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Use of fluorescence imaging to optimize location of tissue sampling in hard-to-heal wounds

INTRODUCTION: Wound microflora in hard-to-heal wounds is invariably complex and diverse. Determining the interfering organisms(s) is therefore challenging. Tissue sampling, particularly in large wounds, is subjective and, when performed, might involve swabbing or biopsy of several locations. Fluores...

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Autores principales: Serena, Thomas E., Snyder, Robert J., Bowler, Philip G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9878329/
https://www.ncbi.nlm.nih.gov/pubmed/36710976
http://dx.doi.org/10.3389/fcimb.2022.1070311
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author Serena, Thomas E.
Snyder, Robert J.
Bowler, Philip G.
author_facet Serena, Thomas E.
Snyder, Robert J.
Bowler, Philip G.
author_sort Serena, Thomas E.
collection PubMed
description INTRODUCTION: Wound microflora in hard-to-heal wounds is invariably complex and diverse. Determining the interfering organisms(s) is therefore challenging. Tissue sampling, particularly in large wounds, is subjective and, when performed, might involve swabbing or biopsy of several locations. Fluorescence (FL) imaging of bacterial loads is a rapid, non-invasive method to objectively locate microbial hotspots (loads >10(4) CFU/gr). When sampling is deemed clinically necessary, imaging may indicate an optimal site for tissue biopsy. This study aimed to investigate the microbiology of wound tissue incisional biopsies taken from sites identified by FL imaging compared with sites selected by clinical judgment. METHODS: A post hoc analysis of the 350-patient FLAAG wound trial was conducted; 78 wounds were included in the present study. All 78 wounds were biopsied at two sites: one at the center of the wound per standard of care (SoC) and one site guided by FL-imaging findings, allowing for comparison of total bacterial load (TBL) and species present. RESULTS: The comparison between the two biopsy sites revealed that clinical uncertainty was higher as wound surface area increased. The sensitivity of a FL-informed biopsy was 98.7% for accurately finding any bacterial loads >10(4) CFU/g, compared to 87.2% for SoC (p=0.0059; McNemar test). Regarding species detected, FL-informed biopsies detected an average of 3 bacterial species per biopsy versus 2.2 species with SoC (p < 0.001; t-test). Microbial hotspots with a higher number of pathogens also included the CDC’s pathogens of interest. CONCLUSIONS & PERSPECTIVE: FL imaging provides a more accurate and relevant microbiological profile that guides optimal wound sampling compared to clinical judgment. This is particularly interesting in large, complex wounds, as evidenced in the wounds studied in this post hoc analysis. In addition, fluorescence imaging enables earlier bacterial detection and intervention, guiding early and appropriate wound hygiene and potentially reducing the need for antibiotic use. When indicated, this diagnostic partnership with antibiotic stewardship initiatives is key to ameliorating the continuing threat of antibiotic resistance.
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spelling pubmed-98783292023-01-27 Use of fluorescence imaging to optimize location of tissue sampling in hard-to-heal wounds Serena, Thomas E. Snyder, Robert J. Bowler, Philip G. Front Cell Infect Microbiol Cellular and Infection Microbiology INTRODUCTION: Wound microflora in hard-to-heal wounds is invariably complex and diverse. Determining the interfering organisms(s) is therefore challenging. Tissue sampling, particularly in large wounds, is subjective and, when performed, might involve swabbing or biopsy of several locations. Fluorescence (FL) imaging of bacterial loads is a rapid, non-invasive method to objectively locate microbial hotspots (loads >10(4) CFU/gr). When sampling is deemed clinically necessary, imaging may indicate an optimal site for tissue biopsy. This study aimed to investigate the microbiology of wound tissue incisional biopsies taken from sites identified by FL imaging compared with sites selected by clinical judgment. METHODS: A post hoc analysis of the 350-patient FLAAG wound trial was conducted; 78 wounds were included in the present study. All 78 wounds were biopsied at two sites: one at the center of the wound per standard of care (SoC) and one site guided by FL-imaging findings, allowing for comparison of total bacterial load (TBL) and species present. RESULTS: The comparison between the two biopsy sites revealed that clinical uncertainty was higher as wound surface area increased. The sensitivity of a FL-informed biopsy was 98.7% for accurately finding any bacterial loads >10(4) CFU/g, compared to 87.2% for SoC (p=0.0059; McNemar test). Regarding species detected, FL-informed biopsies detected an average of 3 bacterial species per biopsy versus 2.2 species with SoC (p < 0.001; t-test). Microbial hotspots with a higher number of pathogens also included the CDC’s pathogens of interest. CONCLUSIONS & PERSPECTIVE: FL imaging provides a more accurate and relevant microbiological profile that guides optimal wound sampling compared to clinical judgment. This is particularly interesting in large, complex wounds, as evidenced in the wounds studied in this post hoc analysis. In addition, fluorescence imaging enables earlier bacterial detection and intervention, guiding early and appropriate wound hygiene and potentially reducing the need for antibiotic use. When indicated, this diagnostic partnership with antibiotic stewardship initiatives is key to ameliorating the continuing threat of antibiotic resistance. Frontiers Media S.A. 2023-01-12 /pmc/articles/PMC9878329/ /pubmed/36710976 http://dx.doi.org/10.3389/fcimb.2022.1070311 Text en Copyright © 2023 Serena, Snyder and Bowler https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cellular and Infection Microbiology
Serena, Thomas E.
Snyder, Robert J.
Bowler, Philip G.
Use of fluorescence imaging to optimize location of tissue sampling in hard-to-heal wounds
title Use of fluorescence imaging to optimize location of tissue sampling in hard-to-heal wounds
title_full Use of fluorescence imaging to optimize location of tissue sampling in hard-to-heal wounds
title_fullStr Use of fluorescence imaging to optimize location of tissue sampling in hard-to-heal wounds
title_full_unstemmed Use of fluorescence imaging to optimize location of tissue sampling in hard-to-heal wounds
title_short Use of fluorescence imaging to optimize location of tissue sampling in hard-to-heal wounds
title_sort use of fluorescence imaging to optimize location of tissue sampling in hard-to-heal wounds
topic Cellular and Infection Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9878329/
https://www.ncbi.nlm.nih.gov/pubmed/36710976
http://dx.doi.org/10.3389/fcimb.2022.1070311
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