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

被引:2
|
作者
Castro, Carlos E. Figueroa [1 ]
Palen, Louis [2 ]
Johnson, Carrie [3 ]
Graham, Mary Beth [1 ]
Letzer, David [3 ]
Ledeboer, Nathan [4 ]
Buchan, Blake [4 ]
Block, Timothy [6 ]
Seliger, Heather [2 ]
Singh, Siddhartha [5 ]
Behrens, Elizabeth [6 ]
Huerta, Susan [6 ]
Munoz-Price, L. Silvia [1 ]
机构
[1] Med Coll Wisconsin, Dept Med, Div Infect Dis, Milwaukee, WI 53226 USA
[2] Froedtert Mem Lutheran Hosp, Infect Prevent & Control Dept, Milwaukee, WI USA
[3] Community Hosp Div, Infect Prevent & Control Dept, Milwaukee, WI USA
[4] Med Coll Wisconsin, Dept Pathol, Milwaukee, WI 53226 USA
[5] Med Coll Wisconsin, Dept Med, Div Hosp Med, Milwaukee, WI 53226 USA
[6] Froedtert Hlth Syst, Milwaukee, WI USA
来源
关键词
ENZYME-IMMUNOASSAY; EPIDEMIOLOGY;
D O I
10.1017/ice.2018.241
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
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.
引用
收藏
页码:1484 / 1486
页数:3
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