Evidence map›Paper›PMID 42130493›Full record

ArticleAntimicrobial stewardship & healthcare epidemiology : ASHE2026

Cycle thresholds and discordant 2-step testing for Clostridioides Difficile: Comparison of clinical characteristics and outcomes among discordant and true positive results.

Michael Rossi, Emerald O'Rourke, Tao Hong, Sara F Geffert, Tiffany L Chargualaf, Andrea Collins, Joshua Ray Tanzer, Francine Touzard-Romo

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Article in Antimicrobial stewardship & healthcare epidemiology : ASHE, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Michael RossiWarren Alpert Medical School of Brown University, USA.ORCID https://orcid.org/0009-0001-2316-8952
Emerald O'RourkeBrown University Health, USA.
Tao HongRhode Island Hospital, USA.ORCID https://orcid.org/0009-0009-6052-0706
Sara F GeffertWarren Alpert Medical School of Brown University, USA.ORCID https://orcid.org/0000-0002-2042-3532
Tiffany L ChargualafBrown University Health, USA.
Andrea CollinsBrown University Health, USA.
Joshua Ray TanzerBrown University Health, USA.
Francine Touzard-RomoWarren Alpert Medical School of Brown University, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: To determine if Toxin B polymerase chain reaction (PCR) cycle threshold (Ct) can help identify which patients with discordant clostridioides difficile (CD) PCR and enzyme immunoassay testing (EIA) may benefit from treatment. Design: Retrospective case series. Setting: Multi-hospital tertiary Academic system. Patients: All admitted adult patients with positive CD PCR over a 6 month period (n = 214). Patients with positive Stool PCR for other pathogens were excluded. Methods: Chart review of all eligible patients. CD testing results, patient demographics, underlying comorbidities, symptoms prompting testing, risk factors for CD, markers of severe disease, treatment regimens, and clinical outcomes including: 30-day all-cause mortality and re-admission, and 60-day CDI repeat testing and treatment were collected. Results: Significant association between mortality and lower Ct values among discordant patients who were not treated compared to those who were (P = 0.042). The association between Ct values and 30-day readmission was significantly stronger among untreated patients compared to those who were treated (P = .034). A similar trend was observed among non-severe, untreated patients with low Ct values and subsequent CDI treatment within 60 days (CT < 26, 49% vs. CT > 26, 18%, P = .063). Conclusions: Untreated patients with lower cycle thresholds had worse clinical outcomes compared to untreated patients with higher Ct, regardless of disease severity. A lower PCR Ct can support treatment in patients with clinical disease, positive PCR and negative toxin EIA.

Identifiers

PMID42130493
PMCPMC13162063

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