P-1025. A Systematic Literature Review and Bayesian Meta-analysis of Clostridioides difficile Primary Prophylaxis with Vancomycin in Stem Cell Transplant Patients

Abstract Background Clostridioides difficile infection (CDI) is common among patients undergoing hematopoietic stem cell transplantation (HSCT). Oral vancomycin prophylaxis may effectively prevent CDI in certain populations. We investigated the effectiveness of primary oral vancomycin prophylaxis in preventing CDI in HSCT patients.Figure 1.Literature search for studies that evaluated the impact of Oral Vancomycin Prophylaxis for Clostridioides difficile Infection in Transplanted Population.Figure 2.Forest plot of Clostridioides difficile Infection with and without Oral Vancomycin Prophylaxis. Methods We conducted a Bayesian meta-analysis. PubMed and Embase databases were searched from inception to March 21, 2025. We included studies comparing the incidence of CDI in HSCT recipients who received primary oral vancomycin prophylaxis versus those who did not. We used the Downs and Black scale for quality assessment. Publication bias was assessed using Robust Bayesian Meta-Analyses and heterogeneity was also calculated. Effect sizes and standard errors were calculated from the sample sizes and reported cases, and a Bayesian random-effects model was used to conduct the meta-analysis. The primary outcome was the frequency of CDI in patients who received primary oral vancomycin prophylaxis compared to those who did not. Secondary outcomes included incidence of positive VRE cultures (from any site), blood stream infections, GVHD, and length of hospital stay. The review was registered on PROSPERO (CRD420251016925).Figure 3.Forest plot of Secondary Outcomes with and without Oral Vancomycin Prophylaxis. Results Six studies (including 2 abstracts) met inclusion criteria with a total of 1,236 patients (620 in the intervention group and 616 in the control). The 4 full-text studies were high quality. Primary oral vancomycin prophylaxis reduced the incidence of CDI (OR 0.31; CrI 0.16–0.59). Secondary outcomes including bloodstream infections (OR 1.10; CrI 0.65–1.81), positive VRE cultures (OR 0.75; CrI 0.31–1.78), GVHD (OR 1.21; CrI 0.59–2.47), and length of hospital stay (OR 0.90; CrI 0.29–2.72) were similar in both groups. We found weak evidence of heterogeneity amongst the studies and moderate publication bias. Conclusion There is weak evidence in favor of primary oral vancomycin prophylaxis in preventing CDI in HSCT patients without significantly affecting secondary outcomes. Further studies are needed to provide stronger evidence, and assess long-term safety, potential effects on antimicrobial resistance and influence on gut microbiome. 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/ofaf695.1221
Primary Topic
Clostridium difficile and Clostridium perfringens research
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article
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article

P-1025. A Systematic Literature Review and Bayesian Meta-analysis of Clostridioides difficile Primary Prophylaxis with Vancomycin in Stem Cell Transplant Patients

Guillermo Rodríguez-Nava, Jorge Salinas, Mindy Marie Sampson, Wajeeha Tariq et al.
Open Forum Infectious Diseases
Clostridium difficile and Clostridium perfringens research
article

P-1025. A Systematic Literature Review and Bayesian Meta-analysis of Clostridioides difficile Primary Prophylaxis with Vancomycin in Stem Cell Transplant Patients

Guillermo Rodríguez-Nava, Jorge Salinas, Mindy Marie Sampson, Wajeeha Tariq, Alexandre Rodrigues Marra, Erika Paola Viana Cardenas, Sa Shen, Mingjun Jiang, Eugenia Miranti
article en

Abstract

Abstract Background Clostridioides difficile infection (CDI) is common among patients undergoing hematopoietic stem cell transplantation (HSCT). Oral vancomycin prophylaxis may effectively prevent CDI in certain populations. We investigated the effectiveness of primary oral vancomycin prophylaxis in preventing CDI in HSCT patients.Figure 1.Literature search for studies that evaluated the impact of Oral Vancomycin Prophylaxis for Clostridioides difficile Infection in Transplanted Population.Figure 2.Forest plot of Clostridioides difficile Infection with and without Oral Vancomycin Prophylaxis. Methods We conducted a Bayesian meta-analysis. PubMed and Embase databases were searched from inception to March 21, 2025. We included studies comparing the incidence of CDI in HSCT recipients who received primary oral vancomycin prophylaxis versus those who did not. We used the Downs and Black scale for quality assessment. Publication bias was assessed using Robust Bayesian Meta-Analyses and heterogeneity was also calculated. Effect sizes and standard errors were calculated from the sample sizes and reported cases, and a Bayesian random-effects model was used to conduct the meta-analysis. The primary outcome was the frequency of CDI in patients who received primary oral vancomycin prophylaxis compared to those who did not. Secondary outcomes included incidence of positive VRE cultures (from any site), blood stream infections, GVHD, and length of hospital stay. The review was registered on PROSPERO (CRD420251016925).Figure 3.Forest plot of Secondary Outcomes with and without Oral Vancomycin Prophylaxis. Results Six studies (including 2 abstracts) met inclusion criteria with a total of 1,236 patients (620 in the intervention group and 616 in the control). The 4 full-text studies were high quality. Primary oral vancomycin prophylaxis reduced the incidence of CDI (OR 0.31; CrI 0.16–0.59). Secondary outcomes including bloodstream infections (OR 1.10; CrI 0.65–1.81), positive VRE cultures (OR 0.75; CrI 0.31–1.78), GVHD (OR 1.21; CrI 0.59–2.47), and length of hospital stay (OR 0.90; CrI 0.29–2.72) were similar in both groups. We found weak evidence of heterogeneity amongst the studies and moderate publication bias. Conclusion There is weak evidence in favor of primary oral vancomycin prophylaxis in preventing CDI in HSCT patients without significantly affecting secondary outcomes. Further studies are needed to provide stronger evidence, and assess long-term safety, potential effects on antimicrobial resistance and influence on gut microbiome. Disclosures All Authors: No reported disclosures

Open Forum Infectious DiseasesVol. 13(Supplement_1)
Palo Alto University (US), University of Iowa Hospitals and Clinics (US), Quantitative BioSciences (US), Stanford Medicine (US), Stanford University (US)
Openalex Percentile: Top 91%
Clostridium difficile and Clostridium perfringens research
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