Osteomyelitis due to methicillin-resistant successfully treated by an oral combination of minocycline and trimethoprim–sulfamethoxazole

Most of the anti-methicillin-resistant Staphylococcus aureus drugs available in Japan are administered intravenously, except for linezolid, which can also be administered orally. Here, we report a lupus patient with methicillin-resistant S. aureus– induced osteomyelitis. Linezolid had to be stopped...

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Main Authors: Kojiro Sato, Hiroaki Yazawa, Daisuke Ikuma, Takashi Maruyama, Hiroshi Kajiyama, Toshihide Mimura
Format: Article
Language:English
Published: SAGE Publishing 2019-04-01
Series:SAGE Open Medical Case Reports
Online Access:https://doi.org/10.1177/2050313X19841465
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spelling doaj-02823cc9dfc94deeba3ea2f6061b82622020-11-25T03:24:17ZengSAGE PublishingSAGE Open Medical Case Reports2050-313X2019-04-01710.1177/2050313X19841465Osteomyelitis due to methicillin-resistant successfully treated by an oral combination of minocycline and trimethoprim–sulfamethoxazoleKojiro SatoHiroaki YazawaDaisuke IkumaTakashi MaruyamaHiroshi KajiyamaToshihide MimuraMost of the anti-methicillin-resistant Staphylococcus aureus drugs available in Japan are administered intravenously, except for linezolid, which can also be administered orally. Here, we report a lupus patient with methicillin-resistant S. aureus– induced osteomyelitis. Linezolid had to be stopped due to severe anemia. In an effort to treat her on an outpatient basis, we planned to use a combination of minocycline and trimethoprim–sulfamethoxazole that exhibited in vitro sensitivity against the methicillin-resistant S. aureus detected, and rifampicin is used against methicillin-resistant S. aureus in certain cases. The use of rifampicin increased the level of C-reactive protein even though the prednisolone dose used was doubled, so we gave up using it. The combined application of oral minocycline and trimethoprim–sulfamethoxazole, however, controlled the inflammation, and the patient was able to be discharged. Fourteen months later, we discontinued the administration of both drugs and there has been no relapse more than a year. This combination of antibiotics may be useful, especially when patients want to be treated on an outpatient basis.https://doi.org/10.1177/2050313X19841465
collection DOAJ
language English
format Article
sources DOAJ
author Kojiro Sato
Hiroaki Yazawa
Daisuke Ikuma
Takashi Maruyama
Hiroshi Kajiyama
Toshihide Mimura
spellingShingle Kojiro Sato
Hiroaki Yazawa
Daisuke Ikuma
Takashi Maruyama
Hiroshi Kajiyama
Toshihide Mimura
Osteomyelitis due to methicillin-resistant successfully treated by an oral combination of minocycline and trimethoprim–sulfamethoxazole
SAGE Open Medical Case Reports
author_facet Kojiro Sato
Hiroaki Yazawa
Daisuke Ikuma
Takashi Maruyama
Hiroshi Kajiyama
Toshihide Mimura
author_sort Kojiro Sato
title Osteomyelitis due to methicillin-resistant successfully treated by an oral combination of minocycline and trimethoprim–sulfamethoxazole
title_short Osteomyelitis due to methicillin-resistant successfully treated by an oral combination of minocycline and trimethoprim–sulfamethoxazole
title_full Osteomyelitis due to methicillin-resistant successfully treated by an oral combination of minocycline and trimethoprim–sulfamethoxazole
title_fullStr Osteomyelitis due to methicillin-resistant successfully treated by an oral combination of minocycline and trimethoprim–sulfamethoxazole
title_full_unstemmed Osteomyelitis due to methicillin-resistant successfully treated by an oral combination of minocycline and trimethoprim–sulfamethoxazole
title_sort osteomyelitis due to methicillin-resistant successfully treated by an oral combination of minocycline and trimethoprim–sulfamethoxazole
publisher SAGE Publishing
series SAGE Open Medical Case Reports
issn 2050-313X
publishDate 2019-04-01
description Most of the anti-methicillin-resistant Staphylococcus aureus drugs available in Japan are administered intravenously, except for linezolid, which can also be administered orally. Here, we report a lupus patient with methicillin-resistant S. aureus– induced osteomyelitis. Linezolid had to be stopped due to severe anemia. In an effort to treat her on an outpatient basis, we planned to use a combination of minocycline and trimethoprim–sulfamethoxazole that exhibited in vitro sensitivity against the methicillin-resistant S. aureus detected, and rifampicin is used against methicillin-resistant S. aureus in certain cases. The use of rifampicin increased the level of C-reactive protein even though the prednisolone dose used was doubled, so we gave up using it. The combined application of oral minocycline and trimethoprim–sulfamethoxazole, however, controlled the inflammation, and the patient was able to be discharged. Fourteen months later, we discontinued the administration of both drugs and there has been no relapse more than a year. This combination of antibiotics may be useful, especially when patients want to be treated on an outpatient basis.
url https://doi.org/10.1177/2050313X19841465
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