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Detection of AmpC β-lactamase producing bacteria isolated in neonatal sepsis

OBJECTIVE: The objective of this study was to determine the occurrence and antimicrobial profile of AmpC β-lactamase producing bacteria. METHODS: The study was conducted at The Children’s Hospital and The Institute of Child Health Lahore, Pakistan, during September 2011 to June 2012. A total number...

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Autores principales: Salamat, Sonia, Ejaz, Hasan, Zafar, Aizza, Javed, Humera
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Professional Medical Publications 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5216311/
https://www.ncbi.nlm.nih.gov/pubmed/28083055
http://dx.doi.org/10.12669/pjms.326.10861
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author Salamat, Sonia
Ejaz, Hasan
Zafar, Aizza
Javed, Humera
author_facet Salamat, Sonia
Ejaz, Hasan
Zafar, Aizza
Javed, Humera
author_sort Salamat, Sonia
collection PubMed
description OBJECTIVE: The objective of this study was to determine the occurrence and antimicrobial profile of AmpC β-lactamase producing bacteria. METHODS: The study was conducted at The Children’s Hospital and The Institute of Child Health Lahore, Pakistan, during September 2011 to June 2012. A total number of 1,914 blood samples of suspected neonatal septicemia were processed. Isolates were identified using Gram’s staining, API 20E and API 20NE tests. Gram negative isolates were screened for AmpC β-lactamase production against ceftazidime, cefotaxime and cefoxitin resistance and confirmed by inhibitor based method. RESULTS: Total number of 54 (8.49%) Gram positive and 582 (91.5%) Gram negative bacteria were identified. Among Gram negative isolates 141 (22%) were AmpC producers and found to be 100% resistant to co-amoxiclav, cefoxitin, ceftazidime, cefotaxime, cefuroxime, cefixime, ceftriaxone, cefpodoxime, gentamicin, amikacin and aztreonam. Less resistance was observed against cefepime (30.4%), sulbactam-cefoperazone (24.8%), piperacillin-tazobactam (10.6%), ciprofloxacin (20.5%) and meropenem (2.1%). All the isolates were found sensitive to imipenem. The patients harbored AmpC β-lactamases were on various interventions in which intravenous line was noted among (51.1%), naso-gastric tube (37.6%), ambu bag (8.5%), endotracheal tube (3.5%), ventilator (2.1%) and surgery (0.7%). CONCLUSION: Extensive use of invasive procedures and third generation cephalosporins should be restricted to avoid the emergence of AmpC beta-lactamases in neonates.
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spelling pubmed-52163112017-01-12 Detection of AmpC β-lactamase producing bacteria isolated in neonatal sepsis Salamat, Sonia Ejaz, Hasan Zafar, Aizza Javed, Humera Pak J Med Sci Original Article OBJECTIVE: The objective of this study was to determine the occurrence and antimicrobial profile of AmpC β-lactamase producing bacteria. METHODS: The study was conducted at The Children’s Hospital and The Institute of Child Health Lahore, Pakistan, during September 2011 to June 2012. A total number of 1,914 blood samples of suspected neonatal septicemia were processed. Isolates were identified using Gram’s staining, API 20E and API 20NE tests. Gram negative isolates were screened for AmpC β-lactamase production against ceftazidime, cefotaxime and cefoxitin resistance and confirmed by inhibitor based method. RESULTS: Total number of 54 (8.49%) Gram positive and 582 (91.5%) Gram negative bacteria were identified. Among Gram negative isolates 141 (22%) were AmpC producers and found to be 100% resistant to co-amoxiclav, cefoxitin, ceftazidime, cefotaxime, cefuroxime, cefixime, ceftriaxone, cefpodoxime, gentamicin, amikacin and aztreonam. Less resistance was observed against cefepime (30.4%), sulbactam-cefoperazone (24.8%), piperacillin-tazobactam (10.6%), ciprofloxacin (20.5%) and meropenem (2.1%). All the isolates were found sensitive to imipenem. The patients harbored AmpC β-lactamases were on various interventions in which intravenous line was noted among (51.1%), naso-gastric tube (37.6%), ambu bag (8.5%), endotracheal tube (3.5%), ventilator (2.1%) and surgery (0.7%). CONCLUSION: Extensive use of invasive procedures and third generation cephalosporins should be restricted to avoid the emergence of AmpC beta-lactamases in neonates. Professional Medical Publications 2016 /pmc/articles/PMC5216311/ /pubmed/28083055 http://dx.doi.org/10.12669/pjms.326.10861 Text en Copyright: © Pakistan Journal of Medical Sciences http://creativecommons.org/licenses/by/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Salamat, Sonia
Ejaz, Hasan
Zafar, Aizza
Javed, Humera
Detection of AmpC β-lactamase producing bacteria isolated in neonatal sepsis
title Detection of AmpC β-lactamase producing bacteria isolated in neonatal sepsis
title_full Detection of AmpC β-lactamase producing bacteria isolated in neonatal sepsis
title_fullStr Detection of AmpC β-lactamase producing bacteria isolated in neonatal sepsis
title_full_unstemmed Detection of AmpC β-lactamase producing bacteria isolated in neonatal sepsis
title_short Detection of AmpC β-lactamase producing bacteria isolated in neonatal sepsis
title_sort detection of ampc β-lactamase producing bacteria isolated in neonatal sepsis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5216311/
https://www.ncbi.nlm.nih.gov/pubmed/28083055
http://dx.doi.org/10.12669/pjms.326.10861
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