Evidence map›Paper›PMID 41127168›Full record

ArticleAntimicrobial stewardship & healthcare epidemiology : ASHE2025

A systematic literature review and bayesian meta-analysis of oral vancomycin primary prophylaxis for

Erika Viana-Cardenas, Eugenia Miranti, Wajeeha Tariq, Guillermo Rodriguez-Nava, Sa Shen, Evans Whitaker, Mingjun Jiang, Mindy M Sampson, Andrew Rezvani, Ami S Bhatt and 2 more

Abstract read
In one paragraph

Article in Antimicrobial stewardship & healthcare epidemiology : ASHE, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Erika Viana-CardenasDivision of Infectious Diseases and Geographic Medicine, Stanford University School of Medicine, Stanford, CA, USA.ORCID https://orcid.org/0000-0002-6399-890X
Eugenia MirantiDivision of Infectious Diseases and Geographic Medicine, Stanford University School of Medicine, Stanford, CA, USA.ORCID https://orcid.org/0000-0002-0654-8937
Wajeeha TariqDivision of Infectious Diseases and Geographic Medicine, Stanford University School of Medicine, Stanford, CA, USA.
Guillermo Rodriguez-NavaDivision of Infectious Diseases and Geographic Medicine, Stanford University School of Medicine, Stanford, CA, USA.
Sa ShenQuantitative Sciences Unit, Stanford University, Stanford, CA, USA.
Evans WhitakerLane Medical Library, Stanford University School of Medicine, Stanford, CA, USA.ORCID https://orcid.org/0000-0003-1326-4374
Mingjun JiangDepartment Civil and Environmental Engineering, Stanford University, Stanford, CA, USA.
Mindy M SampsonDivision of Infectious Diseases and Geographic Medicine, Stanford University School of Medicine, Stanford, CA, USA.ORCID https://orcid.org/0000-0001-5724-5875
Andrew RezvaniDivision of Blood and Marrow Transplantation, Stanford University School of Medicine, Stanford, CA, USA.
Ami S BhattDepartment of Medicine (Hematology) and of Genetics, Stanford University School of Medicine, Stanford, CA, USA.
Alexandre R MarraDepartment of Internal Medicine, University of Iowa Carver College of Medicine, Iowa City, IA, USA.ORCID https://orcid.org/0000-0002-7577-7688
Jorge L SalinasDivision of Infectious Diseases and Geographic Medicine, Stanford University School of Medicine, Stanford, CA, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Methods: We searched six databases from inception to March 21, 2025, for studies comparing the incidence of CDI in HSCT patients who received oral vancomycin primary prophylaxis versus those who did not. We built a Bayesian random-effects model for meta-analysis. The primary outcome was the incidence of CDI. Secondary outcomes included incidence of positive vancomycin-resistant Results: Six studies met inclusion criteria with a total of 1,236 patients. Four of the studies were of fair to good quality. Oral vancomycin primary prophylaxis reduced the incidence of CDI during hospitalization (OR 0.31; 95%CrI 0.16-0.59). Studies were weakly heterogeneous but had strong publication bias. Oral vancomycin primary prophylaxis reduced the odds of CDI by 12% after accounting for publication bias (OR 0.88; 95%CrI 0.32-1.16), although this reduction was not statistically significant. Secondary outcomes were similar in both groups. Conclusion: Oral vancomycin primary prophylaxis prevented CDI in HSCT patients without significantly affecting secondary outcomes. However, after controlling for publication bias, these findings were no longer significant. Further studies are needed to provide stronger evidence for or against this intervention, assess long-term safety, and assess potential effects on antimicrobial resistance.

Identifiers

PMID41127168
PMCPMC12538368

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.