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Rheumatology (Oxford). 2007 Jan;46(1):161-8. Epub 2006 Jun 20.

The impact of a coordinated transitional care programme on adolescents with juvenile idiopathic arthritis.

Author information

  • 1Division of Reproductive and Child Health, University of Birmingham, Institute of Child Health, Steelhouse Lane, Birmingham B4 6NH, UK. j.e.mcdonagh@bham.ac.uk

Abstract

OBJECTIVE:

There is an extensive evidence base for the need of transitional care, but a paucity of robust outcome data. The aim of the study was to determine whether the quality of life of adolescents with juvenile idiopathic arthritis (JIA) could be improved by a co-ordinated, evidence-based programme of transitional care.

METHODS:

Adolescents with JIA aged 11, 14 and 17 yrs and their parents were recruited from 10 rheumatology centres in the UK. Data were collected at baseline, 6 and 12 months including core outcome variables. The primary outcome measure was health-related quality of life (HRQL): Juvenile Arthritis Quality of Life Questionnaire (JAQQ). Secondary outcome measures included: knowledge, satisfaction, independent health behaviours and pre-vocational experience.

RESULTS:

Of the 359 families invited to participate, 308 (86%) adolescents and 303 (84%) parents accepted. A fifth of them had persistent oligoarthritis. Median disease duration was 5.7 (0-16) yrs. Compared with baseline values, significant improvements in JAQQ scores were reported for adolescent and parent ratings at 6 and 12 months and for most secondary outcome measures with no significant deteriorations between 6 and 12 months. Continuous improvement was observed for both adolescent and parent knowledge with significantly greater improvement in the younger age groups at 12 months (P = 0.002).

CONCLUSIONS:

This study represents the first objective evaluation of an evidence-based transitional care programme and demonstrates that such care can potentially improve adolescents' HRQL.

PMID:
16790451
DOI:
10.1093/rheumatology/kel198
[PubMed - indexed for MEDLINE]
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