首页> 外文期刊>Journal of orthopaedic science : >Development of the patient-based outcome instrument for foot and ankle: part 2: results from the second field survey: validity of the outcome instrument for the foot and ankle version 2.
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Development of the patient-based outcome instrument for foot and ankle: part 2: results from the second field survey: validity of the outcome instrument for the foot and ankle version 2.

机译:基于患者的足踝结局指标工具的开发:第2部分:第二次现场调查的结果:足踝第2版结局指标的有效性。

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BACKGROUND: The Clinical Outcomes Committee of the Japanese Society for Surgery of the Foot (JSSF) has conducted the second Field Survey of the Outcome Instrument for the Foot and Ankle version 2. METHODS: The survey of the Outcome Instrument version 2, which was composed of 43 items, was performed in 313 patients (154 men and 159 women) who had pathological conditions related to the foot and ankle. Optional sports items in the Outcome Instrument version 2 were analyzed in 123 patients. Internal consistency and construct validity of the Outcome Instrument version 2 were assessed. Correlation of the Outcome Instrument version 2 score with Short Form 36 (SF36) and JSSF scores was analyzed to evaluate criterion validity. RESULTS: Both the EFA and CFA demonstrated good alignment of questionnaire items with their intended subscales in most cases. Sports items were not clearly classified into subgroups. Therefore, it seemed reasonable to use those as a set of questions in a single subscale. The present subscales, having similar names as the SF36 subscales, were closely correlated with the respective subscales. In those cases, the magnitude of the correlation coefficient was >0.6 (p < 0.001) except the present subscale called General Health and Well-being. Comparison of the present scores with JSSF evaluation scores showed satisfactory results except in patients with rheumatoid arthritis. CONCLUSIONS: The Outcome Instrument version 2 demonstrated acceptable psychometric performances as outcome measures for patients with pathological conditions related to the foot and ankle. This outcome instrument would be helpful to evaluate patients with foot and/or ankle impairment. However, the analyses of the test-retest reliability and the influence of background factors such as age and gender, etc., on Outcome Instrument version 2 are needed in the third field survey.
机译:背景:日本足外科学会临床结果委员会(JSSF)已对脚和踝关节版本2的结果仪器进行了第二次现场调查。方法:对结果仪器2的调查是由在313例(与男性和女性有关的病理状况)患者中进行了43项检查,其中154例男性和159例女性。在123例患者中分析了结果器械版本2中的可选运动项目。评估了成果工具第2版的内部一致性和构建效度。分析结果工具第2版得分与简短表格36(SF36)和JSSF得分的相关性,以评估标准的有效性。结果:在大多数情况下,EFA和CFA都显示出问卷项目与其预期的子量表的良好一致性。体育项目没有明确分类为亚组。因此,在单个分量表中将这些问题用作一组问题似乎是合理的。本子量表与SF36子量表具有相似的名称,与各自的子量表密切相关。在那些情况下,相关系数的幅度大于> 0.6(p <0.001),但目前称为“总体健康与福祉”的子量表除外。当前评分与JSSF评分的比较显示,除类风湿关节炎患者外,结果令人满意。结论:成果仪器第2版显示了可接受的心理测量表现,作为与脚和踝有关的病理状况患者的结局指标。该结果仪器将有助于评估患有脚和/或踝关节损伤的患者。但是,在第三次现场调查中,需要分析重测信度以及背景因素(例如年龄和性别等)对结果仪器版本2的影响。

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