Evidence map›Paper›PMID 25564777›Full record

ReviewGut microbes2014

The potential for emerging therapeutic options for Clostridium difficile infection.

Harsh Mathur, Mary C Rea, Paul D Cotter, R Paul Ross, Colin Hill

Abstract readReview
In one paragraph

Review in Gut microbes, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing 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

22 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Encapsulation protocol for fecal microbiota transplantation.Frontiers in cellular and infection microbiology · 2024
    Article
  5. Article
  6. Bacteriocins: Properties and potential use as antimicrobials.Journal of clinical laboratory analysis · 2022
    Review
  7. Article
  8. Bacteriocins From LAB and Other Alternative Approaches for the Control ofFrontiers in bioengineering and biotechnology · 2020
    Review
  9. Recent advances in the treatment ofInfection and drug resistance · 2019
    Article
  10. Review
  11. Article
  12. Frontiers in cellular and infection microbiology · 2018
    Review
  13. Novel Antimicrobials for the Treatment ofFrontiers in medicine · 2018
    Review
  14. Control ofMicrobiology spectrum · 2017
    Review
  15. Review
  16. Article
  17. Article
  18. Review
  19. Article
  20. 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

5 authors.

Harsh Mathura School of Microbiology ; University College Cork ; Cork , Ireland.
Mary C Rea
Paul D Cotter
R Paul Ross
Colin Hill

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Clostridium difficile is mainly a nosocomial pathogen and is a significant cause of antibiotic-associated diarrhea. It is also implicated in the majority of cases of pseudomembranous colitis. Recently, advancements in next generation sequencing technology (NGS) have highlighted the extent of damage to the gut microbiota caused by broad-spectrum antibiotics, often resulting in C. difficile infection (CDI). Currently the treatment of choice for CDI involves the use of metronidazole and vancomycin. However, recurrence and relapse of CDI, even after rounds of metronidazole/vancomycin administration is a problem that must be addressed. The efficacy of alternative antibiotics such as fidaxomicin, rifaximin, nitazoxanide, ramoplanin and tigecycline, as well as faecal microbiota transplantation has been assessed and some have yielded positive outcomes against C. difficile. Some bacteriocins have also shown promising effects against C. difficile in recent years. In light of this, the potential for emerging treatment options and efficacy of anti-C. difficile vaccines are discussed in this review.

Indexed as

AnimalsAnti-Bacterial AgentsBacterial VaccinesClostridioides difficileClostridium InfectionsHumansAnti-Bacterial AgentsBacterial VaccinesantibioticsATCC, American Type Culture CollectionCDI, Clostridium difficile infectionCdtLoc, binary toxin locusClostridium difficileDNA, deoxyribonucleic acidDPC, Dairy Products CollectionESCMID, European Society of Clinical Microbiology and Infectious DiseasesETEC, enterotoxigenic E. colifaecal microbiota transplantationFDA, Food and Drug AdministrationFMT, faecal microbiota transplantationGIT, gastrointestinal tractHIV, human immunodeficiency virusIDSA, Infectious Diseases Society of AmericaIgG, immunoglobulin GLTA, lipoteichoic acidM21V, methionine to valine substitution at residue 21MIC, minimum inhibitory concentrationNGS, next generation sequencingNVB, Novacta Biosystems LtdPaLoc, pathogenicity locusPMC, pseudomembranous colitisR027, ribotype 027RBDRBS, ribosome binding sitereceptor binding domainRNA, ribonucleic acidSHEA, Society for Healthcare Epidemiology of AmericatoxinsV15F, valine to phenylalanine substitution at residue 15vaccines

Identifiers

PMID25564777
PMCPMC4615897

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.