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β-内酰胺类抗生素治疗革兰氏阴性感染的延长输注:原理和证据基础。

Prolonged infusion of beta-lactam antibiotics for Gram-negative infections: rationale and evidence base.

机构信息

University of Queensland Centre for Clinical Research (UQCCR), Faculty of Medicine, The University of Queensland, Brisbane, Queensland, Australia.

Division of Infectious Diseases, IRCCS Ospedale Policlinico San Martino, Genoa.

出版信息

Curr Opin Infect Dis. 2020 Dec;33(6):501-510. doi: 10.1097/QCO.0000000000000681.

DOI:10.1097/QCO.0000000000000681
PMID:33009140
Abstract

PURPOSE OF REVIEW

The aim of this review is to discuss the rationale of and current evidence for prolonged beta-lactam infusion in the management of Gram-negative infections.

RECENT FINDINGS

Pharmacokinetic/pharmacodynamic (PK/PD) data from various in-vitro and in-vivo experimental studies conclusively support prolonged infusion over intermittent infusion in terms of achieving effective beta-lactam exposure for maximal bacterial killing. Superior PK/PD target attainment has been demonstrated with prolonged beta-lactam infusion in patient populations that are more likely to have less susceptible Gram-negative infections. These populations include critically ill patients, cystic fibrosis patients and patients with malignant diseases. The clinical impact of prolonged beta-lactam infusion is likely to be the greatest in these patient groups: critically ill patients with a high level of illness severity who are not receiving renal replacement therapy; patients with nonfermenting Gram-negative bacilli infection and patients with respiratory infection. Critically ill patients with augmented renal clearance may not achieve effective beta-lactam exposure even with the use of prolonged infusion. Maximizing the effectiveness of prolonged beta-lactam infusion via therapeutic drug monitoring is becoming a more common strategy in the management of critically ill patients with Gram-negative infection.

SUMMARY

Prolonged beta-lactam infusion may not benefit all patients but only for those who are critically ill and/or immunocompromised, who are also more likely to have less susceptible Gram-negative infections.

摘要

目的综述

本综述旨在讨论延长β-内酰胺输注在治疗革兰氏阴性感染中的原理和当前证据。

最近的发现

来自各种体外和体内实验研究的药代动力学/药效学(PK/PD)数据明确支持在实现最大杀菌效果的有效β-内酰胺暴露方面,与间歇性输注相比,延长输注。在更有可能发生耐药革兰氏阴性感染的患者人群中,延长β-内酰胺输注已被证明具有更好的 PK/PD 目标达成率。这些人群包括重症患者、囊性纤维化患者和恶性疾病患者。在这些患者群体中,延长β-内酰胺输注的临床影响可能最大:病情严重程度高且未接受肾脏替代治疗的重症患者;患有非发酵革兰氏阴性杆菌感染和呼吸道感染的患者。即使使用延长输注,清除增强的重症患者也可能无法达到有效的β-内酰胺暴露。通过治疗药物监测来最大化延长β-内酰胺输注的效果,在治疗革兰氏阴性感染的重症患者中越来越成为一种常见策略。

总结

延长β-内酰胺输注可能并非对所有患者都有益,而只是对那些病情严重和/或免疫功能低下的患者有益,这些患者也更有可能发生耐药的革兰氏阴性感染。

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