茴香菌素
伏立康唑
棘白菌素
米卡芬金
卡斯波芬金
泊沙康唑
医学
人口
药理学
重症监护医学
抗真菌
氟康唑
皮肤病科
环境卫生
作者
Susanne Perkhofer,Cornelia Lass‐Flörl
标识
DOI:10.1517/13543780903160658
摘要
The incidence of invasive fungal infections has been increasing since the 1980s due to a growing population of immunocompromised and critically ill patients with associated risk factors including immunosuppressive chemotherapy, prolonged periods on intensive care units and infection with HIV. Persons who are severely immunocompromised are particularly vulnerable to infection from molds and yeasts that are often found naturally in the environment. In recent years, several new systemic antifungal agents have been released, significantly increasing options for the treatment of the most serious fungal infections. Newly available drugs as those in the echinocandin class include caspofungin, micafungin and anidulafungin, as well as the newer generation triazoles, voriconazole and posaconazole. In this review, the in vitro and in vivo activity of anidulafungin and voriconazole, both new antimycotic substances with a different mode of action, are analyzed.
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