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Development and validation of a set of patient reported outcome measures to assess effectiveness of asthma prophylaxis

机译:一套患者的开发和验证报告的结果措施,以评估哮喘预防效果的疗效

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In the local setting, asthma control is assessed by symptoms and signs elicited by clinicians because of the limited availability of spirometry. Hence, we intended to develop a patient reported outcome measure (PROM) with more holistic interpretation that could also serve as a tool to measure the asthma control in resource limited settings. Therefore, this study was carried out in Northern Sri Lanka to develop and validate the Asthma Control PROM (AC-PROM) Tamil to measure the effectiveness of asthma prophylaxis based on symptoms, exacerbation and limitation of activity which could also serve as an easy measure of asthma control to the provider. The AC-PROM Tamil was developed in 3 steps: item generation, item reduction and psychometric evaluation. Items were generated through thematic analysis from focus group discussions among patients with asthma. Items were converted to an interviewer administered questionnaire in Tamil in the format of 5-point Likert scale. Item reduction was done by two rounds of online Delphi surveys among 10 experts and an exploratory factor analysis among 200 patients with asthma. The face and content validity were assessed by a panel of experts during Delphi survey and patients during the pre-test of the tool. Criterion validity of the tool was assessed against the forced expiratory volume in one second of 187 patients with asthma. The cut-off value to assess the asthma control was determined by receiver operating characteristic curve. Reliability was verified by Cronbach’s alpha coefficient. From thematic analysis of focus group discussions 10 items were generated. One item was removed during Delphi survey. Exploratory factor analysis indicated removal of another item with 8 items categorised into two factors. Cronbach’s alpha coefficient of factors 1 and 2 were 0.821 and 0.903 respectively, indicating good reliability. Observations made by experts and responses made by patients were incorporated to improve the clarity and relevance of the items. Criterion validity was demonstrated by significant correlation between the AC-PROM Tamil and forced expiratory volume in one second (r?=?0.66, p?=?0.001). The cut-off value of the AC-PROM Tamil to detect asthma control was 28.5 with 79% (95% CI 71.3–86.9) sensitivity and 71% (95% CI 61.9–79.6) specificity. The AC-PROM Tamil showed moderate accuracy (the area under the receiver operating characteristic curve?=?0.796; 95% CI 0.73–0.86). Response rate of the AC-PROM Tamil was 100% and time taken to complete was 3–4?min. The AC-PROM Tamil is a simple, feasible and reasonably accurate tool to assesses the effectiveness of asthma prophylaxis, particularly in resource limited settings.
机译:在局部环境中,由于肺活量测量的可用性有限,临床医生引发的症状和标志评估了哮喘控制。因此,我们打算开发报告的患者报告的结果措施(PROM),具有更多的整体解释,也可以作为测量资源限制环境中哮喘控制的工具。因此,这项研究是在斯里兰卡北部开发和验证哮喘控制舞会(AC-PROM)泰米尔,以根据症状,加重和活动限制来测量哮喘预防的有效性,这也可以作为一种简单的衡量标准哮喘控制到提供者。 AC-PROM泰米尔在3步开发:物品生成,物品减少和心理评估。通过患有哮喘患者的焦点组讨论的主题分析来产生项目。物品被转换为在泰米尔泰米尔的面试官以5分李克特规模的格式进行了调查员。物品还原是通过10个专家的两轮在线德尔福调查完成,200名哮喘患者的探索性因子分析。在工具预测试期间,在Delphi调查和患者期间,通过专家组评估面部和内容有效性。在187名哮喘患者的一秒钟内评估工具的标准有效性。评估哮喘控制的截止值由接收器操作特性曲线测定。 Cronbach的alpha系数验证了可靠性。从对焦组讨论的主题分析,产生了10个项目。在Delphi调查期间被删除了一个项目。探索性因子分析表明,另外的另一件商品分为两个因素。 Cronbach的alpha系数1和2分别为0.821和0.903,表明可靠性良好。患者提出的专家和反应的观察结果纳入,以提高物品的清晰度和相关性。通过在一秒钟内的AC-PROM泰米尔和强迫呼气量之间的显着相关性来证明标准有效性(R?= 0.66,P?= 0.001)。 AC-PROM泰米尔检测哮喘控制的截止值为28.5,79%(95%CI 71.3-86.9)敏感性,71%(95%CI 61.9-79.6)特异性。 AC-PROM泰米尔显示中等精度(接收器下的区域操作特征曲线?= 0.796; 95%CI 0.73-0.86)。 AC-PROM泰米尔的响应率为100%,完成时间为3-4分钟。 AC-PROM泰米尔是一种简单,可行和合理的准确工具,可以评估哮喘预防的有效性,特别是在资源有限的环境中。

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