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How common is remission in juvenile idiopathic arthritis: A systematic review

OBJECTIVES: The ideal goal of treatment for juvenile idiopathic arthritis (JIA) is disease remission. However, many sets of remission criteria have been developed and no systematic review of remission in JIA exists. The current systematic review investigated (1) how remission has been defined across...

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Autores principales: Shoop-Worrall, Stephanie J.W., Kearsley-Fleet, Lianne, Thomson, Wendy, Verstappen, Suzanne M.M., Hyrich, Kimme L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: W.B. Saunders 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5687936/
https://www.ncbi.nlm.nih.gov/pubmed/28625712
http://dx.doi.org/10.1016/j.semarthrit.2017.05.007
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author Shoop-Worrall, Stephanie J.W.
Kearsley-Fleet, Lianne
Thomson, Wendy
Verstappen, Suzanne M.M.
Hyrich, Kimme L.
author_facet Shoop-Worrall, Stephanie J.W.
Kearsley-Fleet, Lianne
Thomson, Wendy
Verstappen, Suzanne M.M.
Hyrich, Kimme L.
author_sort Shoop-Worrall, Stephanie J.W.
collection PubMed
description OBJECTIVES: The ideal goal of treatment for juvenile idiopathic arthritis (JIA) is disease remission. However, many sets of remission criteria have been developed and no systematic review of remission in JIA exists. The current systematic review investigated (1) how remission has been defined across JIA clinical cohorts and (2) the frequency of remission overall and within disease categories. METHODS: Studies using prospective inception cohorts published after 1972 were selected if they estimated remission in cohorts of ≥50 patients. Articles focusing on specific medical interventions, not defining remission clearly or not reporting disease duration at remission assessment were excluded. Studies were selected from Medline, Embase, PubMed and bibliographies of selected articles. Risks of selection, missing outcome data and outcome reporting biases were assessed. RESULTS: Within 17 studies reviewed, 88% had majority female participants and patient disease duration ranged from 0.5 to 17 years. Thirteen sets of criteria for clinically inactive disease and remission were identified. Uptake of Wallace’s preliminary criteria was good in studies recruiting or following patients after their publication (78%). Remission frequencies increased with longer disease duration from 7% within 1.5 years to 47% by 10 years following diagnosis. Patients with persistent oligoarticular and rheumatoid-factor positive polyarticular JIA were most and least likely to achieve remission, respectively. CONCLUSIONS: Achievement of remission increased with longer disease duration, but many patients remain in active disease, even in contemporary cohorts. Multiple sets of outcome criteria limited comparability between studies.
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spelling pubmed-56879362017-12-01 How common is remission in juvenile idiopathic arthritis: A systematic review Shoop-Worrall, Stephanie J.W. Kearsley-Fleet, Lianne Thomson, Wendy Verstappen, Suzanne M.M. Hyrich, Kimme L. Semin Arthritis Rheum Article OBJECTIVES: The ideal goal of treatment for juvenile idiopathic arthritis (JIA) is disease remission. However, many sets of remission criteria have been developed and no systematic review of remission in JIA exists. The current systematic review investigated (1) how remission has been defined across JIA clinical cohorts and (2) the frequency of remission overall and within disease categories. METHODS: Studies using prospective inception cohorts published after 1972 were selected if they estimated remission in cohorts of ≥50 patients. Articles focusing on specific medical interventions, not defining remission clearly or not reporting disease duration at remission assessment were excluded. Studies were selected from Medline, Embase, PubMed and bibliographies of selected articles. Risks of selection, missing outcome data and outcome reporting biases were assessed. RESULTS: Within 17 studies reviewed, 88% had majority female participants and patient disease duration ranged from 0.5 to 17 years. Thirteen sets of criteria for clinically inactive disease and remission were identified. Uptake of Wallace’s preliminary criteria was good in studies recruiting or following patients after their publication (78%). Remission frequencies increased with longer disease duration from 7% within 1.5 years to 47% by 10 years following diagnosis. Patients with persistent oligoarticular and rheumatoid-factor positive polyarticular JIA were most and least likely to achieve remission, respectively. CONCLUSIONS: Achievement of remission increased with longer disease duration, but many patients remain in active disease, even in contemporary cohorts. Multiple sets of outcome criteria limited comparability between studies. W.B. Saunders 2017-12 /pmc/articles/PMC5687936/ /pubmed/28625712 http://dx.doi.org/10.1016/j.semarthrit.2017.05.007 Text en © 2017 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Shoop-Worrall, Stephanie J.W.
Kearsley-Fleet, Lianne
Thomson, Wendy
Verstappen, Suzanne M.M.
Hyrich, Kimme L.
How common is remission in juvenile idiopathic arthritis: A systematic review
title How common is remission in juvenile idiopathic arthritis: A systematic review
title_full How common is remission in juvenile idiopathic arthritis: A systematic review
title_fullStr How common is remission in juvenile idiopathic arthritis: A systematic review
title_full_unstemmed How common is remission in juvenile idiopathic arthritis: A systematic review
title_short How common is remission in juvenile idiopathic arthritis: A systematic review
title_sort how common is remission in juvenile idiopathic arthritis: a systematic review
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5687936/
https://www.ncbi.nlm.nih.gov/pubmed/28625712
http://dx.doi.org/10.1016/j.semarthrit.2017.05.007
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