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Establishment of a reliable in-vivo model of implant-associated infection to investigate innovative treatment options

The increasing number of implant-associated infections and of multiresistant pathogens is a major problem in the daily routine. In the field of osteomyelitis, it is difficult to manage a valid clinical study because of multiple influencing factors. Therefore, models of osteomyelitis with a simulatio...

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Autores principales: Kreis, C., Aschenbrenner, F. K., Günther, D., Tholema-Hans, N., Koeppe, J., Rosslenbroich, S. B., Raschke, M. J., Fuchs, T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8913616/
https://www.ncbi.nlm.nih.gov/pubmed/35273202
http://dx.doi.org/10.1038/s41598-022-07673-8
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author Kreis, C.
Aschenbrenner, F. K.
Günther, D.
Tholema-Hans, N.
Koeppe, J.
Rosslenbroich, S. B.
Raschke, M. J.
Fuchs, T.
author_facet Kreis, C.
Aschenbrenner, F. K.
Günther, D.
Tholema-Hans, N.
Koeppe, J.
Rosslenbroich, S. B.
Raschke, M. J.
Fuchs, T.
author_sort Kreis, C.
collection PubMed
description The increasing number of implant-associated infections and of multiresistant pathogens is a major problem in the daily routine. In the field of osteomyelitis, it is difficult to manage a valid clinical study because of multiple influencing factors. Therefore, models of osteomyelitis with a simulation of the pathophysiology to evaluate treatment options for implant-associated infections are necessary. The aim of this study is to develop a standardized and reproducible osteomyelitis model in-vivo to improve treatment options. This study analyses the influence of a post-infectious implant exchange one week after infection and the infection progress afterward in combination with a systemic versus a local antibiotic treatment in-vivo. Therefore, the implant exchange, the exchange to a local drug-delivery system with gentamicin, and the implant removal are examined. Furthermore, the influence of an additional systemic antibiotic therapy is evaluated. An in-vivo model concerning the implant exchange is established that analyzes clinic, radiologic, microbiologic, histologic, and immunohistochemical diagnostics to obtain detailed evaluation and clinical reproducibility. Our study shows a clear advantage of the combined local and systemic antibiotic treatment in contrast to the implant removal and to a non-combined antibiotic therapy. Group genta/syst. showed the lowest infection rate with a percentage of 62.5% concerning microbiologic analysis, which is in accordance with the immunohistochemical, cytochemical, histologic, and radiologic analysis. Our in-vivo rat model has shown valid and reproducible results, which will lead to further investigations regarding treatment options and influencing factors concerning the therapy of osteomyelitis and implant-associated infections.
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spelling pubmed-89136162022-03-11 Establishment of a reliable in-vivo model of implant-associated infection to investigate innovative treatment options Kreis, C. Aschenbrenner, F. K. Günther, D. Tholema-Hans, N. Koeppe, J. Rosslenbroich, S. B. Raschke, M. J. Fuchs, T. Sci Rep Article The increasing number of implant-associated infections and of multiresistant pathogens is a major problem in the daily routine. In the field of osteomyelitis, it is difficult to manage a valid clinical study because of multiple influencing factors. Therefore, models of osteomyelitis with a simulation of the pathophysiology to evaluate treatment options for implant-associated infections are necessary. The aim of this study is to develop a standardized and reproducible osteomyelitis model in-vivo to improve treatment options. This study analyses the influence of a post-infectious implant exchange one week after infection and the infection progress afterward in combination with a systemic versus a local antibiotic treatment in-vivo. Therefore, the implant exchange, the exchange to a local drug-delivery system with gentamicin, and the implant removal are examined. Furthermore, the influence of an additional systemic antibiotic therapy is evaluated. An in-vivo model concerning the implant exchange is established that analyzes clinic, radiologic, microbiologic, histologic, and immunohistochemical diagnostics to obtain detailed evaluation and clinical reproducibility. Our study shows a clear advantage of the combined local and systemic antibiotic treatment in contrast to the implant removal and to a non-combined antibiotic therapy. Group genta/syst. showed the lowest infection rate with a percentage of 62.5% concerning microbiologic analysis, which is in accordance with the immunohistochemical, cytochemical, histologic, and radiologic analysis. Our in-vivo rat model has shown valid and reproducible results, which will lead to further investigations regarding treatment options and influencing factors concerning the therapy of osteomyelitis and implant-associated infections. Nature Publishing Group UK 2022-03-10 /pmc/articles/PMC8913616/ /pubmed/35273202 http://dx.doi.org/10.1038/s41598-022-07673-8 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Kreis, C.
Aschenbrenner, F. K.
Günther, D.
Tholema-Hans, N.
Koeppe, J.
Rosslenbroich, S. B.
Raschke, M. J.
Fuchs, T.
Establishment of a reliable in-vivo model of implant-associated infection to investigate innovative treatment options
title Establishment of a reliable in-vivo model of implant-associated infection to investigate innovative treatment options
title_full Establishment of a reliable in-vivo model of implant-associated infection to investigate innovative treatment options
title_fullStr Establishment of a reliable in-vivo model of implant-associated infection to investigate innovative treatment options
title_full_unstemmed Establishment of a reliable in-vivo model of implant-associated infection to investigate innovative treatment options
title_short Establishment of a reliable in-vivo model of implant-associated infection to investigate innovative treatment options
title_sort establishment of a reliable in-vivo model of implant-associated infection to investigate innovative treatment options
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8913616/
https://www.ncbi.nlm.nih.gov/pubmed/35273202
http://dx.doi.org/10.1038/s41598-022-07673-8
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