Evidence map›Paper›PMID 35944176›Full record

ArticleJournal of clinical laboratory analysis2022

Colistin resistance screening by 3 μg/ml colistin agar in Carbapenemase-producing Enterobacterales.

Claudia Soria-Segarra, Carmen Soria-Segarra, Michelle Andrade-Soriano, Tamara Nuñez Quezada, Monica C Gestal, Jose Gutierrez-Fernandez

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical laboratory analysis, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.2field-weighted citation impact, top 60% of its field
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

3 citing papers in PubMed, 3 citations in OpenAlex.

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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

6 authors at 3 institutions in 3 countries.

Claudia Soria-SegarraSosecali, Medical Services, Guayaquil, Ecuador.ORCID https://orcid.org/0000-0003-0896-6291
Carmen Soria-SegarraSosecali, Medical Services, Guayaquil, Ecuador.
Michelle Andrade-SorianoSosecali, Medical Services, Guayaquil, Ecuador.
Tamara Nuñez QuezadaDepartment of Internal Medicine, School of Medicine, Universidad Católica de Santiago de Guayaquil, Guayaquil, Ecuador.
Monica C GestalDepartment of Microbiology and Immunology, LSU Health Shreveport, Shreveport, Louisiana, USA.
Jose Gutierrez-FernandezDepartment of Microbiology, School of Medicine and PhD Program in Clinical Medicine and Public Health, University of Granada & ibs, Granada, Spain.ORCID https://orcid.org/0000-0001-6146-9740
Universidad de Granada · ESLouisiana State University Health Sciences Center Shreveport · USUniversity of Guayaquil · EC

Funding

Sosecali Medical Services. C.Ltda 001-020Universidad Catolica de Santiago de Guayaquil SIU#510-298
6 · The paper itself

Abstract

backgroundIn low- and middle-income countries, the use of colistin in therapeutic regimens is common, to treat infections produced for Carbapenemase-producing Enterobacterales (CPE) due to limited access to the recently discovered-approved antibiotics. Furthermore, the technical limitations to perform colistin susceptibility tests make it difficult to assess the suitability of this treatment for each patient, as well as to monitor the rates of resistance. In the present study, we describe the use of agar dilution using a unique colistin concentration of 3 μg/ml to discriminate isolates with colistin resistance in CPE obtained from clinical samples.

methodsClinical Laboratory Standards Institute (CLSI) colistin broth microdilution method and dilution agar with a colistin concentration of 3 μg/ml were performed in 168 isolates of CPE obtained from clinical samples in Guayaquil, Ecuador. Broth microdilution was considered our gold standard using CLSI breakpoints as reference (≤2 μg/ml intermediate and ≥4 μg/ml resistant). Categorical agreement was defined as obtaining a reading within the same category with both methodologies.

resultsIsolates obtained from respiratory samples were the most prevalent (26.19%; n = 44). Klebsiella pneumoniae was the predominant specie (94.04%; n = 158). KPC-like carbapenemase was present in all the isolates, and interestingly, colistin resistance was not mediated by MCR-1 production. Categorical agreement between both methods resulted in 97.02%.

conclusionWe propose the use of dilution agar with a colistin concentration of 3 μg/ml, as a valid method for screening colistin resistance in low- and middle-income countries to monitor resistance and to perform epidemiological studies.

Indexed as

beta-LactamasesColistinAgarAnti-Bacterial AgentsBacterial ProteinsDrug Resistance, BacterialHumansKlebsiella pneumoniaeMicrobial Sensitivity TestsAgarAnti-Bacterial AgentsBacterial Proteinsbeta-LactamasescarbapenemaseColistinbroth microdilutionCarbapenemase-producing Enterobacteralescolistin dilution agarcolistin resistancesurveillance

Identifiers

PMID35944176
PMCPMC9459281
OpenAlexW4292457872

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.