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Histological Quantification to Determine Lung Fungal Burden in Experimental Aspergillosis
Published on: March 9, 2018
Aerosolized amphotericin for the treatment of allergic bronchopulmonary aspergillosis
Don Hayes1, Brian S Murphy, James E Lynch
1Department of Pediatrics, University of Kentucky College of Medicine, C424 University of Kentucky Medical Center, Lexington, KY, USA. don.hayes@uky.edu
Abstract:
Allergic bronchopulmonary aspergillosis (ABPA) is a complex hypersensitivity reaction to Aspergillus fumigatus that occur frequently in patients with cystic fibrosis (CF). Recurrent episodes of bronchial obstruction, inflammation, and mucoid impaction occur in ABPA and results in bronchiectasis, fibrosis, and respiratory failure. The treatment of ABPA includes corticosteroids to reduce the acute inflammation and intraconazole to reduce the fungal colonization load in order to reduce lung injury. This case discusses the successful use of aerosolized amphotericin B for the treatment of ABPA in a 14-year-old patient with CF listed for lung transplant. The patient required fewer hospitalizations, and both oral corticosteroids and anti-fungal therapy were eventually stopped.
Insights
Aerosolized amphotericin B successfully treated allergic bronchopulmonary aspergillosis (ABPA) in a cystic fibrosis (CF) patient, reducing hospitalizations and allowing cessation of other therapies.
Area of Science:
- Pulmonology
- Mycology
- Immunology
Background:
- Allergic bronchopulmonary aspergillosis (ABPA) is a hypersensitivity reaction to Aspergillus fumigatus, common in cystic fibrosis (CF) patients.
- ABPA leads to bronchial obstruction, inflammation, mucoid impaction, bronchiectasis, fibrosis, and respiratory failure.
- Current treatments involve corticosteroids and intraconazole, aiming to reduce inflammation and fungal load.
Observation:
- A 14-year-old cystic fibrosis patient with ABPA, awaiting lung transplant, was treated with aerosolized amphotericin B.
- This novel approach was administered as a potential alternative or adjunct therapy.
Findings:
- The patient experienced a successful treatment outcome with aerosolized amphotericin B.
- Hospitalizations were significantly reduced during the treatment period.
- The patient was eventually able to discontinue both oral corticosteroids and systemic anti-fungal medications.
Implications:
- Aerosolized amphotericin B presents a promising therapeutic option for ABPA in cystic fibrosis patients.
- This approach may reduce the need for systemic corticosteroids and other anti-fungal agents.
- Further research into aerosolized amphotericin B for ABPA management is warranted.
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