Allergic bronchopulmonary aspergillosis (ABPA) may affect from 1% to 15% of patients with cystic fibrosis (CF).1 This disease results from hypersensitivity to Aspergillus antigens, and afflicted patients may present with airway inflammation, bronchiectasis, and bronchoconstriction. Corticosteroids are the acknowledged first-line therapy for this condition. Itraconazole is often added to therapy if there is a slow or poor response to corticosteroids.
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Parisi et al. (2019) studied this question.
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