Cargando…
Chlorhexidine and octenidine susceptibility of bacterial isolates from clinical samples in a three-armed cluster randomised decolonisation trial
BACKGROUND: Routine use of chlorhexidine or octenidine for antiseptic bathing may have unintended consequences. Our analysis aimed to assess the phenotypic susceptibility of bacterial isolates from clinical samples to chlorhexidine and octenidine collected from intensive care units (ICU) that routin...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9749986/ https://www.ncbi.nlm.nih.gov/pubmed/36516147 http://dx.doi.org/10.1371/journal.pone.0278569 |
_version_ | 1784850149472731136 |
---|---|
author | Denkel, Luisa A. Kramer, Tobias S. Schwab, Frank Golembus, Jennifer Wolke, Solvy Gastmeier, Petra Geffers, Christine |
author_facet | Denkel, Luisa A. Kramer, Tobias S. Schwab, Frank Golembus, Jennifer Wolke, Solvy Gastmeier, Petra Geffers, Christine |
author_sort | Denkel, Luisa A. |
collection | PubMed |
description | BACKGROUND: Routine use of chlorhexidine or octenidine for antiseptic bathing may have unintended consequences. Our analysis aimed to assess the phenotypic susceptibility of bacterial isolates from clinical samples to chlorhexidine and octenidine collected from intensive care units (ICU) that routinely used 2% chlorhexidine-impregnated wash cloths or 0.08% octenidine wash mitts (intervention) or water and soap (control) for daily patient care. METHODS: This study was conducted within the context of a three armed cluster-randomised controlled decolonisation trial (Registration number DRKS00010475, registration date August 18, 2016). Bacterial isolates were collected prior to and at the end of a 12-month-intervention period from patients with ≥ 3 days length of stay at an ICU assigned to one of two intervention groups or the control group. Phenotypic susceptibility to chlorhexidine and octenidine was assessed by an accredited contract research laboratory determining minimal inhibitory concentrations (MIC) as percentage of extraction solutions used. MIC were reported as estimated concentrations in μg/ml derived from the chlorhexidine and octenidine extraction solutions. Statistical analyses including generalized estimating equation models were applied. RESULTS: In total, 790 ICU-attributable bacterial isolates from clinical samples (e.g. blood, urine, tracheal aspirate) were eligible for all analyses. Pathogens included were Staphylococcus aureus (n = 155), coagulase-negative staphylococci (CoNS, n = 122), Escherichia coli (n = 227), Klebsiella spp. (n = 150) and Pseudomonas aeruginosa (n = 136). For all species, chlorhexidine and octenidine MIC did not increase from baseline to intervention period in the antiseptic bathing groups. For proportions of bacterial isolates with elevated chlorhexidine / octenidine MIC (≥ species-specific chlorhexidine / octenidine MIC(50)), adjusted incidence rate ratios (aIRR) showed no differences between the intervention groups and the control group (intervention period). CONCLUSION: We found no evidence for reduced phenotypic susceptibilities of bacterial isolates from clinical samples to chlorhexidine or octenidine in ICUs 12 months after implementation of routine antiseptic bathing with the respective substances. |
format | Online Article Text |
id | pubmed-9749986 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-97499862022-12-15 Chlorhexidine and octenidine susceptibility of bacterial isolates from clinical samples in a three-armed cluster randomised decolonisation trial Denkel, Luisa A. Kramer, Tobias S. Schwab, Frank Golembus, Jennifer Wolke, Solvy Gastmeier, Petra Geffers, Christine PLoS One Research Article BACKGROUND: Routine use of chlorhexidine or octenidine for antiseptic bathing may have unintended consequences. Our analysis aimed to assess the phenotypic susceptibility of bacterial isolates from clinical samples to chlorhexidine and octenidine collected from intensive care units (ICU) that routinely used 2% chlorhexidine-impregnated wash cloths or 0.08% octenidine wash mitts (intervention) or water and soap (control) for daily patient care. METHODS: This study was conducted within the context of a three armed cluster-randomised controlled decolonisation trial (Registration number DRKS00010475, registration