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Detection of bacteria with molecular methods in prosthetic joint infection: sonication fluid better than periprosthetic tissue

BACKGROUND AND PURPOSE: The correct diagnosis of prosthetic joint infection (PJI) can be difficult because bacteria form a biofilm on the surface of the implant. The sensitivity of culture from sonication fluid is better than that from periprosthetic tissue, but no comparison studies using molecular...

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Autores principales: Rak, Mitja, KavčIč, Martina, Trebše, Rihard, CőR, Andrej
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4967274/
https://www.ncbi.nlm.nih.gov/pubmed/27123818
http://dx.doi.org/10.3109/17453674.2016.1165558
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author Rak, Mitja
KavčIč, Martina
Trebše, Rihard
CőR, Andrej
author_facet Rak, Mitja
KavčIč, Martina
Trebše, Rihard
CőR, Andrej
author_sort Rak, Mitja
collection PubMed
description BACKGROUND AND PURPOSE: The correct diagnosis of prosthetic joint infection (PJI) can be difficult because bacteria form a biofilm on the surface of the implant. The sensitivity of culture from sonication fluid is better than that from periprosthetic tissue, but no comparison studies using molecular methods on a large scale have been performed. We assessed whether periprosthetic tissue or sonication fluid should be used for molecular analysis. PATIENTS AND METHODS: Implant and tissue samples were retrieved from 87 patients who underwent revision operation of total knee or total hip arthroplasty. Both sample types were analyzed using broad-range (BR-) PCR targeting the 16S rRNA gene. The results were evaluated based on the definition of periprosthetic joint infection from the Workgroup of the Musculoskeletal Infection Society. RESULTS: PJI was diagnosed in 29 patients, whereas aseptic failure was diagnosed in 58 patients. Analysis of sonication fluid using BR-PCR detected bacteria in 27 patients, whereas analysis of periprosthetic tissue by BR-PCR detected bacteria in 22 patients. In 6 of 7 patients in whom BR-PCR analysis of periprosthetic tissue was negative, low-virulence bacteria were present. The sensitivity and specificity values for periprosthetic tissue were 76% and 93%, respectively, and the sensitivity and specificity values for sonication fluid were 95% and 97%. INTERPRETATION: Our results suggest that sonication fluid may be a more appropriate sample than periprosthetic tissue for BR-PCR analysis in patients with PJI. However, further investigation is required to improve detection of bacteria in patients with so-called aseptic failure.
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spelling pubmed-49672742017-01-11 Detection of bacteria with molecular methods in prosthetic joint infection: sonication fluid better than periprosthetic tissue Rak, Mitja KavčIč, Martina Trebše, Rihard CőR, Andrej Acta Orthop Articles BACKGROUND AND PURPOSE: The correct diagnosis of prosthetic joint infection (PJI) can be difficult because bacteria form a biofilm on the surface of the implant. The sensitivity of culture from sonication fluid is better than that from periprosthetic tissue, but no comparison studies using molecular methods on a large scale have been performed. We assessed whether periprosthetic tissue or sonication fluid should be used for molecular analysis. PATIENTS AND METHODS: Implant and tissue samples were retrieved from 87 patients who underwent revision operation of total knee or total hip arthroplasty. Both sample types were analyzed using broad-range (BR-) PCR targeting the 16S rRNA gene. The results were evaluated based on the definition of periprosthetic joint infection from the Workgroup of the Musculoskeletal Infection Society. RESULTS: PJI was diagnosed in 29 patients, whereas aseptic failure was diagnosed in 58 patients. Analysis of sonication fluid using BR-PCR detected bacteria in 27 patients, whereas analysis of periprosthetic tissue by BR-PCR detected bacteria in 22 patients. In 6 of 7 patients in whom BR-PCR analysis of periprosthetic tissue was negative, low-virulence bacteria were present. The sensitivity and specificity values for periprosthetic tissue were 76% and 93%, respectively, and the sensitivity and specificity values for sonication fluid were 95% and 97%. INTERPRETATION: Our results suggest that sonication fluid may be a more appropriate sample than periprosthetic tissue for BR-PCR analysis in patients with PJI. However, further investigation is required to improve detection of bacteria in patients with so-called aseptic failure. Taylor & Francis 2016-08 2016-04-28 /pmc/articles/PMC4967274/ /pubmed/27123818 http://dx.doi.org/10.3109/17453674.2016.1165558 Text en © 2016 The Author(s). Published by Taylor & Francis on behalf of the Nordic Orthopedic Federation. https://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution-Non-Commercial License (https://creativecommons.org/licenses/by-nc/3.0)
spellingShingle Articles
Rak, Mitja
KavčIč, Martina
Trebše, Rihard
CőR, Andrej
Detection of bacteria with molecular methods in prosthetic joint infection: sonication fluid better than periprosthetic tissue
title Detection of bacteria with molecular methods in prosthetic joint infection: sonication fluid better than periprosthetic tissue
title_full Detection of bacteria with molecular methods in prosthetic joint infection: sonication fluid better than periprosthetic tissue
title_fullStr Detection of bacteria with molecular methods in prosthetic joint infection: sonication fluid better than periprosthetic tissue
title_full_unstemmed Detection of bacteria with molecular methods in prosthetic joint infection: sonication fluid better than periprosthetic tissue
title_short Detection of bacteria with molecular methods in prosthetic joint infection: sonication fluid better than periprosthetic tissue
title_sort detection of bacteria with molecular methods in prosthetic joint infection: sonication fluid better than periprosthetic tissue
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4967274/
https://www.ncbi.nlm.nih.gov/pubmed/27123818
http://dx.doi.org/10.3109/17453674.2016.1165558
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