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抗真菌药敏试验。技术现状、局限性与标准化

Antifungal susceptibility testing. Current state of technology, limitations, and standardization.

作者信息

Pfaller M A, Rinaldi M G

机构信息

Department of Pathology, Oregon Health Sciences University, Portland.

出版信息

Infect Dis Clin North Am. 1993 Jun;7(2):435-44.

PMID:8345178
Abstract

In parallel with the escalating incidence of serious, invasive fungal infections in the immune-compromised host has been the development and use of new, potentially efficacious antifungal agents as well as recognition of both primary and secondary resistance to such drugs by the etiologic mycotic agents. These findings have generated considerable enthusiasm for a reproducible and standardized means for the laboratory evaluation of antifungal drugs. For over a decade, global investigations have ensued in the hope of generating laboratory methods analogous to those used for antibacterial drugs that may predict the optimal therapeutic choice for clinicians treating mycoses. This article reviews the background, history, and development of in vitro antifungal susceptibility efforts, details the problems inherent in this area of laboratory medicine/infectious diseases, and assesses the contemporary aspects of standardization.

摘要

在免疫功能低下宿主中,严重侵袭性真菌感染的发病率不断上升的同时,新的、可能有效的抗真菌药物得到了开发和应用,并且病原真菌对这类药物的原发性和继发性耐药性也得到了认识。这些发现激发了人们对用于抗真菌药物实验室评估的可重复且标准化方法的极大热情。十多年来,全球范围内都在进行研究,希望能开发出类似于用于抗菌药物的实验室方法,从而为治疗真菌病的临床医生预测最佳治疗选择。本文回顾了体外抗真菌药敏试验的背景、历史和发展,详述了检验医学/传染病领域中该方法所固有的问题,并评估了标准化的现状。

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