date August 18, 2016). Bacterial isolates were collected prior to and at the end of a 12-month-intervention period from patients with ≥ 3 days length of stay at an ICU assigned to one of two intervention groups or the control group. Phenotypic susceptibility to chlorhexidine and octenidine was assessed by an accredited contract research laboratory determining minimal inhibitory concentrations (MIC) as percentage of extraction solutions used. MIC were reported as estimated concentrations in μg/ml derived from the chlorhexidine and octenidine extraction solutions. Statistical analyses including generalized estimating equation models were applied. RESULTS: In total, 790 ICU-attributable bacterial isolates from clinical samples (e.g. blood, urine, tracheal aspirate) were eligible for all analyses. Pathogens included were Staphylococcus aureus (n = 155), coagulase-negative staphylococci (CoNS, n = 122), Escherichia coli (n = 227), Klebsiella spp. (n = 150) and Pseudomonas aeruginosa (n = 136). For all species, chlorhexidine and octenidine MIC did not increase from baseline to intervention period in the antiseptic bathing groups. For proportions of bacterial isolates with elevated chlorhexidine / octenidine MIC (≥ species-specific chlorhexidine / octenidine MIC(50)), adjusted incidence rate ratios (aIRR) showed no differences between the intervention groups and the control group (intervention period). CONCLUSION: We found no evidence for reduced phenotypic susceptibilities of bacterial isolates from clinical samples to chlorhexidine or octenidine in ICUs 12 months after implementation of routine antiseptic bathing with the respective substances. Public Library of Science 2022-12-14 /pmc/articles/PMC9749986/ /pubmed/36516147 http://dx.doi.org/10.1371/journal.pone.0278569 Text en © 2022 Denkel et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Denkel, Luisa A. Kramer, Tobias S. Schwab, Frank Golembus, Jennifer Wolke, Solvy Gastmeier, Petra Geffers, Christine Chlorhexidine and octenidine susceptibility of bacterial isolates from clinical samples in a three-armed cluster randomised decolonisation trial |
title | Chlorhexidine and octenidine susceptibility of bacterial isolates from clinical samples in a three-armed cluster randomised decolonisation trial |
title_full | Chlorhexidine and octenidine susceptibility of bacterial isolates from clinical samples in a three-armed cluster randomised decolonisation trial |
title_fullStr | Chlorhexidine and octenidine susceptibility of bacterial isolates from clinical samples in a three-armed cluster randomised decolonisation trial |
title_full_unstemmed | Chlorhexidine and octenidine susceptibility of bacterial isolates from clinical samples in a three-armed cluster randomised decolonisation trial |
title_short | Chlorhexidine and octenidine susceptibility of bacterial isolates from clinical samples in a three-armed cluster randomised decolonisation trial |
title_sort | chlorhexidine and octenidine susceptibility of bacterial isolates from clinical samples in a three-armed cluster randomised decolonisation trial |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9749986/ https://www.ncbi.nlm.nih.gov/pubmed/36516147 http://dx.doi.org/10.1371/journal.pone.0278569 |
work_keys_str_mv | AT denkelluisaa chlorhexidineandoctenidinesusceptibilityofbacterialisolatesfromclinicalsamplesinathreearmedclusterrandomiseddecolonisationtrial AT kramertobiass chlorhexidineandoctenidinesusceptibilityofbacterialisolatesfromclinicalsamplesinathreearmedclusterrandomiseddecolonisationtrial AT schwabfrank chlorhexidineandoctenidinesusceptibilityofbacterialisolatesfromclinicalsamplesinathreearmedclusterrandomiseddecolonisationtrial AT golembusjennifer chlorhexidineandoctenidinesusceptibilityofbacterialisolatesfromclinicalsamplesinathreearmedclusterrandomiseddecolonisationtrial AT wolkesolvy chlorhexidineandoctenidinesusceptibilityofbacterialisolatesfromclinicalsamplesinathreearmedclusterrandomiseddecolonisationtrial AT gastmeierpetra chlorhexidineandoctenidinesusceptibilityofbacterialisolatesfromclinicalsamplesinathreearmedclusterrandomiseddecolonisationtrial AT gefferschristine chlorhexidineandoctenidinesusceptibilityofbacterialisolatesfromclinicalsamplesinathreearmedclusterrandomiseddecolonisationtrial |