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头孢他啶-阿维巴坦用于重症患者:一项多中心观察性研究。

Ceftazidime-Avibactam in Critically Ill Patients: A Multicenter Observational Study.

作者信息

Silvia Olivieri, Mazzanti Sara, Gelo Signorino Gabriele, Pallotta Francesco, Ficola Andrea, Canovari Benedetta, Di Muzio Vanessa, Di Prinzio Michele, Cerutti Elisabetta, Donati Abele, Giacometti Andrea, Barchiesi Francesco, Brescini Lucia

机构信息

Infectious Diseases, Via Murri, 15, 63023 Fermo, Italy.

Infectious Diseases Clinic, Via Conca 71, 60126 Torrette, Italy.

出版信息

Antibiotics (Basel). 2025 Aug 5;14(8):797. doi: 10.3390/antibiotics14080797.

Abstract

UNLABELLED

Ceftazidime-avibactam (CAZ-AVI) is a second-generation intravenous β-lactam/β-lactamase inhibitor combination. In recent years, substantial evidence has emerged regarding the efficacy and safety of CAZ-AVI. However, data on its use in critically ill patients remain limited.

BACKGROUND/OBJECTIVES: This multicenter, retrospective, observational cohort study was conducted across four Intensive Care Units (ICUs) in three hospitals in the Marche region of Italy. The primary objective was to evaluate the 30-day clinical outcomes and identify risk factors associated with 30-day clinical failure-defined as death, microbiological recurrence, or persistence within 30 days after discontinuation of therapy-in critically ill patients treated with CAZ-AVI.

METHODS

The study included all adult critically ill patients admitted to the participating ICUs between January 2020 and September 2023 who received CAZ-AVI for at least 72 h for the treatment of a confirmed or suspected Gram-negative bacterial (GNB) infection.

RESULTS

Among the 161 patients included in the study, CAZ-AVI treatment resulted in a positive clinical outcome (i.e., clinical improvement and 30-day survival) in 58% of cases (n = 93/161), while the overall mortality rate was 24% (n = 38/161). Relapse or persistent infection occurred in a substantial proportion of patients (25%, n = 41/161). Notably, acquired resistance to CAZ-AVI was observed in 26% of these cases, likely due to suboptimal use of the drug in relation to its pharmacokinetic/pharmacodynamic (PK/PD) properties in critically ill patients. Furthermore, treatment failure was more frequent among immunosuppressed individuals, particularly liver transplant recipients.

CONCLUSIONS

This study demonstrates that the mortality rate among ICU patients treated with this novel antimicrobial combination is consistent with findings from other studies involving heterogeneous populations. However, the rapid emergence of resistance underscores the need for vigilant surveillance and the implementation of robust antimicrobial stewardship strategies.

摘要

未标注

头孢他啶-阿维巴坦(CAZ-AVI)是第二代静脉用β-内酰胺/β-内酰胺酶抑制剂组合。近年来,出现了大量关于CAZ-AVI疗效和安全性的证据。然而,其在重症患者中使用的数据仍然有限。

背景/目的:这项多中心、回顾性、观察性队列研究在意大利马尔凯地区三家医院的四个重症监护病房(ICU)进行。主要目的是评估30天临床结局,并确定与30天临床失败相关的危险因素,30天临床失败定义为在接受CAZ-AVI治疗的重症患者停药后30天内死亡、微生物复发或持续感染。

方法

该研究纳入了2020年1月至2023年9月期间入住参与研究的ICU并接受CAZ-AVI治疗至少72小时以治疗确诊或疑似革兰氏阴性菌(GNB)感染的所有成年重症患者。

结果

在纳入研究的161例患者中,CAZ-AVI治疗在58%的病例(n = 93/161)中产生了积极的临床结局(即临床改善和30天生存),而总死亡率为24%(n = 38/161)。相当一部分患者(25%,n = 41/161)出现复发或持续感染。值得注意的是,在这些病例中有26%观察到对CAZ-AVI获得性耐药,这可能是由于在重症患者中药物的药代动力学/药效学(PK/PD)特性使用不当。此外,免疫抑制个体,特别是肝移植受者中治疗失败更为常见。

结论

这项研究表明,使用这种新型抗菌药物组合治疗的ICU患者死亡率与其他涉及异质人群的研究结果一致。然而,耐药性的迅速出现凸显了进行警惕监测和实施强有力的抗菌药物管理策略的必要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc85/12383002/e817a55612c2/antibiotics-14-00797-g001.jpg

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