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

被引:55
作者
Shoop-Worrall, Stephanie J. W. [1 ,2 ,3 ]
Kearsley-Fleet, Lianne [1 ]
Thomson, Wendy [2 ,3 ,4 ]
Verstappen, Suzanne M. M. [1 ,2 ,3 ]
Hyrich, Kimme L. [1 ,2 ,3 ]
机构
[1] Univ Manchester, Inst Inflammat & Repair, Div Musculoskeletal & Dermatol Sci,Fac Biol Med &, Arthrit Res UK Ctr Epidemiol,Ctr Musculoskeletal, Manchester, Lancs, England
[2] Cent Manchester Univ Hosp NHS Fdn Trust, NIHR Manchester Musculoskeletal Biomed Res Unit, Manchester, Lancs, England
[3] Univ Manchester Partnership, Manchester, Lancs, England
[4] Univ Manchester, Inst Inflammat & Repair, Div Musculoskeletal & Dermatol Sci,Fac Biol Med &, Arthrit Res UK Ctr Genet & Genom,Ctr Musculoskele, Manchester, Lancs, England
基金
英国医学研究理事会;
关键词
Juvenile idiopathic arthritis; Remission; Clinically inactive disease; Paediatric rheumatology; Systematic review; DISEASE-ACTIVITY; RHEUMATOID-ARTHRITIS; SELECT CATEGORIES; CLINICAL REMISSION; DEFINING CRITERIA; INACTIVE DISEASE; COHORT; PREDICTORS; SPONDYLOARTHROPATHY; CLASSIFICATION;
D O I
10.1016/j.semarthrit.2017.05.007
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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 poly articular 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. (C) 2017 The Authors. Published by Elsevier HS Journals, Inc.
引用
收藏
页码:331 / 337
页数:7
相关论文
共 44 条
  • [1] Outcome following onset of juvenile idiopathic inflammatory arthritis: I. Frequency of different outcomes
    Adib, N
    Silman, A
    Thomson, W
    [J]. RHEUMATOLOGY, 2005, 44 (08) : 995 - 1001
  • [2] [Anonymous], RHEUMATOLOGY
  • [3] [Anonymous], STAND CAR CHILDR YOU
  • [4] [Anonymous], ARTHRITIS CARE RES H
  • [5] [Anonymous], GUID US ET TREATM IU
  • [6] [Anonymous], COCHR COLL TOOL ASS
  • [7] HLA-B27 Predicts a More Chronic Disease Course in an 8-year Followup Cohort of Patients with Juvenile Idiopathic Arthritis
    Bemtson, Lillemor
    Nordal, Ellen
    Aalto, Kristiina
    Peltoniemi, Suvi
    Herlin, Troels
    Zak, Marek
    Nielsen, Susan
    Rygg, Marite
    [J]. JOURNAL OF RHEUMATOLOGY, 2013, 40 (05) : 725 - 731
  • [8] Berntson L, 2007, J RHEUMATOL, V34, P2106
  • [9] Anti-type II collagen antibodies, anti-CCP, IgA RF and IgM RF are associated with joint damage, assessed eight years after onset of juvenile idiopathic arthritis (JIA)
    Berntson, Lillemor
    Nordal, Ellen
    Fasth, Anders
    Aalto, Kristiina
    Herlin, Troels
    Nielsen, Susan
    Rygg, Marite
    Zak, Marek
    Ronnelid, Johan
    [J]. PEDIATRIC RHEUMATOLOGY, 2014, 12
  • [10] A 5-year prospective population-based study of juvenile chronic arthritis: onset, disease process, and outcome
    Bertilsson, L.
    Andersson-Gare, B.
    Fasth, A.
    Forsblad-d'Elia, H.
    [J]. SCANDINAVIAN JOURNAL OF RHEUMATOLOGY, 2012, 41 (05) : 379 - 382