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      Patterns of pain over time among children with juvenile idiopathic arthritis

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          Abstract

          Objectives

          Pain is a very common symptom of juvenile idiopathic arthritis (JIA). Disease activity alone cannot explain symptoms of pain in all children, suggesting other factors may be relevant. The objectives of this study were to describe the different patterns of pain experienced over time in children with JIA and to identify predictors of which children are likely to experience ongoing pain.

          Methods

          This study used longitudinal-data from patients (aged 1–16 years) with new-onset JIA. Baseline and up to 5-year follow-up pain data from the Childhood Arthritis Prospective Study (CAPS) were used. A two-step approach was adopted. First, pain trajectories were modelled using a discrete mixture model. Second, multinomial logistic regression was used to determine the association between variables and trajectories.

          Results

          Data from 851 individuals were included (4 years, median follow-up). A three-group trajectory model was identified: consistently low pain (n=453), improved pain (n=254) and consistently high pain (n=144). Children with improved pain or consistently high pain differed on average at baseline from consistently low pain. Older age at onset, poor function/disability and longer disease duration at baseline were associated with consistently high pain compared with consistently low pain. Early increases in pain and poor function/disability were also associated with consistently high pain compared with consistently low pain.

          Conclusions

          This study has identified routinely collected clinical factors, which may indicate those individuals with JIA at risk of poor pain outcomes earlier in disease. Identifying those at highest risk of poor pain outcomes at disease onset may enable targeted pain management strategies to be implemented early in disease thus reducing the risk of poor pain outcomes.

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          Most cited references30

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          Prevalence and incidence of juvenile idiopathic arthritis: a systematic review.

          To conduct a systematic literature review on incidence and prevalence of juvenile idiopathic arthritis and to estimate these figures in Europe for 2010. Articles on incidence or prevalence of juvenile idiopathic arthritis were searched in Medline. Pooled incidence and prevalence were calculated overall, by gender, age, classification and arthritis categories. We used the available age and gender pooled rates to standardize the incidence and prevalence on the 2010 European population and estimate the number of cases in Europe in 2010. Forty-three articles (33 on incidence, 29 on prevalence) were included. Incidence rates varied from 1.6 to 23 and prevalence from 3.8 to 400/100,000. Pooled incidence and prevalence were higher for girls (10.0 [9.4-10.7] and 19.4 [18.3-20.6]/100,000) than boys (5.7 [5.3-6.2] and 11.0 [10.2-11.9]/100,000). Oligoarthritis was the most frequent form (pooled incidence rate 3.7 [3.5-3.9] and prevalence 16.8 [15.9-17.7]/100,000). The direct standardized incidence rate was 8.2 [7.5-9.0] and prevalence 70.2 [62.9-78.1]/100,000. In Europe in 2010, the estimated number of incident cases was 6896 [5481-8578] and 59,175 [44,256-76,983] prevalent cases. Incidence and prevalence varied greatly among published reports of juvenile idiopathic arthritis, which may be explained by methodological issues, classification used, and time. Estimating the number of affected children can be useful, especially with the new treatment possibilities. Copyright © 2013 Société française de rhumatologie. Published by Elsevier SAS. All rights reserved.
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            DEVELOPMENTAL TRAJECTORY GROUPS: FACT OR A USEFUL STATISTICAL FICTION?*

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              Daily pain and symptoms in children with polyarticular arthritis.

              To analyze patterns of daily pain, stiffness, and fatigue related to juvenile arthritis; to examine the relationships of demographics, disease severity, and psychological adjustment to daily disease symptoms; and to examine daily disease symptoms as predictors of reduced participation in school and social activity. For a 2-month period, 41 children with polyarticular juvenile arthritis completed daily diaries that included measures of symptoms and function. Children also underwent an initial evaluation and 4 followup evaluations that included a joint count, laboratory testing, and completion of questionnaires assessing physical and psychosocial functioning. Children reported having pain an average of 73% of days, with the majority of children (76%) reporting pain on >60% of all days. On average, children described the intensity of their daily pain as being in the mild to moderate range; however, a significant subgroup (31%) reported pain in the severe range. Higher physician global assessment ratings, increased functional disability, and increased anxiety were significantly associated with increased daily pain and other daily symptoms. Multilevel random-effects analyses indicated that increased daily symptoms of pain, stiffness, and fatigue were significant predictors of reduced participation in school and social activities. Physicians should consider treating pain more aggressively in children with arthritis, in order to preserve function in school and social domains, as well as physical function. Moreover, optimal pain management in children with arthritis should include therapeutic regimens addressing anxiety as well as standard pharmacologic interventions.
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                Author and article information

