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Validity Test of the Indonesia Version of Revised American Pain Society Outcome Questionnaire (APS-POQ-R) to Evaluate Postoperative Management Quality

机译:印度尼西亚版修订的美国痛苦社会结果问卷(APS-POQ-R)的有效性测试,以评估术后管理质量

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The Revised American Pain Society Patient Outcome Questionnaire (APS-POQ-R) is the most commonly used instrument to assess the quality of pain management in many countries but the validity and reliability of this instrument has not been verified in Indonesia. This is a descriptive,cross-sectional psychometric study to test the validity and reliability of Indonesia version of APS-POQ-R instrument to evaluate postoperative pain management quality. The APS-POQ-R was translated into Bahasa Indonesia according to international guidelines. The translation result was testedin 102 patients who underwent elective surgery at Cipto Mangunkusumo Hospital from March to April 2017. Coefficient Aiken V formula was used for content validity test while factor analysis and corrected item total correlation were used for construction validity test. Reliability was testedusing internal consistency (Chronbach α ). Aiken V formula showed the Indonesian version of APS-POQ-R was valid with score of 0.8–1 (scale V was ≥0.5). Factor analysis generated five main factors out of 18 instrument questions: activity and sleep disturbances, impact ofpain to emotion, side effects, pain management perception, and pain scale. Construction validity test with corrected item total correlation showed all questions has good correlation, which ranged between 0.244–0.799 (correlation ≥0.3). Correlation between each factors of the Indonesianversion of APS-POQ-R ranged 0.319–0.407. Internal consistency test showed the Indonesian version of APS-POQ-R was reliable with score of 0.663 (α > 0.5). The Indonesian version of APS-POQ-R is valid and reliable to measure postoperative pain management quality.
机译:修订后的美国痛苦社会患者结果调查问卷(APS-POQ-R)是评估许多国家疼痛管理质量的最常用的工具,但该仪器的有效性和可靠性尚未在印度尼西亚核实。这是一个描述性的横截面心理学研究,用于测试印度尼西亚版APS-POQ-R仪器的有效性和可靠性,以评估术后疼痛管理质量。根据国际指南,APS-POQ-R被翻译成Bahasa印度尼西亚。翻译结果是测试in 102患者在2017年3月至4月的Cipto Mangunkusumo医院接受选修手术的患者。系数艾肯V公式用于内容有效性测试,而因素分析和纠正物品总相关性用于施工有效性测试。可靠性测试内部一致性(Chronbach α)。 AIKEN V公式显示,APS-POQ-R的印尼版本有效,得分为0.8-1(尺寸v≥0.5)。因子分析产生了18个仪器问题的五个主要因素:活动和睡眠障碍,对情绪的影响,副作用,疼痛管理感知和疼痛量表。施工有效性试验与校正项目总相关性显示所有问题都具有良好的相关性,范围为0.244-0.799(相关≥0.3)。 APS-POQ-R印度尼西亚透视的每个因素之间的相关性范围为0.319-0.407。内部一致性测试显示,APS-POQ-R的印度尼西亚版本可靠,得分为0.663(α> 0.5)。 APS-POQ-R的印尼版本有效可靠,以测量术后疼痛管理质量。

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