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Multicentre Evaluation of a Commercial Test for the Rapid Diagnosis of Clostridium difficile-Mediated Antibiotic-Associated Diarrhoea

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European Journal of Clinical Microbiology and Infectious Diseases Aims and scope Submit manuscript

Abstract

 An immunoassay for the detection of Clostridium difficile toxin A in stool samples (Clearview C. DIFF A; Unipath, UK) was evaluated against the cell cytotoxicity assay using 407 stool samples from patients suspected to have, or considered at risk of, antibiotic-associated diarrhoea. Of the samples tested, 98 were positive and 280 were negative by both tests (sensitivity 83.1%, specificity 96.9%). Following resolution of the 29 discrepant results, the sensitivity and specificity of the immunoassay were 91% and 98%, respectively, and the sensitivity for the cell cytotoxicity assay was calculated as 91.5%, with a specificity of 99%. The Clearview C. DIFF A test proved to be a rapid simple assay for the detection of Clostridium difficile toxin A in stool samples. The test was equally suited to single or batch testing, required minimal sample handling, and provided results within 30 min of applying the sample to the test unit.

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Bentley, A., Patel, N., Sidorczuk, M. et al. Multicentre Evaluation of a Commercial Test for the Rapid Diagnosis of Clostridium difficile-Mediated Antibiotic-Associated Diarrhoea. EJCMID 17, 788–790 (1998). https://doi.org/10.1007/s100960050187

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  • DOI: https://doi.org/10.1007/s100960050187

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