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脑和脊髓刺激疗法治疗幻肢痛:系统评价。

Brain and spinal stimulation therapies for phantom limb pain: a systematic review.

机构信息

Centre for Reviews and Dissemination (CRD), University of York, York, UK.

James Cook University Hospital, South Tees Hospitals NHS Foundation Trust, Middlesborough, UK.

出版信息

Health Technol Assess. 2018 Nov;22(62):1-94. doi: 10.3310/hta22620.

Abstract

BACKGROUND

Although many treatments exist for phantom limb pain (PLP), the evidence supporting them is limited and there are no guidelines for PLP management. Brain and spinal cord neurostimulation therapies are targeted at patients with chronic PLP but have yet to be systematically reviewed.

OBJECTIVE

To determine which types of brain and spinal stimulation therapy appear to be the best for treating chronic PLP.

DESIGN

Systematic reviews of effectiveness and epidemiology studies, and a survey of NHS practice.

POPULATION

All patients with PLP.

INTERVENTIONS

Invasive interventions - deep brain stimulation (DBS), motor cortex stimulation (MCS), spinal cord stimulation (SCS) and dorsal root ganglion (DRG) stimulation. Non-invasive interventions - repetitive transcranial magnetic stimulation (rTMS) and transcranial direct current stimulation (tDCS).

MAIN OUTCOME MEASURES

Phantom limb pain and quality of life.

DATA SOURCES

Twelve databases (including MEDLINE and EMBASE) and clinical trial registries were searched in May 2017, with no date limits applied.

REVIEW METHODS

Two reviewers screened titles and abstracts and full texts. Data extraction and quality assessments were undertaken by one reviewer and checked by another. A questionnaire was distributed to clinicians via established e-mail lists of two relevant clinical societies. All results were presented narratively with accompanying tables.

RESULTS

Seven randomised controlled trials (RCTs), 30 non-comparative group studies, 18 case reports and 21 epidemiology studies were included. Results from a good-quality RCT suggested short-term benefits of rTMS in reducing PLP, but not in reducing anxiety or depression. Small randomised trials of tDCS suggested the possibility of modest, short-term reductions in PLP. No RCTs of invasive therapies were identified. Results from small, non-comparative group studies suggested that, although many patients benefited from short-term pain reduction, far fewer maintained their benefits. Most studies had important methodological or reporting limitations and few studies reported quality-of-life data. The evidence on prognostic factors for the development of chronic PLP from the longitudinal studies also had important limitations. The results from these studies suggested that pre-amputation pain and early PLP intensity are good predictors of chronic PLP. Results from the cross-sectional studies suggested that the proportion of patients with severe chronic PLP is between around 30% and 40% of the chronic PLP population, and that around one-quarter of chronic PLP patients find their PLP to be either moderately or severely limiting or bothersome. There were 37 responses to the questionnaire distributed to clinicians. SCS and DRG stimulation are frequently used in the NHS but the prevalence of use of DBS and MCS was low. Most responders considered SCS and DRG stimulation to be at least sometimes effective. Neurosurgeons had mixed views on DBS, but most considered MCS to rarely be effective. Most clinicians thought that a randomised trial design could be successfully used to study neurostimulation therapies.

LIMITATION

There was a lack of robust research studies.

CONCLUSIONS

Currently available studies of the efficacy, effectiveness and safety of neurostimulation treatments do not provide robust, reliable results. Therefore, it is uncertain which treatments are best for chronic PLP.

FUTURE WORK

Randomised crossover trials, randomised N-of-1 trials and prospective registry trials are viable study designs for future research.

STUDY REGISTRATION

The study is registered as PROSPERO CRD42017065387.

FUNDING

The National Institute for Health Research Health Technology Assessment programme.

摘要

背景

尽管有许多治疗幻肢痛(PLP)的方法,但支持这些方法的证据有限,并且没有针对 PLP 管理的指南。脑和脊髓神经刺激疗法针对的是慢性 PLP 患者,但尚未进行系统评价。

目的

确定哪些类型的脑和脊髓刺激疗法似乎最适合治疗慢性 PLP。

设计

有效性系统评价和流行病学研究,以及对英国国家医疗服务体系(NHS)实践的调查。

人群

所有 PLP 患者。

干预措施

侵入性干预 - 深部脑刺激(DBS)、运动皮层刺激(MCS)、脊髓刺激(SCS)和背根神经节刺激(DRG)。非侵入性干预 - 重复经颅磁刺激(rTMS)和经颅直流电刺激(tDCS)。

主要结局测量

幻肢痛和生活质量。

数据来源

2017 年 5 月,12 个数据库(包括 MEDLINE 和 EMBASE)和临床试验注册库进行了检索,未设定日期限制。

研究方法

两名审查员筛选标题和摘要以及全文。数据提取和质量评估由一名审查员进行,另一名审查员进行核对。通过两个相关临床学会的既定电子邮件列表向临床医生分发了一份问卷。所有结果均以叙述性方式呈现,并附有相应的表格。

结果

纳入了 7 项随机对照试验(RCT)、30 项非对照组研究、18 例病例报告和 21 项流行病学研究。一项高质量 RCT 的结果表明,rTMS 短期治疗可减轻 PLP,但不能减轻焦虑或抑郁。tDCS 的小型随机试验提示 PLP 可能有适度的短期减轻。未发现针对侵入性治疗的 RCT。来自小型非对照组研究的结果表明,尽管许多患者的疼痛短期减轻,但很少有患者能维持疗效。大多数研究都存在重要的方法学或报告局限性,很少有研究报告生活质量数据。来自纵向研究的关于慢性 PLP 发生的预后因素的证据也存在重要局限性。这些研究的结果表明,截肢前疼痛和早期 PLP 强度是慢性 PLP 的良好预测指标。来自横断面研究的结果表明,严重慢性 PLP 患者的比例在慢性 PLP 人群中约为 30%至 40%,约四分之一的慢性 PLP 患者认为他们的 PLP 存在中度或严重的限制或困扰。向临床医生分发的问卷得到了 37 份回复。SCS 和 DRG 刺激在 NHS 中经常使用,但 DBS 和 MCS 的使用频率较低。大多数应答者认为 SCS 和 DRG 刺激至少有时有效。神经外科医生对 DBS 的看法不一,但大多数人认为 MCS 很少有效。大多数临床医生认为,随机试验设计可以成功用于研究神经刺激疗法。

局限性

缺乏强有力的研究。

结论

目前关于神经刺激治疗的疗效、有效性和安全性的研究结果并不提供可靠、可靠的结果。因此,尚不确定哪些治疗方法最适合慢性 PLP。

未来工作

随机交叉试验、随机 N-of-1 试验和前瞻性登记试验是未来研究的可行设计。

研究注册

该研究在 PROSPERO 注册为 CRD42017065387。

资金来源

英国国家卫生研究院卫生技术评估计划。

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