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酷刑幸存者持续性疼痛的治疗干预措施。

Interventions for treating persistent pain in survivors of torture.

作者信息

Baird Emma, Williams Amanda C de C, Hearn Leslie, Amris Kirstine

机构信息

University Hospitals of Morecambe Bay, Lancaster, UK.

出版信息

Cochrane Database Syst Rev. 2017 Aug 18;8(8):CD012051. doi: 10.1002/14651858.CD012051.pub2.

Abstract

BACKGROUND

Persistent (chronic) pain is a frequent complaint in survivors of torture, particularly but not exclusively pain in the musculoskeletal system. Torture survivors may have no access to health care; where they do, they may not be recognised when they present, and the care available often falls short of their needs. There is a tendency in state and non-governmental organisations' services to focus on mental health, with poor understanding of persistent pain, while survivors may have many other legal, welfare, and social problems that take precedence over health care.

OBJECTIVES

To assess the efficacy of interventions for treating persistent pain and associated problems in survivors of torture.

SEARCH METHODS

We searched for randomised controlled trials (RCTs) published in any language in CENTRAL, MEDLINE, Embase, Web of Science, CINAHL, LILACS, and PsycINFO, from database inception to 1 February 2017. We also searched trials registers and grey literature databases.

SELECTION CRITERIA

RCTs of interventions of any type (medical, physical, psychological) compared with any alternative intervention or no intervention, and with a pain outcome. Studies needed to have at least 10 participants in each arm for inclusion.

DATA COLLECTION AND ANALYSIS

We identified 3578 titles in total after deduplication; we selected 24 full papers to assess for eligibility. We requested data from two completed trials without published results.We used standard methodological procedures expected by Cochrane. We assessed risk of bias and extracted data. We calculated standardised mean difference (SMD) and effect sizes with 95% confidence intervals (CI). We assessed the evidence using GRADE and created a 'Summary of findings' table.

MAIN RESULTS

Three small published studies (88 participants) met the inclusion criteria, but one had been retracted from publication because of ethical problems concerned with confidentiality and financial irregularities. Since these did not affect the data, the study was retained in this review. Despite the search including any intervention, only two types were represented in the eligible studies: two trials used cognitive behavioural therapy (CBT) with biofeedback versus waiting list on unspecified persistent pain (58 participants completed treatment), and one examined the effect of complex manual therapy versus self-treatment on low back pain (30 participants completed treatment). Excluded studies were largely either not RCTs or did not report pain as an outcome.There was no difference for the outcome of pain relief at the end of treatment between CBT and waiting list (two trials, 58 participants; SMD -0.05, 95% CI -1.23 to 1.12) (very low quality evidence); one of these reported a three-month follow-up with no difference between intervention and comparison (28 participants; SMD -0.03, 95% CI -0.28 to 0.23) (very low quality evidence). The manual therapy trial also reported no difference between complex manual therapy and self-treatment (30 participants; SMD -0.48, 95% CI -9.95 to 0.35) (very low quality evidence). Two studies reported dropouts, one with partial information on reasons; none of the studies reported adverse effects.There was no information from any study on the outcomes of use of analgesics or quality of life.Reduction in disability showed no difference at the end of treatment between CBT and waiting list (two trials, 57 participants; SMD -0.39, 95% CI -1.17 to 0.39) (very low quality evidence); one of these reported a three-month follow-up with no difference between intervention and comparison (28 participants; SMD 0, 95% CI -0.74 to 0.74) (very low quality evidence). The manual therapy trial reported superiority of complex manual therapy over self-treatment for reducing disability (30 participants; SMD -1.10, 95% CI - 1.88 to -0.33) (very low quality evidence).Reduction in distress showed no difference at the end of treatment between CBT and waiting list (two trials, 58 participants; SMD 0.07, 95% CI -0.46 to 0.60) (very low quality evidence); one of these reported a three-month follow-up with no difference between intervention and comparison (28 participants; SMD -0.24, 95% CI -0.50 to 0.99) (very low quality evidence). The manual therapy trial reported superiority of complex manual therapy over self-treatment for reducing distress (30 participants; SMD -1.26, 95% CI - 2.06 to -0.47) (very low quality evidence).The risk of bias was considered high given the small number of trials, small size of trials, and the likelihood that each was underpowered for the comparisons it reported. We primarily downgraded the quality of the evidence due to small numbers in trials, lack of intention-to-treat analyses, high unaccounted dropout, lack of detail on study methods, and CIs around effect sizes that included no effect, benefit, and harm.

