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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
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. Methods: We conducted a retrospective observational study of patients with Nocardia species isolated from clinical specimens at a tertiary-care academic hospital in Japan between January 2015 and April 2025. Clinical characteristics, antimicrobial therapy, adverse events, and outcomes were reviewed.
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
発行日
2026-10
出版物タイトル
International Journal of Antimicrobial Agents
67巻
10号
出版者
Elsevier BV
開始ページ
107906
ISSN
0924-8579
NCID
AA10778078
資料タイプ
学術雑誌論文
言語
英語
OAI-PMH Set
岡山大学
著作権者
© 2026 The Author(s).
論文のバージョン
publisher
PubMed ID
DOI
Web of Science KeyUT
関連URL
isVersionOf https://doi.org/10.1016/j.ijantimicag.2026.107906
ライセンス
http://creativecommons.org/licenses/by/4.0/