Long Linda, Briscoe Simon, Cooper Chris, Hyde Chris, Crathorne Louise
Peninsula Technology Assessment Group (PenTAG), Evidence Synthesis and Modelling for Health Improvement (ESMI), University of Exeter Medical School, Exeter, UK.
Health Technol Assess. 2015 Jan;19(8):1-134. doi: 10.3310/hta19080.
Lateral elbow tendinopathy (LET) is a common complaint causing characteristic pain in the lateral elbow and upper forearm, and tenderness of the forearm extensor muscles. It is thought to be an overuse injury and can have a major impact on the patient's social and professional life. The condition is challenging to treat and prone to recurrent episodes. The average duration of a typical episode ranges from 6 to 24 months, with most (89%) reporting recovery by 1 year.
This systematic review aims to summarise the evidence concerning the clinical effectiveness and cost-effectiveness of conservative interventions for LET.
A comprehensive search was conducted from database inception to 2012 in a range of databases including MEDLINE, EMBASE and Cochrane Databases.
We conducted an overview of systematic reviews to summarise the current evidence concerning the clinical effectiveness and a systematic review for the cost-effectiveness of conservative interventions for LET. We identified additional randomised controlled trials (RCTs) that could contribute further evidence to existing systematic reviews. We searched MEDLINE, EMBASE, Allied and Complementary Medicine Database, Cumulative Index to Nursing and Allied Health Literature, Web of Science, The Cochrane Library and other important databases from inception to January 2013.
A total of 29 systematic reviews published since 2003 matched our inclusion criteria. These were quality appraised using the Assessment of Multiple Systematic Reviews (AMSTAR) checklist; five were considered high quality and evaluated using a Grading of Recommendations, Assessment, Development and Evaluation approach. A total of 36 RCTs were identified that were not included in a systematic review and 29 RCTs were identified that had only been evaluated in an included systematic review of intermediate/low quality. These were then mapped to existing systematic reviews where further evidence could provide updates. Two economic evaluations were identified.
The summary of findings from the review was based only on high-quality evidence (scoring of > 5 AMSTAR). Other limitations were that identified RCTs were not quality appraised and dichotomous outcomes were also not considered. Economic evaluations took effectiveness estimates from trials that had small sample sizes leading to uncertainty surrounding the effect sizes reported. This, in turn, led to uncertainty of the reported cost-effectiveness and, as such, no robust recommendations could be made in this respect.
Clinical effectiveness evidence from the high-quality systematic reviews identified in this overview continues to suggest uncertainty as to the effectiveness of many conservative interventions for the treatment of LET. Although new RCT evidence has been identified with either placebo or active controls, there is uncertainty as to the size of effects reported within them because of the small sample size. Conclusions regarding cost-effectiveness are also unclear. We consider that, although updated or new systematic reviews may also be of value, the primary focus of future work should be on conducting large-scale, good-quality clinical trials using a core set of outcome measures (for defined time points) and appropriate follow-up. Subgroup analysis of existing RCT data may be beneficial to ascertain whether or not certain patient groups are more likely to respond to treatments.
This study is registered as PROSPERO CRD42013003593.
The National Institute for Health Research Health Technology Assessment programme.
外侧肘肌腱病(LET)是一种常见病症,可导致外侧肘部和前臂上部出现特征性疼痛,以及前臂伸肌压痛。它被认为是一种过度使用性损伤,会对患者的社交和职业生活产生重大影响。这种病症治疗具有挑战性,且容易复发。典型发作的平均持续时间为6至24个月,大多数患者(89%)报告在1年内康复。
本系统评价旨在总结有关LET保守干预措施的临床有效性和成本效益的证据。
从数据库建立至2012年,在一系列数据库中进行了全面检索,包括MEDLINE、EMBASE和Cochrane数据库。
我们对系统评价进行了概述,以总结有关临床有效性的现有证据,并对LET保守干预措施的成本效益进行了系统评价。我们识别出了其他随机对照试验(RCT),这些试验可为现有系统评价提供更多证据。我们检索了MEDLINE、EMBASE、补充与替代医学数据库、护理及相关健康文献累积索引、科学引文索引、Cochrane图书馆以及其他重要数据库,检索时间从数据库建立至2013年1月。
自2003年以来发表的共29篇系统评价符合我们的纳入标准。使用多项系统评价评估(AMSTAR)清单对这些评价进行了质量评估;其中5篇被认为是高质量的,并采用推荐分级、评估、制定与评价方法进行了评估。共识别出36项未纳入系统评价的RCT,以及29项仅在纳入的中/低质量系统评价中进行过评估的RCT。然后将这些研究映射到现有的系统评价中,在这些评价中,更多证据可提供更新信息。识别出两项经济评价。
评价结果总结仅基于高质量证据(AMSTAR评分>5)。其他局限性包括,识别出的RCT未进行质量评估,且未考虑二分法结局。经济评价采用了样本量较小的试验中的有效性估计值,导致所报告效应大小存在不确定性。这进而导致所报告成本效益的不确定性,因此在这方面无法给出有力的推荐意见。
本概述中识别出的高质量系统评价的临床有效性证据继续表明,许多保守干预措施治疗LET的有效性存在不确定性。尽管已识别出有安慰剂或活性对照的新RCT证据,但由于样本量小,其中报告的效应大小仍存在不确定性。关于成本效益的结论也不明确。我们认为,尽管更新或新的系统评价可能也有价值,但未来工作的主要重点应是使用一组核心结局指标(针对特定时间点)并进行适当随访,开展大规模、高质量的临床试验。对现有RCT数据进行亚组分析可能有助于确定某些患者群体是否更可能对治疗有反应。
本研究注册为PROSPERO CRD42013003593。
英国国家卫生研究院卫生技术评估项目。