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Immediate impact of healthcare-facility–onset Clostridium difficile laboratory-identified events reporting methodology change on standardized infection ratios

  • Carlos E. Figueroa Castro (a1), Louis Palen (a2), Carrie Johnson (a3), Mary Beth Graham (a1), David Letzer (a3), Nathan Ledeboer (a4), Blake Buchan (a4), Timothy Block (a5), Heather Seliger (a2), Siddhartha Singh (a6), Elizabeth Behrens (a5), Susan Huerta (a5) and L. Silvia Munoz-Price (a1)...
Abstract

In 2018, the Clostridium difficile LabID event methodology changed so that hospitals doing 2-step tests, nucleic acid amplification test (NAAT) plus enzyme immunofluorescence assay (EIA), had their adjustment modified to EIA-based tests, and only positive final tests (eg, EIA) were counted in the numerator. We report the immediate impact of this methodological change at 3 Milwaukee hospitals.

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Corresponding author
Author for correspondence: L. Silvia Munoz-Price, MD, PhD, 8701 Watertown Plank Road, Milwaukee, WI 53226. E-mail: smunozprice@mcw.edu
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Cite this article: Figueroa Castro CE et al. (2018). Immediate impact of healthcare-facility–onset Clostridium difficile laboratory-identified events reporting methodology change on standardized infection ratios. Infection Control & Hospital Epidemiology 2018, 39, 1484–1486. doi: 10.1017/ice.2018.241

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Infection Control & Hospital Epidemiology
  • ISSN: 0899-823X
  • EISSN: 1559-6834
  • URL: /core/journals/infection-control-and-hospital-epidemiology
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