Evidence map›Paper›PMID 28721981›Full record

ArticleSaudi journal of gastroenterology : official journal of the Saudi Gastroenterology Association

Detection of

Abiola C Senok, Kamel M Aldosari, Rayan A Alowaisheq, Othman A Abid, Khalid A Alsuhaibani, Mohammad A Khan, Ali M Somily

Abstract readComparative Study
In one paragraph

Article in Saudi journal of gastroenterology : official journal of the Saudi Gastroenterology Association. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Biomedicines · 2025
    Review
  2. Frontiers in pediatrics · 2025
    Review
  3. The Current Knowledge onPathogens (Basel, Switzerland) · 2022
    Review
  4. Article
  5. Review
  6. Frequency of toxin genes and antibiotic resistance pattern ofGastroenterology and hepatology from bed to bench · 2021
    Article
  7. Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society · 2020
    Review
  8. Article
  9. Article
  10. Burden ofIranian journal of public health · 2019
    Review
  11. Article
  12. 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.

Abiola C SenokDepartment of Basic Science, College of Medicine, Mohammed Bin Rashid University of Medicine and Health Sciences, Dubai, United Arab Emirates.
Kamel M AldosariDepartment of Laboratory Medicine, Microbiology Laboratory, Prince Mohammed Bin Abdulaziz Hospital, Riyadh, Kingdom of Saudi Arabia.
Rayan A AlowaisheqCollege of Medicine, King Saud University, Riyadh, Kingdom of Saudi Arabia.
Othman A AbidCollege of Medicine, King Saud University, Riyadh, Kingdom of Saudi Arabia.
Khalid A AlsuhaibaniCollege of Medicine, King Saud University, Riyadh, Kingdom of Saudi Arabia.
Mohammad A KhanDepartment of Laboratory Medicine, Microbiology Laboratory, Prince Mohammed Bin Abdulaziz Hospital, Riyadh, Kingdom of Saudi Arabia.
Ali M SomilyDepartment of Pathology and Laboratory Medicine, College of Medicine, King Saud University and King Saud University Medical City, Riyadh, Kingdom of Saudi Arabia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

aimsAccurate and rapid laboratory diagnosis of Clostridium difficile infections (CDI) remains a significant challenge. A two-step algorithm for detection of toxigenic C. difficile in stool based on initial screening for glutamate dehydrogenase assay followed by confirmation by toxin A+B detection using an enzyme immunoassay (EIA) or molecular assay has been proposed. We aimed to evaluate the C. difficile Quik Chek Complete® (QCC-EIA) versus the GeneXpert® C. difficile polymerase chain reaction (PCR) assay in this two-step algorithm. MATERIALS AND

methodsTwo hundred and ten liquid stool samples obtained between June 2014 and June 2015 from patients suspected of CDI were tested by the QCC-EIA and GeneXpert PCR assay. The GeneXpert assay was used as the reference standard to calculate the QCC-EIA sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV).

resultsOf the 210 stool samples tested, 43 (20.5%) were positive by QCC-EIA, while 31 (14.8%) were positive by GeneXpert assay. The sensitivity and specificity of the QCC-EIA were found to be 100 and 93%, respectively; the PPV and NPV were 72 and 100%, respectively. The binary toxin was detected in 12 (38.7%) and tcdC gene deletion in 3 (9.6%).

conclusionsThe low specificity of QCC-EIA makes it less reliable as a confirmatory test for CDI diagnosis. This test may be used as a screening test in a two-step algorithm when combined with a molecular assay or another confirmatory test.

Indexed as

AdolescentAdultAgedAlgorithmsAntigens, BacterialBacterial ToxinsClostridioides difficileClostridium InfectionsFecesFemaleGlutamate DehydrogenaseHumansImmunoenzyme TechniquesMaleMiddle AgedPolymerase Chain ReactionAntigens, BacterialBacterial ToxinsGlutamate DehydrogenaseReagent Kits, Diagnostic

Identifiers

PMID28721981
PMCPMC5539681

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.