Annals of Clinical Microbiology and Antimicrobials (Apr 2024)

Clinical outcomes and treatment necessity in patients with toxin-negative Clostridioides difficile stool samples

  • Dae Hyeon Cho,
  • Si-Ho Kim,
  • Cheon Hoo Jeon,
  • Hyoung Tae Kim,
  • Kyoung-Jin Park,
  • Junyoung Kim,
  • Jiyeong Kwak,
  • Byung Soo Kwan,
  • Sungmin Kong,
  • Jung Won Lee,
  • Kwang Min Kim,
  • Yu Mi Wi

DOI
https://doi.org/10.1186/s12941-024-00696-1
Journal volume & issue
Vol. 23, no. 1
pp. 1 – 7

Abstract

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Abstract Purpose The clinical significance of negative toxin enzyme immunoassays (EIA) for Clostridioides difficile infections (CDIs) is unclear. Our study aimed to investigate the significance of toxin EIA-negative in the diagnosis and prognosis of CDI. Methods All stool specimens submitted for C. difficile toxin EIA testing were cultured to isolate C. difficile. In-house PCR for tcdA, tcdB, cdtA, and cdtB genes were performed using C. difficile isolates. Stool specimens were tested with C. difficile toxins A and B using EIA kit (RIDASCREEN Clostridium difficile toxin A/B, R-Biopharm AG, Darmstadt, Germany). Characteristics and subsequent CDI episodes of toxin EIA-negative and -positive patients were compared. Results Among 190 C. difficile PCR-positive patients, 83 (43.7%) were toxin EIA-negative. Multivariate analysis revealed independent associations toxin EIA-negative results and shorter hospital stays (OR = 0.98, 95% CI 0.96–0.99, p = 0.013) and less high-risk antibiotic exposure in the preceding month (OR = 0.38, 95% CI 0.16–0.94, p = 0.035). Toxin EIA-negative patients displayed a significantly lower white blood cell count rate (11.0 vs. 35.4%, p < 0.001). Among the 54 patients who were toxin EIA-negative and did not receive CDI treatment, three (5.6%) were diagnosed with CDI after 7–21 days without complication. Conclusion Our study demonstrates that toxin EIA-negative patients had milder laboratory findings and no complications, despite not receiving treatment. Prolonged hospitalisation and exposure to high-risk antibiotics could potentially serve as markers for the development of toxin EIA-positive CDI.

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