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Patient-Reported Outcomes Measurement Information System Tools for Collecting Patient-Reported Outcomes in Children With Juvenile Arthritis.

Authors :
Brandon, Timothy G.
Becker, Brandon D.
Bevans, Katherine B.
Weiss, Pamela F.
Source :
Arthritis Care & Research; Mar2017, Vol. 69 Issue 3, p393-402, 10p
Publication Year :
2017

Abstract

<bold>Objective: </bold>To evaluate the precision and construct validity of pediatric Patient-Reported Outcomes Measurement Information System (PROMIS) instruments in a population of juvenile idiopathic arthritis (JIA) patients and parent proxies.<bold>Methods: </bold>A convenience sample of JIA patients and parents of JIA patients completed PROMIS instruments for 8 domains: anger, anxiety, depressive symptoms, fatigue, mobility, pain interference, peer relationships, and upper-extremity function. Short form and computerized adaptive test (CAT) scores were derived from item bank responses. Raw scores were translated to standardized T scores with corresponding SEs. Discrimination between inactive versus active disease was evaluated as an indicator of each measure's construct validity. SEs were plotted to evaluate each instrument's relative precision. Patient-parent concordance was assessed using intraclass correlations (ICCs).<bold>Results: </bold>A total of 228 patients and 223 parents participated, providing 71-78 responses per domain. Patient- and parent-reported anger, fatigue, mobility, and pain interference scores significantly differed between those with inactive and active disease. Anxiety, depressive symptoms, and peer relationships differed by disease activity levels for parent-report only. Short forms and CATs provided comparable reliability to the full item banks across the full range of each outcome. Patient-parent agreement ranged from ICC 0.3 to 0.8. CATs did not reduce the number of items for any domain compared to the short form.<bold>Conclusion: </bold>Precision and discriminatory abilities of PROMIS instruments depend on health domain and report type (self-report versus parent proxy-report) for children with JIA. Varying levels of patient-parent concordance reinforces the importance of considering both perspectives in comprehensive health outcomes assessments. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
2151464X
Volume :
69
Issue :
3
Database :
Complementary Index
Journal :
Arthritis Care & Research
Publication Type :
Academic Journal
Accession number :
121443474
Full Text :
https://doi.org/10.1002/acr.22937