190. Incidence and Risk Factors for Clostridioides difficile disease (CDI) Progression from Polymerase Chain Reaction (PCR)+/Toxin- to PCR+/Toxin+ in Patients with Cancer: a Single Center Study

Abstract Background Two-step Clostridioides difficile infection (CDI) testing with PCR and EIA has improved diagnostic precision, but longitudinal significance of PCR+/toxin- (P+T-) test in immunocompromised patients is unclear. Our previous study showed P+/T- untreated patients had significantly higher P+/T+ CDI progression within 3 months compared to P+/T- patients who received CDI treatment based on signs or symptoms of CDI without alternate explanation. This study aimed to analyze the risk factors for progression over 3 months from P+/T- to a P+T+ test result. Methods Retrospective review of adult, hospitalized patients with P+T- from 8/18/2021-8/17/2024 was performed (Figure 1). Duplicate tests ≤14 days were excluded. Patient demographics, glutamate dehydrogenase (GDH) test positivity, CDI treatment defined as receiving ≥3 days of CDI treatment at the time of index P+T- test, exposure to proton pump inhibitors/histamine 2 receptor antagonist/ antibiotics were compared between P+T+ progression group and no progression group (Table 1). Logistic regression was performed to identify factors associated with P+T+ CDI progression using SPSS v. 29. Results Among 637 P+T– cases with median age 60, male 52%, hematological malignancies 78%, 38% received CDI treatment and 8% (49/637) progressed to P+T+ CDI within 3 months (Figure 1, Table 1). Compared to those who did not progress, patients who developed confirmed P+T+ CDI within 3 months were more likely to have undergone allogeneic hematopoietic stem cell transplant (HSCT, 69% v. 44%, p=0.003) and less likely to have received CDI treatment at index P+T- result (25% v. 39%, p=0.043). Multivariable regression analysis controlled for age, GDH test positivity, and CDI treatment at the time of index P+T-, identified only allogeneic HSCT (OR 3.020, p< 0.001) as a predictor for P+T+ CDI progression. Conclusion Increased risk of P+T+ CDI progression from P+T- among allogeneic HSCT patients highlights the importance of close monitoring and preventive strategies in high-risk populations. These findings suggest a potential role for prophylaxis as CDI in allogeneic HSCT is independently associated with increased non-relapse mortality and needs to be studied. Disclosures All Authors: No reported disclosures

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Journal
Open Forum Infectious Diseases
Published
2026-01-01
DOI
https://doi.org/10.1093/ofid/ofaf695.065
Primary Topic
Clostridium difficile and Clostridium perfringens research
Type
article
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article

190. Incidence and Risk Factors for Clostridioides difficile disease (CDI) Progression from Polymerase Chain Reaction (PCR)+/Toxin- to PCR+/Toxin+ in Patients with Cancer: a Single Center Study

Rosemary C. She, Jana Dickter, Sanjeet Dadwal, Justine Abella Ross et al.
Open Forum Infectious Diseases
Clostridium difficile and Clostridium perfringens research
article

190. Incidence and Risk Factors for Clostridioides difficile disease (CDI) Progression from Polymerase Chain Reaction (PCR)+/Toxin- to PCR+/Toxin+ in Patients with Cancer: a Single Center Study

Rosemary C. She, Jana Dickter, Sanjeet Dadwal, Justine Abella Ross, Wonhee So, Maryam Jabri, Thu Phu
article en

Abstract

Abstract Background Two-step Clostridioides difficile infection (CDI) testing with PCR and EIA has improved diagnostic precision, but longitudinal significance of PCR+/toxin- (P+T-) test in immunocompromised patients is unclear. Our previous study showed P+/T- untreated patients had significantly higher P+/T+ CDI progression within 3 months compared to P+/T- patients who received CDI treatment based on signs or symptoms of CDI without alternate explanation. This study aimed to analyze the risk factors for progression over 3 months from P+/T- to a P+T+ test result. Methods Retrospective review of adult, hospitalized patients with P+T- from 8/18/2021-8/17/2024 was performed (Figure 1). Duplicate tests ≤14 days were excluded. Patient demographics, glutamate dehydrogenase (GDH) test positivity, CDI treatment defined as receiving ≥3 days of CDI treatment at the time of index P+T- test, exposure to proton pump inhibitors/histamine 2 receptor antagonist/ antibiotics were compared between P+T+ progression group and no progression group (Table 1). Logistic regression was performed to identify factors associated with P+T+ CDI progression using SPSS v. 29. Results Among 637 P+T– cases with median age 60, male 52%, hematological malignancies 78%, 38% received CDI treatment and 8% (49/637) progressed to P+T+ CDI within 3 months (Figure 1, Table 1). Compared to those who did not progress, patients who developed confirmed P+T+ CDI within 3 months were more likely to have undergone allogeneic hematopoietic stem cell transplant (HSCT, 69% v. 44%, p=0.003) and less likely to have received CDI treatment at index P+T- result (25% v. 39%, p=0.043). Multivariable regression analysis controlled for age, GDH test positivity, and CDI treatment at the time of index P+T-, identified only allogeneic HSCT (OR 3.020, p< 0.001) as a predictor for P+T+ CDI progression. Conclusion Increased risk of P+T+ CDI progression from P+T- among allogeneic HSCT patients highlights the importance of close monitoring and preventive strategies in high-risk populations. These findings suggest a potential role for prophylaxis as CDI in allogeneic HSCT is independently associated with increased non-relapse mortality and needs to be studied. Disclosures All Authors: No reported disclosures

Open Forum Infectious DiseasesVol. 13(Supplement_1)
City Of Hope National Medical Center (US), City of Hope (US), Western University of Health Sciences (US)
Good health and well-being
Openalex Percentile: Top 90%
Clostridium difficile and Clostridium perfringens research
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