神经肌肉电刺激能促进急性踝关节扭伤后的恢复吗?一项先导随机对照试验。

IF 1.9 Q2 ORTHOPEDICS
Thomas W Wainwright, Louise C Burgess, Robert G Middleton
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引用次数: 11

摘要

目的:踝关节软组织损伤后,患者常被转诊到门诊进行物理治疗,其症状包括疼痛、活动范围和功能减弱以及水肿。在这项研究中,我们评估了神经肌肉电刺激(NMES)装置作为辅助治疗的使用,以减少I级和II级踝关节扭伤患者的水肿。方法:这是一项单中心、先导随机对照研究,招募踝关节扭伤后进行物理治疗的患者。出现水肿的参与者被随机分配到两个治疗组中的一个:(1)目前的治疗标准和(2)目前的治疗标准加NMES的使用。参与者在急诊科被确定,并在受伤后1至5天转介到物理治疗部门进行治疗,并在7天后返回诊所。结果:22名参与者完成了研究,并有完整的数据集供分析(每组11名)。与标准治疗组相比,干预组的平均容积位移减小(P = 0.011);然而,在8字形测量、功能或疼痛评分方面,组间没有差异。该装置耐受性良好,无器械相关不良事件记录。结论:在这项随机对照试验中,NMES在踝关节扭伤患者中具有良好的耐受性,并且通过液体置换测量显示,NMES在水肿减轻方面具有统计学意义的显著改善。没有观察到其他变化。进一步的工作需要确认临床意义和对踝关节扭伤后长期恢复的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Does Neuromuscular Electrical Stimulation Improve Recovery Following Acute Ankle Sprain? A Pilot Randomised Controlled Trial.

Does Neuromuscular Electrical Stimulation Improve Recovery Following Acute Ankle Sprain? A Pilot Randomised Controlled Trial.

Does Neuromuscular Electrical Stimulation Improve Recovery Following Acute Ankle Sprain? A Pilot Randomised Controlled Trial.

Does Neuromuscular Electrical Stimulation Improve Recovery Following Acute Ankle Sprain? A Pilot Randomised Controlled Trial.

Aim: Following soft tissue ankle injury, patients are often referred for out-patient physiotherapy and present symptoms including pain, reduced range of movement and function, and oedema. In this study, we assess the use of a neuromuscular electrical stimulation (NMES) device as an adjunctive therapy to reduce oedema in patients recovering from grade I and II ankle sprains.

Methods: This was a single-centre, pilot randomised controlled study, recruiting patients referred to physiotherapy following an ankle sprain. Participants presenting with oedema were randomised to one of two treatment groups: (1) the current standard of care and (2) the current standard of care plus NMES use. Participants were identified in an emergency department and referred to a physiotherapy department for treatment 1 to 5 days following the injury and returned to clinic 7 days later.

Results: Twenty-two participants completed the study and had full data sets for analysis (11 in each group). Mean volumetric displacement was reduced in the intervention group in comparison to the standard care group (P = .011); however, there were no between-group differences in figure of eight measurements, function or pain scores. The device was well tolerated, with no device-related adverse events recorded.

Conclusions: In this pilot, randomised controlled trial, NMES was well tolerated by patients following ankle sprain and demonstrated statistically significant improvements in oedema reduction as measured by fluid displacement. No other changes were observed. Further work will need to confirm the clinical significance and effect on longer term recovery post-ankle sprain.

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来源期刊
CiteScore
4.40
自引率
0.00%
发文量
14
审稿时长
8 weeks
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