Evidence map›Paper›PMID 30785934›Full record

ArticlePloS one2019

Carriage and colonization of C. difficile in preterm neonates: A longitudinal prospective study.

Laurent Ferraris, Jeanne Couturier, Catherine Eckert, Johanne Delannoy, Frédéric Barbut, Marie-José Butel, Julio Aires

Abstract read
In one paragraph

Article in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

  1. Microbiology spectrum · 2026
    Article
  2. Article
  3. Antibiotics (Basel, Switzerland) · 2025
    Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Clinical microbiology reviews · 2024
    Review
  9. Diagnostic Guidance for C. difficile Infections.Advances in experimental medicine and biology · 2024
    Article
  10. Gut Microbiota Composition andGut microbes reports · 2024
    Article
  11. Review
  12. Gut Microbiota Diversity of Preterm Neonates Is Associated WithFrontiers in cellular and infection microbiology · 2022
    Article
  13. Gut Dysbiosis andFrontiers in microbiology · 2021
    Review
  14. Characterization of Non-ToxigenicJournal of clinical medicine · 2020
    Article
  15. Review
  16. Article
  17. Case reports in gastroenterology
    Article
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

7 authors.

Laurent FerrarisEA 4065, Faculty of Pharmacy, Paris Descartes University, Hospital University Department Risks in pregnancy, Sorbonne Paris Cité, Paris, France.
Jeanne CouturierEA 4065, Faculty of Pharmacy, Paris Descartes University, Hospital University Department Risks in pregnancy, Sorbonne Paris Cité, Paris, France.
Catherine EckertDepartment of Bacteriology, AP-HP, GH Est Parisien, Paris, France.
Johanne DelannoyEA 4065, Faculty of Pharmacy, Paris Descartes University, Hospital University Department Risks in pregnancy, Sorbonne Paris Cité, Paris, France.
Frédéric BarbutEA 4065, Faculty of Pharmacy, Paris Descartes University, Hospital University Department Risks in pregnancy, Sorbonne Paris Cité, Paris, France.
Marie-José ButelEA 4065, Faculty of Pharmacy, Paris Descartes University, Hospital University Department Risks in pregnancy, Sorbonne Paris Cité, Paris, France.
Julio AiresEA 4065, Faculty of Pharmacy, Paris Descartes University, Hospital University Department Risks in pregnancy, Sorbonne Paris Cité, Paris, France.ORCID 0000-0002-8090-4565

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPremature neonates (PN) present multiple risk factors for high frequencies and high levels of colonization by C. difficile, yet data is missing about this specific pediatric population. Here, we investigated PN C. difficile carriage and colonization dynamics, analyzed the impact of perinatal determinants on colonization, and characterized the isolates.

methodsA one year longitudinal monocentric prospective cohort study was performed on 121 PN. C. difficile strains isolated from fecal samples on selective medium were identified and characterized by PCR (tpi housekeeping gene; tcdA and tcdB, and binary toxin genes), capillary gel-based electrophoresis PCR-ribotyping, and Multi-Locus Variable-number tandem-repeat Analysis (MLVA).

resultsOf the 379 samples analyzed, 199 (52%) were C. difficile culture positive with the mean levels of C. difficile colonization decreasing significantly (P = .027) over time. During hospitalization, C. difficile colonization frequency increased up to 61% with 95% of the strains belonging to both non-toxigenic PCR-ribotypes (RTs) FR082 (35%) and 032 (60%). After hospital discharge, if a higher diversity in RTs was observed, RTs FR082 and 032 remained predominant (respectively 40% and 28%). MLVA showed clonal relationship within each FR082 and 032 RTs. Ten toxigenic strains (5%) were isolated, all tcdA+/tcdB+ except for one tcdA-/tcdB+, and all being acquired after hospitalization. At 1 week, the only factors found to be linked with a higher frequency of C. difficile colonization were a higher gestational age (P = 0.006) and a higher birth weight (P = 0.016).

conclusionThe dynamics of C. difficile colonization in PN followed a specific pattern. C. difficile colonization rapidly occurred after birth with a low diversity of non-toxigenic RTs. After hospitalization, non-toxigenic RTs diversity increased. Sporadic carriage of toxigenic strains was observed after hospitalization.

Indexed as

Clostridioides difficileClostridium InfectionsFecesFemaleHumansInfant, NewbornInfant, PrematureInfant, Premature, DiseasesLongitudinal StudiesMaleProspective StudiesRibotyping

Identifiers

PMID30785934
PMCPMC6382121

What OpenQuestion holds

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Registered trials

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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.