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头孢地尔:一种铁载体头孢菌素。

Cefiderocol: A Siderophore Cephalosporin.

机构信息

Cleveland Clinic Abu Dhabi, United Arab Emirates.

Lebanese American University, School of Phramacy, Byblos Campus, Byblos, Lebanon.

出版信息

Ann Pharmacother. 2020 Dec;54(12):1215-1231. doi: 10.1177/1060028020929988. Epub 2020 Jun 10.

Abstract

OBJECTIVE

This article reviews the available data on the chemistry, spectrum of activity, pharmacokinetic and pharmacodynamic properties, clinical efficacy, and potential place in therapy of cefiderocol.

DATA SOURCES

A literature search through PubMed, Google Scholar, and ClinicalTrials.gov was conducted (2009 to March 2020) using the search terms and . Abstracts presented at recent conferences, prescribing information, and information from the US Food and Drug Administration (FDA) and the manufacturer's website were reviewed.

STUDY SELECTION AND DATA EXTRACTION

All relevant published articles, package inserts, and unpublished meeting abstracts on cefiderocol were reviewed.

DATA SYNTHESIS

Cefiderocol is the first siderophore antibiotic to be approved by the FDA. It was shown to be active against a wide range of resistant Gram-negative pathogens, including multidrug-resistant (MDR) , Enterobacteriaceae, and . Cefiderocol was studied in the treatment of adult patients with complicated urinary tract infections (cUTIs) and nosocomial pneumonia and was well tolerated. In a recently completed prospective study, higher mortality was observed with cefiderocol in the treatment of serious infections caused by carbapenem-resistant (CR) Gram-negative pathogens.

RELEVANCE TO PATIENT CARE AND CLINICAL PRACTICE

The approval of cefiderocol provides a new option in the treatment of cUTIs and potentially treatment of nosocomial pneumonia caused by resistant Gram-negative pathogens. Given the higher mortality observed with cefiderocol, its use in the treatment of CR Gram-negative infections should be carefully considered.

CONCLUSION

Cefiderocol shows promising activity against MDR Gram-negative pathogens. Its use in the treatment of serious infections caused by CR Gram-negative bacteria needs further evaluation in phase III clinical studies.

摘要

目的

本文综述了头孢地尔的化学、活性谱、药代动力学和药效学特性、临床疗效以及在治疗中的潜在地位的现有数据。

资料来源

通过 PubMed、Google Scholar 和 ClinicalTrials.gov 进行文献检索(2009 年至 2020 年 3 月),使用的检索词为 和 。同时检索了近期会议的摘要、说明书以及来自美国食品和药物管理局(FDA)和制造商网站的信息。

研究选择和数据提取

综述了所有关于头孢地尔的已发表文章、说明书和未发表的会议摘要。

综合分析

头孢地尔是 FDA 批准的第一种铁载体抗生素。它被证明对广泛的耐药革兰氏阴性病原体具有活性,包括多药耐药(MDR)、肠杆菌科和 。头孢地尔在治疗成人复杂性尿路感染(cUTI)和医院获得性肺炎方面进行了研究,且耐受性良好。在最近完成的一项前瞻性研究中,在治疗由碳青霉烯类耐药(CR)革兰氏阴性病原体引起的严重感染时,头孢地尔的死亡率更高。

与患者护理和临床实践的相关性

头孢地尔的批准为治疗 cUTI 和潜在治疗耐药革兰氏阴性病原体引起的医院获得性肺炎提供了新的选择。鉴于头孢地尔观察到的死亡率较高,应谨慎考虑其在治疗 CR 革兰氏阴性感染中的应用。

结论

头孢地尔对 MDR 革兰氏阴性病原体表现出有前景的活性。其在治疗 CR 革兰氏阴性细菌引起的严重感染中的应用需要进一步在 III 期临床研究中进行评估。

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