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Consensus on draft OMERACT core domains for clinical trials of Total Joint Replacement outcome by orthopaedic surgeons: a report from the International consensus on outcome measures in TJR trials (I-COMiTT) group

机译:骨科医生进行全关节置换预后临床试验的OMERACT核心域草案共识:国际公认的TJR试验(I-COMiTT)组预后评估报告

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摘要

Background: There are no core outcome domain or measurement sets for Total Joint Replacement (TJR) clinical trials. Our objective was to achieve an International consensus by orthopaedic surgeons on the OMERACT core domain/area set for TJR clinical trials. Methods: We conducted surveys of two orthopaedic surgeon cohorts, which included (1) the leadership of international orthopaedic societies and surgeons (IOS; cohort 1), and (2) the members of the American Academy of Orthopaedic Surgeons' Outcome Special Interest Group (AAOS-Outcome SIG), and/or the Outcome Research Interest Group of the Orthopaedic Research Society (ORS; cohort 2). Participants rated OMERACT-endorsed preliminary core area set for TJR clinical trials on a 1 to 9 scale, indicating 1-3 as domain of limited importance, 4-6 being important, but not critical, and 7-9 being critical. Results: Eighteen survey participants from the IOS group and 69 participants from the AAOS-Outcome SIG/ORS groups completed the survey questionnaire. The median (interquartile range [IQR]) scores were seven or higher for all six proposed preliminary core areas/domains across both groups, IOS and AAOS-Outcome SIG/ORS, respectively: pain, 8 [8, 9] and 8 [7, 9]; function, 8 [8, 8] and 8 [7, 9]; patient satisfaction, 8 [7, 9] and 8 [7, 8]; revision surgery, 7 [6, 9] and 8 [6, 8]; adverse events, 7 [5, 8] and 7 [6, 9]; and death, 7 [7, 9] and 8 [5, 9]. Respective median scores were lower for two additional optional domains: patient participation, 6.5 [5, 7] and 6 [5, 8]; and cost, 6 [5, 7] and 6 [5, 7]. Conclusions: This study showed that two independent surveys dervied from three groups of orthopaedic surgeons with international representation endorsed a preliminary/draft OMERACT core domain/area set for Joint Replacement clinical trials.
机译:背景:没有针对全关节置换(TJR)临床试验的核心结果域或度量标准集。我们的目标是使骨科医生在针对TJR临床试验设定的OMERACT核心领域/领域上达成国际共识。方法:我们对两个骨科医师队列进行了调查,其中包括(1)国际骨科学会和外科医师的领导(IOS;队列1),以及(2)美国骨科医师学会成果特别兴趣小组( AAOS-成果SIG)和/或骨科研究学会(ORS;第二组)的成果研究兴趣小组。参与者对OMERACT认可的用于TJR临床试验的初步核心区域范围进行了1到9的评分,表明1-3是有限的领域,4-6是重要的,但不是关键的,而7-9是关键的。结果:IOS组的18名调查参与者和AAOS结果SIG / ORS组的69名参与者完成了调查问卷。 IOS和AAOS结果SIG / ORS这两个组的所有六个拟议初步核心区域/域的中位数(四分位数范围[IQR])得分均为7分或更高,分别为:疼痛,8 [8、9]和8 [7]。 ,9];功能8 [8,8]和8 [7,9];患者满意度分别为8 [7,9]和8 [7,8];翻修手术,7 [6,9]和8 [6,8];不良事件7 [5,8]和7 [6,9];死亡7 [7,9]和8 [5,9]。另外两个可选领域的中位数得分较低:患者参与度6.5 [5,7]和6 [5,8];和成本分别为6 [5,7]和6 [5,7]。结论:这项研究表明,来自三组具有国际代表性的整形外科医生的独立调查认可了OMERACT核心领域/区域的初步/草案,用于联合置换临床试验。

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