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Management of systemic fungal infections: alternatives to itraconazole
Author(s) -
Raoul Herbrecht,
Yasmine Nivoix,
Cécile Fohrer,
Shanti NatarajanAmé,
V. LetscherBru
Publication year - 2005
Publication title -
journal of antimicrobial chemotherapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.124
H-Index - 194
eISSN - 1460-2091
pISSN - 0305-7453
DOI - 10.1093/jac/dki223
Subject(s) - anidulafungin , micafungin , caspofungin , itraconazole , amphotericin b , posaconazole , voriconazole , flucytosine , fluconazole , medicine , intensive care medicine , amphotericin b deoxycholate , echinocandin , antifungal drug , pharmacology , antifungal , dermatology
For many years, amphotericin B and flucytosine have been the only antifungal agents for invasive fungal infections. Amphotericin B was the standard of care for most of these infections. However, its use was often associated with low efficacy and poor tolerance. Fortunately, the antifungal armamentarium has increased during the past two decades with the addition of several new agents. In addition to itraconazole and fluconazole, lipid formulations of amphotericin B, voriconazole, caspofungin and micafungin have arrived on the market. Other agents are expected to be licensed shortly (anidulafungin, posaconazole). These various antifungal agents differ in their spectrum, pharmacokinetic profile, route of administration, efficacy in clinical trials, safety profile, drug-drug interactions and, importantly, their cost. There is no longer a unique standard agent for all or nearly all invasive fungal infections but a real choice among several agents. The characteristics of these new agents are reviewed to help clinicians in their decision to select an antifungal agent for their patients.

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