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Clinical ineffectiveness of latamoxef for Stenotrophomonas maltophilia infection

OBJECTIVES: Stenotrophomonas maltophilia shows wide-spectrum resistance to antimicrobials and causes various infections in immunocompromised or critically ill patients with high mortality. In this era of antibiotics resistance, a revival of old antibiotics is now featured. We examined the clinical u...

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Autores principales: Hagiya, Hideharu, Tasaka, Ken, Sendo, Toshiaki, Otsuka, Fumio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4621224/
https://www.ncbi.nlm.nih.gov/pubmed/26527890
http://dx.doi.org/10.2147/IDR.S90726
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author Hagiya, Hideharu
Tasaka, Ken
Sendo, Toshiaki
Otsuka, Fumio
author_facet Hagiya, Hideharu
Tasaka, Ken
Sendo, Toshiaki
Otsuka, Fumio
author_sort Hagiya, Hideharu
collection PubMed
description OBJECTIVES: Stenotrophomonas maltophilia shows wide-spectrum resistance to antimicrobials and causes various infections in immunocompromised or critically ill patients with high mortality. In this era of antibiotics resistance, a revival of old antibiotics is now featured. We examined the clinical usefulness of latamoxef (LMOX) for the treatment of S. maltophilia infection. PATIENTS AND METHODS: The observational study was retrospectively performed at Okayama University Hospital (Okayama, Japan) from January 2011 to December 2013. LMOX was administered to 12 patients with S. maltophilia infection, with eleven of those patients being admitted to the intensive care unit. RESULTS: Underlying conditions of the patients included postoperation, hematological transplantation, hepatic transplantation, and burn. Major infectious foci were surgical site infection (six cases), respiratory infection (four cases), blood stream infection (three cases), and burn site infection (one case). The doses of LMOX administered ranged from 1 g/d to 3 g/d for ten adult patients and from 40 mg/kg/d to 80 mg/kg/d for two pediatric patients. Microbiologic failure was seen in five (41.7%) of 12 cases, and 30-day and hospital mortality rates were 25% and 50%, respectively. Minimum inhibitory concentrations of LMOX were higher in the deceased group (4–64 µg/mL) than in the surviving group (1–4 µg/mL). CONCLUSION: LMOX treatment is not recommended for the treatment of S. maltophilia infection. Further investigation would be needed before its clinical use.
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spelling pubmed-46212242015-11-02 Clinical ineffectiveness of latamoxef for Stenotrophomonas maltophilia infection Hagiya, Hideharu Tasaka, Ken Sendo, Toshiaki Otsuka, Fumio Infect Drug Resist Original Research OBJECTIVES: Stenotrophomonas maltophilia shows wide-spectrum resistance to antimicrobials and causes various infections in immunocompromised or critically ill patients with high mortality. In this era of antibiotics resistance, a revival of old antibiotics is now featured. We examined the clinical usefulness of latamoxef (LMOX) for the treatment of S. maltophilia infection. PATIENTS AND METHODS: The observational study was retrospectively performed at Okayama University Hospital (Okayama, Japan) from January 2011 to December 2013. LMOX was administered to 12 patients with S. maltophilia infection, with eleven of those patients being admitted to the intensive care unit. RESULTS: Underlying conditions of the patients included postoperation, hematological transplantation, hepatic transplantation, and burn. Major infectious foci were surgical site infection (six cases), respiratory infection (four cases), blood stream infection (three cases), and burn site infection (one case). The doses of LMOX administered ranged from 1 g/d to 3 g/d for ten adult patients and from 40 mg/kg/d to 80 mg/kg/d for two pediatric patients. Microbiologic failure was seen in five (41.7%) of 12 cases, and 30-day and hospital mortality rates were 25% and 50%, respectively. Minimum inhibitory concentrations of LMOX were higher in the deceased group (4–64 µg/mL) than in the surviving group (1–4 µg/mL). CONCLUSION: LMOX treatment is not recommended for the treatment of S. maltophilia infection. Further investigation would be needed before its clinical use. Dove Medical Press 2015-10-20 /pmc/articles/PMC4621224/ /pubmed/26527890 http://dx.doi.org/10.2147/IDR.S90726 Text en © 2015 Hagiya et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Hagiya, Hideharu
Tasaka, Ken
Sendo, Toshiaki
Otsuka, Fumio
Clinical ineffectiveness of latamoxef for Stenotrophomonas maltophilia infection
title Clinical ineffectiveness of latamoxef for Stenotrophomonas maltophilia infection
title_full Clinical ineffectiveness of latamoxef for Stenotrophomonas maltophilia infection
title_fullStr Clinical ineffectiveness of latamoxef for Stenotrophomonas maltophilia infection
title_full_unstemmed Clinical ineffectiveness of latamoxef for Stenotrophomonas maltophilia infection
title_short Clinical ineffectiveness of latamoxef for Stenotrophomonas maltophilia infection
title_sort clinical ineffectiveness of latamoxef for stenotrophomonas maltophilia infection
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4621224/
https://www.ncbi.nlm.nih.gov/pubmed/26527890
http://dx.doi.org/10.2147/IDR.S90726
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