Patient-Reported Outcomes Measurement Information System Tools for Collecting Patient-Reported Outcomes in Children With Juvenile Arthritis.
Patient-Reported Outcomes Measurement Information System Tools for Collecting Patient-Reported Outcomes in Children With Juvenile Arthritis.
复制标题
DOI:
10.1002/acr.22937
复制
发表时间:
2017-03
影响因子:
4.7
通讯作者:
Weiss, Pamela F.
中科院分区:
文献类型:
--
作者:
Brandon, Timothy G.;Becker, Brandon D.;Bevans, Katherine B.;Weiss, Pamela F.
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. A convenience sample of JIA patients and parents of JIA patients completed PROMIS instruments for eight 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 standard errors (SEs). Discrimination between inactive versus active disease was evaluated as an indicator of each measures’ construct validity. SEs were plotted to evaluate each instrument’s relative precision. Patient-parent concordance was assessed using intraclass correlations (ICC). 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. CAT did not reduce the number of items for any domain compared to the short form. 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.
登录
查看更多内容
影响因子:
--
作者:
HOWE, S;LEVINSON, J;LOVELL, D
通讯作者:
LOVELL, D
影响因子:
3.6
作者:
Irwin, Debra E.;Gross, Heather E.;DeWalt, Darren A.
通讯作者:
DeWalt, Darren A.
DOI:
10.1002/art.22900
发表时间:
2007-08-15
期刊:
ARTHRITIS & RHEUMATISM-ARTHRITIS CARE & RESEARCH
影响因子:
--
作者:
Filocamo, Giovanni;Sztainbok, Flavio;Ravelli, Angelo
通讯作者:
Ravelli, Angelo
影响因子:
7.2
作者:
DeWitt, Esi Morgan;Stucky, Brian D.;Thissen, David;Irwin, Debra E.;Langer, Michelle;Varni, James W.;Lai, Jin-Shei;Yeatts, Karin B.;DeWalt, Darren A.
通讯作者:
DeWalt, Darren A.
影响因子:
5.5
作者:
Filocamo, Giovanni;Schiappapietra, Benedetta;Ravelli, Angelo
通讯作者:
Ravelli, Angelo