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Whole Genome Sequencing of Candida glabrata for Detection of Markers of Antifungal Drug Resistance
Published on: December 28, 2017
Recent advances in antifungal pharmacotherapy for invasive fungal infections
Jason C Gallagher1, Conan MacDougall, Elizabeth S Dodds Ashley
1Hahnemann University Hospital, Broad and Vine Sts, Mail Stop 451, Philadelphia, PA 19102, USA. jason.gallagher@tenethealth.com.
Abstract:
Invasive fungal infections carry significant morbidity and mortality. Candida species have become one of the most frequent causes of bloodstream infections, and infections caused by molds such as Aspergillus are becoming more frequent in immunocompromised patients. As this population grows, more invasive fungal infections can be anticipated. In the past, treatment options have been limited for many of these infections due to toxicity and efficacy concerns with the available antifungals. Fortunately, the past few years have brought exciting developments in antifungal pharmacotherapy. Lipid-based formulations of amphotericin B were introduced in the 1990s to attenuate adverse effects caused by amphotericin B deoxycholate (Fungizone, Bristol-Myers Squibb). Most recently, the echinocandins have been added to our antifungal regimen with the introduction of caspofungin (Cancidas, Merck and Co.) and voriconazole (Vfend, Pfizer), a new triazole, has come to market. The introduction of the echinocandins has invigorated the discussion about combination antifungal therapy. Evidence-based studies using these new agents are accumulating, and they are assuming important roles in the pharmacotherapy of invasive fungal infections in seriously ill and complex patients.
Insights
New antifungal medications, including echinocandins and voriconazole, offer improved treatment options for invasive fungal infections. These advancements are crucial for managing serious infections in immunocompromised patients.
Area of Science:
- Mycology
- Infectious Diseases
- Pharmacology
Background:
- Invasive fungal infections (IFIs) pose significant health risks, with Candida and Aspergillus species being common culprits, especially in immunocompromised individuals.
- Limited efficacy and toxicity of older antifungal agents historically restricted treatment options for IFIs.
- The growing population of immunocompromised patients is expected to increase the incidence of IFIs.
Purpose of the Study:
- To review recent advancements in antifungal pharmacotherapy.
- To discuss the role of new antifungal agents in treating IFIs.
- To explore the implications of new antifungals on combination therapy strategies.
Main Methods:
- Literature review of recent developments in antifungal pharmacotherapy.
- Analysis of clinical evidence for new antifungal agents like echinocandins and voriconazole.
- Discussion of treatment guidelines and emerging therapeutic approaches for IFIs.
Main Results:
- Introduction of lipid formulations of amphotericin B to reduce toxicity.
- Development of echinocandins (e.g., caspofungin) and a new triazole (voriconazole) offering new treatment avenues.
- Accumulating evidence supports the efficacy of these newer agents in managing IFIs.
Conclusions:
- Recent advances in antifungal pharmacotherapy have significantly expanded treatment options for IFIs.
- Newer agents like echinocandins and voriconazole are vital in managing serious fungal infections, particularly in complex and critically ill patients.
- These developments are reshaping the landscape of antifungal combination therapy.
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