Factors associated with "Frequent Exacerbator" phenotype in children with bronchiectasis: The first report on children from the Australian Bronchiectasis Registry. (November 2021)

• Record Type: Journal Article
• Authors: Kapur, Nitin; Stroil-Salama, Enna; Morgan, Lucy; Yerkovich, Stephanie; Holmes-Liew, Chien-Li; King, Paul; Middleton, Peter; Maguire, Graeme; Smith, Daniel; Thomson, Rachel; McCallum, Gabrielle; Owens, Louisa; Chang, Anne B
• Is Part Of: Respiratory medicine. Volume 188(2021)
• Publication Date: 2021-11
• Subjects: Bronchiectasis -- Children -- Registry -- Phenotypes -- Frequent exacerbator; Chest -- Diseases -- Periodicals; Chest -- Diseases -- Great Britain -- Periodicals; Respiratory organs -- Diseases -- Periodicals; Respiratory Tract Diseases -- Periodicals; Appareil respiratoire -- Maladies -- Périodiques; Thorax -- Maladies -- Périodiques; Appareil respiratoire -- Maladies -- Traitement -- Périodiques; Electronic journals; 616.2
• DOI: 10.1016/j.rmed.2021.106627
• Languages: English
• ISSNs: 0954-6111

Abstract

Abstract: Introduction: In adults with bronchiectasis, multicentre data advanced the field including disease characterisation and derivation of phenotypes such as 'frequent exacerbator (FE)' (≥3 exacerbations/year). However, paediatric cohorts are largely limited to single centres and no scientifically derived phenotypes of paediatric bronchiectasis yet exists. Using paediatric data from the Australian Bronchiectasis Registry (ABR), we aimed to: (a) describe the clinical characteristics and compare Indigenous with non-Indigenous children, and (b) determine if a FE phenotype can be identified and if so, its associated factors. Methods: We retrieved data of children (aged <18-years) with radiologically confirmed bronchiectasis, enrolled between March 2016–March 2020. Results: Across five sites, 540 children [288 Indigenous; median age = 8-years (IQR 6–11)] were included. Baseline characteristics revealed past infection/idiopathic was the commonest (70%) underlying aetiology, most had cylindrical bronchiectasis and normal spirometry. Indigenous children (vs. non-Indigenous) had significantly more environmental tobacco smoke exposure (84% vs 32%, p < 0.0001) and lower birth weight (2797 g vs 3260 g, p < 0.0001). FE phenotype present in 162 (30%) children, was associated with being younger (ORadjusted = 0.85, 95%CI 0.81–0.90), more recent diagnosis of bronchiectasis (ORadjusted = 0.67; 95%CI 0.60–0.75), recent hospitalization (ORadj = 4.51; 95%CI 2.45–8.54) and Pseudomonas aeruginosa ( PsA ) infection (ORadjusted = 2.43; 95%CI 1.01–5.78). The FE phenotype were less likely to be Indigenous (ORadjusted = 0.14; 95%CI 0.03–0.65). Conclusion: Even within a single country, the characteristics of children with bronchiectasis differ among cohorts. A paediatric FE phenotype exists and is characterised by being younger with a more recent diagnosis, PsA infection and previous hospitalization. Prospective data to consolidate our findings characterising childhood bronchiectasis phenotypes are required. Highlights: Bronchiectasis in children is an important yet heterogenous chronic respiratory condition with significant knowledge gaps. This is the largest multi-centric study defining clinical phenotypes using a registry-based approach. A Frequent Exacerbator phenotype exists in children with bronchiectasis..