医学
基岩
氯法齐明
指南
重症监护医学
阿奇霉素
养生
乙胺丁醇
内科学
克拉霉素
抗药性
文化转换
阿米卡星
肺结核
抗生素
利福平
结核分枝杆菌
免疫学
痰
病理
幽门螺杆菌
麻风病
微生物学
生物
作者
Masashi Ito,Yasuhiko Koga,Yoshimasa Hachisu,Keisuke Murata,Noriaki Sunaga,Toshitaka Maeno,Takeshi Hisada
标识
DOI:10.1016/j.resinv.2022.05.006
摘要
Diseases caused by Mycobacterium avium complex (MAC) infection in the lungs are increasing worldwide. The recurrence rate of MAC-pulmonary disease (PD) has been reported to be as high as 25–45%. A significant percentage of recurrences occurs because of reinfection with a new genotype from the environment. A focus on reducing exposure to MAC organisms from the environment is therefore an essential component of the management of this disease as well as standard MAC-PD treatment. A macrolide-containing three-drug regimen is recommended over a two-drug regimen as a standard treatment, and azithromycin is recommended rather than clarithromycin . Both the 2007 and 2020 guidelines recommend a treatment duration of MAC-PD of at least one year after the culture conversion. Previous clinical studies have reported that ethambutol could prevent macrolide resistance. Furthermore, the concomitant use of aminoglycoside , amikacin liposomal inhalation, clofazimine , linezolid , bedaquiline , and fluoroquinolone with modification of guideline-based therapy has been studied. Long-term management of MAC-PD remains challenging because of the discontinuation of multi-drug regimens and the acquisition of macrolide resistance. Moreover, the poor compliance of guideline-based therapy for MAC-PD treatment worldwide is concerning since it causes macrolide resistance. Therefore, in this review, we focus on MAC-PD treatment and summarize various treatment options when standard treatment cannot be maintained, with reference to the latest ATS/ERS/ESCMID/IDSA clinical practice guidelines revised in 2020.
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