RTI Health Solutions, Research Triangle Park, NC, USA.
RTI Health Solutions, Ann Arbor, MI, USA.
J Patient Rep Outcomes. 2023 Oct 30;7(1):105. doi: 10.1186/s41687-023-00647-y.
Patient-reported outcome measures that facilitate self-report by children are needed to reduce the bias of proxy report. We previously developed an electronic Pediatric Asthma Symptom Diary (ePASD) to assess the severity of daily asthma symptoms and proximal impacts in children aged 6-11 years with mild to severe asthma. The ePASD, administered via a digital application with visuals, sounds, and text, is uniquely designed to minimize the importance of reading skills on children's ability to self-report accurately. Here, we describe the ePASD's psychometric properties.
Ninety-one children aged 6-11 years with mild to severe asthma and their caregivers participated in 2 study visits, which consisted of training on the provisioned device and completing asthma-specific clinical outcome assessment (COA) questionnaires. The children self-completed the ePASD at home twice daily for 8 consecutive days. The scoring of the ePASD was guided by factor analyses, inter-item correlations, and internal consistencies. Reliability, discriminating ability, construct validity, and responsiveness were evaluated for ePASD items and candidate scores.
All COAs included in the study-the ePASD, Asthma Control Questionnaire (ACQ), Childhood Asthma Control Test, Pediatric Asthma Quality of Life Questionnaire-Standardized (PAQLQ[S]), and global ratings-demonstrated that the children exhibited few asthma-related symptoms and impacts at all timepoints, and consequently, showed little change over time. Internal consistencies (all Cronbach's alphas ≥ 0.52) and test-retest reliabilities (all intraclass correlation coefficients ≥ 0.60) were largely satisfactory. Patterns of convergent and divergent correlations supported the construct validity of ePASD scores. The ePASD symptom scores correlated moderately to strongly with PAQLQ(S) Symptom scores (all correlations ≥ - 0.46) and with ACQ scores (all correlations ≥ 0.42), as predicted. Evidence of the discriminating ability of ePASD items and composite scores was demonstrated by known-groups analyses.
The ePASD is a reliable and valid measure of asthma symptoms and proximal impacts in children aged 6-11 years with mild, moderate, or severe asthma. These results lay the psychometric groundwork for use of the ePASD in future clinical trials for the management of pediatric asthma. An ongoing pediatric asthma treatment trial is anticipated to provide evidence of the ePASD's responsiveness to change.
需要能够促进儿童自我报告的患者报告结局测量工具,以减少代理报告的偏差。我们之前开发了一种电子儿科哮喘症状日记(ePASD),用于评估 6-11 岁患有轻度至重度哮喘的儿童的日常哮喘症状严重程度和近端影响。ePASD 通过带有视觉、声音和文本的数字应用程序进行管理,专门设计用于最大限度地减少阅读技能对儿童准确自我报告能力的重要性。在这里,我们描述了 ePASD 的心理测量特性。
91 名 6-11 岁患有轻度至重度哮喘的儿童及其照顾者参加了 2 次研究访问,包括设备使用培训和完成哮喘特定的临床结局评估(COA)问卷。儿童在家中每天两次自行完成 ePASD,连续 8 天。ePASD 的评分通过因素分析、项目间相关性和内部一致性进行指导。评估了 ePASD 项目和候选评分的可靠性、区分能力、结构有效性和反应性。
研究中包含的所有 COA-ePASD、哮喘控制问卷(ACQ)、儿童哮喘控制测试、儿科哮喘生活质量问卷标准化(PAQLQ[S])和总体评分-均表明,所有儿童在所有时间点均表现出很少的哮喘相关症状和影响,因此随着时间的推移几乎没有变化。内部一致性(所有 Cronbach's alpha 值≥0.52)和测试-重测信度(所有 ICC 值≥0.60)基本令人满意。收敛和发散相关性的模式支持 ePASD 评分的结构有效性。ePASD 症状评分与 PAQLQ[S]症状评分(所有相关性≥-0.46)和 ACQ 评分(所有相关性≥0.42)中度至高度相关,这与预测一致。通过已知组分析证明了 ePASD 项目和综合评分的区分能力。
ePASD 是一种可靠且有效的 6-11 岁轻度、中度或重度哮喘儿童哮喘症状和近端影响的测量工具。这些结果为未来儿科哮喘管理的临床试验中使用 ePASD 奠定了心理测量基础。预计正在进行的儿科哮喘治疗试验将提供 ePASD 对变化的反应性证据。