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: 10

The Utility of Screening for Infectious Diseases in Recipients of Anti-TNF-α Therapy

Kristal Choi1, Lester Mertz2, Russell Heigh3, James Yiannias4 and Janis Blair5, 1Internal Medicine, Mayo Clinic Arizona, Scottsdale, AZ, 2Rheumatology, Mayo Clinic Arizona, Scottsdale, AZ, 3Gastroenterology, Mayo Clinic Arizona, Scottsdale, AZ, 4Dermatology, Mayo Clinic Arizona, Scottsdale, AZ, 5Infectious Diseases, Mayo Clinic Arizona, Scottsdale, AZ

Meeting: 2016 ACR/ARHP Annual Meeting

Date of first publication: September 28, 2016

Keywords: Biologic agents, Hepatitis, infection and tuberculosis

  • Tweet
  • Email
  • Print
Session Information

Date: Sunday, November 13, 2016

Title: Epidemiology and Public Health - Poster I

Session Type: ACR Poster Session A

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

The Utility of Screening for Infectious Diseases in Recipients of Anti-TNF-α Therapy   Choi, Kristal, Mertz, Lester, Heigh, Russell, Yiannias, James, Blair, Janis

Background/Purpose: Tumor necrosis factor-α inhibitors (TNF-I) are commonly used today to treat a wide variety of immune-mediated disorders. These medications are linked with an increased risk of mycobacterial, viral, and fungal infections, and some society guidelines recommend screening for tuberculosis (TB), hepatitis B (HBV) and C (HCV), human immunodeficiency virus (HIV), and active life-threatening fungal infections. The aim of our study was to determine the number of patients with infectious diseases identified on screening; and to describe what evaluation, treatment, and follow-up transpired for these individuals.  

Methods: We electronically searched for all patients receiving TNF-I from 9/4/2010 to 4/22/2015.  The records for patients screening positive for HBV, HCV, TB, and HIV were then reviewed in detail.  

Results: 2218 individuals received TNF-I during the study period. 656 patients had at least one of the following laboratory tests checked: hepatitis B surface antibody (HBsAb), hepatitis B surface antigen (HBsAg), and hepatitis B core antibodies (HBc total Ab). Of these, 37 (5.6%) were positive for HBsAb only, 1 (0.1%) was positive for HBsAg only, 3 (0.5%) were positive for HBc total Ab only, and 5 (0.8%) were positive for both HBsAb and HBc total Ab. One patient had a known history of chronic HBV prior to the initiation of a TNF-I, and one patient was tested due to the development of symptoms only. Thus, there were 7 (1.0%) new diagnoses of HBV diagnosed by screening. All 7 cases were maintained or eventually started on their TNF-I. One case received treatment with lamivudine when started on a TNF-I.             662 patients were tested for HCV via antibody test, and 2 (0.3%) were found to be positive on pre-screening. Follow-up RNA testing was negative in one case and positive in the other. The latter patient was referred to Hepatology, and the initiation of the TNF-I was delayed due to the new diagnosis.                   557 were tested for TB via the QuantiFERON-TB Gold In-Tube assay, and 13 (2.3%) were positive. After excluding patients who had a known history of latent TB and those who were tested due to the development of symptoms only, there were a total of 7 (1.3%) new diagnoses of TB found on screening. Five (71.4%) cases were diagnosed with latent TB, and were appropriately treated. TNF-I was initiated in 4/5 cases after > 1 month of treatment with isoniazid. Two positive assays found on pre-screening were thought to be false positives, and TNF-I was initiated with no TB treatment.             Two patients were screened for HIV with an antigen and antibody combination assay, and both were negative.

Conclusion: Few new cases, and no active cases, of HBV, HCV, TB, and HIV are identified in recipients of TNF-I therapy during routine screening.  

 

HBV

HCV

TB

HIV

Total number screened

656

662

557

2

Total new cases diagnosed on screening (%)

7 (1.0%)

2 (0.3%)

7 (1.3%)

0 (0%)

      Pre-screening

4

2

5

0

      Annual screening

3

0

2

0

TNF-I delayed or held

0

1

4

0

Treatment initiated for infection

1

0

5

0

Sub-specialty referral

6

1

7

0

 


Disclosure: K. Choi, None; L. Mertz, None; R. Heigh, None; J. Yiannias, None; J. Blair, None.

To cite this abstract in AMA style:

Choi K, Mertz L, Heigh R, Yiannias J, Blair J. The Utility of Screening for Infectious Diseases in Recipients of Anti-TNF-α Therapy [abstract]. Arthritis Rheumatol. 2016; 68 (suppl 10). https://acrabstracts.org/abstract/the-utility-of-screening-for-infectious-diseases-in-recipients-of-anti-tnf-%ce%b1-therapy/. Accessed .
  • Tweet
  • Email
  • Print

« Back to 2016 ACR/ARHP Annual Meeting

ACR Meeting Abstracts - https://acrabstracts.org/abstract/the-utility-of-screening-for-infectious-diseases-in-recipients-of-anti-tnf-%ce%b1-therapy/

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