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The validity and precision of the leicester cough questionnaire in COPD patients with chronic cough

机译:莱斯特咳嗽问卷在慢性阻塞性肺病慢性咳嗽患者中的有效性和准确性

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Background A validated instrument to assess the effects of chronic cough on health status in patients with chronic obstructive pulmonary disease ( COPD ) is currently not available. The Leicester Cough Questionnaire (LCQ) is a cough-specific health status questionnaire which is originally validated for a population of general patients presenting with chronic cough. We examined the psychometric performance of the LCQ in patients with COPD and chronic productive cough. Methods Concurrent validity, internal consistency, reproducibility and responsiveness were determined. The St. George's Respiratory Questionnaire (SGRQ) and the Short Form-36 (SF-36) were used as external criteria. Questionnaires were completed at the start of the study. After 2 and 12 weeks the LCQ was repeated, together with a global rating of change. Results In total 54 patients were included. Concurrent validity analysis showed significant correlations between corresponding domains of the LCQ and the SGRQ (rs -0.31 to -0.60). Corresponding domains of the LCQ and the SF-36 showed weaker correlations (rs 0.04 to 0.41). Internal consistency was adequate for two of the three domains (Cronbach's α 0.74 - 0.86). Test-retest reliability in stable patients was high (intraclass correlation coefficients 0.79 - 0.93). The mean difference after two weeks was 0.73 (± 1.75). Responsiveness analysis indicated that the LCQ was able to detect changes after 12 weeks. Conclusion The LCQ is a valid, reliable, responsive instrument to measure health status in COPD patients with chronic productive cough. Trial Registration ClinicalTrials.gov: NCT01071161
机译:背景技术目前尚没有一种有效的评估慢性咳嗽对慢性阻塞性肺疾病(COPD)患者健康状况影响的仪器。莱斯特咳嗽问卷(LCQ)是一种针对特定咳嗽的健康状况调查表,最初是针对患有慢性咳嗽的一般患者人群进行验证的。我们检查了慢性阻塞性肺病和慢性生产性咳嗽患者的LCQ心理测验表现。方法确定并发有效性,内部一致性,可重复性和反应性。圣乔治呼吸问卷(SGRQ)和简短表格36(SF-36)被用作外部标准。在研究开始时完成问卷调查。 2周和12周后,将再次进行LCQ,同时对总体变化进行评分。结果共纳入54例患者。并发有效性分析表明,LCQ和SGRQ的相应域之间存在显着相关性(r s -0.31至-0.60)。 LCQ和SF-36的相应域显示出较弱的相关性(r s 0.04至0.41)。内部一致性对于三个域中的两个域是足够的(Cronbachα0.74-0.86)。稳定患者的重测信度很高(类内相关系数为0.79-0.93)。两周后的平均差异为0.73(±1.75)。响应性分析表明,LCQ能够在12周后检测到变化。结论LCQ是一种有效,可靠,反应迅速的仪器,可用于测量COPD慢性生产性咳嗽患者的健康状况。试验注册ClinicalTrials.gov:NCT01071161

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