澳大利亚对 "类风湿关节炎-RA-患者报告体验测量法"(CQRA-RA-PREM)进行改编和外部验证。

IF 2.1 Q3 RHEUMATOLOGY
Rheumatology Advances in Practice Pub Date : 2024-08-17 eCollection Date: 2024-01-01 DOI:10.1093/rap/rkae099
Madeleine J Bryant, Rachel J Black, Susan Lester, Vibhasha Chand, Claire Barrett, Rachelle Buchbinder, Marissa Lassere, Lyn March, Catherine L Hill
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引用次数: 0

摘要

目的评估改编后的类风湿关节炎-RA-患者报告体验测量法(Commissioning for Quality in Rheumatoid Arthritis-RA-Patient-Reported Experience Measure,CQRA-RA-PREM)的可靠性和有效性,以评估澳大利亚风湿病门诊病人队列中的护理体验:方法:对患者进行个别访谈,检查 CQRA-RA-PREM 的语言和完成时间,然后进行修改。澳大利亚风湿病学协会数据库(ARAD)的参与者完成了CQRA-PREM-澳大利亚版(CQRA-PREM-AU)(22个项目,5个领域)、疾病活动度测量(RAPID-3,BASDAI)和生活质量评估(AQOL-6D)指数。探索性因子分析(EFA)评估了项目相关性。Cronbach's α 评估内部一致性:患者个人访谈(n = 8,62% 为男性,平均年龄 50 岁,平均病程 4.5 年)为 CQRA-RA-PREM 的修改提供了依据。ARAD调查回复率为707/1124(63%);459(65%)名RA患者,134(19%)名PsA患者,114(16%)名AS患者;67%为女性,平均年龄62岁,平均病程22年。完成问卷的时间中位数为 299 秒(四分位数间距为 284-414 秒)。通过对回答进行评分,得出平均总分。EFA 提取出五个因子:所有项目在因子 1 上的载荷相似,表明总分有效。CQRA-PREM-AU得分与AQOL-6D得分相关(ρ = 0.23,P P = 0.45),表明具有发散有效性。不同疾病亚组之间的信度相当(Cronbach's α >0.94)。不同疾病亚组的平均总分没有差异[4.1(s.d. 0.6,P = 0.73)],也没有地板/天花板效应:结论:CQRA-PREM-AU是衡量澳大利亚风湿病患者自我报告护理经验的有效而可靠的工具,可解释为平均总分。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Australian adaptation and external validation of Commissioning for Quality in Rheumatoid Arthritis-RA-Patient Reported Experience Measure (CQRA-RA-PREM).

Objectives: To evaluate the reliability and validity of an adapted Commissioning for Quality in Rheumatoid Arthritis-RA-Patient-Reported Experience Measure (CQRA-RA-PREM) for assessing care experience in an Australian rheumatology outpatient cohort.

Methods: Individual patient interviews were performed to check the language and completion time of the CQRA-RA-PREM before modification. Australian Rheumatology Association Database (ARAD) participants completed the CQRA-PREM-Australian version (CQRA-PREM-AU) (22 items, 5 domains), disease activity measure (RAPID-3, BASDAI) and Assessment of Quality of Life (AQOL-6D) index. Exploratory factor analysis (EFA) assessed item correlation. Cronbach's α assessed internal consistency.

Results: Individual patient interviews (n = 8, 62% male, mean age 50 years, mean disease duration 4.5 years) informed CQRA-RA-PREM modification. The ARAD survey response rate was 707/1124 (63%); 459 (65%) RA, 134 (19%) PsA, 114 (16%) AS; 67% female, mean age 62 years, mean disease duration 22 years. The median instrument completion time was 299 s (interquartile range 284-414). Scoring of responses allowed an averaged overall score. EFA extracted five factors: all items loading similarly onto factor 1, indicating validity of the overall score. The CQRA-PREM-AU score correlated with the AQOL-6D score (ρ = 0.23, P < 0.01); partial correlation with disease activity was not significant (ρ = 0.03, P = 0.45), indicating divergent validity. Reliability was comparable across disease subgroups (Cronbach's α >0.94). The mean overall score did not differ by disease subgroup [4.1 (s.d. 0.6, P = 0.73) and there was no floor/ceiling effect.

Conclusion: CQRA-PREM-AU is a valid and reliable instrument to measure self-reported care experience in Australian rheumatology patients and may be interpreted as an average overall numerical score.

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来源期刊
Rheumatology Advances in Practice
Rheumatology Advances in Practice Medicine-Rheumatology
CiteScore
3.60
自引率
3.20%
发文量
197
审稿时长
11 weeks
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