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Published in: Pediatric Rheumatology 1/2018

Open Access 01-12-2018 | Research article

Juvenile idiopathic arthritis managed in the new millennium: one year outcomes of an inception cohort of Australian children

Authors: Georgina Tiller, Joanne Buckle, Roger Allen, Jane Munro, Peter Gowdie, Angela Cox, Jonathan Akikusa

Published in: Pediatric Rheumatology | Issue 1/2018

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Abstract

Background

The advent of new treatments for Juvenile Idiopathic Arthritis (JIA) has prompted interest in systematically studying the outcomes of patients treated in the ‘modern era’. Such data provide both benchmarks for assessing local outcomes and important information for use in counselling families of newly diagnosed patients. While data are available for cohorts in Europe and North America, no such data exist for Australian patients.
The aim was to examine the demographics, treatment and outcomes at 12 months of an inception cohort of newly diagnosed patients with JIA at a single tertiary referral paediatric rheumatology centre in Australia.

Methods

Retrospective review of prospectively collected data from patients newly diagnosed with JIA between 2010 and 2014 at the Royal Children’s Hospital in Melbourne.

Results

One hundred thirty four patients were included (62% female). Oligoarthritis was the single largest category of JIA (36%) and rheumatoid factor positive polyarthritis the least common (2%). Undifferentiated JIA accounted for 13% of patients and was the third largest category. Across the cohort 94% received NSAIDs, 53% oral steroids, 62% methotrexate and 15% a biologic DMARD. Intra-articular steroids were used in 62%, most commonly in the oligoarticular subtype (94%). 95% of patients achieved a joint count of zero at a median of 4.1 months, however flares occurred in 42%. At 12 months 65% had no active joint disease, though more than half remained on medication.

