Cefiderocol treatment for patients infected by Stenotrophomonas maltophilia, Burkholderia cepacia complex and Achromobacter spp.: subgroup analysis from the PERSEUS study.

IF 3.7 3区 医学 Q2 INFECTIOUS DISEASES
Julian Torre-Cisneros, Ricard Ferrer, Carmen De La Fuente Martos, Jessica Sarda, A Javier Gonzalez Calvo, Stefano Verardi, Andreas Karas, Alex Soriano
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Abstract

Purpose: This subgroup analysis of the PERSEUS study aimed to describe the effectiveness of cefiderocol treatment in the early access programme in Spain in patients infected by Stenotrophomonas maltophilia, Burkholderia cepacia complex (Bcc) or Achromobacter species.

Methods: In the retrospective, observational, multicentre PERSEUS study in Spain, the effectiveness and safety of cefiderocol treatment administered for at least 72 h up to 28 days in patients infected by Gram-negative bacteria, except Acinetobacter spp., in the early access programme was investigated. Patient demographics and baseline clinical characteristics, cefiderocol use, clinical cure at end of treatment, all-cause mortality at Day 28 were the main outcomes.

Results: A total of 20 patients had S. maltophilia infections, and 14 patients had other rare glucose non-fermenters (Bcc 8, Achromobacter spp. 5, Ralstonia mannitolilytica 1). The median (interquartile range [IQR]) age was 60.5 (48.0-65.5) years and 49.5 (33.0-59.0) years for patients with S. maltophilia and other rare non-fermenters, respectively. The majority of patients had respiratory tract infections (S. maltophilia 55%; other rare non-fermenters 71.4%), and median (IQR) duration of cefiderocol treatment was 10.0 (6.5-13.5) days and 8.0 (6-14) days, respectively. Clinical cure rates were 70%, 62.5% and 80.0% for patients with S. maltophilia, Bcc and Achromobacter spp., respectively. Corresponding 28-day all-cause mortality rates were 30.0%, 37.5% and 40.0%, respectively. One patient with R. mannitolilytica had clinical cure and survived to Day 28.

Conclusions: Cefiderocol is an important addition to the limited treatment options for patients infected by these rare glucose non-fermenting Gram-negative bacteria.

Trial registration: ClinicalTrials.gov: NCT05789199 (Registration date: 16 February 2023).

头孢地罗治疗嗜麦芽窄养单胞菌、洋葱伯克霍尔德菌复合菌和无色杆菌感染患者:来自PERSEUS研究的亚组分析
目的:对PERSEUS研究进行亚组分析,旨在描述头孢地罗治疗西班牙嗜麦芽窄养单胞菌、洋葱伯克霍尔德菌复合菌(Bcc)或无色杆菌感染患者的早期获取计划的有效性。方法:在西班牙的一项回顾性、观察性、多中心PERSEUS研究中,对早期获取计划中感染革兰氏阴性菌(不动杆菌除外)的患者给予头孢地罗治疗至少72小时至28天的有效性和安全性进行了调查。患者人口统计学和基线临床特征、头孢地罗使用、治疗结束时的临床治愈、第28天的全因死亡率是主要结局。结果:嗜麦芽葡萄球菌感染20例,其他罕见葡萄糖非发酵菌(Bcc 8、Achromobacter spp. 5、Ralstonia mannitololtica 1)感染14例。嗜麦芽葡萄球菌和其他罕见非发酵菌的中位年龄(四分位数间距[IQR])分别为60.5(48.0 ~ 65.5)岁和49.5(33.0 ~ 59.0)岁。大多数患者有呼吸道感染(嗜麦芽葡萄球菌55%;其他罕见非发酵剂71.4%),头孢地罗治疗的中位(IQR)持续时间分别为10.0(6.5-13.5)天和8.0(6-14)天。嗜麦芽葡萄球菌临床治愈率为70%,嗜麦芽葡萄球菌临床治愈率为62.5%,嗜麦芽葡萄球菌临床治愈率为80.0%。相应的28天全因死亡率分别为30.0%、37.5%和40.0%。1例患者临床治愈并存活至第28天。结论:对于这些罕见的葡萄糖非发酵革兰氏阴性菌感染的患者,头孢地罗是有限治疗选择的重要补充。试验注册:ClinicalTrials.gov: NCT05789199(注册日期:2023年2月16日)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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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