Gartner-Schmidt Jackie L, Shembel Adrianna C, Zullo Thomas G, Rosen Clark A
Department of Otolaryngology, University of Pittsburgh Voice Center, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
Department of Otolaryngology, University of Pittsburgh Voice Center, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
J Voice. 2014 Nov;28(6):775-82. doi: 10.1016/j.jvoice.2013.12.017. Epub 2014 Oct 12.
To (1) develop and validate the Dyspnea Index (DI); (2) quantify severity of symptoms in upper airway dyspnea; and (3) validate the DI as an outcome measure.
Survey development and validation.
Three hundred sixty-nine participants were recruited for different phases of the study. Two hundred participants with chief complaints of dyspnea were given a 41-item questionnaire addressing common symptoms of dyspnea related to the upper airway. The questions were then reduced based on principal component analysis (PCA) and internal consistency resulting in a 10-item questionnaire. Cognitive interviews were conducted with 15 participants. Test-retest reliability and discriminant validity were measured from 51 participants. The DI was further validated by administering the index to 57 healthy controls (HC). Validation of the DI as a treatment outcome tool occurred with 46 participants' pre- and post-treatment scores.
PCA revealed that only a single factor was being measured in both the original 41- and 10-item questionnaires. Additional cognitive interviewing suggested that no modification was needed to the DI. Test-retest reliability was r = 0.83. Discriminant validity was r = 0.62. The Mann-Whitney test demonstrated significant differences between healthy/symptomatic participants. Scores from the HC cohort resulted in a mean of 3.12 (SEM = 0.484; SD = 3.65) for the normative values.
The DI is an effective and efficient instrument to quantify patients' symptoms of upper airway dyspnea. It is a statistically robust index, with significant reliability and validity, and can be dependably used as a treatment outcome measure.
(1)开发并验证呼吸困难指数(DI);(2)对上气道呼吸困难的症状严重程度进行量化;(3)验证DI作为一项结局指标的有效性。
调查开发与验证。
369名参与者被招募参与该研究的不同阶段。200名以呼吸困难为主诉的参与者接受了一份包含41个条目的问卷,该问卷涉及与上气道相关的常见呼吸困难症状。随后基于主成分分析(PCA)和内部一致性对问题进行缩减,最终形成一份10个条目的问卷。对15名参与者进行了认知访谈。对51名参与者测量了重测信度和判别效度。通过对57名健康对照者(HC)应用该指数进一步验证DI。通过46名参与者治疗前和治疗后的得分对DI作为治疗结局工具的有效性进行了验证。
PCA显示,在最初的41个条目和10个条目的问卷中测量的均只是单一因素。额外的认知访谈表明DI无需修改。重测信度r = 0.83。判别效度r = 0.62。曼-惠特尼检验显示健康/有症状参与者之间存在显著差异。HC队列的得分得出规范值的均值为3.12(标准误=0.484;标准差=3.65)。
DI是一种有效且高效的工具,可用于量化患者的上气道呼吸困难症状。它是一个统计学上稳健的指数,具有显著的信度和效度,并且可以可靠地用作治疗结局指标。