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西班牙新型隐球菌新型变种临床分离株中的抗真菌耐药率。

Rates of antifungal resistance among Spanish clinical isolates of Cryptococcus neoformans var. neoformans.

作者信息

Perkins Alexander, Gomez-Lopez Alicia, Mellado Emilia, Rodriguez-Tudela Juan L, Cuenca-Estrella Manuel

机构信息

Servicio de Micología, Centro Nacional de Microbiología, Instituto de Salud Carlos III, Ctra Majadahonda-Pozuelo Km 2. 28220 Majadahonda (Madrid), Spain.

出版信息

J Antimicrob Chemother. 2005 Dec;56(6):1144-7. doi: 10.1093/jac/dki393. Epub 2005 Nov 9.

Abstract

OBJECTIVES

Activities in vitro of six antifungal agents were tested against a collection of 317 Cryptococcus neoformans var. neoformans clinical isolates.

METHODS

The procedure described in document 7.1 by the European Committee on Antibiotic Susceptibility Testing with minor modifications was employed.

RESULTS

Amphotericin B, itraconazole, voriconazole and ravuconazole exhibited a potent activity with geometric mean (GM) MICs under 0.26 mg/L. The GM MIC of flucytosine was 7.33 mg/L and that of fluconazole was 4.16 mg/L. The rates of antifungal resistance were 5.3% for amphotericin B, 0.9% for voriconazole and 3.1% for ravuconazole. Fifteen point eight per cent of strains had itraconazole MICs > or = 1 mg/L, and 46% of strains had flucytosine MICs > or = 8 mg/L. Fluconazole susceptibility (MIC < or = 8 mg/L) stood at 53.4%.

CONCLUSIONS

The percentage of fluconazole susceptibility was significantly lower than that in other surveys. Cross-resistance to itraconazole was common (33.8%) but almost the whole collection was susceptible to voriconazole and ravuconazole. These results should be confirmed with prospective and population-based surveillance programmes.

摘要

目的

检测六种抗真菌药物对317株新型隐球菌新型变种临床分离株的体外活性。

方法

采用欧洲抗生素敏感性试验委员会文件7.1中所述方法并略作修改。

结果

两性霉素B、伊曲康唑、伏立康唑和雷夫康唑表现出强效活性,几何平均(GM)最低抑菌浓度(MIC)低于0.26mg/L。氟胞嘧啶的GM MIC为7.33mg/L,氟康唑的GM MIC为4.16mg/L。两性霉素B的抗真菌耐药率为5.3%,伏立康唑为0.9%,雷夫康唑为3.1%。15.8%的菌株伊曲康唑MIC≥1mg/L,46%的菌株氟胞嘧啶MIC≥8mg/L。氟康唑敏感性(MIC≤8mg/L)为53.4%。

结论

氟康唑敏感性百分比显著低于其他调查结果。对伊曲康唑的交叉耐药很常见(33.8%),但几乎所有菌株对伏立康唑和雷夫康唑敏感。这些结果应通过前瞻性和基于人群的监测计划加以证实。

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