Literature DB >> 2059234

Development of a disability measurement tool for juvenile rheumatoid arthritis. The Juvenile Arthritis Functional Assessment Report for Children and their Parents.

S Howe1, J Levinson, E Shear, S Hartner, G McGirr, M Schulte, D Lovell.   

Abstract

Two questionnaires were developed for measuring disability due to juvenile rheumatoid arthritis (JRA), one based on patient reports and one on parent reports. These questionnaires were termed the Juvenile Arthritis Functional Assessment Report for Children (JAFAR-C) and for Parents (JAFAR-P). The questionnaires were administered to 72 JRA patients ages 7-18 years and to their parents. Respondents rated the patient's recent ability to perform 23 activities. Patient reports and parent reports were found to correlate highly with each other and with an objective assessment performed by therapists. Questionnaire scores did not correlate significantly with the age of the patient. The JAFAR appears to be a convenient, reliable, and valid measure of disability in patients with JRA.

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Year:  1991        PMID: 2059234     DOI: 10.1002/art.1780340713

Source DB:  PubMed          Journal:  Arthritis Rheum        ISSN: 0004-3591


  71 in total

Review 1.  Juvenile rheumatoid arthritis--assessment.

Authors:  T B Graham; E H Giannini
Journal:  Indian J Pediatr       Date:  1996 May-Jun       Impact factor: 1.967

Review 2.  Outcome measures and medical progress: why outcome measures are needed in childhood arthritis.

Authors:  Francesco Zulian
Journal:  Curr Rheumatol Rep       Date:  2003-12       Impact factor: 4.592

Review 3.  Evidence-based assessment of health-related quality of life and functional impairment in pediatric psychology.

Authors:  Tonya M Palermo; Anna C Long; Amy S Lewandowski; Dennis Drotar; Alexandra L Quittner; Lynn S Walker
Journal:  J Pediatr Psychol       Date:  2008-04-22

Review 4.  Quality of life in children with systemic lupus erythematosus.

Authors:  L Nandini Moorthy; Margaret Peterson; Karen B Onel; Melanie J Harrison; Thomas J A Lehman
Journal:  Curr Rheumatol Rep       Date:  2005-12       Impact factor: 4.592

5.  Comparison between Children with Juvenile Idiopathic Arthritis (JIA) and their parents concerning perceived Quality of Life.

Authors:  Karine Toupin April; Debbie Ehrmann Feldman; Robert W Platt; Ciarán M Duffy
Journal:  Qual Life Res       Date:  2006-05       Impact factor: 4.147

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

Authors:  Timothy G Brandon; Brandon D Becker; Katherine B Bevans; Pamela F Weiss
Journal:  Arthritis Care Res (Hoboken)       Date:  2017-03       Impact factor: 4.794

7.  The primary role of steroids on the osteoporosis in juvenile rheumatoid patients evaluated by dual energy X-ray absorptiometry.

Authors:  F Falcini; S Trapani; R Civinini; A Capone; M Ermini; G Bartolozzi
Journal:  J Endocrinol Invest       Date:  1996-03       Impact factor: 4.256

8.  Evaluation of response to methotrexate by a functional index in juvenile chronic arthritis.

Authors:  A Ravelli; S Viola; B Ramenghi; G Di Fuccia; N Ruperto; L Zonta; A Martini
Journal:  Clin Rheumatol       Date:  1995-05       Impact factor: 2.980

Review 9.  Using Patient-Reported Outcome Measures to Capture the Patient's Voice in Research and Care of Juvenile Idiopathic Arthritis.

Authors:  Aimee O Hersh; Parissa K Salimian; Elissa R Weitzman
Journal:  Rheum Dis Clin North Am       Date:  2016-03-18       Impact factor: 2.670

10.  Functional disability in children with hemophilic arthropathy.

Authors:  Eda Gurcay; Emel Eksioglu; Ustun Ezer; Reyhan Tuncay; Aytul Cakci
Journal:  Rheumatol Int       Date:  2006-02-17       Impact factor: 2.631

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