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头孢地尔在临床实践中的作用。

The role of cefiderocol in clinical practice.

机构信息

Emilio Maseda, Servicio de Anestesia y Reanimación. Hospital Valdecilla, Santander, Spain.

出版信息

Rev Esp Quimioter. 2022 Sep;35 Suppl 2(Suppl 2):39-44. doi: 10.37201/req/s02.06.2022. Epub 2022 Oct 4.

Abstract

Cefiderocol is a new antimicrobial with a chemical structure similar to ceftazidime and cefepime. In this review we will focus on the role of cefiderocol in different clinical scenarios produced by resistant Gram-negative microorganisms, especially to carbapenems. In infections caused by Gram-negative microorganisms, inappropriate antibiotic treatment increased the risk of mortality almost fourfold. In patients with hospital-acquired infection and septic shock; with sepsis and poor functional reserve due to fragility; in immunocompromised patients; and in those with local ecology, individual history of colonization or previous infection and risk factors for carbapenem-resistant Enterobacteriaceae (CRE) such as the presence of chronic multi-morbidities, the best option would be to start an active empirical treatment against gram-negative bacteria resistant to carbapenems and later in 24-36 h with the information obtained from the cultures we could decide on a definitive empirical or directed treatment and avoid unnecessary overuse of these antibiotics. Cefiderocol would be in these cases a good candidate due to its excellent in vitro activity against all classes of beta-lactamase-producing Gram-negatives (including carbapenemase class A, B and D producers), as well as against non-fermenting Gram-negatives such as P. aeruginosa, Acinetobacter spp. and S. maltophilia. It is necessary to optimize the use of new antibiotics such as cefiderocol, guaranteeing the best available treatment to patients while delaying the emergence and spread of resistance.

摘要

头孢地尔是一种新型抗菌药物,其化学结构类似于头孢他啶和头孢吡肟。在这篇综述中,我们将重点介绍头孢地尔在由耐药革兰氏阴性微生物引起的不同临床情况下的作用,尤其是对碳青霉烯类药物的耐药性。在由革兰氏阴性微生物引起的感染中,不适当的抗生素治疗使死亡率增加了近四倍。在医院获得性感染和感染性休克患者;有败血症和因脆弱而导致的功能储备不良;免疫功能低下的患者;以及具有局部生态、个体定植史或既往感染和碳青霉烯类耐药肠杆菌科(CRE)危险因素(如慢性多病共存)的患者,最佳选择是开始针对耐碳青霉烯类药物的革兰氏阴性细菌进行积极的经验性治疗,然后在 24-36 小时内根据培养物获得的信息决定进行明确的经验性或靶向治疗,并避免这些抗生素的不必要过度使用。头孢地尔在这些情况下是一个很好的候选药物,因为它对所有产β-内酰胺酶的革兰氏阴性菌(包括产 A、B 和 D 型碳青霉烯酶的菌株)以及非发酵革兰氏阴性菌(如铜绿假单胞菌、不动杆菌属和嗜麦芽窄食单胞菌)具有出色的体外活性。有必要优化新型抗生素如头孢地尔的使用,在延缓耐药性的出现和传播的同时,为患者提供最佳的现有治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11a0/9632056/9765f3b71203/revespquimioter-35-suppl-2-39-g001.jpg

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