Evidence map›Paper›PMID 26131411›Full record

ArticleAnnals of laboratory medicine2015

Isolation and Identification of Clostridium difficile Using ChromID C. difficile Medium Combined With Gram Staining and PRO Disc Testing: A Proposal for a Simple Culture Process.

Kyung Sun Park, Chang-Seok Ki, Nam Yong Lee

Abstract readEvaluation Study
In one paragraph

Article in Annals of laboratory medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Optimized Surveillance Testing for ToxigenicmedRxiv : the preprint server for health sciences · 2026
    Article
  2. Article
  3. Prevalence of Non-ToxigenicAntibiotics (Basel, Switzerland) · 2023
    Article
  4. Article
  5. Article
  6. Article
  7. Simultaneous Detection ofAnnals of laboratory medicine · 2019
    Article
  8. Review
  9. Article
  10. 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

3 authors.

Kyung Sun ParkDepartment of Laboratory Medicine and Genetics, Sungkyunkwan University School of Medicine, Seoul, Korea.
Chang-Seok KiDepartment of Laboratory Medicine and Genetics, Sungkyunkwan University School of Medicine, Seoul, Korea.
Nam Yong LeeDepartment of Laboratory Medicine and Genetics, Sungkyunkwan University School of Medicine, Seoul, Korea.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundChromID C. difficile agar (CDIF; bioMérieux, France), a chromogenic medium, allows for the isolation and identification of Clostridium difficile strains within 24 hr regardless of pretreatment of stool specimens with heat or alcohol shock. In the present study, we designed and evaluated a simple procedure for the implementation C. difficile cultures using CDIF medium in a tertiary hospital setting.

methodsWe designed a simple protocol for untreated stool specimens using CDIF medium followed by Gram staining and PRO disc (PRO disc K1532B, Key Scientific Products, USA) testing for the identification of C. difficile in colonies produced on CDIF agar. A total of 1,402 prospectively collected stool specimens from patients with suspected C. difficile infection were tested. The protocol was evaluated by phenotypic or molecular identification of C. difficile using Vitek 2 ANC card (bioMérieux) or 16S rDNA/tpi gene sequencing, respectively.

resultsOf 1,402 stool specimens, 650 isolates were cultured in CDIF. Overall, 235 (36.2%, 235/650) strains could be presumptively identified as C. difficile by using Gram staining and PRO disc testing. Of those, 231 (98.3%, 231/235) isolates were confirmed as true C. difficile by molecular assays.

conclusionsThe use of CDIF combined with Gram staining and PRO disc testing of untreated stool specimens would allow for isolation and accurate identification of C. difficile strains and would be advantageous in reducing the multistep process for C. difficile culture.

Indexed as

Bacterial ProteinsBacterial ToxinsBacteriological TechniquesClostridioides difficileCulture MediaEnterotoxinsFecesGentian VioletHumansImmunoassayPhenazinesPhenotypeRNA, Ribosomal, 16SSequence Analysis, DNABacterial ProteinsBacterial ToxinsCulture MediaEnterotoxinsGentian VioletGram's stainPhenazinesRNA, Ribosomal, 16StcdA protein, Clostridium difficiletoxB protein, Clostridium difficileClostridium difficileCultureIsolation

Identifiers

PMID26131411
PMCPMC4446578

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