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首页> 外文期刊>Clinical rheumatology >How well are the ASAS/OMERACT core outcome sets for ankylosing spondylitis implemented in randomized clinical trials? A systematic literature review
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How well are the ASAS/OMERACT core outcome sets for ankylosing spondylitis implemented in randomized clinical trials? A systematic literature review

机译:在随机临床试验中对强直性脊柱炎实施ASAS / OMERACT核心结果集的效果如何?系统的文献综述

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This study aims to investigate how well the Assessment of SpondyloArthritis international Society (ASAS)/Outcome Measures in Rheumatology Clinical Trials (OMERACT) core set and response criteria for ankylosing spondylitis (AS) have been implemented in randomized controlled trials (RCTs) testing pharmacological and non-pharmacological interventions. A systematic literature search was performed up to June 2013 looking for RCTs in patients with axial spondyloarthritis (SpA) (AS and non-radiographic axial SpA). The assessed domains and instruments belonging to the core sets for disease-controlling anti-rheumatic therapy (DC-ART) and symptom-modifying anti-rheumatic drugs (SMARDs) were extracted. Results were reported separately for those trials published until 2 years after the publication of the core set (1 April 2001; 'control trials') and those trials published at least 2 years after the publication date ('implementation trials'). One hundred twenty-three articles from 99 RCTs were included in the analysis, comparing 48 'control trials' and 51 'implementation trials'. Regarding DC-ART core set, the following domains were significantly more frequently assessed in the 'implementation group' in comparison to the 'control group': 'physical function' (100 vs 41.7 %; p≤0.001), 'peripheral joints/entheses' (100 vs 33.3 %; p≤0.001) and 'fatigue' (100 vs 0 %; p≤0.001). Three instruments were significantly more used in the 'implementation group': Bath Ankylosing Spondylitis Functional Index (BASFI) (100 vs 8.3 %; p=≤0.001), CRP (92.3 vs 58.3 %; p=0.01) and Bath Ankylosing Spondylitis Metrology Index (BASMI) (53.8 vs 0 %; p=0.001). Regarding SMARD core set domains, physical function (92 vs 23 %; p≤0.001) and fatigue (84 vs 17 %; p≤0.001), as well as the instruments BASFI (88 vs 14 %; p≤0.001) and BASMI (52 vs 0 %; p≤0.001), increased significantly in the 'implementation group'. Twenty per cent of trials from the 'implementation group' but none from the 'control group' included all domains of the core set. In conclusion, this study provides evidence for the implementation of the ASAS/OMERACT core set in RCTs of both DC-ART and SMARD. This applies to the use of the domains and, to a lesser extent, to the specific instruments.
机译:这项研究的目的是调查国际上对脊椎关节炎的评估(ASAS)/风湿病临床试验结果指标(OMERACT)的核心设置和强直性脊柱炎(AS)的反应标准在随机对照试验(RCT)中的药理和临床试验非药物干预。进行了系统的文献检索,直至2013年6月,以寻找轴性脊椎关节炎(SpA)(AS和非放射线性轴颈SpA)患者的RCT。提取了评估领域和仪器,这些领域和仪器属于疾病控制抗风湿疗法(DC-ART)和症状缓解抗风湿药(SMARDs)的核心集。在核心组公布后两年(2001年4月1日;“对照试验”)之前发表的那些试验和在发表之日起至少两年后发表的那些试验(“实施试验”)分别报告了结果。分析中包括来自99个RCT的123篇文章,比较了48个“对照试验”和51个“实施试验”。关于DC-ART核心集,与“对照组”相比,在“实施组”中评估以下领域的频率更高:“身体机能”(100比41.7%;p≤0.001),“外周关节/主体” '(100 vs 33.3%;p≤0.001)和'疲劳'(100 vs 0%;p≤0.001)。 “实施组”中使用了三种工具:巴斯强直性脊柱炎功能指数(BASFI)(100 vs 8.3%; p =≤0.001),CRP(92.3 vs 58.3%; p = 0.01)和巴斯强直性脊柱炎计量指标(BASMI)(53.8 vs 0%; p = 0.001)。关于SMARD核心设置域,物理功能(92%vs 23%;p≤0.001)和疲劳(84%vs 17%;p≤0.001),以及BASFI仪器(88%vs 14%;p≤0.001)和BASMI( 52 vs 0%;p≤0.001),在“实施组”中显着增加。来自“实施组”的试验有20%,但没有来自“对照组”的试验,涵盖了核心组的所有领域。总之,这项研究为DC-ART和SMARD的RCT中ASAS / OMERACT核心集的实施提供了证据。这适用于域的使用,并且在较小程度上适用于特定工具。

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