ACR Meeting Abstracts

ACR Meeting Abstracts

  • Home
  • Meetings Archive
    • ACR Convergence 2021
    • ACR Convergence 2020
    • 2020 ACR/ARP PRSYM
    • 2019 ACR/ARP Annual Meeting
    • 2018 ACR/ARHP Annual Meeting
    • 2017 ACR/ARHP Annual Meeting
    • 2017 ACR/ARHP PRSYM
    • 2016-2009 Meetings
    • Download Abstracts
  • Keyword Index
  • Advanced Search
  • Your Favorites
    • Favorites
    • Login
    • View and print all favorites
    • Clear all your favorites
  • Meeting Resource Center

Abstract Number: 54

Treatment and 1-year outcomes of an inception cohort of Australian children with JIA

Georgina Tiller1, Jo Buckle2, Jane Munro3, Angela Cox2, Peter Gowdie2, Roger Allen4 and Jonathan Akikusa5,6, 1Rheumatology, Royal Childrens Hospital, Parkville, Australia, 2Rheumatology, Royal Children's Hospital, Melbourne, Australia, 3Rheumatology, Royal Children's Hospital, Parkville, Australia, 4Paediatric Consulting Centre, Royal Childrens Hospital, Melbourne, VIC, Australia, 5Arthritis and Rheumatology Research, Murdoch Childrens Research Institute, Parkville, Australia, 63 West Clinical Offices, Royal, Royal Children's Hospital, Melbourne, Australia

Meeting: 2017 Pediatric Rheumatology Symposium

Keywords: Juvenile Arthritis

  • Tweet
  • Email
  • Print
Session Information

Date: Thursday, May 18, 2017

Session Title: Clinical and Therapeutic Poster Session

Session Type: Abstract Submissions

Session Time: 5:30PM-7:00PM

Background/Purpose:  Recent studies have provided insight into the short and intermediate term outcomes of cohorts of children with JIA managed with contemporary treatments in North America and Europe. There are no such data for Australasia.

The objective is to describe the treatment and 1-year clinical outcomes of an inception cohort of newly diagnosed Australian children with juvenile idiopathic arthritis (JIA) followed at a tertiary paediatric centre.

Methods:  Retrospective review of prospectively collected clinical data from a specifically designed electronic rheumatology database on all patients newly diagnosed with JIA at the Royal Children’s Hospital, Melbourne, between October 2010 and October 2014.

Results:

134 patients were included. Sixty two percent were female. The mean age at diagnosis was 8.3 years. The distribution of patients by subtype was:Oligoarticular 36%; RF + Polyarticular 2%; RF – Polyarticular 25%; Systemic 7%; Enthesitis Related 10%; Psoriatic 7% and Undifferentiated 13%. Ninety five percent of patients achieved a zero joint count at least once in the first year of follow-up, however, just 66% had a zero joint count at 1 year. The median time to a zero joint count was 4.1 months in patients achieving this outcome in the first year of follow-up. The systemic subtype had the shortest time to zero joint count at 1.7 months, psoriatic the longest at 7.6 months. For the 11% of patients who did not achieve a zero joint count in the first year of follow-up, the median time to this outcomewas 18.5 months.

Sixty two percent of patients were commenced on a conventional DMARD (cDMARD), most commonly methotrexate. The median time to commencement of a cDMARD was 0.9 months. 15% were commenced on a biologic DMARD (bDMARD). The median time to commencement of a bDMARD was 4.9 months. 55% were treated with oral corticosteroids. 17% were on oral corticosteroids at 1 year. 62% were treated with intra-articular steroids, most commonly the oligoarticular subtype, of whom 94% had at least one joint injection. 7% of children developed uveitis, with the highest incidence in the oligoarticular subtype, 17%.

Of patients with inactive arthritis at 12 months, 61% were on and 39% were off treatment.

Conclusion:  This study demonstrates that children with JIA in Australia have demographic features and short term outcomes similar to those described in international cohorts. At twelve months, two thirds of the cohort had a zero joint count and over a third of these were on no medications. When compared to international cohorts there was some variation in management, with a higher proportion having intra-articular steroid therapy.


Disclosure: G. Tiller, None; J. Buckle, None; J. Munro, None; A. Cox, None; P. Gowdie, None; R. Allen, None; J. Akikusa, None.

To cite this abstract in AMA style:

Tiller G, Buckle J, Munro J, Cox A, Gowdie P, Allen R, Akikusa J. Treatment and 1-year outcomes of an inception cohort of Australian children with JIA [abstract]. Arthritis Rheumatol. 2017; 69 (suppl 4). https://acrabstracts.org/abstract/treatment-and-1-year-outcomes-of-an-inception-cohort-of-australian-children-with-jia/. Accessed May 17, 2022.
  • Tweet
  • Email
  • Print

« Back to 2017 Pediatric Rheumatology Symposium

ACR Meeting Abstracts - https://acrabstracts.org/abstract/treatment-and-1-year-outcomes-of-an-inception-cohort-of-australian-children-with-jia/

Advanced Search

Your Favorites

You can save and print a list of your favorite abstracts during your browser session by clicking the “Favorite” button at the bottom of any abstract. View your favorites »

ACR Pediatric Rheumatology Symposium 2020

© COPYRIGHT 2022 AMERICAN COLLEGE OF RHEUMATOLOGY

Wiley

  • Home
  • Meetings Archive
  • Advanced Search
  • Meeting Resource Center
  • Online Journal
  • Privacy Policy
  • Permissions Policies
loading Cancel
Post was not sent - check your email addresses!
Email check failed, please try again
Sorry, your blog cannot share posts by email.