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Tissue adhesives for bacterial inhibition in extracorporeal membrane oxygenation cannulae

BACKGROUND: One of the most serious complications of extracorporeal membrane oxygenation (ECMO) therapy is ECMO cannulae infection, which can occur at quadruple the rate of central venous catheter infections, and significantly impact morbidity and paediatric mortality. The objective of this in vitro...

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Detalles Bibliográficos
Autores principales: Pearse, India, Corley, Amanda, Qu, Yue, Fraser, John
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8107059/
https://www.ncbi.nlm.nih.gov/pubmed/33969444
http://dx.doi.org/10.1186/s40635-021-00388-6
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author Pearse, India
Corley, Amanda
Qu, Yue
Fraser, John
author_facet Pearse, India
Corley, Amanda
Qu, Yue
Fraser, John
author_sort Pearse, India
collection PubMed
description BACKGROUND: One of the most serious complications of extracorporeal membrane oxygenation (ECMO) therapy is ECMO cannulae infection, which can occur at quadruple the rate of central venous catheter infections, and significantly impact morbidity and paediatric mortality. The objective of this in vitro observational study was to assess antimicrobial properties of two n-butyl-2-octyl cyanoacrylate tissue adhesive (TA) formulations for bacterial inhibition at peripheral ECMO cannulae insertion sites. METHODS: Antimicrobial properties were assessed using modified agar disk-diffusion (n = 3) and simulated agar cannulation insertion site (n = 20) models. Both assays used Staphylococcus epidermidis which was seeded at the edge of the TA or dressing. Microorganism inhibition was visually inspected and evidenced by the presence or absence of a TA bacterial inhibition zone at 24 and 72 h. RESULTS: Both TAs provided effective barriers to bacterial migration under cannula dressings, to cannula insertion sites and down cannula tunnels. Additionally, both TAs demonstrated distinct zones of inhibition produced when left to polymerise onto agar plates seeded with S. epidermidis. CONCLUSIONS: N-Butyl-2-octyl cyanoacrylate TA appears to inhibit bacterial growth and migration of S. epidermidis. Application of TA to cannulae insertion sites may therefore be a potential bedside strategy for infection prevention in ECMO cannulae, but requires further testing before being used clinically for this purpose.
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spelling pubmed-81070592021-05-10 Tissue adhesives for bacterial inhibition in extracorporeal membrane oxygenation cannulae Pearse, India Corley, Amanda Qu, Yue Fraser, John Intensive Care Med Exp Research Articles BACKGROUND: One of the most serious complications of extracorporeal membrane oxygenation (ECMO) therapy is ECMO cannulae infection, which can occur at quadruple the rate of central venous catheter infections, and significantly impact morbidity and paediatric mortality. The objective of this in vitro observational study was to assess antimicrobial properties of two n-butyl-2-octyl cyanoacrylate tissue adhesive (TA) formulations for bacterial inhibition at peripheral ECMO cannulae insertion sites. METHODS: Antimicrobial properties were assessed using modified agar disk-diffusion (n = 3) and simulated agar cannulation insertion site (n = 20) models. Both assays used Staphylococcus epidermidis which was seeded at the edge of the TA or dressing. Microorganism inhibition was visually inspected and evidenced by the presence or absence of a TA bacterial inhibition zone at 24 and 72 h. RESULTS: Both TAs provided effective barriers to bacterial migration under cannula dressings, to cannula insertion sites and down cannula tunnels. Additionally, both TAs demonstrated distinct zones of inhibition produced when left to polymerise onto agar plates seeded with S. epidermidis. CONCLUSIONS: N-Butyl-2-octyl cyanoacrylate TA appears to inhibit bacterial growth and migration of S. epidermidis. Application of TA to cannulae insertion sites may therefore be a potential bedside strategy for infection prevention in ECMO cannulae, but requires further testing before being used clinically for this purpose. Springer International Publishing 2021-05-10 /pmc/articles/PMC8107059/ /pubmed/33969444 http://dx.doi.org/10.1186/s40635-021-00388-6 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Articles
Pearse, India
Corley, Amanda
Qu, Yue
Fraser, John
Tissue adhesives for bacterial inhibition in extracorporeal membrane oxygenation cannulae
title Tissue adhesives for bacterial inhibition in extracorporeal membrane oxygenation cannulae
title_full Tissue adhesives for bacterial inhibition in extracorporeal membrane oxygenation cannulae
title_fullStr Tissue adhesives for bacterial inhibition in extracorporeal membrane oxygenation cannulae
title_full_unstemmed Tissue adhesives for bacterial inhibition in extracorporeal membrane oxygenation cannulae
title_short Tissue adhesives for bacterial inhibition in extracorporeal membrane oxygenation cannulae
title_sort tissue adhesives for bacterial inhibition in extracorporeal membrane oxygenation cannulae
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8107059/
https://www.ncbi.nlm.nih.gov/pubmed/33969444
http://dx.doi.org/10.1186/s40635-021-00388-6
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