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Daptomycin treatment in patients with resistant staphylococcal periprosthetic joint infection 

BACKGROUND: Resistant staphylococcal organisms remain a serious problem in the treatment of periprosthetic joint infection (PJI). Higher failure rates have been reported when vancomycin was used. The purpose of this study was to assess the clinical dosage, effect, and safety of daptomycin in patient...

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Autores principales: Chang, Yu-Jui, Lee, Mel S., Lee, Chen-Hsiang, Lin, Po-Chun, Kuo, Feng-Chih
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5707892/
https://www.ncbi.nlm.nih.gov/pubmed/29187163
http://dx.doi.org/10.1186/s12879-017-2842-6
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author Chang, Yu-Jui
Lee, Mel S.
Lee, Chen-Hsiang
Lin, Po-Chun
Kuo, Feng-Chih
author_facet Chang, Yu-Jui
Lee, Mel S.
Lee, Chen-Hsiang
Lin, Po-Chun
Kuo, Feng-Chih
author_sort Chang, Yu-Jui
collection PubMed
description BACKGROUND: Resistant staphylococcal organisms remain a serious problem in the treatment of periprosthetic joint infection (PJI). Higher failure rates have been reported when vancomycin was used. The purpose of this study was to assess the clinical dosage, effect, and safety of daptomycin in patients with resistant staphylococcal PJI. METHODS: We retrospectively enrolled patients with hip or knee PJI who were treated with daptomycin in our institution (n = 16) from January 2013 to December 2014 with a minimum follow-up of 2 years. The patients received daptomycin when glycopeptide could not be used due to multiple resistance, any adverse reaction, chronic kidney disease stage 3 or worse, and previous treatment failure with glycopeptide or empirical therapy. RESULTS: These patients received daptomycin at a median dose of 8.3 mg∕kg per day for a median duration of 14 days. The overall treatment success rate was 87.5% (14 of 16 cases) after a median follow-up period of 27 months. In the subgroups of acute and chronic PJI, the success rate was 80% and 91%, respectively. One patient developed asymptomatic transient serum aspartate transaminase (AST) elevation. No severe side effects such as myositis, acute renal failure due to rhabdomyolysis or eosinophilic pneumonia were found in our series. CONCLUSION: Relatively high daptomycin doses combined with adequate surgical intervention were effective in treating resistant staphylococcal PJI. Daptomycin is an option worthy of consideration in PJI patients for whom glycopeptide treatment is unsuitable. Further prospective randomized comparative study is needed in the future.
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spelling pubmed-57078922017-12-06 Daptomycin treatment in patients with resistant staphylococcal periprosthetic joint infection  Chang, Yu-Jui Lee, Mel S. Lee, Chen-Hsiang Lin, Po-Chun Kuo, Feng-Chih BMC Infect Dis Research Article BACKGROUND: Resistant staphylococcal organisms remain a serious problem in the treatment of periprosthetic joint infection (PJI). Higher failure rates have been reported when vancomycin was used. The purpose of this study was to assess the clinical dosage, effect, and safety of daptomycin in patients with resistant staphylococcal PJI. METHODS: We retrospectively enrolled patients with hip or knee PJI who were treated with daptomycin in our institution (n = 16) from January 2013 to December 2014 with a minimum follow-up of 2 years. The patients received daptomycin when glycopeptide could not be used due to multiple resistance, any adverse reaction, chronic kidney disease stage 3 or worse, and previous treatment failure with glycopeptide or empirical therapy. RESULTS: These patients received daptomycin at a median dose of 8.3 mg∕kg per day for a median duration of 14 days. The overall treatment success rate was 87.5% (14 of 16 cases) after a median follow-up period of 27 months. In the subgroups of acute and chronic PJI, the success rate was 80% and 91%, respectively. One patient developed asymptomatic transient serum aspartate transaminase (AST) elevation. No severe side effects such as myositis, acute renal failure due to rhabdomyolysis or eosinophilic pneumonia were found in our series. CONCLUSION: Relatively high daptomycin doses combined with adequate surgical intervention were effective in treating resistant staphylococcal PJI. Daptomycin is an option worthy of consideration in PJI patients for whom glycopeptide treatment is unsuitable. Further prospective randomized comparative study is needed in the future. BioMed Central 2017-11-29 /pmc/articles/PMC5707892/ /pubmed/29187163 http://dx.doi.org/10.1186/s12879-017-2842-6 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Chang, Yu-Jui
Lee, Mel S.
Lee, Chen-Hsiang
Lin, Po-Chun
Kuo, Feng-Chih
Daptomycin treatment in patients with resistant staphylococcal periprosthetic joint infection 
title Daptomycin treatment in patients with resistant staphylococcal periprosthetic joint infection 
title_full Daptomycin treatment in patients with resistant staphylococcal periprosthetic joint infection 
title_fullStr Daptomycin treatment in patients with resistant staphylococcal periprosthetic joint infection 
title_full_unstemmed Daptomycin treatment in patients with resistant staphylococcal periprosthetic joint infection 
title_short Daptomycin treatment in patients with resistant staphylococcal periprosthetic joint infection 
title_sort daptomycin treatment in patients with resistant staphylococcal periprosthetic joint infection 
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5707892/
https://www.ncbi.nlm.nih.gov/pubmed/29187163
http://dx.doi.org/10.1186/s12879-017-2842-6
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