Update on the epidemiology, risk factors and disease outcomes of Juvenile idiopathic arthritis

被引:46
|
作者
Palman, Jason [1 ]
Shoop-Worrall, Stephanie [2 ]
Hyrich, Kimme [2 ]
McDonagh, Janet E. [2 ]
机构
[1] Royal Manchester Childrens Hosp, Dept Paediat Rheumatol, Oxford Rd, Manchester M13 9WL, Lancs, England
[2] Univ Manchester, ARUK Ctr Epidemiol, Div Musculoskeletal & Dermatol Sci, Stopford Bldg, Manchester M13 9PT, Lancs, England
来源
基金
英国医学研究理事会;
关键词
Juvenile idiopathic arthritis; Outcomes; Adults with JIA; Transitional care; Proxy reporting; Patient-reported outcome measures; QUALITY-OF-LIFE; TERM FOLLOW-UP; RHEUMATOID-ARTHRITIS; SOCIOECONOMIC-STATUS; SEASONAL-VARIATION; HEALTH OUTCOMES; PARVOVIRUS B19; YOUNG-ADULTS; CHILDREN; POPULATION;
D O I
10.1016/j.berh.2018.10.004
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Juvenile idiopathic arthritis (JIA) is the most common inflammatory joint condition of childhood and represents seven JIA subtypes characterised by distinct clinical and laboratory variables. Genetic and environmental factors are known to influence JIA, although many unanswered questions remain. Measurement of health outcomes in JIA is imperative for both clinical practice and research. Patient -reported outcomes present particular challenges in paediatric rheumatology in view of the importance of collecting reports from both the child/ young person and the parent. Another challenge is the need for continuity of outcome measurement across the paediatric adult interface during the process of transition in terms of both measurement tools and the mechanisms in the system to facilitate tracking of the young person into adult care. Finally, the need for adults with JIA to be seen as a distinct group in adult rheumatology practice is important for both service provision and outcome research. Crown Copyright (C) 2018 Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:206 / 222
页数:17
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