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两种用于临床试验的哮喘症状日记量表的测量特性。

Measurement characteristics of two asthma symptom diary scales for use in clinical trials.

作者信息

Santanello N C, Barber B L, Reiss T F, Friedman B S, Juniper E F, Zhang J

机构信息

Dept of Epidemiology, Merck Research Laboratories, West Point, PA 19486-004, USA.

出版信息

Eur Respir J. 1997 Mar;10(3):646-51.

PMID:9072999
Abstract

The measurement characteristics of two asthma symptom diary scales developed for use as health outcome measures in clinical trials of asthma therapy were investigated. A daytime diary scale was designed to capture the frequency and inconvenience of daytime asthma symptoms and their effects on activities, and a nocturnal asthma symptom diary scale was designed to capture awakenings with asthma symptoms. The internal consistency, reliability, validity and responsiveness of both asthma diary scales were assessed in 346 adult asthma patients in two placebo-controlled clinical trials of an investigational asthma therapy, a leukotriene biosynthesis inhibitor. The daytime symptom scale showed sufficient internal consistency (0.90-0.92), and the daytime and nocturnal symptom scales showed sufficient test retest reliability (0.69-0.87). Construct validity was demonstrated by generally moderate-to-strong correlations for changes in the diary scales with changes in other measures of asthma status, such as forced expiratory volume in one second (FEV1), peak expiratory flow (PEF), and puffs of beta-agonist inhaler. Both scales demonstrated significant responsiveness to change in asthma due to therapy in one of the clinical trials. Based on these results, the daytime and nocturnal asthma symptom diary scales show measurement characteristics appropriate for use as asthma outcome measures in clinical trials of asthma therapy.

摘要

对开发用于哮喘治疗临床试验中作为健康结局指标的两种哮喘症状日记量表的测量特性进行了研究。日间日记量表旨在记录日间哮喘症状的频率、不便程度及其对活动的影响,夜间哮喘症状日记量表旨在记录因哮喘症状而导致的觉醒情况。在一项关于研究性哮喘治疗药物(一种白三烯生物合成抑制剂)的两项安慰剂对照临床试验中,对346名成年哮喘患者评估了两种哮喘日记量表的内部一致性、可靠性、有效性和反应性。日间症状量表显示出足够的内部一致性(0.90 - 0.92),日间和夜间症状量表显示出足够的重测信度(0.69 - 0.87)。日记量表的变化与哮喘状态的其他指标(如一秒用力呼气容积(FEV1)、呼气峰值流速(PEF)和β - 激动剂吸入器的使用次数)的变化之间通常存在中度至高度相关性,证明了结构效度。在其中一项临床试验中,两种量表均显示出对哮喘治疗引起的变化有显著反应性。基于这些结果,日间和夜间哮喘症状日记量表显示出适合在哮喘治疗临床试验中用作哮喘结局指标的测量特性。

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