ACR Meeting Abstracts

ACR Meeting Abstracts

  • Meetings
    • 2026 ACR/ARP PRSYM
    • ACR Convergence 2025
    • ACR Convergence 2024
    • ACR Convergence 2023
    • 2023 ACR/ARP PRSYM
    • ACR Convergence 2022
    • ACR Convergence 2021
    • 2020-2009 Meetings
    • Download Abstracts
  • Keyword Index
  • Advanced Search
  • Your Favorites
    • Favorites
    • Login
    • View and print all favorites
    • Clear all your favorites
  • ACR Meetings

Abstract Number: 085

Outcomes of Oligoarticular Juvenile Idiopathic Arthritis Patients Treated with Intra-articular Glucocorticoids: Can We Predict Successful Treatment?

Andrew Kung1, Kimberly Hays1, Lisabeth Scalzi2, Catherine Bingham3, Ferris Troy Yu Asensi4 and Timothy Hahn1, 1Penn State Childrens Hospital, Hershey, PA, 2Penn State Childrens Hospital, Hummelstown, PA, 3Penn State Childrens Hospital, 4Penn State Childrens Hospital, Jacksonville, FL

Meeting: 2026 Pediatric Rheumatology Symposium

  • Tweet
  • Email a link to a friend (Opens in new window) Email
  • Print (Opens in new window) Print
Session Information

Date: Friday, March 20, 2026

Title: Posters: Clinical and Therapeutic Aspects II

Session Time: 5:00PM-6:00PM

Background/Purpose: Intra-articular glucocorticoids (IAGCs) are a common first-line therapy for patients with oligoarticular juvenile arthritis. Limited data exist on rates and predictors of treatment escalation following initial IAGC use.
Avramovic et al. (2024) reported that 46% of patients treated with IAGC initially required systemic therapy. Younger age, ANA positivity, and HLA-B27 presence were predictive factors for systemic therapy use.
This study aimed to determine the percentage of patients requiring systemic therapy within 6 and 12 months of diagnosis after receiving IAGCs as initial treatment and to identify clinical factors associated with treatment escalation.

Methods: We conducted a single-center retrospective review of patients with JIA initially treated with IAGCs only. Patients with uveitis were excluded. Systemic therapy was defined as the use of either conventional or biologic disease-modifying antirheumatic drug. Statistical analysis included Fisher’s exact and Chi-square tests. 

Results: Ninety-two patients met inclusion criteria (Table 1).
Overall, 33% required systemic therapy within 6 months and 46% required systemic therapy within 12 months. 
Age ≤ 6 years at diagnosis was not significantly associated with risk of systemic therapy at either timepoint.
Patients presenting with 3–5 joints were significantly more likely to require systemic therapy at 6 months and 12 months than those presenting with 1–2 joints.
Use of triamcinolone acetonide for the initial procedure was associated with higher rates of systemic therapy initiation at both timepoints compared with triamcinolone hexacetonide.
ANA positivity did not predict systemic therapy at 6 months but became significant at 12 months (Table 2).
Among patients with early-onset arthritis and 1-2 joints treated with triamcinolone hexacetonide, ANA status did not significantly influence the need for systemic therapy at either timepoint (Table 3). 

Conclusion: In this cohort, 33% and 46% of patients required systemic therapy within 6 months and 12 months from diagnosis, respectively.
Two factors emerged as predictors of treatment escalation: involvement of 3-5 joints at diagnosis and use of triamcinolone acetonide rather than triamcinolone hexacetonide. This suggests that a presentation at the higher end of the oligoarticular range could indicate either a more aggressive phenotype with reduced likelihood of remission from local therapy alone or increased likelihood of IAGC refractory joints.
While ANA positivity was not associated with systemic therapy at 6 months, it became a statistically significant predictor for requirement of systemic therapy by 12 months. Among patients with 1-2 joints, ANA status showed a trend toward higher risk at both timepoints, though not statistically significant. The results of this study may help guide decision-making for clinicians managing new onset oligoarticular JIA. IAGCs are likely to be more successful in patients with 1-2 joints involved, negative ANA status, and when triamcinolone hexacetonide is available. 

Table 1. Patient DemographicsSupporting image 1

Table 2. Results Supporting image 2

Table 3. Early Onset Arthritis AnalysisSupporting image 3


Disclosures: A. Kung: None; K. Hays: None; L. Scalzi: None; C. Bingham: None; F. Yu Asensi: None; T. Hahn: None.

To cite this abstract in AMA style:

Kung A, Hays K, Scalzi L, Bingham C, Yu Asensi F, Hahn T. Outcomes of Oligoarticular Juvenile Idiopathic Arthritis Patients Treated with Intra-articular Glucocorticoids: Can We Predict Successful Treatment? [abstract]. Arthritis Rheumatol. 2026; 78 (suppl 3). https://acrabstracts.org/abstract/outcomes-of-oligoarticular-juvenile-idiopathic-arthritis-patients-treated-with-intra-articular-glucocorticoids-can-we-predict-successful-treatment/. Accessed .
  • Tweet
  • Email a link to a friend (Opens in new window) Email
  • Print (Opens in new window) Print

« Back to 2026 Pediatric Rheumatology Symposium

ACR Meeting Abstracts - https://acrabstracts.org/abstract/outcomes-of-oligoarticular-juvenile-idiopathic-arthritis-patients-treated-with-intra-articular-glucocorticoids-can-we-predict-successful-treatment/

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 »

Embargo Policy

All abstracts accepted to PRYSM are under media embargo once the ACR has notified presenters of their abstract’s acceptance. They may be presented at other meetings or published as manuscripts after this time but should not be discussed in non-scholarly venues or outlets. The following embargo policies are strictly enforced by the ACR.

Accepted abstracts are made available to the public online in advance of the meeting and are published in a special online supplement of our scientific journal, Arthritis & Rheumatology. Information contained in those abstracts may not be released until the abstracts appear online. In an exception to the media embargo, academic institutions, private organizations, and companies with products whose value may be influenced by information contained in an abstract may issue a press release to coincide with the availability of an ACR abstract on the ACR website. However, the ACR continues to require that information that goes beyond that contained in the abstract (e.g., discussion of the abstract done as part of editorial news coverage) is under media embargo until 6:00 PM CT on March 18. Journalists with access to embargoed information cannot release articles or editorial news coverage before this time. Editorial news coverage is considered original articles/videos developed by employed journalists to report facts, commentary, and subject matter expert quotes in a narrative form using a variety of sources (e.g., research, announcements, press releases, events, etc.).

Violation of this policy may result in the abstract being withdrawn from the meeting and other measures deemed appropriate. Authors are responsible for notifying colleagues, institutions, communications firms, and all other stakeholders related to the development or promotion of the abstract about this policy. If you have questions about the ACR abstract embargo policy, please contact ACR abstracts staff at [email protected].

Wiley

  • Online Journal
  • Privacy Policy
  • Permissions Policies
  • Cookie Preferences

© Copyright 2026 American College of Rheumatology