Zeng Chengbo, Hays Ron D, Rodriguez Anthony, Hanmer Janel, Herman Patricia M, Edelen Maria Orlando
Patient Reported Outcomes, Value and Experience (PROVE) Center, Department of Surgery, Brigham and Women's Hospital, Boston, MA, USA.
Division of General Internal Medicine and Health Services Research, UCLA Department of Medicine, Los Angeles, CA, USA.
Qual Life Res. 2025 Jan;34(1):27-34. doi: 10.1007/s11136-024-03747-4. Epub 2024 Aug 14.
This study evaluates the interpretability of Patient-Reported Outcomes Measurement Information System (PROMIS)-16 profile domain scores (physical function, ability to participate in social roles and activities, anxiety, depression, sleep disturbance, pain interference, cognitive function - abilities, and fatigue) compared to the PROMIS-29 scores and a 5-item PROMIS cognitive function score. The study aims to provide insights into using these measures in clinical and research settings.
Analyses were conducted using data from 4130 adults from a nationally representative, probability-based internet panel between September and October 2022. A subset of 1256 individuals with back pain was followed up at six months. We compared the PROMIS-16 profile with the corresponding domain scores from the PROMIS-29 and a custom five-item cognitive function measure. We evaluated (1) reliability through inter-item correlations within each domain and (2) criterion validity by comparing PROMIS-16 profile with the corresponding longer PROMIS measures: (a) standardized mean differences in domain scores, (b) correlations, and (c) concordance of change (i.e., got worse, stayed the same, got better) among those with back pain from baseline to six months later using the reliable change index. We report the Kappa coefficient of agreement and the frequency and percentage of participants with concordant classifications.
Inter-item correlations for the PROMIS-16 domains ranged from 0.65 in cognitive function to 0.92 in pain interference. Standardized mean differences between PROMIS-16 and the scores for the corresponding longer PROMIS domains were minimal (< 0.2). Correlations among the corresponding domain scores ranged from 0.82 for sleep disturbance to 0.98 for pain interference. The percentage of concordance in change groups ranged from 63% for sleep disturbance to 88% for pain interference. Except for sleep disturbance, the change groups derived from the PROMIS-16 showed moderate to substantial agreement with scores estimated from the longer PROMIS measures (Kappa coefficients ≥ 0.41).
The PROMIS-16 domain scores perform similarly to the longer PROMIS measures and can be interpreted in the same way. This similarity indicates that PROMIS-16 can be useful for research as a brief health-related quality-of-life profile measure.
本研究评估患者报告结局测量信息系统(PROMIS)-16简表领域得分(身体功能、参与社会角色和活动的能力、焦虑、抑郁、睡眠障碍、疼痛干扰、认知功能——能力和疲劳)与PROMIS-29得分以及5项PROMIS认知功能得分相比的可解释性。该研究旨在深入了解在临床和研究环境中使用这些测量方法的情况。
使用来自2022年9月至10月全国代表性的基于概率的互联网面板的4130名成年人的数据进行分析。对1256名背痛患者的子集进行了为期6个月的随访。我们将PROMIS-16简表与PROMIS-29相应领域得分以及一项定制的五项认知功能测量进行了比较。我们评估了:(1)通过每个领域内的项目间相关性来评估信度,以及(2)通过将PROMIS-16简表与相应的更长的PROMIS测量进行比较来评估效标效度:(a)领域得分的标准化均值差异,(b)相关性,以及(c)使用可靠变化指数比较背痛患者从基线到6个月后变化的一致性(即变差、不变、变好)。我们报告了一致性的Kappa系数以及分类一致的参与者的频率和百分比。
PROMIS-16领域的项目间相关性范围从认知功能的0.65到疼痛干扰的0.92。PROMIS-16与相应更长的PROMIS领域得分之间的标准化均值差异最小(<0.2)。相应领域得分之间的相关性范围从睡眠障碍的0.82到疼痛干扰的0.98。变化组的一致性百分比范围从睡眠障碍的63%到疼痛干扰的88%。除睡眠障碍外,PROMIS-16得出的变化组与更长的PROMIS测量估计得分显示出中度到高度的一致性(Kappa系数≥ 0.41)。
PROMIS-16领域得分与更长的PROMIS测量表现相似,并且可以以相同的方式进行解释。这种相似性表明PROMIS-16作为一种简短的健康相关生活质量简表测量方法在研究中可能有用。