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Mapping bacterial biofilm on explanted orthopedic hardware: An analysis of 14 consecutive cases

Hardware implanted during primary total joint arthroplasty carries a serious risk for periprosthetic joint infection (PJI). The formation of bacterial biofilms, which are highly tolerant of antibiotics and host immunity, is recognized as being a major barrier to treatment. It is not known whether so...

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Autores principales: BROOKS, JACOB R., CHONKO, DOUGLAS J., PIGOTT, MATTHEW, SULLIVAN, ANNE C., MOORE, KELLY, STOODLEY, PAUL
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10012203/
https://www.ncbi.nlm.nih.gov/pubmed/36656746
http://dx.doi.org/10.1111/apm.13295
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author BROOKS, JACOB R.
CHONKO, DOUGLAS J.
PIGOTT, MATTHEW
SULLIVAN, ANNE C.
MOORE, KELLY
STOODLEY, PAUL
author_facet BROOKS, JACOB R.
CHONKO, DOUGLAS J.
PIGOTT, MATTHEW
SULLIVAN, ANNE C.
MOORE, KELLY
STOODLEY, PAUL
author_sort BROOKS, JACOB R.
collection PubMed
description Hardware implanted during primary total joint arthroplasty carries a serious risk for periprosthetic joint infection (PJI). The formation of bacterial biofilms, which are highly tolerant of antibiotics and host immunity, is recognized as being a major barrier to treatment. It is not known whether some components and their surface features are more prone to biofilm than others. This study attempted to map biofilm on different components and features of orthopedic hardware recovered during revision. Implant surface culture (ISC) was used on 53 components from 14 hip and knee revisions. ISC achieves a thin agar coating over components, followed by incubation and observation for colony outgrowth over 9 days. Recovered organisms were identified by selective culture and 16s rRNA sequencing. Outcomes were compared with clinical culturing and PJI diagnosis based on 2013 Musculoskeletal Infection Society criteria. ISC paralleled clinical culturing with a sensitivity of 100% and a specificity of 57.1%. When compared to Musculoskeletal Infection Society criteria, sensitivity remained at 100% while specificity was 80%. Biofilm accumulation was patchy and heterogeneous throughout different prostheses, though notably the non-articulating surfaces between the tibial tray and polyethylene insert showed consistent growth. On individual components, ridges and edges consistently harbored biofilm, while growth elsewhere was case dependent. ISC successfully identified microbial growth with high sensitivity while also revealing that biofilm growth was commonly localized to particular locations. Understanding where biofilm formation occurs most often on implanted hardware will help guide debridement, retention choices, and implant design.
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spelling pubmed-100122032023-04-01 Mapping bacterial biofilm on explanted orthopedic hardware: An analysis of 14 consecutive cases BROOKS, JACOB R. CHONKO, DOUGLAS J. PIGOTT, MATTHEW SULLIVAN, ANNE C. MOORE, KELLY STOODLEY, PAUL APMIS Article Hardware implanted during primary total joint arthroplasty carries a serious risk for periprosthetic joint infection (PJI). The formation of bacterial biofilms, which are highly tolerant of antibiotics and host immunity, is recognized as being a major barrier to treatment. It is not known whether some components and their surface features are more prone to biofilm than others. This study attempted to map biofilm on different components and features of orthopedic hardware recovered during revision. Implant surface culture (ISC) was used on 53 components from 14 hip and knee revisions. ISC achieves a thin agar coating over components, followed by incubation and observation for colony outgrowth over 9 days. Recovered organisms were identified by selective culture and 16s rRNA sequencing. Outcomes were compared with clinical culturing and PJI diagnosis based on 2013 Musculoskeletal Infection Society criteria. ISC paralleled clinical culturing with a sensitivity of 100% and a specificity of 57.1%. When compared to Musculoskeletal Infection Society criteria, sensitivity remained at 100% while specificity was 80%. Biofilm accumulation was patchy and heterogeneous throughout different prostheses, though notably the non-articulating surfaces between the tibial tray and polyethylene insert showed consistent growth. On individual components, ridges and edges consistently harbored biofilm, while growth elsewhere was case dependent. ISC successfully identified microbial growth with high sensitivity while also revealing that biofilm growth was commonly localized to particular locations. Understanding where biofilm formation occurs most often on implanted hardware will help guide debridement, retention choices, and implant design. 2023-04 2023-02-14 /pmc/articles/PMC10012203/ /pubmed/36656746 http://dx.doi.org/10.1111/apm.13295 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Article
BROOKS, JACOB R.
CHONKO, DOUGLAS J.
PIGOTT, MATTHEW
SULLIVAN, ANNE C.
MOORE, KELLY
STOODLEY, PAUL
Mapping bacterial biofilm on explanted orthopedic hardware: An analysis of 14 consecutive cases
title Mapping bacterial biofilm on explanted orthopedic hardware: An analysis of 14 consecutive cases
title_full Mapping bacterial biofilm on explanted orthopedic hardware: An analysis of 14 consecutive cases
title_fullStr Mapping bacterial biofilm on explanted orthopedic hardware: An analysis of 14 consecutive cases
title_full_unstemmed Mapping bacterial biofilm on explanted orthopedic hardware: An analysis of 14 consecutive cases
title_short Mapping bacterial biofilm on explanted orthopedic hardware: An analysis of 14 consecutive cases
title_sort mapping bacterial biofilm on explanted orthopedic hardware: an analysis of 14 consecutive cases
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10012203/
https://www.ncbi.nlm.nih.gov/pubmed/36656746
http://dx.doi.org/10.1111/apm.13295
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