School of Allied Health, College of Science, Health and Engineering, La Trobe University, Victoria, Australia.
Department of Family Practice, Centre for Hip Health and Mobility, University of British Columbia, Vancouver, Canada.
Br J Sports Med. 2018 Sep;52(17):1130-1136. doi: 10.1136/bjsports-2016-096776. Epub 2017 Mar 3.
Patellofemoral pain and osteoarthritis are prevalent and associated with substantial pain and functional impairments. Patient-reported outcome measures (PROMs) are recommended for research and clinical use, but no PROMs are specific for patellofemoral osteoarthritis, and existing PROMs for patellofemoral pain have methodological limitations. This study aimed to develop a new subscale of the Knee injury and Osteoarthritis Outcome Score for patellofemoral pain and osteoarthritis (KOOS-PF), and evaluate its measurement properties.
Items were generated using input from 50 patients with patellofemoral pain and/or osteoarthritis and 14 health and medical clinicians. Item reduction was performed using data from patellofemoral cohorts (n=138). We used the COnsesus-based Standards for the selection of health Measurements INstruments guidelines to evaluate reliability, validity, responsiveness and interpretability of the final version of KOOS-PF and other KOOS subscales.
From an initial 80 generated items, the final subscale included 11 items. KOOS-PF items loaded predominantly on one factor, pain during activities that load the patellofemoral joint. KOOS-PF had good internal consistency (Cronbach's α 0.86) and adequate test-retest reliability (intraclass correlation coefficient 0.86). Hypothesis testing supported convergent, divergent and known-groups validity. Responsiveness was confirmed, with KOOS-PF demonstrating a moderate correlation with Global Rating of Change scores (r 0.52) and large effect size (Cohen's d 0.89). Minimal detectable change was 2.3 (groups) and 16 (individuals), while minimal important change was 16.4. There were no floor or ceiling effects.
The 11-item KOOS-PF, developed in consultation with patients and clinicians, demonstrated adequate measurement properties, and is recommended for clinical and research use in patients with patellofemoral pain and osteoarthritis.
髌股疼痛和骨关节炎普遍存在,并与大量疼痛和功能障碍相关。患者报告的结局测量(PROM)被推荐用于研究和临床使用,但没有专门针对髌股骨关节炎的 PROM,而现有的髌股疼痛 PROM 存在方法学限制。本研究旨在开发一种新的髌股疼痛和骨关节炎膝关节损伤和骨关节炎结局评分(KOOS-PF)子量表,并评估其测量性能。
使用 50 名髌股疼痛和/或骨关节炎患者和 14 名健康和医疗临床医生的输入生成项目。使用髌股队列的数据(n=138)进行项目减少。我们使用基于共识的健康测量仪器选择标准指南来评估 KOOS-PF 和其他 KOOS 子量表的最终版本的可靠性、有效性、反应性和可解释性。
从最初的 80 个生成项目中,最终子量表包括 11 个项目。KOOS-PF 项目主要加载在一个因子上,即髌股关节负荷活动时的疼痛。KOOS-PF 具有良好的内部一致性(Cronbach's α 0.86)和足够的测试-重测可靠性(组内相关系数 0.86)。假设检验支持收敛、发散和已知群体的有效性。反应性得到证实,KOOS-PF 与全球变化评分(r 0.52)和大效应量(Cohen's d 0.89)呈中度相关。最小可检测变化为 2.3(组)和 16(个体),而最小重要变化为 16.4。没有地板或天花板效应。
与患者和临床医生协商制定的 11 项 KOOS-PF 具有足够的测量性能,建议在髌股疼痛和骨关节炎患者的临床和研究中使用。