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氨吡啶用于改善多发性硬化症患者行动不便状况时,物理治疗或可增强其效果:一项非随机两组概念验证性试点研究。

Dalfampridine for Mobility Limitations in People With Multiple Sclerosis May Be Augmented by Physical Therapy: A Non-randomized Two-Group Proof-of-Concept Pilot Study.

作者信息

Plummer Prudence, Markovic-Plese Silva, Giesser Barbara

机构信息

Department of Physical Therapy, MGH Institute of Health Professions, Boston, MA, United States.

Department of Neurology, Thomas Jefferson University, Philadelphia, PA, United States.

出版信息

Front Rehabil Sci. 2022 Jan 11;2:795306. doi: 10.3389/fresc.2021.795306. eCollection 2021.

Abstract

To demonstrate proof-of-concept for a combined physical therapy and pharmacological intervention and obtain preliminary estimates of the therapeutic efficacy of a motor-relearning physical therapy intervention with and without concurrent dalfampridine treatment on gait speed in people with mobility limitations due to multiple sclerosis (MS). Using a non-randomized, two-group design, 4 individuals with MS newly prescribed dalfampridine as part of their routine medical care, and 4 individuals with MS not taking dalfampridine completed a 3-week drug run-in or no-treatment baseline, respectively. After 3 weeks, all participants commenced physical therapy twice weekly for 6 weeks. Participants taking dalfampridine took the medication for the study duration. The physical therapy program comprised functional strengthening, gait training, balance training, and dual-task training. The primary outcome was Timed 25-foot Walk (T25FW) at the end of the 6-week physical therapy program. For the 4 participants taking dalfampridine, average improvement in T25FW on drug only was 12.8% (95% CI 1.2 to 24.4%). During the 6-week physical therapy phase, both groups significantly improved T25FW, but the effect tended to favor the group taking dalfampridine (mean difference = -0.93 s, 95% CI -1.9 to 0.07 s, = 0.064, = 1.6). Whereas the physical therapy group had average T25FW improvement of 10.8% (95% CI 1.0 to 20.5%), the physical therapy plus dalfampridine group demonstrated average improvement of 20.7% (95% CI 3.8 to 37.6%). Further research is warranted to examine whether dalfampridine for mobility impairment may be augmented by physical therapy in people with MS.

摘要

为证明物理治疗与药物干预相结合的概念验证,并初步评估运动再学习物理治疗干预在联合或不联合氨吡啶治疗的情况下,对因多发性硬化症(MS)导致行动不便的患者步态速度的治疗效果。采用非随机、两组设计,4名新开具氨吡啶作为常规医疗护理一部分的MS患者,以及4名未服用氨吡啶的MS患者分别完成了为期3周的药物导入期或无治疗基线期。3周后,所有参与者开始每周进行两次物理治疗,为期6周。服用氨吡啶的参与者在研究期间持续服用该药物。物理治疗方案包括功能强化、步态训练、平衡训练和双任务训练。主要结局是6周物理治疗方案结束时的25英尺定时步行(T25FW)。对于4名服用氨吡啶的参与者,仅使用药物时T25FW的平均改善率为12.8%(95%置信区间1.2%至24.4%)。在6周的物理治疗阶段,两组的T25FW均显著改善,但效果倾向于服用氨吡啶的组(平均差值=-0.93秒,95%置信区间-1.9至0.07秒,P=0.064,效应量=1.6)。物理治疗组的T25FW平均改善率为10.8%(95%置信区间1.0%至20.5%),而物理治疗加氨吡啶组的平均改善率为20.7%(95%置信区间3.8%至37.6%)。有必要进行进一步研究,以检验在MS患者中,物理治疗是否可以增强氨吡啶对行动障碍的治疗效果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ed1/9397954/7fcabd34199a/fresc-02-795306-g0001.jpg

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