了解修订后的 CLSI 2024 米诺环素对嗜麦芽单胞菌敏感性断点的原理和临床影响

IF 3.7 3区 医学 Q2 INFECTIOUS DISEASES
Yamuna Devi Bakthavatchalam, Yuvashri Manoharan, Abirami Shankar, Karthik Gunasekaran, Kamini Walia, Balaji Veeraraghavan
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引用次数: 0

摘要

由于存在多种内在和获得性耐药机制,嗜麦芽糖单胞菌的治疗具有挑战性。TMP-SMZ 是治疗嗜麦芽单胞菌感染的标准疗法;左氧氟沙星和米诺环素是首选的潜在替代药物。最近,CLSI 在 2024 年降低了米诺环素对嗜麦芽糖酵母菌的药敏断点。应用修订后的米诺环素药敏断点≤1 mg/L,米诺环素的药敏率从 77%(以前的断点≤4 mg/L)大幅降至 35%(修订后的断点≤1 mg/L)。由于这一变化,米诺环素在治疗嗜麦芽糖酵母菌感染方面的依赖性受到质疑。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Understanding the rationale and clinical impact of the revised CLSI 2024 minocycline susceptibility breakpoints against Stenotrophomonas maltophilia

Stenotrophomonas maltophilia is challenging to treat due to the presence of multiple intrinsic and acquired resistance mechanisms. TMP-SMZ is the standard care of therapy for treating S. maltophilia infections; levofloxavin and minocycline are the preferred potential alternatives. Recently, in 2024, CLSI has lowered the susceptibility breakpoints for minocycline against S. maltophilia. Applying the revised minocycline’s susceptibility breakpoint of ≤ 1 mg/L, susceptibility to minocycline dropped significantly from 77% (previous breakpoint, ≤ 4 mg/L) to 35% (revised breakpoint of ≤ 1 mg/L). In the wake of this change, minocycline’s dependency has been questioned for treating S. maltophilia infections.

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来源期刊
CiteScore
10.40
自引率
2.20%
发文量
138
审稿时长
1 months
期刊介绍: EJCMID is an interdisciplinary journal devoted to the publication of communications on infectious diseases of bacterial, viral and parasitic origin.
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