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Microbial Persistence, Replacement and Local Antimicrobial Therapy in Recurrent Bone and Joint Infection

We report microbiological results from a cohort of recurrent bone and joint infection to define the contributions of microbial persistence or replacement. We also investigated for any association between local antibiotic treatment and emerging antimicrobial resistance. Microbiological cultures and a...

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Autores principales: Young, Bernadette C., Dudareva, Maria, Vicentine, Margarete P., Hotchen, Andrew J., Ferguson, Jamie, McNally, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10135193/
https://www.ncbi.nlm.nih.gov/pubmed/37107070
http://dx.doi.org/10.3390/antibiotics12040708
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author Young, Bernadette C.
Dudareva, Maria
Vicentine, Margarete P.
Hotchen, Andrew J.
Ferguson, Jamie
McNally, Martin
author_facet Young, Bernadette C.
Dudareva, Maria
Vicentine, Margarete P.
Hotchen, Andrew J.
Ferguson, Jamie
McNally, Martin
author_sort Young, Bernadette C.
collection PubMed
description We report microbiological results from a cohort of recurrent bone and joint infection to define the contributions of microbial persistence or replacement. We also investigated for any association between local antibiotic treatment and emerging antimicrobial resistance. Microbiological cultures and antibiotic treatments were reviewed for 125 individuals with recurrent infection (prosthetic joint infection, fracture-related infection, and osteomyelitis) at two UK centres between 2007 and 2021. At re-operation, 48/125 (38.4%) individuals had an organism from the same bacterial species as at their initial operation for infection. In 49/125 (39.2%), only new species were isolated in culture. In 28/125 (22.4%), re-operative cultures were negative. The most commonly persistent species were Staphylococcus aureus (46.3%), coagulase-negative Staphylococci (50.0%), and Pseudomonas aeruginosa (50.0%). Gentamicin non-susceptible organisms were common, identified at index procedure in 51/125 (40.8%) and at re-operation in 40/125 (32%). Gentamicin non-susceptibility at re-operation was not associated with previous local aminoglycoside treatment (21/71 (29.8%) vs. 19/54 (35.2%); p = 0.6). Emergence of new aminoglycoside resistance at recurrence was uncommon and did not differ significantly between those with and without local aminoglycoside treatment (3/71 (4.2%) vs. 4/54 (7.4%); p = 0.7). Culture-based diagnostics identified microbial persistence and replacement at similar rates in patients who re-presented with infection. Treatment for orthopaedic infection with local antibiotics was not associated with the emergence of specific antimicrobial resistance.
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spelling pubmed-101351932023-04-28 Microbial Persistence, Replacement and Local Antimicrobial Therapy in Recurrent Bone and Joint Infection Young, Bernadette C. Dudareva, Maria Vicentine, Margarete P. Hotchen, Andrew J. Ferguson, Jamie McNally, Martin Antibiotics (Basel) Article We report microbiological results from a cohort of recurrent bone and joint infection to define the contributions of microbial persistence or replacement. We also investigated for any association between local antibiotic treatment and emerging antimicrobial resistance. Microbiological cultures and antibiotic treatments were reviewed for 125 individuals with recurrent infection (prosthetic joint infection, fracture-related infection, and osteomyelitis) at two UK centres between 2007 and 2021. At re-operation, 48/125 (38.4%) individuals had an organism from the same bacterial species as at their initial operation for infection. In 49/125 (39.2%), only new species were isolated in culture. In 28/125 (22.4%), re-operative cultures were negative. The most commonly persistent species were Staphylococcus aureus (46.3%), coagulase-negative Staphylococci (50.0%), and Pseudomonas aeruginosa (50.0%). Gentamicin non-susceptible organisms were common, identified at index procedure in 51/125 (40.8%) and at re-operation in 40/125 (32%). Gentamicin non-susceptibility at re-operation was not associated with previous local aminoglycoside treatment (21/71 (29.8%) vs. 19/54 (35.2%); p = 0.6). Emergence of new aminoglycoside resistance at recurrence was uncommon and did not differ significantly between those with and without local aminoglycoside treatment (3/71 (4.2%) vs. 4/54 (7.4%); p = 0.7). Culture-based diagnostics identified microbial persistence and replacement at similar rates in patients who re-presented with infection. Treatment for orthopaedic infection with local antibiotics was not associated with the emergence of specific antimicrobial resistance. MDPI 2023-04-05 /pmc/articles/PMC10135193/ /pubmed/37107070 http://dx.doi.org/10.3390/antibiotics12040708 Text en © 2023 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
Young, Bernadette C.
Dudareva, Maria
Vicentine, Margarete P.
Hotchen, Andrew J.
Ferguson, Jamie
McNally, Martin
Microbial Persistence, Replacement and Local Antimicrobial Therapy in Recurrent Bone and Joint Infection
title Microbial Persistence, Replacement and Local Antimicrobial Therapy in Recurrent Bone and Joint Infection
title_full Microbial Persistence, Replacement and Local Antimicrobial Therapy in Recurrent Bone and Joint Infection
title_fullStr Microbial Persistence, Replacement and Local Antimicrobial Therapy in Recurrent Bone and Joint Infection
title_full_unstemmed Microbial Persistence, Replacement and Local Antimicrobial Therapy in Recurrent Bone and Joint Infection
title_short Microbial Persistence, Replacement and Local Antimicrobial Therapy in Recurrent Bone and Joint Infection
title_sort microbial persistence, replacement and local antimicrobial therapy in recurrent bone and joint infection
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10135193/
https://www.ncbi.nlm.nih.gov/pubmed/37107070
http://dx.doi.org/10.3390/antibiotics12040708
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