ACR Meeting Abstracts

ACR Meeting Abstracts

  • Meetings
    • ACR Convergence 2024
    • ACR Convergence 2023
    • 2023 ACR/ARP PRSYM
    • ACR Convergence 2022
    • ACR Convergence 2021
    • ACR Convergence 2020
    • 2020 ACR/ARP PRSYM
    • 2019 ACR/ARP Annual Meeting
    • 2018-2009 Meetings
    • Download Abstracts
  • Keyword Index
  • Advanced Search
  • Your Favorites
    • Favorites
    • Login
    • View and print all favorites
    • Clear all your favorites
  • ACR Meetings

Abstract Number: 2761

High-Dose Prednisone Use up to 42 Days Prior to Temporal Artery Biopsy (TAB) Did Not Reduce Yield of Positive Biopsy in the Veterans Health Administration (VHA) Database Cohort

Sarah H. Chung1, Meredith B. Morcos1 and Bernard Ng1,2, 1Division of Rheumatology, University of Washington, Seattle, WA, 2Rheumatology, VA Puget Sound Healthcare System, Seattle, WA

Meeting: 2018 ACR/ARHP Annual Meeting

Keywords: biopsies, giant cell arteritis, prednisolone, prednisone and temporal arteritis

  • Tweet
  • Email
  • Print
Session Information

Date: Tuesday, October 23, 2018

Title: Vasculitis Poster III: Immunosuppressive Therapy in Giant Cell Arteritis and Polymyalgia Rheumatica

Session Type: ACR Poster Session C

Session Time: 9:00AM-11:00AM

Background/Purpose: Temporal artery biopsy (TAB) currently remains the gold-standard confirmatory test for the diagnosis of giant cell arteritis (GCA); positive TAB justifies long-term steroid use and/or immunosuppression. High-dose glucocorticoids are often briskly initiated when GCA is clinically suspected, even before TAB is obtained, to avoid ischemic complications. Historically, this has raised concern over the effect of glucocorticoids on TAB yield. This study aimed to determine if the duration of prednisone use, dosed at 30 mg or more daily, prior to TAB influenced TAB result in subjects with suspected GCA.

Methods: Subjects with a procedure code for TAB between 1999-2017 were queried through the VHA national database. TAB result (positive or negative, presence of granuloma/giant cells) was reviewed manually; indeterminate results (i.e. inconclusive, healed arteritis) were categorized as negative. Prescription data regarding prednisone dosage and dispense date were also extracted for each subject. Days of prednisone use (≥30 mg daily) before TAB were categorized as follows: 0-14, >14-28, >28-42, >42, and prednisone started after TAB. Abnormal ESR and CRP values within 180 days before TAB to 14 days after TAB, as well as age, gender, TAB laterality, and TAB length were also extracted. Logistic regression models were run using Stata.

Results: 3,057 biopsies were reviewed, 306 (10%) of which were deemed positive per pathology report. Prednisone use ≥30 mg daily was identified among 2,012 subjects. Of these, 1,474 (73.3%) initiated prednisone within 14 days prior to TAB. The duration of prednisone use before TAB, as a continuous variable, was not influenced by age, TAB length, TAB laterality, or abnormal ESR or CRP values by linear regression. Male gender had a significant negative correlation with prednisone initiation prior to TAB (coefficient -2.97, CI -5.6 to -0.4, p<0.05). After adjustment for gender, there was no association between positive TAB and time of prednisone initiation up to 42 days prior to TAB. Furthermore, prednisone administration up to 42 days prior to TAB did not influence the presence of granulomatous inflammation. Interestingly, positive TAB was significantly associated with prednisone dosed after TAB date, suggesting that a positive TAB prompted the provider to initiate treatment. Additionally, there was no significant correlation between a positive TAB and abnormal ESR or CRP values within 180 days pre- and 14 days post-TAB after correcting for pre-TAB prednisone exposure.

Conclusion: This is the largest retrospective study to date showing that prednisone ≥30 mg daily initiated up to 42 days prior to a TAB did not influence biopsy yield. This study also demonstrated that abnormal ESR or CRP values prior to TAB were not associated with positive TAB even after corrections for pre-TAB prednisone usage, suggesting that these inflammatory markers may not be independently helpful in the diagnosis of GCA.


Disclosure: S. H. Chung, None; M. B. Morcos, None; B. Ng, None.

To cite this abstract in AMA style:

Chung SH, Morcos MB, Ng B. High-Dose Prednisone Use up to 42 Days Prior to Temporal Artery Biopsy (TAB) Did Not Reduce Yield of Positive Biopsy in the Veterans Health Administration (VHA) Database Cohort [abstract]. Arthritis Rheumatol. 2018; 70 (suppl 9). https://acrabstracts.org/abstract/high-dose-prednisone-use-up-to-42-days-prior-to-temporal-artery-biopsy-tab-did-not-reduce-yield-of-positive-biopsy-in-the-veterans-health-administration-vha-database-cohort/. Accessed .
  • Tweet
  • Email
  • Print

« Back to 2018 ACR/ARHP Annual Meeting

ACR Meeting Abstracts - https://acrabstracts.org/abstract/high-dose-prednisone-use-up-to-42-days-prior-to-temporal-artery-biopsy-tab-did-not-reduce-yield-of-positive-biopsy-in-the-veterans-health-administration-vha-database-cohort/

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 »

All abstracts accepted to ACR Convergence 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 10:00 AM ET on November 14, 2024. 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 2025 American College of Rheumatology