Literature DB >> 24842571

The outcomes of juvenile idiopathic arthritis in children managed with contemporary treatments: results from the ReACCh-Out cohort.

Jaime Guzman1, Kiem Oen2, Lori B Tucker1, Adam M Huber3, Natalie Shiff4, Gilles Boire5, Rosie Scuccimarri6, Roberta Berard7, Shirley M L Tse8, Kimberly Morishita1, Elizabeth Stringer3, Nicole Johnson9, Deborah M Levy8, Karen Watanabe Duffy10, David A Cabral1, Alan M Rosenberg4, Maggie Larché11, Paul Dancey12, Ross E Petty1, Ronald M Laxer8, Earl Silverman8, Paivi Miettunen9, Anne-Laure Chetaille13, Elie Haddad14, Kristin Houghton1, Lynn Spiegel8, Stuart E Turvey1, Heinrike Schmeling9, Bianca Lang3, Janet Ellsworth15, Suzanne Ramsey3, Alessandra Bruns5, Sarah Campillo6, Susanne Benseler9, Gaëlle Chédeville6, Rayfel Schneider8, Rae Yeung8, Ciarán M Duffy10.   

Abstract

OBJECTIVE: To describe clinical outcomes of juvenile idiopathic arthritis (JIA) in a prospective inception cohort of children managed with contemporary treatments.
METHODS: Children newly diagnosed with JIA at 16 Canadian paediatric rheumatology centres from 2005 to 2010 were included. Kaplan-Meier survival curves for each JIA category were used to estimate probability of ever attaining an active joint count of 0, inactive disease (no active joints, no extraarticular manifestations and a physician global assessment of disease activity <10 mm), disease remission (inactive disease >12 months after discontinuing treatment) and of receiving specific treatments.
RESULTS: In a cohort of 1104 children, the probabilities of attaining an active joint count of 0 exceeded 78% within 2 years in all JIA categories. The probability of attaining inactive disease exceeded 70% within 2 years in all categories, except for RF-positive polyarthritis (48%). The probability of discontinuing treatment at least once was 67% within 5 years. The probability of attaining remission within 5 years was 46-57% across JIA categories except for polyarthritis (0% RF-positive, 14% RF-negative). Initial treatment included joint injections and non-steroidal anti-inflammatory drugs for oligoarthritis, disease-modifying antirheumatic drugs (DMARDs) for polyarthritis and systemic corticosteroids for systemic JIA.
CONCLUSIONS: Most children with JIA managed with contemporary treatments attain inactive disease within 2 years of diagnosis and many are able to discontinue treatment. The probability of attaining remission within 5 years of diagnosis is about 50%, except for children with polyarthritis. Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.

Entities:  

Keywords:  Epidemiology; Juvenile Idiopathic Arthritis; Outcomes research; Treatment

Mesh:

Substances:

Year:  2014        PMID: 24842571     DOI: 10.1136/annrheumdis-2014-205372

Source DB:  PubMed          Journal:  Ann Rheum Dis        ISSN: 0003-4967            Impact factor:   19.103


  72 in total

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10.  Different corticosteroid induction regimens in children and young people with juvenile idiopathic arthritis: the SIRJIA mixed-methods feasibility study.

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