Zusammenfassung
Die Einführung von Itraconazol und Fluconazol brachte große Fortschritte in die Therapie opportunistischer Pilzinfektionen. Die Kliniker können heutzutage zwischen 5 verschiedenen systemisch wirksamen Antimykotika wählen, nämlich Amphotericin B (Amph B), liposomales Amphotericin B, 5-Flucytosin (5-FC), Itraconazol (ITRA) und Fluconazol (FLU). Die neuen Triazol-Derivate haben sich neben der Dermatologie und Gynäkologie bei folgenden opportunistischen Pilzinfektionen etabliert: die oropharyngeale und gastrointestinale Candidose spricht gut auf Fluconazol an [14,21]. Beide, Itraconazol [36, 38] und Fluconazol [32], werden erfolgreich bei der Erhaltungstherapie bei Cryptococcose bei AIDS-Patienten eingesetzt. Bei invasiver Aspergillose und beim Aspergillom erzielte ITRA in gewissen Fällen Heilungen, in anderen nicht [9,12, 36, 37]. Für beide Indikationen ist die klinische Prüfung noch nicht ganz abgeschlossen. Doch zeigt sich auch an diesem Horizont ein Lichtblick. Das liposomale Amph B wirkte in mehreren Fällen von therapieresistenten Pilzinfektionen kurativ [41]. Das ideale Antimykotikum zur Bekämpfung opportunistischer Pilzinfektionen existiert aber noch immer nicht. Es bleiben noch viele Probleme zu lösen.
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Polak, A. (1991). Die antimykotische Chemotherapie opportunistischer Pilzinfektionen. In: Staib, F., Huhn, D. (eds) Pilzinfektionen bei abwehrgeschwächten Patienten. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-76845-3_10
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