
| ID | 71134 |
| フルテキストURL | |
| 著者 |
Akazawa, Hidemasa
Department of Infectious Diseases, Okayama University Hospital
Fukushima, Shinnosuke
Department of Infectious Diseases, Okayama University Hospital
Miyahara, Tomoyuki
Department of General Medicine, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
Tsuji, Shuma
Department of Medical Laboratory Science, Okayama University Graduate School of Health Sciences
Gotoh, Kazuyoshi
Department of Medical Laboratory Science, Okayama University Graduate School of Health Sciences
Ogawa, Sakura
Microbiology Division, Clinical Laboratory, Okayama University Hospital
Iio, Koji
Microbiology Division, Clinical Laboratory, Okayama University Hospital
Hagiya, Hideharu
Department of Infectious Diseases, Okayama University Hospital
ORCID
Kaken ID
researchmap
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| 抄録 | Objectives: Nocardiosis often requires prolonged antimicrobial therapy, and trimethoprim–sulfamethoxazole (TMP–SMX) is considered the cornerstone of treatment. However, TMP–SMX–related adverse events frequently complicate long-term therapy, and real-world data regarding treatment continuity and outcomes remain limited.
Results: Eleven cases were enrolled, with a median age of 65 years. The cohort comprised seven patients with severe nocardiosis (disseminated disease, brain abscess, and pneumonia in transplant recipients) and four patients with mild nocardiosis (cutaneous infection and pneumonia). Nine patients received TMP–SMX as part of the initial regimen, of whom seven required modification of therapy within 1 day to 3 months because of adverse events. Following modification of TMP–SMX, patients were treated with alternative regimens, including fluoroquinolone—and minocycline-based therapies, as well as β-lactam–containing combinations. Importantly, no cases of treatment failure or death were observed, and no relapses were identified during the available follow-up period, even among patients with those clinically complex diseases. Conclusions: Although TMP–SMX is the first-line therapy for nocardiosis, the majority of our patients did not tolerate the drug. Nevertheless, favorable outcomes were observed with alternative regimens, even in patients with clinically complex disease, suggesting that alternative regimens may be reasonable options when TMP–SMX is not tolerated. |
| キーワード | Nocardiosis
Treatment
Trimethoprim–sulfamethoxazole
Alternative therapy
Dose modification
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| 発行日 | 2026-10
|
| 出版物タイトル |
International Journal of Antimicrobial Agents
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| 巻 | 67巻
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| 号 | 10号
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| 出版者 | Elsevier BV
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| 開始ページ | 107906
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| ISSN | 0924-8579
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| NCID | AA10778078
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| 資料タイプ |
学術雑誌論文
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| 言語 |
英語
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| OAI-PMH Set |
岡山大学
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| 著作権者 | © 2026 The Author(s).
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| 論文のバージョン | publisher
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| PubMed ID | |
| DOI | |
| Web of Science KeyUT | |
| 関連URL | isVersionOf https://doi.org/10.1016/j.ijantimicag.2026.107906
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| ライセンス | http://creativecommons.org/licenses/by/4.0/
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