Published online by Cambridge University Press: 23 October 2018
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.
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