肌强直的成年患者中用于肌强直治疗的用途,这是一种不同的、不涉及心脏的神经肌肉疾病。由于存在潜在的致心律失常作用,在开始治疗和整个治疗过程中都需要进行心脏评估。传导系统疾病是肌强直性营养不良最常见的心脏表现,因此对于患有这种疾病的患者需要反复进行心脏评估,而当给予米贝地尔时则变得更加重要。一组专家,包括来自法国神经肌肉参考中心的三名神经病学家和五名心脏病专家,参与了一个工作组,制定了一个治疗算法来指导米贝地尔在肌强直性营养不良中的使用。该建议基于对患有肌强直性营养不良的米贝地尔治疗患者安全性的文献综述数据、米贝地尔的同情用药方案以及专家的个人临床经验。专家组的主要结论是,尽管米贝地尔治疗的肌强直性营养不良患者的现有安全性数据令人放心,但与米贝地尔治疗的非营养不良性肌强直患者相比,此类患者应加强心脏评估。该专家意见旨在指导肌强直性营养不良患者的米贝地尔治疗,有助于降低严重不良事件的风险,并促进参与肌强直性营养不良患者常规护理的专家之间的互动。