Characteristics of patients initiated on budesonide/glycopyrronium bromide/formoterol fumarate single inhaler triple therapy for the treatment of chronic obstructive pulmonary disease: a population-based observational study

  • Gaétan Deslee
  • , Caroline Fabry-Vendrand
  • , Elsa Salmi
  • , Nolwenn Poccardi
  • , Adrien Coriat*
  • , Idir Ghout
  • , Caroline Eteve-Pitsaer
  • , Nicola Adderley
  • , Henri Leleu
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

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Abstract

Background: Budesonide/glycopyrronium bromide/formoterol fumarate (BUD/GLY/FOR) single inhaler triple therapy became available to prescribe to patients with severe chronic obstructive pulmonary disease (COPD) in France in 2021. The characteristics of patients prescribed BUD/GLY/FOR triple therapy and guideline adherence have not been previously described in France.

Objective: To describe the characteristics of COPD patients initiated on BUD/GLY/FOR triple therapy, assess adherence to COPD management guidelines, and explore any differences by prescribing physician.

Materials and Methods: A cross-sectional study using data from The Health Improvement Network (THIN®) France database was conducted. Patients with ≥ 2 recorded diagnostic codes for COPD were included. Demographic characteristics, comorbidities, management, COPD-related characteristics, and guideline adherence (Société de Pneumologie de Langue Française (SPLF); Haute Autorité de Santé (HAS)), stratified by initiating physician speciality (general practitioner (GP) or pulmonologist) were described.

Results: A total of 263 patients initiating BUD/GLY/FOR triple therapy were included. Mean (SD) age was 68.8 (11.8) years; 53.6% were male. Mean (SD) COPD duration was 6.4 (5.5) years. Comorbidities were common, with slightly more cardiometabolic and mental health conditions recorded in the GP-initiated group, and more comorbid respiratory conditions recorded in the pulmonologist-initiated group. About 77.2% (n=203) of patients had at least one moderate or severe exacerbation in the 12 months before initiation. About 86.3% had a previous record of dual (n=117, 44.5%) or triple (n=110, 41.8%) therapy. About 68.8% had been initiated on BUD/GLY/FOR triple therapy in line with SPLF guidelines (62.4% and 72.4% in the GP- and pulmonologist-initiated groups, respectively); among those with a record of COPD severity, 75.2% were initiated in line with HAS guidelines (69.2% and 76.3% in the GP- and pulmonologist-initiated groups, respectively).

Conclusion: The majority of COPD patients are prescribed BUD/GLY/FOR triple therapy in accordance with current treatment guidelines, irrespective of whether the therapy is prescribed by a general practitioner or a pulmonologist.
Original languageEnglish
Pages (from-to)1131-1142
Number of pages13
Journal International Journal of Chronic Obstructive Pulmonary Disease
Volume20
DOIs
Publication statusPublished - 18 Apr 2025

Keywords

  • chronic obstructive pulmonary disease
  • triple therapy
  • budesonide/glycopyrronium bromide/formoterol fumarate
  • management

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