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膝关节骨关节炎临床试验的纳入标准:系统评价。

Eligibility criteria in knee osteoarthritis clinical trials: systematic review.

机构信息

Honam Research Center, Medifarm Hospital, Suncheon, South Korea,

出版信息

Clin Rheumatol. 2013 Nov;32(11):1569-74. doi: 10.1007/s10067-013-2342-z. Epub 2013 Jul 23.

Abstract

There is an increasing concern over generalizability of trial results. We investigated eligibility criteria of knee osteoarthritis clinical trials. Eligible trials were randomized, placebo-controlled trials that were identified by searches in MEDLINE, SCOPUS, and the Cochrane Central Register of Controlled Trials. We then attempted to extract data on the eligibility criteria by employing predetermined criteria. From 355 randomized knee osteoarthritis trials, we reviewed data categorized by non-osteoarthritis-related and osteoarthritis-related factors. A variety of items were used in the eligibility criteria. Regarding the non-osteoarthritis-related factors, ethical considerations, such as inability to give an informed consent (79.4 %) or medical conditions potential for risks by test treatments (56.0 %) or by participation in a trial (57.2 %), were the common reasons for excluding patients from a trial. Concerning the osteoarthritis-related factors, most of the trials did not specify age and symptom severity. When trials specifying these items were investigated, patients with 40 to 80 years in age and grade 2 in the Kellgren-Lawrence scale were mostly included into a trial. For the pain intensity, patients with ≥20-40 in the 100-mm visual analog scale and ≥6-8 in the WOMAC pain subscale were commonly enrolled into a trial. These findings warrant further investigation on the generalizability of trial results.

摘要

人们越来越关注试验结果的可推广性。我们调查了膝骨关节炎临床试验的纳入标准。合格的试验是随机、安慰剂对照试验,通过在 MEDLINE、SCOPUS 和 Cochrane 对照试验中心注册库中搜索确定。然后,我们试图通过使用预定的标准提取纳入标准的数据。从 355 项随机膝关节骨关节炎试验中,我们回顾了按非骨关节炎相关因素和骨关节炎相关因素分类的数据。纳入标准中使用了各种项目。关于非骨关节炎相关因素,由于无法获得知情同意(79.4%)或由于试验治疗(56.0%)或参与试验(57.2%)可能带来的风险而排除患者的伦理考虑是试验排除患者的常见原因。关于骨关节炎相关因素,大多数试验没有具体说明年龄和症状严重程度。当调查指定这些项目的试验时,发现大多数试验纳入了年龄在 40 至 80 岁之间、Kellgren-Lawrence 分级为 2 级的患者。对于疼痛强度,100mm 视觉模拟量表中≥20-40 分和 WOMAC 疼痛子量表中≥6-8 分的患者通常会被纳入试验。这些发现需要进一步研究试验结果的可推广性。

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