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碳青霉烯类耐药革兰氏阴性菌的联合治疗。

Combination therapy for carbapenem-resistant Gram-negative bacteria.

机构信息

Infectious Diseases Service, Hospital de Clínicas de Porto Alegre, 2350 Ramiro Barcelos St, Porto Alegre, 90.035-903, Brazil.

出版信息

Expert Rev Anti Infect Ther. 2013 Dec;11(12):1333-53. doi: 10.1586/14787210.2013.845523. Epub 2013 Nov 6.

Abstract

The emergence of resistant to carbapenems Gram-negative bacteria (CR GNB) has severely challenged antimicrobial therapy. Many CR GNB isolates are only susceptible to polymyxins; however, therapy with polymyxins and other potentially active antibiotics presents some drawbacks, which have discouraged their use in monotherapy. In this context, along with strong pre-clinical evidence of benefit in combining antimicrobials against CR GNB, the clinical use of combination therapy has been raised as an interesting strategy to overcome these potential limitations of a single agent. Polymyxins, tigecycline and even carbapenems are usually the cornerstone agents in combination schemes. Optimization of the probability to attain the pharmacokinetic/pharmacodynamic targets by both cornerstone drug and adjuvant drug is of paramount importance to achieve better clinical and microbiological outcomes. Clinical evidence of the major drugs utilized in combination schemes and how they should be prescribed considering pharmacokinetic/pharmacodynamic characteristics against CR GNB will be reviewed in this article.

摘要

耐药碳青霉烯类革兰氏阴性菌(CR GNB)的出现严重挑战了抗菌治疗。许多 CR GNB 分离株仅对多黏菌素敏感;然而,多黏菌素和其他潜在有效抗生素的治疗存在一些缺点,这阻碍了它们在单药治疗中的应用。在这种情况下,鉴于联合使用针对 CR GNB 的抗菌药物具有强有力的临床前获益证据,联合治疗的临床应用已被提为克服单一药物潜在局限性的一种有趣策略。多黏菌素、替加环素甚至碳青霉烯类通常是联合方案中的基石药物。优化基石药物和辅助药物达到药代动力学/药效学目标的概率对于实现更好的临床和微生物学结果至关重要。本文将回顾联合方案中主要药物的临床证据,以及考虑针对 CR GNB 的药代动力学/药效学特征如何对其进行处方。

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