Development and validation of an onset of effect questionnaire for patients with asthma

被引:12
|
作者
Leidy, Nancy K. [1 ]
Mathias, Susan D.
Parasuraman, Bhash M. [2 ,3 ]
Patrick, Donald L.
Pathak, Dev [4 ]
机构
[1] United BioSource Corp, Bethesda, MD 20814 USA
[2] AstraZeneca, Wilmington, DE USA
[3] Univ Washington, Seattle, WA 98195 USA
[4] Univ S Florida, Tampa, FL USA
关键词
Adherence; asthma; bronchodilation; compliance; health outcomes; instrument development; maintenance therapy; noncompliance; qualitative methods; self-management; validity;
D O I
10.2500/aap.2008.29.3164
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
A maintenance medication that patients with asthma can feel working shortly after administration could reinforce daily treatment and improve satisfaction, adherence, and outcomes. This study was performed to develop and test a measure assessing patient perception and satisfaction with feeling an asthma medication working right away. Three studies were conducted to develop and evaluate the measure. Study I involved qualitative patient interviews to understand the concept of feeling a medication working right away and developed the assessment method and item pool (n = 64). Study 2 examined item clarity and content validity through cognitive interviews (n = 39). Study 3 tested reliability and validity through secondary analyses of data from adults participating in a 12-week, multicenter, double-blind, placebo-controlled phase III trial of mild to moderate persistent asthma (n = 245). A five-item Weekly diary, the Onset of Effect Questionnaire, was developed with two items selected as primary: one evaluating whether patients feel their medication working right away and one assessing satisfaction with how quickly they feel their medication begin to work. These items showed 1-week reproducibility (phi = 0.77, 0.70; p < 0.0001), construct validity (relationship with improvement in 15-minute postdose forced expiratory volume in I second [FEV1; p < 0.0001 and symptom severity] p < 0.001) and predictive validity (response after I week of treatment predicted 2-Week 15-minute postdose FEV1 [p < 0.0001], Asthma Quality of Life Questionnaire symptom domain [p < 0.05], and Patient Satisfaction with Asthma Medication overall perception of medication [p < 0.0001] and asthma relief subscales [p < 0.0001)]. Results suggest that the items arc reliable and valid and may be used as end points in clinical trials involving similar patient populations.
引用
收藏
页码:590 / 599
页数:10
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