PLoS ONE (Apr 2011)

The potential influence of common viral infections diagnosed during hospitalization among critically ill patients in the United States.

  • Makesha Miggins,
  • Anjum Hasan,
  • Samuel Hohmann,
  • Frederick Southwick,
  • George Casella,
  • Denise Schain,
  • Huazhi Liu,
  • Azra Bihorac,
  • Lyle Moldawer,
  • Philip Efron,
  • Darwin Ang

DOI
https://doi.org/10.1371/journal.pone.0018890
Journal volume & issue
Vol. 6, no. 4
p. e18890

Abstract

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Viruses are the most common source of infection among immunocompetent individuals, yet they are not considered a clinically meaningful risk factor among the critically ill. This work examines the association of viral infections diagnosed during the hospital stay or not documented as present on admission to the outcomes of ICU patients with no evidence of immunosuppression on admission. This is a population-based retrospective cohort study of University HealthSystem Consortium (UHC) academic centers in the U.S. from the years 2006 to 2009. The UHC is an alliance of over 90% of the non-profit academic medical centers in the U.S. A total of 209,695 critically ill patients were used in this analysis. Eight hospital complications were examined. Patients were grouped into four cohorts: absence of infection, bacterial infection only, viral infection only, and bacterial and viral infection during same hospital admission. Viral infections diagnosed during hospitalization significantly increased the risk of all complications. There was also a seasonal pattern for viral infections. Specific viruses associated with poor outcomes included influenza, RSV, CMV, and HSV. Patients who had both viral and bacterial infections during the same hospitalization had the greatest risk of mortality RR 6.58, 95% CI (5.47, 7.91); multi-organ failure RR 8.25, 95% CI (7.50, 9.07); and septic shock RR 271.2, 95% CI (188.0, 391.3). Viral infections may play a significant yet unrecognized role in the outcomes of ICU patients. They may serve as biological markers or play an active role in the development of certain adverse complications by interacting with coincident bacterial infection.