Discordant <i>Clostridioides difficile</i> diagnostic assay and treatment practice: a cross-sectional study in a tertiary care hospital, Geneva, Switzerland.
cross_sectional · Level IV
Where this comes from
- Record sourced from PubMed, PMID 32928850.
- Also identified by DOI 10.1136/bmjopen-2019-036342 and PMC identifier 7488797.
- Licence recorded as CC BY-NC.
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Abstract
To determine the proportion of patients who received a treatment for <i>Clostridioides difficile</i> infection (CDI) among those presenting a discordant <i>C. difficile</i> diagnostic assay and to identify patient characteristics associated with the decision to treat CDI. Cross-sectional study. Monocentric study in a tertiary care hospital, Geneva, Switzerland. Among 4562 adult patients tested for <i>C. difficile</i> between March 2017 and March 2019, 208 patients with discordant tests' results (positive nucleic acid amplification test (NAAT+)/negative enzyme immunoassay (EIA-)) were included. Treatment for CDI. CDI treatment was administered in 147 (71%) cases. In multivariate analysis, an abdominal CT scan with signs of colitis (OR 14.7; 95% CI 1.96 to 110.8) was the only factor associated with CDI treatment. The proportion of NAAT+/EIA- patients who received treatment questions the contribution of the EIA for the detection of toxin A/B after NAAT to limit overtreatment. Additional studies are needed to investigate if other factors are associated with the decision to treat.
Medical subject headings
- Bacterial Toxins
- Clostridioides difficile
- Clostridium Infections