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念珠菌属临床抗真菌药敏试验的最新进展。

Update on clinical antifungal susceptibility testing for Candida species.

作者信息

Lewis R E, Klepser M E, Pfaller M A

机构信息

College of Pharmacy, University of Iowa, Iowa City 52242-1112, USA.

出版信息

Pharmacotherapy. 1998 May-Jun;18(3):509-15.

PMID:9620102
Abstract

With the emergence of fungi as important nosocomial pathogens, increasing reports of antifungal resistance, and expanding drug therapy options, the need for clinically relevant antifungal susceptibility testing is evident. Over the last decade, the National Committee for Clinical Laboratory Standards (NCCLS) worked to standardize procedures for in vitro susceptibility testing of Candida species against fluconazole, itraconazole, 5-fluorocytosine, and amphotericin B. With the establishment of a reproducible methodology, correlation of antifungal susceptibility in vitro with clinical outcome is a priority. The NCCLS proposed susceptibility breakpoints for the three agents against Candida species, with breakpoints for amphotericin B forthcoming. These breakpoints could provide useful guidance in some clinical situations involving azole or 5-fluorocytosine therapy; however, routine susceptibility testing of fungal isolates should be discouraged.

摘要

随着真菌成为重要的医院病原体,抗真菌耐药性报告不断增加,以及药物治疗选择的扩大,进行临床相关的抗真菌药敏试验的必要性显而易见。在过去十年中,美国国家临床实验室标准委员会(NCCLS)致力于规范念珠菌属对氟康唑、伊曲康唑、5-氟胞嘧啶和两性霉素B的体外药敏试验程序。随着可重复方法的建立,体外抗真菌药敏与临床结果的相关性成为优先事项。NCCLS提出了这三种药物针对念珠菌属的药敏折点,两性霉素B的折点即将出台。这些折点在某些涉及唑类或5-氟胞嘧啶治疗的临床情况下可能提供有用的指导;然而,应不鼓励对真菌分离株进行常规药敏试验。

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