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头孢地尔在治疗革兰氏阴性菌感染患者临床实践中的有效性和安全性:PROVE研究的美国中期结果

Effectiveness and Safety of Cefiderocol in Clinical Practice for Treatment of Patients with Gram-Negative Bacterial Infections: US Interim Results of the PROVE Study.

作者信息

Clancy Cornelius J, Cornely Oliver A, Marcella Stephen W, Nguyen Sean T, Gozalo Laurence, Cai Bin

机构信息

Department of Medicine, University of Pittsburgh, Pittsburgh, PA, USA.

Institute of Translational Research, Cologne Excellence Cluster on Cellular Stress Responses in Aging-Associated Diseases (CECAD), University Hospital Cologne, Faculty of Medicine, University of Cologne, Cologne, Germany.

出版信息

Infect Drug Resist. 2024 Oct 15;17:4427-4443. doi: 10.2147/IDR.S475462. eCollection 2024.

Abstract

PURPOSE

The international PROVE retrospective chart-review study aims to assess the real-world effectiveness and safety of cefiderocol for treatment of patients with carbapenem-resistant Gram-negative infections.

PATIENTS AND METHODS

US centers selected hospitalized patients receiving their first cefiderocol treatment for ≥72 hours for a Gram-negative bacterial infection (November 2020-March 2023). Patient demographics, clinical characteristics, hospitalization, course of infection, antibiotic use, clinical cure (excluding patients with a relapse/reinfection), clinical response at the end of treatment, microbiology, in-hospital all-cause mortality (IH-ACM) at Day 30, and safety were analyzed using descriptive statistics.

RESULTS

This interim analysis included 244 patients. The most frequent infection sites were respiratory tract (55.7%), skin and skin structure (16.8%), and blood (9.8%). The median duration of cefiderocol use was 12 days (interquartile range 8-18.5). Clinical cure was reported for 64.8% (158/244) of patients, clinical response for 74.2% (181/244), and 9.4% (23/244) had relapse/reinfection; 30-day IH-ACM was 18.4% (45/244). Of 82 patients with monomicrobial infections, 64.6% (n = 53) and 74.4% (n = 61) had clinical cure and clinical response, respectively, and 30-day IH-ACM was 25.6%. Among 43 patients with monomicrobial infections, 60.5% (n = 26) and 74.4% (n = 32) had clinical cure and clinical response, respectively, and 30-day IH-ACM was 18.6%. Five patients experienced six adverse drug reactions (one serious event: interstitial nephritis/acute kidney injury), and cefiderocol was discontinued in two cases.

CONCLUSION

Cefiderocol had similar clinical cure and response rates to previous retrospective studies and lower mortality. Cefiderocol was well tolerated in real-world settings in critically ill US patients with problematic Gram-negative pathogens.

摘要

目的

国际PROVE回顾性图表审查研究旨在评估头孢地尔治疗耐碳青霉烯革兰氏阴性菌感染患者的真实世界有效性和安全性。

患者与方法

美国各中心选择2020年11月至2023年3月期间因革兰氏阴性菌感染接受首次头孢地尔治疗≥72小时的住院患者。使用描述性统计分析患者的人口统计学特征、临床特征、住院情况、感染病程、抗生素使用情况、临床治愈情况(不包括复发/再感染患者)、治疗结束时的临床反应、微生物学情况、第30天的院内全因死亡率(IH-ACM)以及安全性。

结果

本次中期分析纳入了244例患者。最常见的感染部位是呼吸道(55.7%)、皮肤及皮肤结构(16.8%)和血液(9.8%)。头孢地尔的中位使用时长为12天(四分位间距8 - 18.5天)。64.8%(158/244)的患者报告临床治愈,74.2%(181/244)有临床反应,9.4%(23/244)出现复发/再感染;30天的IH-ACM为18.4%(45/244)。在82例单一微生物感染患者中,分别有64.6%(n = 53)和74.4%(n = 61)实现临床治愈和临床反应,30天的IH-ACM为25.6%。在43例多重微生物感染患者中,分别有60.5%(n = 26)和74.4%(n = 32)实现临床治愈和临床反应,30天的IH-ACM为18.6%。5例患者发生了6起药物不良反应(1起严重事件:间质性肾炎/急性肾损伤),2例患者停用了头孢地尔。

结论

头孢地尔的临床治愈率和反应率与既往回顾性研究相似,死亡率较低。在美国患有难治性革兰氏阴性病原体的重症患者的真实世界环境中,头孢地尔耐受性良好。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fe2/11490232/4a94c5d8a6eb/IDR-17-4427-g0001.jpg

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