AUTHORS' CONCLUSIONS: There is insufficient evidence to support or refute the use of any intervention for persistent pain in survivors of torture.

摘要

背景

持续性(慢性)疼痛是酷刑幸存者常见的主诉,尤其是但不限于肌肉骨骼系统疼痛。酷刑幸存者可能无法获得医疗保健;即使他们能获得,就医时可能也未被识别,而且现有的护理往往无法满足他们的需求。国家和非政府组织的服务倾向于关注心理健康,对持续性疼痛了解不足,而幸存者可能还有许多其他优先于医疗保健的法律、福利和社会问题。

目的

评估治疗酷刑幸存者持续性疼痛及相关问题的干预措施的疗效。

检索方法

我们检索了CENTRAL、MEDLINE、Embase、Web of Science、CINAHL、LILACS和PsycINFO中从数据库建立至2017年2月1日以任何语言发表的随机对照试验(RCT)。我们还检索了试验注册库和灰色文献数据库。

选择标准

任何类型(医学、物理、心理)干预措施与任何其他替代干预措施或不干预措施相比且有疼痛结局的RCT。每项研究每组至少需要10名参与者才能纳入。

数据收集与分析

去重后共识别出3578个标题;我们选择了24篇全文进行资格评估。我们向两项已完成但未发表结果的试验索取数据。我们采用Cochrane预期的标准方法程序。我们评估偏倚风险并提取数据。我们计算标准化均数差(SMD)和效应量及95%置信区间(CI)。我们使用GRADE评估证据并创建“结果总结”表。

主要结果

三项已发表的小型研究(88名参与者)符合纳入标准,但其中一项因涉及保密和财务违规的伦理问题已从出版物中撤回。由于这些问题未影响数据,该研究仍保留在本综述中。尽管检索涵盖了任何干预措施,但符合条件的研究中仅出现了两种类型:两项试验使用认知行为疗法(CBT)加生物反馈与等待名单对照治疗未明确的持续性疼痛(58名参与者完成治疗),一项研究考察了复杂手法治疗与自我治疗对腰痛的效果(30名参与者完成治疗)。排除的研究大多不是RCT或未将疼痛作为结局报告。CBT与等待名单对照在治疗结束时疼痛缓解结局方面无差异(两项试验,58名参与者;SMD -0.05,95%CI -1.23至1.12)(极低质量证据);其中一项报告了三个月随访,干预组与对照组无差异(28名参与者;SMD -0.03,95%CI -0.28至0.23)(极低质量证据)。手法治疗试验也报告复杂手法治疗与自我治疗无差异(30名参与者;SMD -0.48,95%CI -9.95至0.35)(极低质量证据)。两项研究报告了脱落情况,一项提供了部分脱落原因信息;没有研究报告不良反应。没有任何研究提供关于使用镇痛药结局或生活质量的信息。CBT与等待名单对照在治疗结束时残疾减少方面无差异(两项试验,57名参与者;SMD -0.39,95%CI -1.17至0.39)(极低质量证据);其中一项报告了三个月随访,干预组与对照组无差异(28名参与者;SMD 0,95%CI -0.74至0.74)(极低质量证据)。手法治疗试验报告复杂手法治疗在减少残疾方面优于自我治疗(30名参与者;SMD -1.10,95%CI -1.88至-0.33)(极低质量证据)。CBT与等待名单对照在治疗结束时痛苦减少方面无差异(两项试验,58名参与者;SMD 0.07,95%CI -0.46至0.60)(极低质量证据);其中一项报告了三个月随访,干预组与对照组无差异(28名参与者;SMD -0.24,95%CI -0.50至0.99)(极低质量证据)。手法治疗试验报告复杂手法治疗在减少痛苦方面优于自我治疗(30名参与者;SMD -1.26,95%CI -2.06至-0.47)(极低质量证据)。鉴于试验数量少、试验规模小以及每项试验报告的比较可能效能不足,偏倚风险被认为很高。我们主要因试验数量少、缺乏意向性分析、未解释的高脱落率、研究方法细节不足以及效应量的CI包含无效应及有益和有害情况而降低了证据质量。

作者结论

没有足够的证据支持或反驳对酷刑幸存者持续性疼痛使用任何干预措施。

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