Evidence map›Paper›PMID 24898123›Full record

ArticleBMC infectious diseases2014

Risk factors for recurrent Clostridium difficile infection (CDI) hospitalization among hospitalized patients with an initial CDI episode: a retrospective cohort study.

Marya D Zilberberg, Kimberly Reske, Margaret Olsen, Yan Yan, Erik R Dubberke

2 registry-linked trialsAbstract readEvaluation Study
In one paragraph

Article in BMC infectious diseases, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing 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.

NCT05320068 phase3completednot on this mapstarted 2022, after this paper: background citation

Phase III,randomized,double-blinded Clinical Trial to Evaluate the Effectiveness and Safety of Oral Vancomycin Vs Placebo in the Prevention of Recurrence of C.difficile Infection in Patients Under Treatment with Systemic Antibiotic Therapy

TypeinterventionalSponsorJulia OrígüenRan2022 to 2024Enrolled24ConditionsClostridioides Difficile InfectionArmsOral Vancomycin, Placebo
NCT06979609 phase2 / phase3recruitingnot on this mapstarted 2025, after this paper: background citation

Secondary Prophylaxis of Recurrent Clostridioides Difficile Infections During Systemic Antibiotics With Vancomycin: A Randomized Controlled Trial

TypeinterventionalSponsorMcGill University Health Centre/Research Institute of the McGill University Health CentreRan2025 to 2029Enrolled300ConditionsClostridioides Difficile Infection, Clostridioides Difficile Infection Recurrence, Clostridoides Difficile Associated DiseaseArmsOral Vancomycin Prophylaxis, Placebo
3 · Its place in the literature

Who cites it

20 citing papers in PubMed.

  1. Trial
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  7. Review
  8. Risk factors for recurrent Clostridium difficile infection in a tertiary hospital in Israel.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2018
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Review
  18. Novel risk factors for recurrent Clostridium difficile infection in children.Journal of pediatric gastroenterology and nutrition · 2015
    Article
  19. A prediction model for Clostridium difficile recurrence.Journal of community hospital internal medicine perspectives · 2015
    Article
  20. 2019 update of the WSES guidelines for management ofWorld journal of emergency surgery : WJES
    Review
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

5 authors.

Marya D ZilberbergUniversity of Massachusetts, Amherst, MA, USA. evimedgroup@gmail.com.
Kimberly Reske
Margaret Olsen
Yan Yan
Erik R Dubberke

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRecurrent Clostridium difficile infection (rCDI) is observed in up to 25% of patients with an initial CDI episode (iCDI). We assessed risk factors for rCDI among patients hospitalized with iCDI.

methodsWe performed a retrospective cohort study at Barnes-Jewish Hospital from 1/1/03 to 12/31/09. iCDI was defined as a positive toxin assay for C. difficile with no CDI in previous 60 days, and rCDI as a repeat positive toxin ≤42 days of stopping iCDI treatment. Three demographic, 13 chronic and 12 acute disease characteristics, and 21 processes of care were assessed for association with rCDI. Cox modeling identified independent risk factors for rCDI.

results425 (10.1%) of 4,200 patients enrolled developed rCDI. Of the eight risk factors for rCDI on multivariate analyses, the strongest three were 1) high-risk antimicrobials following completion of iCDI treatment (HR 2.95, 95% CI 2.25-3.86), 2) community-onset healthcare-associated iCDI (HR 1.80, 95% CI 1.41-2.29) and 3) fluoroquinolones after completion of iCDI treatment (HR 1.56, 95% CI 1.63-2.08). Other risk factors included gastric acid suppression, ≥2 hospitalizations within prior 60 days, age, and IV vancomycin after iCDI treatment ended.

conclusionsThe rCDI rate was 10.1%. Recognizing such modifiable risk factors as certain antimicrobial treatments and gastric acid suppression may help optimize prevention efforts.

Indexed as

Clostridioides difficileHospitalizationAdolescentAdultAgedAged, 80 and overAnti-Bacterial AgentsClostridium InfectionsCohort StudiesCross InfectionFemaleHumansMaleMiddle AgedMultivariate AnalysisProportional Hazards ModelsAnti-Bacterial Agents

Identifiers

PMID24898123
PMCPMC4050409

What OpenQuestion holds

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Registered trials

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.