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腕管综合征的夹板固定

Splinting for carpal tunnel syndrome.

作者信息

Page Matthew J, Massy-Westropp Nicola, O'Connor Denise, Pitt Veronica

机构信息

School of Public Health & Preventive Medicine, Monash University, Melbourne, Australia.

出版信息

Cochrane Database Syst Rev. 2012 Jul 11;2012(7):CD010003. doi: 10.1002/14651858.CD010003.

Abstract

BACKGROUND

Carpal tunnel syndrome (CTS) is a condition where one of two main nerves in the wrist is compressed, which can lead to pain in the hand, wrist and sometimes arm, and numbness and tingling in the thumb, index and long finger. Splinting is usually offered to people with mild to moderate symptoms. However, the effectiveness and duration of the benefit of splinting for this condition remain unknown.

OBJECTIVES

To compare the effectiveness of splinting for carpal tunnel syndrome with no treatment, placebo or another non-surgical intervention.

SEARCH METHODS

We searched the Cochrane Neuromuscular Disease Group Specialized Register (10 January 2011), CENTRAL, NHSEED and DARE (The Cochrane Library 2011, Issue 4), MEDLINE (January 1966 to December 2011), EMBASE (January 1980 to January 2012), AMED (January 1985 to January 2012), and CINAHL Plus (January 1937 to January 2012), using no time limits. We searched the reference lists of all included trials and relevant reviews for further relevant studies.

SELECTION CRITERIA

All randomised and quasi-randomised trials comparing splinting with no treatment (or a placebo) or with other non-surgical treatments were eligible for inclusion. We also included studies comparing one splint type or regimen versus another. We excluded studies comparing splinting with surgical treatment. There were no language restrictions. We included all patients diagnosed with carpal tunnel syndrome unless they had undergone surgical release.

DATA COLLECTION AND ANALYSIS

Two review authors independently selected trials for inclusion, and performed data extraction. Two authors also independently performed the assessment of risk of bias. We calculated measures of effect as risk ratios (RR) for dichotomous outcomes and mean differences (MD) for continuous outcomes, with 95% confidence intervals (CI) reported and statistical significance set at P < 0.05 for all outcome comparisons.

MAIN RESULTS

The review included 19 studies randomising 1190 participants with carpal tunnel syndrome. Two studies compared splinting with no treatment, five compared different splint designs, one compared different splint-wearing regimens, seven compared splint delivered as a single intervention with another non-surgical intervention, and five compared splint delivered alongside other non-surgical interventions with another non-surgical intervention. Only three studies reported concealing the allocation sequence, and only one reported blinding of participants. Three studies measured the primary outcome, short-term overall improvement at three months or less. One low quality study with 80 wrists found that compared to no treatment, splints worn at night more than tripled the likelihood of reporting overall improvement at the end of four weeks of treatment (RR 3.86, 95% CI 2.29 to 6.51). However, the lack of patient blinding and unclear allocation concealment suggests this result should be interpreted with caution. A very low quality quasi-randomised trial with 90 wrists found that wearing a neutral splint more than doubled the likelihood of reporting 'a lot or complete relief' at the end of two weeks of treatment compared with an extension splint (RR 2.43, 95% CI 1.12 to 5.28). The third study which measured short-term overall improvement did not report outcome data separately per group. Nine studies measured adverse effects of splinting and all found either no or few participants reporting discomfort or swelling due to splinting; however, the precision of all RRs was very low. Differences between groups in the secondary outcomes - symptoms, function, and neurophysiologic parameters - were most commonly small with 95% CIs incorporating effects in either direction.

AUTHORS' CONCLUSIONS: Overall, there is limited evidence that a splint worn at night is more effective than no treatment in the short term, but there is insufficient evidence regarding the effectiveness and safety of one splint design or wearing regimen over others, and of splint over other non-surgical interventions for CTS. More research is needed on the long-term effects of this intervention for CTS.

摘要

背景

腕管综合征(CTS)是一种手腕部两条主要神经之一受到压迫的病症,可导致手部、腕部疼痛,有时还会引起手臂疼痛,以及拇指、示指和中指麻木、刺痛。通常会为症状轻至中度的患者提供夹板治疗。然而,夹板治疗对这种病症的有效性及受益持续时间尚不清楚。

目的

比较夹板治疗与不治疗、安慰剂或其他非手术干预措施对腕管综合征的有效性。

检索方法

我们检索了Cochrane神经肌肉疾病组专业注册库(2011年1月10日)、Cochrane系统评价数据库、英国国家卫生服务电子图书馆的卫生经济评价数据库和英国护理及健康领域数据库(《Cochrane图书馆》2011年第4期)、医学索引数据库(1966年1月至2011年12月)、荷兰医学文摘数据库(1980年1月至2012年1月)、联合和补充健康护理数据库(1985年1月至2012年1月)以及护理学与健康领域数据库全文版(1937年1月至2012年1月),无时间限制。我们检索了所有纳入试验和相关综述的参考文献列表以查找更多相关研究。

选择标准

所有比较夹板治疗与不治疗(或安慰剂)或其他非手术治疗的随机和半随机试验均符合纳入标准。我们还纳入了比较一种夹板类型或治疗方案与另一种的研究。我们排除了比较夹板治疗与手术治疗的研究。无语言限制。我们纳入了所有诊断为腕管综合征的患者,除非他们已接受手术松解。

数据收集与分析

两位综述作者独立选择纳入试验,并进行数据提取。两位作者还独立进行偏倚风险评估。我们计算了二分类结局的效应量为风险比(RR),连续结局的效应量为均值差(MD),报告95%置信区间(CI),所有结局比较的统计学显著性设定为P<0.05。

主要结果

该综述纳入了19项研究,随机分配了1190例腕管综合征患者。两项研究比较了夹板治疗与不治疗,五项比较了不同的夹板设计,一项比较了不同的夹板佩戴方案,七项比较了作为单一干预措施的夹板与另一种非手术干预措施,五项比较了与其他非手术干预措施联合使用的夹板与另一种非手术干预措施。只有三项研究报告了分配序列隐藏,只有一项报告了对参与者的盲法。三项研究测量了主要结局,即三个月及以内的短期总体改善情况。一项纳入80只手腕的低质量研究发现,与不治疗相比,夜间佩戴夹板使治疗四周结束时报告总体改善的可能性增加了两倍多(RR 3.86,95%CI 2.29至6.51)。然而,由于缺乏对患者的盲法以及分配隐藏不明确,提示该结果应谨慎解读。一项纳入90只手腕的极低质量半随机试验发现,与伸展夹板相比,佩戴中立位夹板使治疗两周结束时报告“大量缓解或完全缓解”的可能性增加了一倍多(RR 2.43,95%CI 1.12至5.28)。第三项测量短期总体改善情况的研究未分别报告每组的结局数据。九项研究测量了夹板治疗的不良反应,均发现没有或只有少数参与者报告因夹板治疗出现不适或肿胀;然而,所有RR的精确性都非常低。次要结局(症状、功能和神经生理参数)在组间的差异通常较小,95%CI包含了两个方向的效应。

作者结论

总体而言,有限的证据表明夜间佩戴夹板在短期内比不治疗更有效,但关于一种夹板设计或佩戴方案相对于其他方案的有效性和安全性,以及夹板相对于其他非手术干预措施治疗腕管综合征的有效性和安全性,证据不足。需要更多关于这种干预措施对腕管综合征长期影响的研究。

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