Towards development of evidence to inform recommendations for the evaluation and management of bronchiectasis
- PMID: 36931575
- DOI: 10.1016/j.rmed.2023.107217
Towards development of evidence to inform recommendations for the evaluation and management of bronchiectasis
Abstract
Bronchiectasis (BE) is a chronic condition characterized by airway dilation as a consequence of a variety of pathogenic processes. It is often associated with persistent airway infection and an inflammatory response resulting in cough productive of purulent sputum, which has an adverse impact on quality of life. The prevalence of BE is increasing worldwide. Treatment guidelines exist for managing BE, but they are generally informed by a paucity of high-quality evidence. This review presents the findings of a scientific advisory board of experts held in the United States in November 2020. The main focus of the meeting was to identify unmet needs in BE and propose ways to identify research priorities for the management of BE, with a view to developing evidence-based treatment recommendations. Key issues identified include diagnosis, patient evaluation, promoting airway clearance and appropriate use of antimicrobials. Unmet needs include effective pharmacological agents to promote airway clearance and reduce inflammation, control of chronic infection, clinical endpoints to be used in the design of BE clinical trials, and more accurate classification of patients using phenotypes and endotypes to better guide treatment decisions and improve outcomes.
Keywords: Antimicrobials; Bronchiectasis; Clinical trials; Evidence-based treatment; Health-related quality of life; Unmet needs.
Copyright © 2023 The Authors. Published by Elsevier Ltd.. All rights reserved.
Conflict of interest statement
Declaration of competing interest Patrick A. Flume has received grant support from Abbvie, Armata, AstraZeneca, Corbus Pharmaceuticals, Cystic Fibrosis Foundation Therapeutics, Insmed, Janssen, Merck, National Institutes of Health, Novartis, Novoteris, Novovax, Proteostasis Therapeutics, Savara, Sound Pharmaceuticals, Inc. and Vertex Pharmaceuticals, Inc., and consultancy fees from Arrevus, Chiesi, Corbus Pharmaceuticals, Eloxx Pharmaceuticals, Hill-Rom, Insmed, Ionis Pharmaceuticals, Janssen Research and Development, McKesson, Merck, Novartis, Polyphor, Proteostasis Therapeutics, Santhera, Savara and Vertex Pharmaceuticals, Inc. Ashwin Basavaraj has acted as a consultant and advisory board participant for Insmed, Hill-Rom, Dymedso, Physioassist and Zambon, is a principal investigator in a clinical trial with Hill-Rom, and has received grant support from Insmed. Bryan Garcia has received grant support from the Cystic Fibrosis Foundation, CHEST Foundation, and consulting honoraria from Zambon, Insmed, Synspira and Resbiotic. Kevin Winthrop has received grant support from Pfizer, BMS, Insmed and the Cystic Fibrosis Foundation, and consulting honoraria from Novartis, Zambon, Insmed, Janssen, Redhills Biopharma, Paratek and Bayer. Emily Di Mango reports receiving advisory board fees from Zambon in 2019 and from Contrafect Pharmaceuticals in 2021. Charles L. Daley has received grant support from the Cystic Fibrosis Foundation, Insmed, Spero, Paratek and BugWorks, and consulted with AstraZeneca, Genentech, Pfizer, Insmed, Spero, Paratek, Beyond Air, AN2, Matinas and Zambon. Julie V. Philley has received grant support from Insmed, AN2, Paratek, Redhill, Electromed, Zambon and Hill Rom, and has been a consultant for Insmed, Paratek, AN2 and Electromed. Emily Henkle has been an advisory board participant for Zambon. Anne E. O'Donnell has received grant support from Insmed, Paratek, Redhill, Zambon, Janssen, and Astra Zeneca and has received consulting honoraria from Insmed, Paratek, Zambon, Boehringer Ingelheim, Astra Zeneca and Electromed. Mark Metersky has been a consultant for Savara, Insmed, International Biophysics, Zambon and Boehringer Ingelheim, and received clinical trial funding from Insmed.
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