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

机译:哮喘患者效果问卷的开发和验证。

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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 1 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 1 second [FEV(1); p < 0.0001 and symptom severity] p < 0.001) and predictive validity (response after 1 week of treatment predicted 2-week 15-minute postdose FEV(1) [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 are reliable and valid and may be used as end points in clinical trials involving similar patient populations.
机译:哮喘患者在服药后不久即可感觉到工作的维持性药物可以加强日常治疗并改善满意度,依从性和结果。进行这项研究是为了开发和测试一种评估患者对立即服用哮喘药物的感知和满意度的措施。进行了三项研究以开发和评估该措施。研究1涉及定性患者访谈,以了解立即感觉到药物正在​​起作用的概念,并开发了评估方法和项目库(n = 64)。研究2通过认知访谈检查了项目的清晰度和内容有效性(n = 39)。研究3通过对来自参加轻度至中度持续性哮喘(n = 245)的12周,多中心,双盲,安慰剂对照III期临床试验的成年人的数据进行二次分析,测试了信度和效度。编写了一份五项每周日记,即《效果调查问卷》,其中有两项被选为主要项目:一项评估患者是否感觉到自己的药物立即起作用,另一项评估他们对自己的药物开始起作用的速度的满意度。这些项目显示1周可重复性(phi = 0.77; 0.70; p <0.0001),构建体有效性(与服药后15分钟强迫呼气量在1秒内改善的关系[FEV(1); p <0.0001和症状严重程度)p <0.001)和预测效度(治疗1周后的反应预测给药后2周15分钟FEV(1)[p <0.0001],哮喘患者生活质量问卷症状域[p <0.05]和患者对哮喘药物的满意度药物的总体感觉[p <0.0001]和哮喘缓解量表[p <0.0001])。结果表明,这些项目可靠且有效,并且可以用作涉及相似患者人群的临床试验的终点。

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