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Incidence of genes encoding vanA/vanB vancomycin resistance in rectal swabs of patients with diagnosed cancer, on the day of admission to hospital, in a non-epidemic period
INTRODUCTION: Rapid diagnosis is important for preventing infections due to vancomycin-resistant enterococci. AIM: To evaluate the status of gastrointestinal colonisation with strains containing vanA/vanB genes in oncological patients. MATERIAL AND METHODS: A total of 167 samples of rectal swabs tak...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Termedia Publishing House
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7509899/ https://www.ncbi.nlm.nih.gov/pubmed/33005267 http://dx.doi.org/10.5114/pg.2020.98537 |
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author | Szymankiewicz, Maria Wróblewska, Joanna Nowikiewicz, Tomasz |
author_facet | Szymankiewicz, Maria Wróblewska, Joanna Nowikiewicz, Tomasz |
author_sort | Szymankiewicz, Maria |
collection | PubMed |
description | INTRODUCTION: Rapid diagnosis is important for preventing infections due to vancomycin-resistant enterococci. AIM: To evaluate the status of gastrointestinal colonisation with strains containing vanA/vanB genes in oncological patients. MATERIAL AND METHODS: A total of 167 samples of rectal swabs taken from 161 patients (mean age: 63, range: 29–93 years) were examined, including 113 patients from surgical wards (70.2%) and 48 patients from non-surgical wards (29.8%), with diagnosed cancer. The tests were carried out within 24 h of admitting the patient to the department, using the Cepheid Xpert vanA/vanB test, with a CE marked GeneXpert(®) Instrument Systems analyser. Samples with positive vanB gene results were additionally seeded on chromogenic media. RESULTS: The presence of the vanA gene was found in 2.7% and 6.3% of the examined patients, respectively, from the surgical and non-surgical departments, which accounted for 3.7% of all the patients examined. The presence of the vanB gene was detected in 21.1% of the patients, but in no case was there any growth of vancomycin-resistant enterococci on the chromogenic medium. CONCLUSIONS: Patients admitted to non-surgical wards were more often colonised with vanA/vanB genes than were patients admitted to surgical wards, but the differences were not statistically significant. |
format | Online Article Text |
id | pubmed-7509899 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Termedia Publishing House |
record_format | MEDLINE/PubMed |
spelling | pubmed-75098992020-09-30 Incidence of genes encoding vanA/vanB vancomycin resistance in rectal swabs of patients with diagnosed cancer, on the day of admission to hospital, in a non-epidemic period Szymankiewicz, Maria Wróblewska, Joanna Nowikiewicz, Tomasz Prz Gastroenterol Original Paper INTRODUCTION: Rapid diagnosis is important for preventing infections due to vancomycin-resistant enterococci. AIM: To evaluate the status of gastrointestinal colonisation with strains containing vanA/vanB genes in oncological patients. MATERIAL AND METHODS: A total of 167 samples of rectal swabs taken from 161 patients (mean age: 63, range: 29–93 years) were examined, including 113 patients from surgical wards (70.2%) and 48 patients from non-surgical wards (29.8%), with diagnosed cancer. The tests were carried out within 24 h of admitting the patient to the department, using the Cepheid Xpert vanA/vanB test, with a CE marked GeneXpert(®) Instrument Systems analyser. Samples with positive vanB gene results were additionally seeded on chromogenic media. RESULTS: The presence of the vanA gene was found in 2.7% and 6.3% of the examined patients, respectively, from the surgical and non-surgical departments, which accounted for 3.7% of all the patients examined. The presence of the vanB gene was detected in 21.1% of the patients, but in no case was there any growth of vancomycin-resistant enterococci on the chromogenic medium. CONCLUSIONS: Patients admitted to non-surgical wards were more often colonised with vanA/vanB genes than were patients admitted to surgical wards, but the differences were not statistically significant. Termedia Publishing House 2020-09-19 2020 /pmc/articles/PMC7509899/ /pubmed/33005267 http://dx.doi.org/10.5114/pg.2020.98537 Text en Copyright © 2020 Termedia http://creativecommons.org/licenses/by-nc-sa/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0). License (http://creativecommons.org/licenses/by-nc-sa/4.0/) |
spellingShingle | Original Paper Szymankiewicz, Maria Wróblewska, Joanna Nowikiewicz, Tomasz Incidence of genes encoding vanA/vanB vancomycin resistance in rectal swabs of patients with diagnosed cancer, on the day of admission to hospital, in a non-epidemic period |
title | Incidence of genes encoding vanA/vanB vancomycin resistance in rectal swabs of patients with diagnosed cancer, on the day of admission to hospital, in a non-epidemic period |
title_full | Incidence of genes encoding vanA/vanB vancomycin resistance in rectal swabs of patients with diagnosed cancer, on the day of admission to hospital, in a non-epidemic period |
title_fullStr | Incidence of genes encoding vanA/vanB vancomycin resistance in rectal swabs of patients with diagnosed cancer, on the day of admission to hospital, in a non-epidemic period |
title_full_unstemmed | Incidence of genes encoding vanA/vanB vancomycin resistance in rectal swabs of patients with diagnosed cancer, on the day of admission to hospital, in a non-epidemic period |
title_short | Incidence of genes encoding vanA/vanB vancomycin resistance in rectal swabs of patients with diagnosed cancer, on the day of admission to hospital, in a non-epidemic period |
title_sort | incidence of genes encoding vana/vanb vancomycin resistance in rectal swabs of patients with diagnosed cancer, on the day of admission to hospital, in a non-epidemic period |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7509899/ https://www.ncbi.nlm.nih.gov/pubmed/33005267 http://dx.doi.org/10.5114/pg.2020.98537 |
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