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Published on: February 14, 2018
Antifungal prophylaxis and pre-emptive therapy: When and how?
Rosanne Sprute1, Julia A Nacov1, Dionysios Neofytos2
1University of Cologne, Faculty of Medicine and University Hospital Cologne, Translational Research, Cologne Excellence Cluster on Cellular Stress Responses in Aging-Associated Diseases (CECAD), Cologne, Germany; University of Cologne, Faculty of Medicine and University Hospital Cologne, Department I of Internal Medicine, Center for Integrated Oncology Aachen Bonn Cologne Duesseldorf (CIO ABCD) and Excellence Center for Medical Mycology (ECMM), Cologne, Germany; German Centre for Infection Research (DZIF), Partner Site Bonn-Cologne, Cologne, Germany.
Abstract:
The growing pool of critically ill or immunocompromised patients leads to a constant increase of life-threatening invasive infections by fungi such as Aspergillus spp., Candida spp. and Pneumocystis jirovecii. In response to this, prophylactic and pre-emptive antifungal treatment strategies have been developed and implemented for high-risk patient populations. The benefit by risk reduction needs to be carefully weighed against potential harm caused by prolonged exposure against antifungal agents. This includes adverse effects and development of resistance as well as costs for the healthcare system. In this review, we summarise evidence and discuss advantages and downsides of antifungal prophylaxis and pre-emptive treatment in the setting of malignancies such as acute leukaemia, haematopoietic stem cell transplantation, CAR-T cell therapy, and solid organ transplant. We also address preventive strategies in patients after abdominal surgery and with viral pneumonia as well as individuals with inherited immunodeficiencies. Notable progress has been made in haematology research, where strong recommendations regarding antifungal prophylaxis and pre-emptive treatment are backed by data from randomized controlled trials, whereas other critical areas still lack high-quality evidence. In these areas, paucity of definitive data translates into centre-specific strategies that are based on interpretation of available data, local expertise, and epidemiology. The development of novel immunomodulating anticancer drugs, high-end intensive care treatment and the development of new antifungals with new modes of action, adverse effects and routes of administration will have implications on future prophylactic and pre-emptive approaches.
Insights
Antifungal prophylaxis and pre-emptive treatment are crucial for high-risk patients but require careful risk-benefit assessment. Evidence is strongest in hematology, with other areas needing more research for optimal strategies.
Area of Science:
- Infectious Diseases
- Clinical Pharmacy
- Hematology
Background:
- Critically ill and immunocompromised patients face increased risk of invasive fungal infections (e.g., Aspergillus, Candida, Pneumocystis jirovecii).
- Prophylactic and pre-emptive antifungal strategies are implemented for high-risk populations, necessitating a balance between risk reduction and potential harm.
Purpose of the Study:
- To review evidence on the advantages and disadvantages of antifungal prophylaxis and pre-emptive treatment.
- To discuss current strategies in various patient groups, including those with malignancies, post-surgery, viral pneumonia, and immunodeficiencies.
Main Methods:
- Literature review summarizing evidence on antifungal prophylaxis and pre-emptive treatment.
- Discussion of benefits, harms, and current practices across different clinical settings.
Main Results:
- Strong evidence and recommendations exist for antifungal strategies in hematology, supported by randomized controlled trials.
- Other clinical areas lack high-quality data, leading to center-specific approaches based on local epidemiology and expertise.
Conclusions:
- Future antifungal strategies will be influenced by novel anticancer drugs, intensive care advancements, and new antifungal agents.
- Balancing benefits and harms of antifungal interventions remains critical, especially where high-quality evidence is limited.
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