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首页> 外文期刊>The journal of asthma >Measurement properties of an asthma symptom and rescue medication use diary
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Measurement properties of an asthma symptom and rescue medication use diary

机译:哮喘症状的测量性质和急救药物使用日记

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Introduction: Assessment of symptoms and rescue medication use are well-established endpoints for clinical trials evaluating asthma treatment. Objective: To evaluate the measurement properties of an asthma symptom and rescue medication use (ASRMU) diary for clinical trials involving asthma patients aged >= 12 years. Methods: Interviews with 35 patients were conducted to confirm the importance of key concepts in the ASRMU diary. Scores of symptom and rescue medication use were converted to symptom-free days (SFD) and rescue-free days (RFD). Test-retest reliability and equivalence (based on intra-class correlation coefficients [ICCs]) between paper-and-pencil and electronic (eDiary) versions were evaluated in a prospective study in 47 patients. Responsiveness of the ASRMU diary was evaluated through differences in percentage of SFD and of RFD by treatment group in eight asthma clinical trials that assessed inhaled corticosteroids (ICS) and long-acting beta(2)-agonists (LABA), alone or in combination. A ninth placebo-controlled study calculated effect sizes. Minimal important differences (MID) were determined using anchor-based methods from two trials and by interviewing 11 patients. Results: Patient interviews supported content validity for the ASRMU diary. Test-retest reliability was acceptable for SFD (ICC: 0.70-0.75), but varied for RFD (ICC: 0.58-0.78). Paper-and-pencil and eDiary modes of administration were equivalent (SFD, ICC = 0.84; RFD, ICC = 0.70). ICS/LABA had the largest percentage of SFD and RFD, followed by monotherapy and then placebo. MIDs were 7.7-14.7% for SFD and 8.4-15.6% for RFD. Conclusions: The ASRMU diary captures the disease-specific concepts of greatest importance to asthma patients and provides important information for asthma diagnosis and treatment evaluation.
机译:简介:症状评估和急救药物的使用是评估哮喘治疗的临床试验的既定终点。目的:评估哮喘症状和急救药物使用(ASRMU)日记在涉及≥12岁哮喘患者的临床试验中的测量性能。方法:采访了35名患者,以确认ASRMU日记中关键概念的重要性。将症状和急救药物的使用分数转换为无症状天数(SFD)和无急救天数(RFD)。一项前瞻性研究在47位患者中评估了纸笔型和电子版(eDiary)之间的重测信度和等效性(基于类内相关系数[ICC])。在八项哮喘临床试验中,通过评估吸入皮质类固醇(ICS)和长效β(2)-激动剂(LABA)的单独使用或联合使用,通过治疗组的SFD和RFD百分比差异来评估ASRMU日记的反应性。第九个安慰剂对照研究计算了效应量。使用两项研究中基于锚的方法并采访11位患者,确定了最小重要差异(MID)。结果:患者访谈支持ASRMU日记的内容有效性。重试可靠性对于SFD(ICC:0.70-0.75)是可以接受的,但对于RFD(ICC:0.58-0.78)是可以接受的。纸笔和电子日记的给药方式相同(SFD,ICC = 0.84; RFD,ICC = 0.70)。 ICS / LABA的SFD和RFD百分比最高,其次是单一疗法,然后是安慰剂。 SFD的MID为7.7-14.7%,RFD的MID为8.4-15.6%。结论:ASRMU日记记录了对哮喘患者最重要的疾病特定概念,并为哮喘诊断和治疗评估提供重要信息。

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