Evidence map›Paper›PMID 42769880›Full record

ReviewFrontiers in medicine2026

Aerosolized antifungal therapy in pulmonary fungal disease: pharmacology, drug delivery and emerging clinical applications.

Massimo Caracciolo, Sarah Antonella Caracciolo, Maria Francesca Stagno, Simona Pellicano, Antonino Ripepi, Nadia Pellicano, Clara Scopelliti, Angela Elvira Serranò, Antonino Loddo, Stefano La Scala

Abstract readReview
In one paragraph

Review in Frontiers in medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Massimo CaraccioloAnesthesia and Post-Operative Care Unit, Villa Sant'Anna Hospital, Reggio Calabria, Italy.
Sarah Antonella CaraccioloDepartment of Anesthesia and Intensive Care, Santa Maria Nuova Hospital, Reggio Emilia, Italy.
Maria Francesca StagnoUOSD Post-Operative Intensive Care Unit, Great Metropolitan Hospital "Bianchi Melacrino Morelli", Reggio Calabria, Italy.
Simona PellicanoUOSD Post-Operative Intensive Care Unit, Great Metropolitan Hospital "Bianchi Melacrino Morelli", Reggio Calabria, Italy.
Antonino RipepiUOSD Post-Operative Intensive Care Unit, Great Metropolitan Hospital "Bianchi Melacrino Morelli", Reggio Calabria, Italy.
Nadia PellicanoUOSD Post-Operative Intensive Care Unit, Great Metropolitan Hospital "Bianchi Melacrino Morelli", Reggio Calabria, Italy.
Clara ScopellitiUOSD Post-Operative Intensive Care Unit, Great Metropolitan Hospital "Bianchi Melacrino Morelli", Reggio Calabria, Italy.
Angela Elvira SerranòUOSD Post-Operative Intensive Care Unit, Great Metropolitan Hospital "Bianchi Melacrino Morelli", Reggio Calabria, Italy.
Antonino LoddoUOSD Post-Operative Intensive Care Unit, Great Metropolitan Hospital "Bianchi Melacrino Morelli", Reggio Calabria, Italy.
Stefano La ScalaUOSD Post-Operative Intensive Care Unit, Great Metropolitan Hospital "Bianchi Melacrino Morelli", Reggio Calabria, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pulmonary fungal diseases remain associated with substantial morbidity and mortality, particularly in immunocompromised individuals, transplant recipients, and critically ill patients. Although systemic antifungal therapy remains the cornerstone of treatment, its effectiveness may be limited by suboptimal penetration into selected pulmonary compartments, while systemic toxicity, drug-drug interactions, and prolonged treatment requirements may restrict therapeutic options. Aerosolized antifungal therapy provides a pharmacologically attractive approach to increase local pulmonary drug exposure while limiting systemic exposure. Among currently available formulations, liposomal amphotericin B has the most extensive clinical experience for inhaled administration, supported by favorable pulmonary retention, respiratory tolerability, and compatibility with contemporary nebulization technologies. Advances in vibrating mesh nebulizers and aerosol delivery during invasive mechanical ventilation and high-flow respiratory support have further improved the technical feasibility of targeted pulmonary drug administration. Current clinical evidence is strongest for prophylaxis of invasive pulmonary aspergillosis in selected high-risk populations, particularly patients with prolonged neutropenia. Aerosolized amphotericin B formulations are also incorporated into prophylactic strategies after lung transplantation, although protocols remain heterogeneous and evidence is predominantly observational. By contrast, therapeutic applications beyond prophylaxis remain investigational. The potential role of aerosolized therapy differs substantially among pulmonary fungal diseases according to pathogen biology, anatomical distribution, host characteristics, and accessibility of the affected pulmonary compartment. Chronic pulmonary aspergillosis may provide a rationale for localized drug delivery, but cavitary disease and heterogeneous ventilation may limit aerosol deposition. For pulmonary mucormycosis, cryptococcosis,

Indexed as

aerosolized antifungal therapychronic pulmonary aspergillosisinhaled antifungal therapyinvasive pulmonary aspergillosislung transplantationnebulizationpulmonary drug deliverypulmonary fungal diseasevibrating mesh nebulizer

Identifiers

PMID42769880
PMCPMC13591464

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.