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Related Concept Videos

Antifungal Agents01:15

Antifungal Agents

Amphotericin B is a broad-spectrum antifungal agent that exploits structural differences between fungal and mammalian cell membranes. Its amphipathic structure—featuring a hydrophobic polyene-lactone ring and a hydrophilic region containing mycosamine and carboxylic acid groups—enables selective binding to ergosterol, a sterol predominantly found in fungal plasma membranes. This selective interaction underlies the drug’s antifungal activity, although weak binding to cholesterol contributes to...
Combined Effects of Drugs: Synergism01:27

Combined Effects of Drugs: Synergism

Synergism is a useful mechanism where combining two or more drugs is more effective than each constituent used alone. Such combinations are also called supra-additive interactions. The drugs collectively enhance the final therapeutic effect by acting on different targets. Another advantage is that the low dose of each constituent drug is sufficient to achieve the desired effect. This helps reduce the duration of therapy and lower the adverse effects of these drugs.
Such synergistic combinations...
Antiprotozoal Agents01:21

Antiprotozoal Agents

Leishmaniasis is a widespread parasitic disease caused by several Leishmania species. It affects millions of people each year and remains a major public health problem in endemic regions. First-line treatment relies on pentavalent antimonials, including meglumine antimoniate and sodium stibogluconate. Even so, how these drugs work has not been fully clear, especially their interaction with parasite-specific biochemical pathways. One key target is trypanothione reductase (TR), an enzyme that...
Pharmaceutical Alternatives: Stability-Related Therapeutic Nonequivalence01:22

Pharmaceutical Alternatives: Stability-Related Therapeutic Nonequivalence

Generic intravenous (IV) drugs are considered bioequivalent to their branded counterparts due to their 100% bioavailability upon administration. However, variations in stability among different drug products can significantly influence their therapeutic performance, even if they are pharmaceutically equivalent.Cefuroxime, a prophylactic antimicrobial, is often used as a single-dose IV injection for patients undergoing coronary artery bypass grafting surgery. A 3 g dose typically provides...
Antimicrobial Effectiveness01:28

Antimicrobial Effectiveness

The effectiveness of antimicrobial agents depends on various factors influencing their ability to eliminate microbial populations. Larger microbial populations require more time for complete eradication, emphasizing the importance of population size analysis when evaluating antimicrobial efficacy.Microbial resistance to antimicrobial agents varies significantly. Highly resilient microorganisms include endospores, gram-negative bacteria, and non-enveloped viruses, while prions are exceptionally...
Anthelminthic Agents01:15

Anthelminthic Agents

Anthelmintic drugs differ significantly from antiparasitic therapies targeting protozoa, primarily due to differences in parasite biology. Whereas most protozoal treatments act on proliferating cells, anthelmintics are typically directed against mature, nonproliferative helminths. The therapeutic approach considers the helminth's reliance on neuromuscular coordination, glucose metabolism, and microtubular integrity for survival, reproduction, and localization within the host. Most anthelmintics...

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Updated: Jun 14, 2026

Whole Genome Sequencing of Candida glabrata for Detection of Markers of Antifungal Drug Resistance
08:45

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Published on: December 28, 2017

EUCAST breakpoints for antifungals.

Juan L Rodríguez-Tudela1, Maiken C Arendrup, Manuel Cuenca-Estrella

  • 1Micology Service, National Microbiology Center, Carlos III Health Institute, Madrid, Spain. jlrtudela@isciii.es

Drug News & Perspectives
|April 7, 2010
PubMed
Summary

The European Committee on Antibiotic Susceptibility Testing (EUCAST) outlines its method for establishing antifungal susceptibility testing breakpoints. This process ensures accurate interpretation of antifungal resistance in clinical settings.

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Area of Science:

  • Medical Mycology
  • Clinical Microbiology
  • Pharmacology

Background:

  • Invasive fungal infections are increasing, alongside the development of new antifungals and reports of resistance.
  • Accurate antifungal susceptibility testing and interpretative breakpoints are crucial for effective treatment.

Purpose of the Study:

  • To describe the European Committee on Antibiotic Susceptibility Testing (EUCAST) process for setting antifungal breakpoints.
  • To detail the methodology used by EUCAST in developing standards for antifungal susceptibility testing.

Main Methods:

  • Evaluation of common European drug dosages.
  • Definition of wild-type microbial populations and epidemiological cutoffs.
  • Analysis of drug pharmacokinetics, pharmacodynamics (including Monte Carlo simulations), and MIC-clinical outcome correlations.

Main Results:

  • EUCAST has developed standards for yeast and mold susceptibility testing.
  • Proposed breakpoints for fluconazole and voriconazole against Candida species have been established.
  • Epidemiological cutoff values are recommended when clinical outcome data are insufficient for breakpoint determination.

Conclusions:

  • The EUCAST breakpoint setting process is a comprehensive evaluation of multiple factors.
  • This systematic approach aims to improve the clinical utility of antifungal susceptibility testing.
  • The process ensures that breakpoints are based on robust scientific evidence and clinical relevance.