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恶唑烷酮类药物是否名副其实?该抗菌药物类别的未来展望。

Have the oxazolidinones lived up to their billing? Future perspectives for this antibacterial class.

作者信息

Nilius Angela M

机构信息

Abbott Laboratories, Abbott Park, IL 60064-3537, USA.

出版信息

Curr Opin Investig Drugs. 2003 Feb;4(2):149-55.

Abstract

Linezolid was the first antibacterial oxazolidinone to be approved for clinical use. Oxazolidinones meet a growing medical need to treat multidrug-resistant, methicillin-resistant staphylococci, vancomycin-resistant enterococci, and penicillin-non-susceptible pneumococci in hospitalized patients. They also offer a treatment option for patients who are intolerant of vancomycin and other antibacterial agents, or who have infections that are refractory or resistant to other therapies. Two main concerns, however, have arisen as linezolid use has increased. The first is the incidence of myelosuppression, in particular thrombocytopenia, which appears to be greater than that seen during clinical trials. Secondly, linezolid-resistant Staphylococcus aureus and enterococci have emerged during linezolid treatment, which can be transmitted from patient-to-patient. This review will discuss the mechanism of action, the mechanism of resistance, and the antibacterial spectrum and potency of the oxazolidinones. In addition, the efficacy and safety of linezolid derived from clinical experience will be presented.

摘要

利奈唑胺是首个被批准用于临床的抗菌恶唑烷酮类药物。恶唑烷酮类药物满足了日益增长的医疗需求,可用于治疗住院患者中耐多药、耐甲氧西林葡萄球菌、耐万古霉素肠球菌以及对青霉素不敏感的肺炎球菌。它们还为不耐受万古霉素和其他抗菌药物的患者,或对其他治疗方法难治或耐药的感染患者提供了一种治疗选择。然而,随着利奈唑胺使用的增加,出现了两个主要问题。第一个是骨髓抑制的发生率,尤其是血小板减少症,其发生率似乎高于临床试验期间观察到的情况。其次,在利奈唑胺治疗期间出现了耐利奈唑胺金黄色葡萄球菌和肠球菌,它们可在患者之间传播。本综述将讨论恶唑烷酮类药物的作用机制、耐药机制以及抗菌谱和效力。此外,还将介绍来自临床经验的利奈唑胺的疗效和安全性。

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