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A Porcine Model for the Development and Testing of Preoperative Skin Preparations
Clinical preoperative skin preparations (PSPs) do not eradicate skin flora dwelling in the deepest dermal regions. Survivors constitute a persistent infection risk. In search of solutions, we created a porcine model intended for PSP developmental testing. This model employed microbiological techniqu...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9146673/ https://www.ncbi.nlm.nih.gov/pubmed/35630283 http://dx.doi.org/10.3390/microorganisms10050837 |
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author | Duffy, Hannah R. Godfrey, Rose W. Williams, Dustin L. Ashton, Nicholas N. |
author_facet | Duffy, Hannah R. Godfrey, Rose W. Williams, Dustin L. Ashton, Nicholas N. |
author_sort | Duffy, Hannah R. |
collection | PubMed |
description | Clinical preoperative skin preparations (PSPs) do not eradicate skin flora dwelling in the deepest dermal regions. Survivors constitute a persistent infection risk. In search of solutions, we created a porcine model intended for PSP developmental testing. This model employed microbiological techniques sensitive to the deep-dwelling microbial flora as these microorganisms are frequently overlooked when using institutionally-entrenched testing methodologies. Clinical gold-standard PSPs were assessed. Ten Yorkshire pigs were divided into two groups: prepared with either povidone iodine (PVP-I) or chlorhexidine gluconate (CHG) PSP. Bioburdens were calculated on square, 4 cm by 4 cm, full-thickness skin samples homogenized in neutralizing media. Endogenous bioburden of porcine skin (3.3 log(10) CFU/cm(2)) was consistent with natural flora numbers in dry human skin. On-label PSP scrub kits with PVP-I (n = 39) or CHG (n = 40) failed the 2–3 log(10)-reduction criteria established for PSPs by the Food and Drug Administration (FDA), resulting in a 1.46 log(10) and 0.58 log(10) reduction, respectively. Porcine dermal microbiota mirrored that of humans, displaying abundant staphylococcal species. Likewise, histological sections showed similarity in hair follicle depths and sebaceous glands (3.2 ± 0.7 mm). These shared characteristics and the considerable fraction of bacteria which survived clinical PSPs make this model useful for developmental work. |
format | Online Article Text |
id | pubmed-9146673 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-91466732022-05-29 A Porcine Model for the Development and Testing of Preoperative Skin Preparations Duffy, Hannah R. Godfrey, Rose W. Williams, Dustin L. Ashton, Nicholas N. Microorganisms Article Clinical preoperative skin preparations (PSPs) do not eradicate skin flora dwelling in the deepest dermal regions. Survivors constitute a persistent infection risk. In search of solutions, we created a porcine model intended for PSP developmental testing. This model employed microbiological techniques sensitive to the deep-dwelling microbial flora as these microorganisms are frequently overlooked when using institutionally-entrenched testing methodologies. Clinical gold-standard PSPs were assessed. Ten Yorkshire pigs were divided into two groups: prepared with either povidone iodine (PVP-I) or chlorhexidine gluconate (CHG) PSP. Bioburdens were calculated on square, 4 cm by 4 cm, full-thickness skin samples homogenized in neutralizing media. Endogenous bioburden of porcine skin (3.3 log(10) CFU/cm(2)) was consistent with natural flora numbers in dry human skin. On-label PSP scrub kits with PVP-I (n = 39) or CHG (n = 40) failed the 2–3 log(10)-reduction criteria established for PSPs by the Food and Drug Administration (FDA), resulting in a 1.46 log(10) and 0.58 log(10) reduction, respectively. Porcine dermal microbiota mirrored that of humans, displaying abundant staphylococcal species. Likewise, histological sections showed similarity in hair follicle depths and sebaceous glands (3.2 ± 0.7 mm). These shared characteristics and the considerable fraction of bacteria which survived clinical PSPs make this model useful for developmental work. MDPI 2022-04-19 /pmc/articles/PMC9146673/ /pubmed/35630283 http://dx.doi.org/10.3390/microorganisms10050837 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Duffy, Hannah R. Godfrey, Rose W. Williams, Dustin L. Ashton, Nicholas N. A Porcine Model for the Development and Testing of Preoperative Skin Preparations |
title | A Porcine Model for the Development and Testing of Preoperative Skin Preparations |
title_full | A Porcine Model for the Development and Testing of Preoperative Skin Preparations |
title_fullStr | A Porcine Model for the Development and Testing of Preoperative Skin Preparations |
title_full_unstemmed | A Porcine Model for the Development and Testing of Preoperative Skin Preparations |
title_short | A Porcine Model for the Development and Testing of Preoperative Skin Preparations |
title_sort | porcine model for the development and testing of preoperative skin preparations |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9146673/ https://www.ncbi.nlm.nih.gov/pubmed/35630283 http://dx.doi.org/10.3390/microorganisms10050837 |
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