Antifungal Agents Spectrum of Activity, Pharmacology, and Clinical Indications

被引:250
|
作者
Nett, Jeniel E. [1 ,2 ]
Andes, David R. [1 ,2 ]
机构
[1] Univ Wisconsin, Dept Med, Madison, WI 53705 USA
[2] Univ Wisconsin, Dept Med Microbiol & Immunol, Madison, WI 53705 USA
关键词
Antifungal; Spectrum of activity; Azole; Echinocandins; Amphotericin B; Pharmacokinetics; Indications; Toxicity; IN-VITRO ACTIVITIES; INFECTIOUS-DISEASES-SOCIETY; LIPOSOMAL AMPHOTERICIN-B; ITRACONAZOLE ORAL SOLUTION; INVASIVE FUNGAL-INFECTIONS; MURINE CANDIDIASIS MODEL; CENTRAL-NERVOUS-SYSTEM; AZOLE-REFRACTORY OROPHARYNGEAL; RANDOMIZED-CONTROLLED-TRIALS; CELL TRANSPLANT RECIPIENTS;
D O I
10.1016/j.idc.2015.10.012
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The currently available antifungal therapies vary significantly in terms of spectrum of activity, pharmacologic properties, toxicity, and potential for drug-drug interactions. This article provides a history of antifungal development and discusses the characteristics of individual drugs and drug classes, including the amphotericin B formulations, the triazoles, the echinocandins, and flucytosine. For each drug, the clinically relevant pharmacokinetics are reviewed, the spectrum of activity described, and the Food and Drug Administration-approved clinical indications examined. Anti fungal side-effects, therapeutic drug monitoring, and drug-drug interactions are summarized. The variations among different formulations are highlighted.
引用
收藏
页码:51 / +
页数:34
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