Abstract
Introduction: Patient perspectives are essential to establish relevant outcomes in trials assessing COPD treatments.
Aim: To assess which trial outcomes for exacerbation treatments are most important for patients with COPD.
Methods: Patients with COPD underwent semi-structured interviews where they stated what outcomes should be prioritised in clinical trials. Comparisons were made between patients with at least one COPD hospitalisation and patients with no hospitalisations in the preceding year.
Results: Semi-structured interviews were conducted for 70 patients in 11 countries across 4 continents (average age 66.7 years, 79.2% male). 45 patients had at least 1 admission in the previous year. 8 out of the 10 most frequently chosen outcomes focussed on chronic symptoms, such as dyspnoea (90.0%), and specific aspects affecting quality of life and function, such as reduced walking distance (70.0%) and impact on social life (57.1%). Patients with recent hospitalisations more frequently prioritised specific components of quality of life and function (Figure 1). Dyspnoea was most prioritised in both groups.
Conclusions: COPD exacerbations trials should more consistently assess the individual outcomes which contribute to overall quality of life and function, including dyspnoea. The outcomes highlighted align with the ERS statement on a core outcome set for trials on COPD exacerbation treatments.
Aim: To assess which trial outcomes for exacerbation treatments are most important for patients with COPD.
Methods: Patients with COPD underwent semi-structured interviews where they stated what outcomes should be prioritised in clinical trials. Comparisons were made between patients with at least one COPD hospitalisation and patients with no hospitalisations in the preceding year.
Results: Semi-structured interviews were conducted for 70 patients in 11 countries across 4 continents (average age 66.7 years, 79.2% male). 45 patients had at least 1 admission in the previous year. 8 out of the 10 most frequently chosen outcomes focussed on chronic symptoms, such as dyspnoea (90.0%), and specific aspects affecting quality of life and function, such as reduced walking distance (70.0%) and impact on social life (57.1%). Patients with recent hospitalisations more frequently prioritised specific components of quality of life and function (Figure 1). Dyspnoea was most prioritised in both groups.
Conclusions: COPD exacerbations trials should more consistently assess the individual outcomes which contribute to overall quality of life and function, including dyspnoea. The outcomes highlighted align with the ERS statement on a core outcome set for trials on COPD exacerbation treatments.
| Original language | English |
|---|---|
| Article number | PA356 |
| Book series | European Respiratory Journal. Supplement |
| Volume | 66 |
| Issue number | Suppl. 69 |
| ISSN | 0904-1850 |
| DOIs | |
| Publication status | Published - 2025 |
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