Prevalence, Diagnostic Utility and Associated Characteristics of Bronchodilator Responsiveness.

asthma; bronchodilator responsiveness; chronic obstructive pulmonary disease; diagnosis

Journal

American journal of respiratory and critical care medicine
ISSN: 1535-4970
Titre abrégé: Am J Respir Crit Care Med
Pays: United States
ID NLM: 9421642

Informations de publication

Date de publication:
29 Nov 2023
Historique:
medline: 29 11 2023
pubmed: 29 11 2023
entrez: 29 11 2023
Statut: aheadofprint

Résumé

The prevalence and diagnostic utility of bronchodilator responsiveness (BDR) in a real-life setting is unclear. We explored this uncertainty in patients aged ≥12 years with physician-assigned diagnoses of asthma, asthma and COPD, or COPD in NOVELTY, a prospective cohort study in primary and secondary care in 18 countries. The proportion of patients with a positive BDR test in each diagnostic category was calculated using 2005 (∆FEV1 or ∆FVC ≥12% and ≥200mL) and 2021 (∆FEV1 or ∆FVC >10% predicted) ERS/ATS criteria. We studied 3,519 patients with physician-assigned diagnosis of asthma, 833 with asthma+COPD, and 2,436 with COPD. The prevalence of BDR was 19.7% (asthma), 29.6% (asthma+COPD) and 24.7% (COPD) using 2005 criteria; 18.1%, 23.3% and 18.0% respectively using 2021 criteria. Using 2021 criteria, in patients diagnosed with asthma, BDR was associated with higher FeNO, lower lung function, higher symptom burden, more frequent hospital admissions, greater use of triple therapy, oral corticosteroids or biologics; in patients diagnosed with COPD, BDR (2021) was associated with lower lung function and higher symptom burden. BDR prevalence in patients with chronic airway diseases on treatment ranges from 18-30%, being modestly lower with the 2021 compared with 2005 ERS/ATS criteria, and is associated with lower lung function and greater symptom burden. These observations question the validity of BDR as a key diagnostic tool for asthma managed in clinical practice or as a standard inclusion criterion for clinical trials of asthma, and instead suggest BDR be considered a treatable trait for chronic airways disease.

Sections du résumé

BACKGROUND BACKGROUND
The prevalence and diagnostic utility of bronchodilator responsiveness (BDR) in a real-life setting is unclear. We explored this uncertainty in patients aged ≥12 years with physician-assigned diagnoses of asthma, asthma and COPD, or COPD in NOVELTY, a prospective cohort study in primary and secondary care in 18 countries.
METHODS METHODS
The proportion of patients with a positive BDR test in each diagnostic category was calculated using 2005 (∆FEV1 or ∆FVC ≥12% and ≥200mL) and 2021 (∆FEV1 or ∆FVC >10% predicted) ERS/ATS criteria.
RESULTS RESULTS
We studied 3,519 patients with physician-assigned diagnosis of asthma, 833 with asthma+COPD, and 2,436 with COPD. The prevalence of BDR was 19.7% (asthma), 29.6% (asthma+COPD) and 24.7% (COPD) using 2005 criteria; 18.1%, 23.3% and 18.0% respectively using 2021 criteria. Using 2021 criteria, in patients diagnosed with asthma, BDR was associated with higher FeNO, lower lung function, higher symptom burden, more frequent hospital admissions, greater use of triple therapy, oral corticosteroids or biologics; in patients diagnosed with COPD, BDR (2021) was associated with lower lung function and higher symptom burden.
CONCLUSIONS CONCLUSIONS
BDR prevalence in patients with chronic airway diseases on treatment ranges from 18-30%, being modestly lower with the 2021 compared with 2005 ERS/ATS criteria, and is associated with lower lung function and greater symptom burden. These observations question the validity of BDR as a key diagnostic tool for asthma managed in clinical practice or as a standard inclusion criterion for clinical trials of asthma, and instead suggest BDR be considered a treatable trait for chronic airways disease.

Identifiants

pubmed: 38029294
doi: 10.1164/rccm.202308-1436OC
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Auteurs

Richard Beasley (R)

Medical Research Institute of New ZealandWellington School of Medicine, Wellington, New Zealand; richard.beasley@mrinz.ac.nz.

Rod Hughes (R)

External Scientific Engagement, BioPharmaceuticals Medical, AstraZeneca, Cambridge, United Kingdom of Great Britain and Northern Ireland.

Alvar Agusti (A)

University of Barcelona Faculty of Medicine and Health Sciences, 73071, Barcelona, Spain.

Peter Calverley (P)

University of Liverpool, Liverpool, United Kingdom of Great Britain and Northern Ireland.

Bradley Chipps (B)

Capital Allergy and Respiratory Disease Centre, Sacramento, United States.

Ricardo Del Olmo (R)

Rehabilitation Hospital Pulmonary Diseases Maria Ferrer, 433288, Buenos Aires, Argentina.

Alberto Papi (A)

University of Ferrara, Research Centre on Asthma and COPD, Ferrara, Italy.

David Price (D)

Optimum Patient Care, Cambridge, United Kingdom of Great Britain and Northern Ireland.
University of Aberdeen, 1019, Division of Applied Health Sciences, Aberdeen, United Kingdom of Great Britain and Northern Ireland.
Observational and Pragmatic Research Institute, Singapore, Singapore.

Helen Reddel (H)

Woolcock Institute of Medical Research, 104349, Glebe, New South Wales, Australia.
Macquarie University, 7788, Sydney, New South Wales, Australia.

Hana Mullerova (H)

External Scientific Engagement, BioPharmaceuticals Medical, AstraZeneca, Cambridge, United Kingdom of Great Britain and Northern Ireland.

Eleni Rapsomaniki (E)

External Scientific Engagement, BioPharmaceuticals Medical, AstraZeneca, Cambridge, United Kingdom of Great Britain and Northern Ireland.

Classifications MeSH