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药敏试验是头孢地尔治疗成功的关键:一项回顾性队列研究。

Susceptibility Testing Is Key for the Success of Cefiderocol Treatment: A Retrospective Cohort Study.

作者信息

Bleibtreu Alexandre, Dortet Laurent, Bonnin Remy A, Wyplosz Benjamin, Sacleux Sophie-Caroline, Mihaila Liliana, Dupont Hervé, Junot Helga, Bunel Vincent, Grall Nathalie, Razazi Keyvan, Duran Clara, Tattevin Pierre, Dinh Aurélien, The Cefiderocol French Study Group On Behalf Of

机构信息

Infectious Disease Unit, La Pitié-Salpétrière University Hospital, AP-HP, University of Paris, 75013 Paris, France.

Microbiology Laboratory, Bicêtre University Hospital, AP-HP Paris Saclay University, 94270 Le Kremlin-Bicêtre, France.

出版信息

Microorganisms. 2021 Jan 30;9(2):282. doi: 10.3390/microorganisms9020282.

Abstract

Cefiderocol is a novel siderophore cephalosporin, which has proven in vitro activity against carbapenem-resistant (CR) Gram-negative pathogens and stability towards all carbapenemases. The aim of this study was to describe the first cases of prescriptions and the efficacy of cefiderocol for compassionate use in the 2 months following its access in France. We performed a national retrospective study of all patients who received at least one dose of cefiderocol from 2 November 2018 to 5 November 2019. We collected clinical characteristics and outcome through a standard questionnaire. Bacterial isolates from 12 patients were centralized and analyzed in the French National Reference Center for Antimicrobial Resistance, and sequenced using Illumina technology. Finally, 13 patients from 7 French university hospitals were included in the study. The main type of infection treated by cefiderocol was respiratory tract infections (RTI, = 10). The targeted bacteria were ( = 12), including carbapenemase-producing ( = 9), ( = 2), ( = 1), and ( = 1). Overall, of the 12 patients whose samples were analyzed, 5 strains were not susceptible to cefiderocol (4 categorized as resistant and 1 as intermediate) according to Clinical and Laboratory Standards Institute (CLSI) breakpoints. If considering susceptible strains, the cure rate was 6/7, while being 0/5 among not-susceptible strains. This study underlines the necessity to test strains in adequate conditions.

摘要

头孢地尔是一种新型的铁载体头孢菌素,已证明其对耐碳青霉烯类革兰氏阴性病原体具有体外活性,并且对所有碳青霉烯酶都具有稳定性。本研究的目的是描述法国批准使用头孢地尔后头两个月内同情用药的首例处方情况及其疗效。我们对2018年11月2日至2019年11月5日期间接受至少一剂头孢地尔的所有患者进行了一项全国性回顾性研究。我们通过标准问卷收集了临床特征和治疗结果。从12例患者中分离出的细菌菌株被集中送至法国国家抗微生物药物耐药性参考中心进行分析,并使用Illumina技术进行测序。最终,来自法国7所大学医院的13例患者被纳入研究。头孢地尔治疗的主要感染类型是呼吸道感染(RTI,n = 10)。目标细菌为肺炎克雷伯菌(n = 12),包括产碳青霉烯酶的肺炎克雷伯菌(n = 9)、大肠埃希菌(n = 2)、鲍曼不动杆菌(n = 1)和铜绿假单胞菌(n = 1)。总体而言,根据临床和实验室标准协会(CLSI)的断点,在分析样本的12例患者中,有5株肺炎克雷伯菌对头孢地尔不敏感(4株分类为耐药,1株为中介)。如果考虑敏感菌株,治愈率为6/7,而在不敏感菌株中治愈率为0/5。本研究强调了在适当条件下对菌株进行检测的必要性。

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