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用于治疗侵袭性真菌感染的新型及研究性三唑类药物。

New and investigational triazole agents for the treatment of invasive fungal infections.

作者信息

De Sarro A, La Camera E, Fera M T

机构信息

Dipartimento Clinico e Sperimentale di Medicina e Farmacologia, Università degli Studi di meddina, Itally.

出版信息

J Chemother. 2008 Dec;20(6):661-71. doi: 10.1179/joc.2008.20.6.661.

Abstract

The incidence of invasive fungal infections (IFIs) caused by both common and uncommon opportunistic fungi is increasing along with emerging fungal resistance. Since traditional agents (amphotericin B, fluconazole, itraconazole) are limited by an inadequate spectrum of activity, drug resistance or toxicity, there is a great interest in the development of new antifungal agents for treatment of IFIs in high-risk populations. In recent years a number of systemic antifungal drugs have become available and options for treatment of IFIs have expanded. A new generation of triazole agents (voriconazole, posaconazole, isavuconazole, ravuconazole and albaconazole), with a broad spectrum of activity and sufficient improvements in potency to overcome resistance have emerged and represent an alternative to conventional antifungals for the prevention and treatment of IFIs. This article focuses on the microbiology, pharmacology, clinical efficacy and safety of the new antifungal triazole generation.

摘要

随着真菌耐药性的不断出现,由常见和不常见的机会性真菌引起的侵袭性真菌感染(IFI)的发生率正在上升。由于传统药物(两性霉素B、氟康唑、伊曲康唑)存在抗菌谱不足、耐药性或毒性等局限性,因此开发用于治疗高危人群IFI的新型抗真菌药物备受关注。近年来,一些全身性抗真菌药物已可供使用,IFI的治疗选择也有所增加。新一代三唑类药物(伏立康唑、泊沙康唑、艾沙康唑、雷夫康唑和阿巴康唑)已出现,它们具有广谱抗菌活性,且在效力方面有足够的改进以克服耐药性,是预防和治疗IFI的传统抗真菌药物的替代品。本文重点介绍新一代抗真菌三唑类药物的微生物学、药理学、临床疗效和安全性。

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