首页> 外文OA文献 >Validity, reliability, and responsiveness of the Self-reported Foot and Ankle Score (SEFAS) in forefoot, hindfoot, and ankle disorders.
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Validity, reliability, and responsiveness of the Self-reported Foot and Ankle Score (SEFAS) in forefoot, hindfoot, and ankle disorders.

机译:自我报告的足踝评分(sEFas)在前足,后足和踝关节疾病中的有效性,可靠性和反应性。

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摘要

Background and purpose - The self-reported foot and ankle score (SEFAS) is a questionnaire designed to evaluate disorders of the foot and ankle, but it is only validated for arthritis in the ankle. We validated SEFAS in patients with forefoot, midfoot, hindfoot, and ankle disorders. Patients and methods - 118 patients with forefoot disorders and 106 patients with hindfoot or ankle disorders completed the SEFAS, the foot and ankle outcome score (FAOS), SF-36, and EQ-5D before surgery. We evaluated construct validity for SEFAS versus FAOS, SF-36, and EQ-5D; floor and ceiling effects; test-retest reliability (ICC); internal consistency; and agreement. Responsiveness was evaluated by effect size (ES) and standardized response mean (SRM) 6 months after surgery. The analyses were done separately in patients with forefoot disorders and hindfoot/ankle disorders. Results - Comparing SEFAS to the other scores, convergent validity (when correlating foot-specific questions) and divergent validity (when correlating foot-specific and general questions) were confirmed. SEFAS had no floor and ceiling effects. In patients with forefoot disorders, ICC was 0.92 (CI: 0.85-0.96), Cronbach's α was 0.84, ES was 1.29, and SRM was 1.27. In patients with hindfoot or ankle disorders, ICC was 0.93 (CI: 0.88-0.96), Cronbach's α was 0.86, ES was 1.05, and SRM was 0.99. Interpretation - SEFAS has acceptable validity, reliability, and responsiveness in patients with various forefoot, hindfoot, and ankle disorders. SEFAS is therefore an appropriate patient- reported outcome measure (PROM) for these patients, even in national registries.
机译:背景和目的-自我报告的足踝评分(SEFAS)是一种旨在评估足踝疾病的问卷,但仅针对踝关节炎进行了验证。我们验证了前足,中足,后足和踝关节疾病患者的SEFAS。患者和方法-术前118例前足疾病患者和106例后足或踝关节疾病患者完成了SEFAS,足踝结局评分(FAOS),SF-36和EQ-5D。我们评估了SEFAS与FAOS,SF-36和EQ-5D的构建体效度;地板和天花板效果;重测可靠性(ICC);内部一致性和协议。术后6个月通过疗效量(ES)和标准疗效平均值(SRM)评估疗效。对患有前脚异常和后足/踝关节异常的患者分别进行分析。结果-将SEFAS与其他分数进行比较,确认了收敛效度(关联脚特定问题时)和发散效度(关联脚特定问题和一般问题时)。 SEFAS没有地板和天花板的影响。前足疾病患者的ICC为0.92(CI:0.85-0.96),Cronbach'sα为0.84,ES为1.29,SRM为1.27。后足或踝关节疾病患者的ICC为0.93(CI:0.88-0.96),Cronbach'sα为0.86,ES为1.05,SRM为0.99。解释-SEFAS在患有各种前脚,后足和踝关节疾病的患者中具有可接受的有效性,可靠性和反应性。因此,即使在国家注册机构中,SEFAS也是适合这些患者的患者报告结局指标(PROM)。

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