Validation of Patient‐Reported Outcomes Measurement Information System Short Forms for Use in Childhood‐Onset Systemic Lupus Erythematosus

Arthritis Care and Research - Tập 69 Số 1 - Trang 133-142 - 2017
Jordan T. Jones1, Adam C. Carle2, Janet Wootton3, Brianna Liberio4, Jiha Lee4, Laura E. Schanberg3, Jun Ying4, Esi Morgan DeWitt5, Hermine I. Brunner5
1University of Missouri–Kansas City and Children's Mercy Hospitals and Clinics, Kansas City, and University of Cincinnati College of Medicine and Cincinnati Children's Hospital Medical Center Cincinnati Ohio
2University of Cincinnati College of Medicine, Cincinnati Children's Hospital Medical Center, and College of Arts and Sciences Cincinnati Ohio
3Duke University Medical Center, Durham, North Carolina
4University of Cincinnati College of Medicine, Cincinnati, Ohio
5University of Cincinnati College of Medicine and Cincinnati Children's Hospital Medical Center Cincinnati Ohio

Tóm tắt

ObjectiveTo validate the pediatric Patient‐Reported Outcomes Measurement Information System short forms (PROMIS‐SFs) in childhood‐onset systemic lupus erythematosus (SLE) in a clinical setting.MethodsAt 3 study visits, childhood‐onset SLE patients completed the PROMIS‐SFs (anger, anxiety, depressive symptoms, fatigue, physical function‐mobility, physical function‐upper extremity, pain interference, and peer relationships) using the PROMIS assessment center, and health‐related quality of life (HRQoL) legacy measures (Pediatric Quality of Life Inventory, Childhood Health Assessment Questionnaire, Simple Measure of Impact of Lupus Erythematosus in Youngsters [SMILEY], and visual analog scales [VAS] of pain and well‐being). Physicians rated childhood‐onset SLE activity on a VAS and completed the Systemic Lupus Erythematosus Disease Activity Index 2000. Using a global rating scale of change (GRC) between study visits, physicians rated change of childhood‐onset SLE activity (GRC‐MD1: better/same/worse) and change of patient overall health (GRC‐MD2: better/same/worse). Questionnaire scores were compared in support of validity and responsiveness to change (external standards: GRC‐MD1, GRC‐MD2).ResultsIn this population‐based cohort (n = 100) with a mean age of 15.8 years (range 10–20 years), the PROMIS‐SFs were completed in less than 5 minutes in a clinical setting. The PROMIS‐SF scores correlated at least moderately (Pearson's r ≥ 0.5) with those of legacy HRQoL measures, except for the SMILEY. Measures of childhood‐onset SLE activity did not correlate with the PROMIS‐SFs. Responsiveness to change of the PROMIS‐SFs was supported by path, mixed‐model, and correlation analyses.ConclusionTo assess HRQoL in childhood‐onset SLE, the PROMIS‐SFs demonstrated feasibility, internal consistency, construct validity, and responsiveness to change in a clinical setting.

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Arthritis Care and Research

Tập 69 Số 1

133-142

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