Outcomes in patients with inflammatory bowel disease and acute gastrointestinal symptoms who test indeterminate for Clostridioides difficile

Inflammatory bowel disease (IBD) and infection (CDI) can present with similar symptoms. The current preferred method for diagnosing CDI is the nucleic acid amplification test (NAAT) for in stool, followed by reflex toxin enzyme immunoassay (EIA) when NAAT is positive. The clinical significance of NA...

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Veröffentlicht in:Annals of gastroenterology 2022-03, Vol.35 (2), p.135-139
Hauptverfasser: Johnson, Lauren K, Munoz-Price, Silvia, Patel, Poonam Beniwal, Patel, Amir, Stein, Daniel J, Yarur, Andres J
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Sprache:eng
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Zusammenfassung:Inflammatory bowel disease (IBD) and infection (CDI) can present with similar symptoms. The current preferred method for diagnosing CDI is the nucleic acid amplification test (NAAT) for in stool, followed by reflex toxin enzyme immunoassay (EIA) when NAAT is positive. The clinical significance of NAAT(+)/EIA(-) in the IBD population is uncertain. This retrospective cohort included IBD patients who presented with acute onset of gastrointestinal symptoms and a NAAT(+) test. The primary outcome was recurrence within 12 months. Other outcomes examined included hospital admissions within 30 days of CDI, change of IBD maintenance therapy within 90 days of CDI, and complications such as bowel resection or death. A total of 71 patients were included. Eighty-four percent of the tests were EIA(-) and among the EIA(-) 88% were treated with antibiotics. Outcomes between EIA(+) and EIA(-) were not significantly different in terms of recurrences, admissions, changes to IBD medications or complications. Outcomes were also similar when comparing those who received antibiotic therapy to those who did not. Our cohort did not demonstrate a significant difference in outcomes between EIA(+) and EIA(-) patients. Treatment for EIA(-) patients did not improve outcomes. Even though there may be a role for antibiotic therapy in IBD patients who test NAAT(+)/EIA(-) for , further studies will be needed to identify that subpopulation.
ISSN:1108-7471
1792-7463
1792-7463
DOI:10.20524/aog.2022.0690