Psychometric Validation of the EQ-5D-3L in Patients with Nontuberculous Mycobacterial (NTM) Lung Disease Caused by Mycobacterium avium Complex (MAC).

IF 1.8 Q3 HEALTH CARE SCIENCES & SERVICES Patient Related Outcome Measures Pub Date : 2021-02-25 eCollection Date: 2021-01-01 DOI:10.2147/PROM.S272075
Anuj Shah, Xinyi Ng, Ruchit Shah, Caitlyn Solem, Ping Wang, Marko Obradovic
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Abstract

Purpose: This analysis evaluated the psychometric properties of the EQ-5D-3L among patients with Mycobacterium avium complex lung disease (MAC-LD).

Methods: Data from the Phase III CONVERT trial were analyzed. Study measures including the EQ-5D-3L, St. George's Respiratory Questionnaire (SGRQ), the 6-minute walk test (6MWT), and percent predicted forced expiratory volume in 1 second (ppFEV1) were collected at baseline, month 3 (M3), month 4 (M4; only 6MWT), and month 6 (M6). Item characteristics and validity were evaluated at baseline. Test-retest reliability was assessed using intraclass correlation coefficients (ICC) and a weighted kappa statistic among a subgroup of stable patients. Validity was tested by evaluating correlations of the EQ-5D-3L index/visual analogue scale (VAS) scores with SGRQ and 6MWT and comparing mean index/VAS scores across known groups defined using 6MWT and ppFEV1. Responsiveness of the EQ-5D-3L was assessed using 6MWT, SGRQ, ppFEV1, and culture conversion as anchors.

Results: The index score was subject to ceiling effects, with 32.6% of patients reporting perfect health at baseline. ICCs for the index (0.80) and VAS (0.85) scores and weighted kappas for the domains (0.5-0.72) indicated adequate test-retest reliability. Correlations between the index/VAS scores and related domains of the SGRQ and 6MWT were as hypothesized (0.31-0.62), and the mean index/VAS scores were significantly different between the 6MWT and ppFEV1 known groups (p<0.05), supporting the validity of the EQ-5D-3L. No evidence was found supporting the responsiveness of the EQ-5D-3L to changes in any of the anchors.

Conclusion: EQ-5D-3L exhibited evidence of validity and reliability but poor responsiveness to clinically meaningful changes in patients with MAC-LD.

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由复合分枝杆菌 (MAC) 引起的非结核分枝杆菌 (NTM) 肺病患者的 EQ-5D-3L 心理计量学验证。
目的:本分析评估了复合分枝杆菌肺病(MAC-LD)患者的 EQ-5D-3L 心理测量学特性:方法: 分析了 CONVERT III 期试验的数据。在基线、第 3 个月 (M3)、第 4 个月 (M4; 仅 6MWT) 和第 6 个月 (M6) 收集了研究测量数据,包括 EQ-5D-3L、圣乔治呼吸问卷 (SGRQ)、6 分钟步行测试 (6MWT) 和 1 秒内预测用力呼气容积百分比 (ppFEV1)。在基线时对项目特征和有效性进行了评估。使用类内相关系数(ICC)和加权卡帕统计量评估了稳定期患者亚群的重测可靠性。通过评估 EQ-5D-3L 指数/视觉模拟量表 (VAS) 评分与 SGRQ 和 6MWT 的相关性,并比较使用 6MWT 和 ppFEV1 界定的已知组别中的指数/VAS 平均分,对有效性进行了检验。以 6MWT、SGRQ、ppFEV1 和文化转换为锚,评估了 EQ-5D-3L 的响应性:结果:指数得分受上限效应的影响,32.6% 的患者在基线时报告完全健康。指数(0.80)和 VAS(0.85)得分的 ICC 值和各领域的加权卡方值(0.5-0.72)表明测试重复可靠性足够高。指数/VAS 评分与 SGRQ 和 6MWT 的相关领域之间的相关性符合假设(0.31-0.62),指数/VAS 评分的平均值在 6MWT 组和 ppFEV1 已知组之间存在显著差异(pConclusion):EQ-5D-3L在MAC-LD患者中显示出有效性和可靠性,但对有临床意义的变化反应迟钝。
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来源期刊
Patient Related Outcome Measures
Patient Related Outcome Measures HEALTH CARE SCIENCES & SERVICES-
自引率
4.80%
发文量
27
审稿时长
16 weeks
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