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Comparison of four laboratory tests for diagnosis ofClostridium difficile-associated diarrhea
Authors:J. Jacobs  B. Rudensky  J. Dresner  A. Berman  M. Sonnenblick  Y. van Dijk  A. M. Yinnon
Affiliation:(1) Department of Geriatrics, Shaare Zedek Medical Center, PO Box 3235, 91031 Jerusalem, Israel;(2) Clinical Microbiological Laboratory, Shaare Zedek Medical Center, PO Box 3235, 91031 Jerusalem, Israel;(3) Department of Medicine, Shaare Zedek Medical Center, PO Box 3235, 91031 Jerusalem, Israel;(4) Infectious Diseases Unit, Shaare Zedek Medical Center, PO Box 3235, 91031 Jerusalem, Israel
Abstract:Four different laboratory tests for diagnosis ofClostridium difficile-associated diarrhea were compared to determine the optimal one for management of patients with hospital-acquired diarrhea. Stool samples from 231 patients with diarrhea were tested by the following methods: culture forClostridium difficile with subsequent determination of exotoxin production, with a toxigenicClostridium difficile positive (TCP) result considered truly positive; enzyme immunoassay (EIA); latex agglutination test; and an immunobinding blot assay. The rates of positive results were as follows: EIA 5.5%, TCP 7.3%, latex agglutination 16.7%, and immunobinding blot assay 26.1%. Compared to the TCP results, the sensitivity and specificity were, respectively, 61 and 98% for EIA, 47 and 85% for latex agglutination, and 60 and 76% for the immunobinding blot assay. Samples from patients with ge 6 stools/day were TCP and EIA positive in 27 and 17% of cases, respectively, whereas in patients with < 6 stools/day, these percentages decreased to 2 and 3%, respectively (p < 0.001). In hospitalized patients with ge 6 stools/day, EIA appears to be the optimal test for diagnosis ofClostridium difficile-associated diarrhea, with a 73% positive predictive value and a 97% negative predictive value. However, in patients with < 6 stools/day, the prevalence ofClostridium difficile is low, and laboratory detection of this organism remains problematic.
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