GeneralAspectsofFungalDisease 357
&Azoles.Theseagentsdisruptergosterolbiosynthesis.Theireffectismainly
fungistaticwithpossiblegastrointestinalsideeffects.Hepaticfunctional
parametersshouldbemonitoredduringtherapy:
— Ketoconazole.Oneofthefirstazoles.Nolongerusedbecauseofside
effects.
— Fluconazole.Oralorintravenousapplication.Forthetreatmentofsurface
andsystemicmycosesandcryptococcalmeningitisinAIDSpatients.
— Itraconazole.Oralandintravenousapplication.Useinsystemicandcuta-
neousmycosesandalsoforthetreatmentofaspergillosis.
— Voriconazole.Oralandintravenousapplication.Goodactivityagainst
CandidaandAspergillus.NoacitivityagainstMucorales.
&Antimetabolites.5-Fluorocytosine.InterfereswithDNAsynthesis(base
analog).Givenbyoralapplicationincandidiasis,aspergillosis,andcryptococ-
cosis.Itisnecessarytomonitorthecourseoftherapyforthedevelopmentof
resistance.ThetoxicityofamphotericinBisreducedincombinationwith5-
fluorocytosine.
&Allylamines.Terbinafine.Byoralandtopicalapplicationtotreatderma-
tomycoses.Inhibitionofergosterolbiosynthesis.
&Echinocandins.Caspofunginhasbeenapprovedasasalvagetherapyin
refractoryaspergillosis.Itisusefulalsoinoropharyngealandesophagealcan-
didiasis.Inhibitionofthebiosynthesisofglucanofthecellwall.
&Griseofulvin.Thisisanolderantibioticusedintreatmentofdermatomy-
coses.Byoralapplication,therapymustoftenbecontinuedformonths.
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Kayser, Medical Microbiology © 2005 Thieme