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An antibiotic loaded ceramic sternum to treat destroyed infected sternum: 4 cases

BACKGROUND: After its destruction during refractory deep sternal wound infection (DSWI), current sternum reconstructions mainly rely on muscle flaps technique, but such technique have pitfalls and limits. To tackle the limited possibilities to use device implantation because of the risk of infection...

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Autores principales: Tricard, Jeremy, Chermat, Anaëlle, El Balkhi, Souleiman, Denes, Eric, Bertin, François
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7138964/
https://www.ncbi.nlm.nih.gov/pubmed/32274086
http://dx.doi.org/10.21037/jtd.2020.01.70
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author Tricard, Jeremy
Chermat, Anaëlle
El Balkhi, Souleiman
Denes, Eric
Bertin, François
author_facet Tricard, Jeremy
Chermat, Anaëlle
El Balkhi, Souleiman
Denes, Eric
Bertin, François
author_sort Tricard, Jeremy
collection PubMed
description BACKGROUND: After its destruction during refractory deep sternal wound infection (DSWI), current sternum reconstructions mainly rely on muscle flaps technique, but such technique have pitfalls and limits. To tackle the limited possibilities to use device implantation because of the risk of infection, we developed a self-protected device allowing its implantation in an infected area. METHODS: We used gentamicin alone or in combination with vancomycin loaded in a porous ceramic sternum to replace sternums destroyed during DSWI. The aim was to mechanically replace the sternum and to secure the implantation by killing the remaining bacteria in the wound thanks to the loaded antibiotic. RESULTS: This device was implanted in four infected patients during DWSI with sternal dehiscence. No complication occurred during surgeries, and wound healing was obtained quickly. Local antibiotic concentrations largely exceeded the ones needed for their efficacy while no antibiotic was found in the blood. All patients are well-being. However previously unknown gentamicin resistant bacteria, present in the surgical wound at the time of positioning, required sternal implant removal for one patient after 19 months. For all patients, pulmonary function tests (PFT) improved after implantation. CONCLUSIONS: The ceramic sternum played its role consolidating the thoracic cage without stiffening. The antibiotic loaded in the sternum allowed a secure implantation, killing bacteria before the colonization of the implant even in this infected area. These four implantations are promising for patients with sternal destruction after DSWI.
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spelling pubmed-71389642020-04-09 An antibiotic loaded ceramic sternum to treat destroyed infected sternum: 4 cases Tricard, Jeremy Chermat, Anaëlle El Balkhi, Souleiman Denes, Eric Bertin, François J Thorac Dis Original Article BACKGROUND: After its destruction during refractory deep sternal wound infection (DSWI), current sternum reconstructions mainly rely on muscle flaps technique, but such technique have pitfalls and limits. To tackle the limited possibilities to use device implantation because of the risk of infection, we developed a self-protected device allowing its implantation in an infected area. METHODS: We used gentamicin alone or in combination with vancomycin loaded in a porous ceramic sternum to replace sternums destroyed during DSWI. The aim was to mechanically replace the sternum and to secure the implantation by killing the remaining bacteria in the wound thanks to the loaded antibiotic. RESULTS: This device was implanted in four infected patients during DWSI with sternal dehiscence. No complication occurred during surgeries, and wound healing was obtained quickly. Local antibiotic concentrations largely exceeded the ones needed for their efficacy while no antibiotic was found in the blood. All patients are well-being. However previously unknown gentamicin resistant bacteria, present in the surgical wound at the time of positioning, required sternal implant removal for one patient after 19 months. For all patients, pulmonary function tests (PFT) improved after implantation. CONCLUSIONS: The ceramic sternum played its role consolidating the thoracic cage without stiffening. The antibiotic loaded in the sternum allowed a secure implantation, killing bacteria before the colonization of the implant even in this infected area. These four implantations are promising for patients with sternal destruction after DSWI. AME Publishing Company 2020-03 /pmc/articles/PMC7138964/ /pubmed/32274086 http://dx.doi.org/10.21037/jtd.2020.01.70 Text en 2020 Journal of Thoracic Disease. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Original Article
Tricard, Jeremy
Chermat, Anaëlle
El Balkhi, Souleiman
Denes, Eric
Bertin, François
An antibiotic loaded ceramic sternum to treat destroyed infected sternum: 4 cases
title An antibiotic loaded ceramic sternum to treat destroyed infected sternum: 4 cases
title_full An antibiotic loaded ceramic sternum to treat destroyed infected sternum: 4 cases
title_fullStr An antibiotic loaded ceramic sternum to treat destroyed infected sternum: 4 cases
title_full_unstemmed An antibiotic loaded ceramic sternum to treat destroyed infected sternum: 4 cases
title_short An antibiotic loaded ceramic sternum to treat destroyed infected sternum: 4 cases
title_sort antibiotic loaded ceramic sternum to treat destroyed infected sternum: 4 cases
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7138964/
https://www.ncbi.nlm.nih.gov/pubmed/32274086
http://dx.doi.org/10.21037/jtd.2020.01.70
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