ITRACONAZOLE - A NEW TRIAZOLE ANTIFUNGAL AGENT

被引:0
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作者
ZUCKERMAN, JM [1 ]
TUNKEL, AR [1 ]
机构
[1] MED COLL PENN, DIV INFECT DIS, 3300 HENRY AVE, PHILADELPHIA, PA 19129 USA
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R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
The azole antifungal agents represent a major advance in the management of superficial and systemic fungal infections. Itraconazole appears to have a broad spectrum of in vitro activity and is the first azole antifungal agent to have activity against Aspergillus species. Itraconazole acts primarily by impairing the synthesis of ergosterol, resulting in a defective fungal cell membrane with altered permeability and function. It is effective for a wide variety of mycotic infections and some fungal meningeal infections. Most adverse effects have been relatively minor and do not lead to discontinuation of therapy (Infect Control Hosp Epidemiol 1994;15:397-410).
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页码:397 / 410
页数:14
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