Understanding the rationale and clinical impact of the revised CLSI 2024 minocycline susceptibility breakpoints against Stenotrophomonas maltophilia

IF 3.7 3区 医学 Q2 INFECTIOUS DISEASES
Yamuna Devi Bakthavatchalam, Yuvashri Manoharan, Abirami Shankar, Karthik Gunasekaran, Kamini Walia, Balaji Veeraraghavan
{"title":"Understanding the rationale and clinical impact of the revised CLSI 2024 minocycline susceptibility breakpoints against Stenotrophomonas maltophilia","authors":"Yamuna Devi Bakthavatchalam, Yuvashri Manoharan, Abirami Shankar, Karthik Gunasekaran, Kamini Walia, Balaji Veeraraghavan","doi":"10.1007/s10096-024-04932-6","DOIUrl":null,"url":null,"abstract":"<p><i>Stenotrophomonas maltophilia</i> 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 <i>S. maltophilia</i> infections; levofloxavin and minocycline are the preferred potential alternatives. Recently, in 2024, CLSI has lowered the susceptibility breakpoints for minocycline against <i>S. maltophilia</i>. 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 <i>S. maltophilia</i> infections.</p>","PeriodicalId":11782,"journal":{"name":"European Journal of Clinical Microbiology & Infectious Diseases","volume":"10 1","pages":""},"PeriodicalIF":3.7000,"publicationDate":"2024-09-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"European Journal of Clinical Microbiology & Infectious Diseases","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1007/s10096-024-04932-6","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"INFECTIOUS DISEASES","Score":null,"Total":0}
引用次数: 0

Abstract

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.

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
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。
求助全文
约1分钟内获得全文 求助全文
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.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信