                Journal
                Arch Dis Child
                Arch. Dis. Child
                archdischild
                adc
                Archives of Disease in Childhood
                BMJ Publishing Group (BMA House, Tavistock Square, London, WC1H 9JR )
                0003-9888
                1468-2044
                May 2018
                25 November 2017
                : 103
                : 5
                : 437-443
                Affiliations
                [1 ] departmentArthritis Research UK Centre for Epidemiology , The University of Manchester , Manchester, UK
                [2 ] departmentNIHR Manchester Musculoskeletal Biomedical Research Unit, Manchester Academic Health Science Centre , Central Manchester University Hospitals NHS Foundation Trust , Manchester, UK
                [3 ] departmentMusculoskeletal Research Group , Institute Cellular Medicine, Newcastle University , Newcastle, UK
                [4 ] departmentPaediatric Rheumatology , Great North Children’s Hospital , Newcastle, UK
                [5 ] departmentPaediatric Rheumatology , Alder Hey Children’s NHS Foundation Trust , Liverpool, UK
                [6 ] departmentPaediatric Rheumatology , Royal Manchester Children’s Hospital , Manchester, UK
                [7 ] departmentPaediatric Rheumatology , Royal Hospital for Children , Glasgow, UK
                [8 ] departmentPaediatric Rheumatology , Royal Hospital for Sick Children , Edinburgh, UK
                [9 ] University College London (UCL) GOS Institute of Child Health, Great Ormond Street Hospital For Children NHS Trust , London, UK
                [10 ] departmentARUK Centre for Adolescent Rheumatology , University College London , London, UK
                [11 ] departmentThe NIHR Biomedical Research Centre , Great Ormond Street Hospital for Children NHS Trust , London, UK
                [12 ] departmentArthritis Research UK Center for Genetics and Genomics , The University of Manchester , London, UK
                Author notes
                [Correspondence to ] Professor Wendy Thomson, Arthritis Research UK Centre for Genetics and Genomics, Centre for Musculoskeletal Research, Faculty of Biology, Medicine and Health, The University of Manchester, Manchester Academic Health Science Centre, Manchester M13 9PT, UK; wendy.thomson@ 123456manchester.ac.uk
                Author information
                http://orcid.org/0000-0001-8242-9262
                Article
                archdischild-2017-313337
                10.1136/archdischild-2017-313337
                5916104
                29175824
                e0733887-7ae3-4e12-8883-177be8191033
                © Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2018. All rights reserved. No commercial use is permitted unless otherwise expressly granted.

                This is an Open Access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 4.0) license, which permits others to distribute, remix, adapt and build upon this work, for commercial use, provided the original work is properly cited. See: http://creativecommons.org/licenses/by/4.0/

                History
                : 05 May 2017
                : 25 September 2017
                : 25 October 2017
                Funding
                Funded by: NIHR Clinical Research Network Portfolio;
                Funded by: NIHR Biomedical Research Centre Funding Scheme;
                Funded by: FundRef http://dx.doi.org/10.13039/501100000341, Arthritis Research UK;
                Funded by: NIHR Manchester Musculoskeletal Biomedical Research Unit;
                Categories
                Original Article
                1506
                655
                Custom metadata
                unlocked

                Medicine
                pain,adolescent health,epidemiology,musculo-skeletal,rheumatology
                Medicine
                pain, adolescent health, epidemiology, musculo-skeletal, rheumatology

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