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Systemic antifungal agents.

W Abuhammour1, E Habte-Gabr

  • 1Department of Pediatrics, Hurley Medical Centre, Michigan State University-College of Human Medicine, Flint, Michigan, USA. wabuham1@hurleymc.com

Indian Journal of Pediatrics
|August 25, 2001
PubMed
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Systematic antifungal agents like amphotericin B and azoles are crucial for treating fungal infections. Newer formulations of amphotericin B reduce kidney toxicity, while triazoles are preferred for systemic therapy due to fewer side effects.

Area of Science:

  • Pharmacology
  • Mycology
  • Infectious Diseases

Background:

  • Systematic antifungal agents are vital for managing invasive fungal infections.
  • Amphotericin B, discovered in 1955, remains a primary treatment despite resistance in some fungi.
  • Newer liposomal amphotericin B formulations offer reduced nephrotoxicity.

Purpose of the Study:

  • To review systematic antifungal agents.
  • To discuss the properties and applications of amphotericin B, azoles, flucytosine, and griseofulvin.
  • To highlight advancements in antifungal drug development.

Main Methods:

  • Literature review of systematic antifungal agents.
  • Classification of antifungals into major groups.
  • Discussion of drug mechanisms, spectrum of activity, and clinical uses.

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Main Results:

  • Amphotericin B is effective against most fungi but has resistance issues with certain species.
  • Azoles are divided into imidazoles (superficial mycoses) and triazoles (systemic therapy).
  • Flucytosine is used adjunctively, and griseofulvin treats dermatophyte infections.

Conclusions:

  • Systematic antifungal agents encompass a range of drugs with distinct applications and resistance profiles.
  • Advancements in drug formulation, such as liposomal amphotericin B, improve safety.
  • Appropriate selection of antifungals is crucial for effective treatment of various mycoses.