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Safety profile of drugs used in non-cystic fibrosis bronchiectasis: a narrative review. | LitMetric

AI Article Synopsis

  • - Non-cystic fibrosis bronchiectasis is a chronic lung disease causing symptoms like a persistent cough and frequent flare-ups, with no approved medications specifically for treatment.
  • - Current therapies often involve off-label use of drugs, including antibiotics and mucoactive treatments, although their safety has not been confirmed through randomized trials.
  • - This review examines the safety of commonly used drugs in treating bronchiectasis and highlights some new treatments under development for the condition.

Article Abstract

Non-cystic fibrosis bronchiectasis is a long-term lung disease characterised by abnormal dilatation of the bronchi, with patients experiencing chronic productive cough and recurrent exacerbations. Currently, there are no licensed drugs for use in bronchiectasis while clinical trials have been conducted to either test new drugs or repurpose existing ones. These drugs target the underlying pathophysiology of bronchiectasis which is known to include infection, inflammation, mucus hypersecretion and retention. Most of the drugs used in daily clinical practice for bronchiectasis are off-label with no randomised trials exploring their safety. This review aims at exploring the safety profile of drugs frequently used in clinical practice to manage bronchiectasis, including antibiotics (e.g. macrolides, aminoglycosides, polymyxins, fluoroquinolones, aztreonam), mucoactive therapy (e.g. hypertonic saline, mannitol, DNase and carbocisteine), anti-inflammatory therapy (inhaled corticosteroids) and drugs currently in development for use in bronchiectasis (e.g. brensocatib, benralizumab and itepekimab).

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11450733PMC
http://dx.doi.org/10.1177/20420986241279213DOI Listing

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