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外侧肘肌腱病以患者为中心的结局:对英国人群现有证据的系统评价。

Patient-centred outcomes in lateral elbow tendinopathy: A systematic review of available evidence in UK populations.

作者信息

Evans Jonathan P, Smith Chris, Porter Ian, Gangannagaripalli Jaheeda, Goodwin Vicki, Valderas Jose

机构信息

Royal Devon and Exeter NHS Foundation Trust, Exeter, UK.

Health Services and Policy Research Group, University of Exeter, Exeter, UK.

出版信息

Shoulder Elbow. 2019 Dec;11(6):440-449. Epub 2018 Aug 16.

Abstract

BACKGROUND

For Patient-Reported Outcome Measures to be useful, they must have evidenced reliability, validity and responsiveness in both the condition and population of interest. The aim of this study is to systematically review the evidence for Patient-Reported Outcome Measures in UK patients with lateral elbow tendinopathy.

METHODS

A systematic search was performed in Ovid MEDLINE, Embase and CINAHL. Studies were included if reporting administration of Patient-Reported Outcome Measures in UK populations with lateral elbow tendinopathy. Patient-Reported Outcome Measures characteristics and target populations were assessed using a structured classification system. Patient-Reported Outcome Measures reporting in randomised controlled trials was assessed against Consolidated Standards of Reporting Trials (CONSORT) standards (Patient-Reported Outcome extension).

RESULTS

A total of 16 articles were included. Out of seven different Patient-Reported Outcome Measures, there was evidence of partial validation for five. The assessment of validity, reliability and responsiveness of all Patient-Reported Outcome Measures in lateral elbow tendinopathy UK populations extended to just 20 individual patients. No articles conformed to the CONSORT Patient-Reported Outcome extension standards.

CONCLUSION

There exists a paucity of data on the psychometrics of Patient-Reported Outcome Measures in UK lateral elbow tendinopathy populations. Without these data, trial design and interpretation are significantly hindered. The high prevalence of this condition and significant volume of studies being conducted into novel treatments highlight the need for this knowledge gap to be resolved.

摘要

背景

为使患者报告结局测量指标有用,它们必须在相关疾病和目标人群中具备可靠性、有效性及反应性的证据。本研究旨在系统回顾英国外侧肘肌腱病患者报告结局测量指标的相关证据。

方法

在Ovid MEDLINE、Embase和CINAHL中进行系统检索。纳入报告在英国外侧肘肌腱病患者中应用患者报告结局测量指标的研究。使用结构化分类系统评估患者报告结局测量指标的特征和目标人群。根据报告试验的统一标准(CONSORT)标准(患者报告结局扩展版)评估随机对照试验中的患者报告结局测量指标报告情况。

结果

共纳入16篇文章。在七种不同的患者报告结局测量指标中,有五种有部分效度验证的证据。在英国外侧肘肌腱病患者人群中,所有患者报告结局测量指标的效度、信度和反应性评估仅涉及20名个体患者。没有文章符合CONSORT患者报告结局扩展标准。

结论

关于英国外侧肘肌腱病患者人群中患者报告结局测量指标的心理测量学数据匮乏。没有这些数据,试验设计和解读会受到严重阻碍。这种疾病的高患病率以及针对新疗法开展的大量研究凸显了解决这一知识空白的必要性。

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