Gastroenterology
Volume 134, Issue 4 , Pages 929-936, April 2008

Risk Factors for Opportunistic Infections in Patients With Inflammatory Bowel Disease

  • Murat Toruner

      Affiliations

    • Division of Gastroenterology and Hepatology, Mayo Clinic College of Medicine, Rochester, Minnesota
  • ,
  • Edward V. Loftus Jr

      Affiliations

    • Division of Gastroenterology and Hepatology, Mayo Clinic College of Medicine, Rochester, Minnesota
  • ,
  • W. Scott Harmsen

      Affiliations

    • Division of Biostatistics, Mayo Clinic College of Medicine, Rochester, Minnesota
  • ,
  • Alan R. Zinsmeister

      Affiliations

    • Division of Biostatistics, Mayo Clinic College of Medicine, Rochester, Minnesota
  • ,
  • Robert Orenstein

      Affiliations

    • Division of Infectious Diseases, Mayo Clinic College of Medicine, Rochester, Minnesota
  • ,
  • William J. Sandborn

      Affiliations

    • Division of Gastroenterology and Hepatology, Mayo Clinic College of Medicine, Rochester, Minnesota
  • ,
  • Jean–Frederic Colombel

      Affiliations

    • Department of Hepato-Gastroenterology, Centre Hospitalier Regional Universitaire De Lille, France
  • ,
  • Laurence J. Egan

      Affiliations

    • Division of Gastroenterology and Hepatology, Mayo Clinic College of Medicine, Rochester, Minnesota
    • Department of Pharmacology & Therapeutics, National University of Ireland, Galway, Ireland
    • Corresponding Author InformationAddress requests for reprints to: Laurence J. Egan, MD, Department of Pharmacology and Therapeutics, University College Hospital, Galway, Ireland. fax: (353)91495572.

Received 24 June 2007; accepted 4 January 2008. published online 15 January 2008.

Background & Aims: We sought to identify and quantify the clinical factors that were associated with opportunistic infections in inflammatory bowel disease patients. Methods: We identified 100 consecutive IBD patients with opportunistic infections. For each case, 2 matched IBD patients who did not have a history of opportunistic infection were selected as controls. Conditional logistic regression was used to assess associations between putative risk factors and opportunistic infections, presented as odds ratios (OR) and 95% confidence intervals (CIs). Results: In univariate analysis, use of corticosteroids (OR, 3.4; 95% CI, 1.8–6.2), azathioprine/6-mercaptopurine (OR, 3.1; 95% CI, 1.7–5.5), and infliximab (OR, 4.4; 95% CI, 1.2–17.1) were associated individually with significantly increased odds for opportunistic infection. Multivariate analysis indicated that use of any one of these drugs yielded an OR of 2.9 (95% CI, 1.5–5.3), whereas use of 2 or 3 of these drugs yielded an OR of 14.5 (95% CI, 4.9–43) for opportunistic infection. The relative risk of opportunistic infection was greatest in IBD patients seen at older than 50 years of age (OR, 3.0; 95% CI, 1.2–7.2, relative to those 24 years or younger). No patient died from opportunistic infection. Conclusions: Immunosuppressive medications, especially when used in combination, and older age are associated with increased risk of opportunistic infections. The absolute risk of opportunistic infection in IBD patients remains to be determined, as does any potential benefit of any preventive strategy.

Abbreviations used in this paper: AZA/6-MP, azathioprine/6-mercaptopurine, CI, confidence interval, OR, odds ratio

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PII: S0016-5085(08)00051-6

doi:10.1053/j.gastro.2008.01.012

Refers to article:

  • Continuing Medical Education Exam 2: April 2008

    Gastroenterology April 2008 (Vol. 134, Issue 4, Page 1239)

Gastroenterology
Volume 134, Issue 4 , Pages 929-936, April 2008