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[氨吡啶对多发性硬化症(MS)患者步态的影响]

[The effect of fampridine on gait in people with Multiple sclerosis (MS)].

作者信息

Gudjonsdottir Bjorg, Hjaltason Haukur, Andresdottir Gudbjorg Thora

机构信息

Department of Physical Therapy, School of Health Sciences, University of Iceland.

Faculty of Medicine, School of Health Sciences, University of Iceland, Department of Neurology, National University Hospital, Iceland.

出版信息

Laeknabladid. 2021 Apr;107(4):179-184. doi: 10.17992/lbl.2021.04.630.

DOI:10.17992/lbl.2021.04.630
PMID:33769308
Abstract

INTRODUCTION

Fampridine is a drug for people with Multiple Sclerosis (MS). It is a broad-spectrum voltage-dependent potassium channel blocker that enhances synaptic transmission. The drug has been shown to be able to enhance conduction in demyelinated axons, thereby leading to improved gait in patients with MS. The purpose of this study was to examine the effect of fampridine on gait function in people with MS in the end of a 2 weeks trial drug period and to observe how many patients continued drug therapy.

MATERIAL AND METHODS

Data from 41 individuals with MS was collected retrospectively for this study. Measurements were administered by physiotherapists and the results from the Timed 25-Foot Walk (T25FW) and 12-item Multiple Sclerosis Walking Scale (MSWS-12) were obtained from medical records from The National University Hospital of Iceland.

RESULTS

The results showed a significant difference in walking speed before and at the end of trial period (p<0.0001). The average improvement in walking speed was 22%. Results also demonstrated a significant difference in MSWS-12 scores before and at the end of treatment (p<0.0001). The average improvement in MSWS-12 was 11.4 points. Eighteen individuals (43.9%) continued treatment after the trial period.

CONCLUSION

Fampridine can have a positive effect on impaired gait function in people with MS and can be an important adjunct to treatment.

摘要

引言

氨吡啶是一种用于治疗多发性硬化症(MS)患者的药物。它是一种广谱电压依赖性钾通道阻滞剂,可增强突触传递。已证明该药物能够增强脱髓鞘轴突的传导,从而改善MS患者的步态。本研究的目的是在为期2周的药物试验期结束时,研究氨吡啶对MS患者步态功能的影响,并观察有多少患者继续接受药物治疗。

材料与方法

本研究回顾性收集了41例MS患者的数据。测量由物理治疗师进行,25英尺定时步行(T25FW)和12项多发性硬化症步行量表(MSWS-12)的结果来自冰岛国立大学医院的医疗记录。

结果

结果显示试验期开始和结束时的步行速度存在显著差异(p<0.0001)。步行速度的平均改善率为22%。结果还表明治疗开始和结束时MSWS-12评分存在显著差异(p<0.0001)。MSWS-12的平均改善为11.4分。18名患者(43.9%)在试验期后继续接受治疗。

结论

氨吡啶可对MS患者受损的步态功能产生积极影响,并且可以成为治疗的重要辅助手段。

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1
[The effect of fampridine on gait in people with Multiple sclerosis (MS)].[氨吡啶对多发性硬化症(MS)患者步态的影响]
Laeknabladid. 2021 Apr;107(4):179-184. doi: 10.17992/lbl.2021.04.630.
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Real-life experience with fampridine (Fampyra®) for patients with multiple sclerosis and gait disorders.对于患有多发性硬化症和步态障碍的患者使用氨吡啶(Fampyra®)的实际经验。
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Fampridine response in MS patients with gait impairment in a real-world setting: Need for new response criteria?在现实环境中,具有步态障碍的 MS 患者对 Fampridine 的反应:是否需要新的反应标准?
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A guide to treating gait impairment with prolonged-release fampridine (Fampyra) in patients with multiple sclerosis.多发性硬化症患者使用缓释氨吡啶(法吡拉)治疗步态障碍指南。
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Sustained-released fampridine in multiple sclerosis: effects on gait parameters, arm function, fatigue, and quality of life.多发性硬化症中的缓释金刚烷胺:对步态参数、手臂功能、疲劳和生活质量的影响。
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Evaluation of functional outcome measures after fampridine treatment in patients with multiple sclerosis - An interventional follow-up study.多发性硬化症患者服用氨吡啶治疗后功能结局指标的评估——一项干预性随访研究。
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Sustained-release oral fampridine in multiple sclerosis: a randomised, double-blind, controlled trial.缓释口服法吡酯治疗多发性硬化症:一项随机、双盲、对照试验
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