Conclusion

Australian children with JIA managed in the modern era have similar characteristics and achieve short term outcomes comparable to cohorts in Europe and North America, with high rates of joint remission in the first 12 months of follow-up but with a significant relapse rate and requirement for ongoing medication.
Literature
1.
go back to reference Ravelli A. Juvenile idiopathic arthritis. Lancet (North American ed.). 2007;369(9563):767.CrossRef Ravelli A. Juvenile idiopathic arthritis. Lancet (North American ed.). 2007;369(9563):767.CrossRef
2.
go back to reference Petty RE. Epidemiology of juvenile rheumatoid arthritis World. Pediatr Child Care. 1987;3:205–10. Petty RE. Epidemiology of juvenile rheumatoid arthritis World. Pediatr Child Care. 1987;3:205–10.
3.
go back to reference Oen K, et al. Early outcomes and improvement of patients with juvenile idiopathic arthritis enrolled in a Canadian multicenter inception cohort. Arthritis care & research. 2010;62(4):527–36.CrossRef Oen K, et al. Early outcomes and improvement of patients with juvenile idiopathic arthritis enrolled in a Canadian multicenter inception cohort. Arthritis care & research. 2010;62(4):527–36.CrossRef
4.
go back to reference Sengler C, et al. The majority of newly diagnosed patients with juvenile idiopathic arthritis reach an inactive disease state within the first year of specialised care: data from a German inception cohort. RMD Open. 2015;1(1):e000074.CrossRef Sengler C, et al. The majority of newly diagnosed patients with juvenile idiopathic arthritis reach an inactive disease state within the first year of specialised care: data from a German inception cohort. RMD Open. 2015;1(1):e000074.CrossRef
5.
go back to reference Guzman J, et al. The outcomes of juvenile idiopathic arthritis in children managed with contemporary treatments: results from the ReACCh-out cohort. Ann Rheum Dis. 2015;74(10):1854–60.CrossRef Guzman J, et al. The outcomes of juvenile idiopathic arthritis in children managed with contemporary treatments: results from the ReACCh-out cohort. Ann Rheum Dis. 2015;74(10):1854–60.CrossRef
6.
go back to reference Nordal E, et al. Ongoing disease activity and changing categories in a long-term nordic cohort study of juvenile idiopathic arthritis. Arthritis & Rheumatism. 2011;63(9):2809–18.CrossRef Nordal E, et al. Ongoing disease activity and changing categories in a long-term nordic cohort study of juvenile idiopathic arthritis. Arthritis & Rheumatism. 2011;63(9):2809–18.CrossRef
7.
go back to reference Bartoli M, et al. The magnitude of early response to methotrexate therapy predicts long-term outcome of patients with juvenile idiopathic arthritis. Ann Rheum Dis. 2008;67(3):370–4.CrossRef Bartoli M, et al. The magnitude of early response to methotrexate therapy predicts long-term outcome of patients with juvenile idiopathic arthritis. Ann Rheum Dis. 2008;67(3):370–4.CrossRef
8.
go back to reference Wallace CA, et al. Trial of early aggressive therapy in polyarticular juvenile idiopathic arthritis. Arthritis & Rheumatism. 2012;64(6):2012–21.CrossRef Wallace CA, et al. Trial of early aggressive therapy in polyarticular juvenile idiopathic arthritis. Arthritis & Rheumatism. 2012;64(6):2012–21.CrossRef
10.
go back to reference Manners P, Bower C. Worldwide prevalence of juvenile arthritis—why does it vary so much? J Rheumatol. 2002;29(7):1520–30.PubMed Manners P, Bower C. Worldwide prevalence of juvenile arthritis—why does it vary so much? J Rheumatol. 2002;29(7):1520–30.PubMed
11.
go back to reference Bowyer SL, et al. Health status of patients with juvenile rheumatoid arthritis at 1 and 5 years after diagnosis. J Rheumatol. 2003;30(2):394–400.PubMed Bowyer SL, et al. Health status of patients with juvenile rheumatoid arthritis at 1 and 5 years after diagnosis. J Rheumatol. 2003;30(2):394–400.PubMed
12.
go back to reference Behrens EM, et al. Evaluation of the presentation of systemic onset juvenile rheumatoid arthritis: data from the Pennsylvania systemic onset juvenile arthritis registry (PASOJAR). J Rheumatol. 2008;35(2):343–8.PubMed Behrens EM, et al. Evaluation of the presentation of systemic onset juvenile rheumatoid arthritis: data from the Pennsylvania systemic onset juvenile arthritis registry (PASOJAR). J Rheumatol. 2008;35(2):343–8.PubMed
13.
go back to reference Ringold S K.Y, Schanberg LE, Natter MD, Xie F, Ilowite N, Jones J, Mieszkalski K, Beukelman T, Patterns of Medication Use in Children with Juvenile Idiopathic Arthritis: Results from the Childhood Arthritis & Rheumatology Research Alliance Registry [abstract]. 2016: Arthritis Rheumatol. Ringold S K.Y, Schanberg LE, Natter MD, Xie F, Ilowite N, Jones J, Mieszkalski K, Beukelman T, Patterns of Medication Use in Children with Juvenile Idiopathic Arthritis: Results from the Childhood Arthritis & Rheumatology Research Alliance Registry [abstract]. 2016: Arthritis Rheumatol.
15.
go back to reference Kimura Y, et al. Pilot study comparing the Childhood Arthritis & Rheumatology Research Alliance (CARRA) systemic juvenile idiopathic arthritis consensus treatment plans. Pediatr Rheumatol. 2017;15(1):23.CrossRef Kimura Y, et al. Pilot study comparing the Childhood Arthritis & Rheumatology Research Alliance (CARRA) systemic juvenile idiopathic arthritis consensus treatment plans. Pediatr Rheumatol. 2017;15(1):23.CrossRef
16.
go back to reference Nigrovic PA, et al. Anakinra as first-line disease-modifying therapy in systemic juvenile idiopathic arthritis: report of forty-six patients from an international multicenter series. Arthritis & rheumatism. 2011;63(2):545–55.CrossRef Nigrovic PA, et al. Anakinra as first-line disease-modifying therapy in systemic juvenile idiopathic arthritis: report of forty-six patients from an international multicenter series. Arthritis & rheumatism. 2011;63(2):545–55.CrossRef
17.
go back to reference Anink J, et al. Two-year outcome of juvenile idiopathic arthritis in current daily practice: what can we tell our patients? Clinical & Experimental Rheumatology. 2012;30(6):972–8. Anink J, et al. Two-year outcome of juvenile idiopathic arthritis in current daily practice: what can we tell our patients? Clinical & Experimental Rheumatology. 2012;30(6):972–8.
18.
go back to reference Tynjala P, et al. Aggressive combination drug therapy in very early polyarticular juvenile idiopathic arthritis (ACUTE-JIA): a multicentre randomised open-label clinical trial. Ann Rheum Dis. 2011;70(9):1605–12.CrossRef Tynjala P, et al. Aggressive combination drug therapy in very early polyarticular juvenile idiopathic arthritis (ACUTE-JIA): a multicentre randomised open-label clinical trial. Ann Rheum Dis. 2011;70(9):1605–12.CrossRef
19.
go back to reference Boers M. Understanding the window of opportunity concept in early rheumatoid arthritis. Arthritis & Rheumatology. 2003;48(7):1771–4.CrossRef Boers M. Understanding the window of opportunity concept in early rheumatoid arthritis. Arthritis & Rheumatology. 2003;48(7):1771–4.CrossRef
20.
go back to reference Wallace CA, Ruperto N, Giannini E. Preliminary criteria for clinical remission for select categories of juvenile idiopathic arthritis. J Rheumatol. 2004;31(11):2290–4.PubMed Wallace CA, Ruperto N, Giannini E. Preliminary criteria for clinical remission for select categories of juvenile idiopathic arthritis. J Rheumatol. 2004;31(11):2290–4.PubMed
21.
go back to reference Van Mater HA, et al. Psychometric characteristics of outcome measures in juvenile idiopathic arthritis: a systematic review. Arthritis care & research. 2012;64(4):554–62.CrossRef Van Mater HA, et al. Psychometric characteristics of outcome measures in juvenile idiopathic arthritis: a systematic review. Arthritis care & research. 2012;64(4):554–62.CrossRef
22.
go back to reference Consolaro A, et al. Development and validation of a composite disease activity score for juvenile idiopathic arthritis. Arthritis & Rheumatism. 2009;61(5):658–66.CrossRef Consolaro A, et al. Development and validation of a composite disease activity score for juvenile idiopathic arthritis. Arthritis & Rheumatism. 2009;61(5):658–66.CrossRef
Metadata
Title
Juvenile idiopathic arthritis managed in the new millennium: one year outcomes of an inception cohort of Australian children
Authors
Georgina Tiller
Joanne Buckle
Roger Allen
Jane Munro
Peter Gowdie
Angela Cox
Jonathan Akikusa
Publication date
01-12-2018
Publisher
BioMed Central
Published in
Pediatric Rheumatology / Issue 1/2018
Electronic ISSN: 1546-0096
DOI
https://doi.org/10.1186/s12969-018-0288-z

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