Suboptimal Peak Inspiratory Flow, COPD Exacerbations, Hospitalisations, and Disease Burden: A Longitudinal Follow-Up in a Multicentre Real-World Study

Background Peak Inspiratory Flow (PIF) is a critical determinant of dry powder inhaler (DPI) effectiveness in managing patients with Chronic Obstructive Pulmonary Disease (COPD). Suboptimal PIF may compromise drug delivery and clinical outcomes. Objective To evaluate the association between repeated PIF measures and disease exacerbations, hospitalisations, and symptom burden in patients with stable COPD. Methods In this multi-country, observational cohort, 415 participants aged ≥40 years with confirmed COPD and a smoking history underwent PIF measurements at their prescribed inhaler's resistance, and low-, and high-resistance levels using the In-Check DIAL G16. Clinical assessments occurred at 3 months (Follow-Up 1, FU1) and 6 months (Follow-Up 2, FU2) including spirometry, COPD Assessment Test (CAT) scores, medication use, and exacerbation/hospitalisation rates. Results At FU1, 29.4% (n=113/384) had typical suboptimal PIF and 28.6% (n=108/377) remained suboptimal at FU2. Participants with suboptimal PIF were more often female and current smokers, with consistently poorer lung function across both visits: lower FEV1 (% predicted: 33.7±9.1% versus 45.7±9.2%, p=0.01), actual FVC and inspiratory capacity were observed. Suboptimal PIF significantly predicted moderate (p=0.03) and severe (p=0.01) exacerbations, was associated with higher hospitalisation risks (p=0.05), and with greater use of short-acting beta agonist, oral corticosteroid, and triple therapy. Conclusions Suboptimal PIF is a stable, clinically meaningful marker of worse COPD outcomes and may guide more personalised inhaler selection.

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Publication Details

Journal
ERJ Open Research
Published
2026-06-25
DOI
https://doi.org/10.1183/23120541.00343-2026
Primary Topic
Chronic Obstructive Pulmonary Disease (COPD) Research
Type
article
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article

Suboptimal Peak Inspiratory Flow, COPD Exacerbations, Hospitalisations, and Disease Burden: A Longitudinal Follow-Up in a Multicentre Real-World Study

Annie Navarro, Ji‐Yong Moon, Pietro Pirina, Chin Kook Rhee et al.
ERJ Open Research
Chronic Obstructive Pulmonary Disease (COPD) Research
article

Suboptimal Peak Inspiratory Flow, COPD Exacerbations, Hospitalisations, and Disease Burden: A Longitudinal Follow-Up in a Multicentre Real-World Study

Annie Navarro, Ji‐Yong Moon, Pietro Pirina, Chin Kook Rhee, Tiew Pei Yee, Bernardino Alcázar Navarrete, Caroline Gouder, Valeria Perugini, Virginia Almadana Pacheco, Marc Miravitlles, Chee Hong Loh, Matevž Harlander, Seung Won, Omar Usmani, Naval Elsa, Kwang Ha Yoo, Thérèse S. Lapperre
article en

Abstract

Background Peak Inspiratory Flow (PIF) is a critical determinant of dry powder inhaler (DPI) effectiveness in managing patients with Chronic Obstructive Pulmonary Disease (COPD). Suboptimal PIF may compromise drug delivery and clinical outcomes. Objective To evaluate the association between repeated PIF measures and disease exacerbations, hospitalisations, and symptom burden in patients with stable COPD. Methods In this multi-country, observational cohort, 415 participants aged ≥40 years with confirmed COPD and a smoking history underwent PIF measurements at their prescribed inhaler's resistance, and low-, and high-resistance levels using the In-Check DIAL G16. Clinical assessments occurred at 3 months (Follow-Up 1, FU1) and 6 months (Follow-Up 2, FU2) including spirometry, COPD Assessment Test (CAT) scores, medication use, and exacerbation/hospitalisation rates. Results At FU1, 29.4% (n=113/384) had typical suboptimal PIF and 28.6% (n=108/377) remained suboptimal at FU2. Participants with suboptimal PIF were more often female and current smokers, with consistently poorer lung function across both visits: lower FEV1 (% predicted: 33.7±9.1% versus 45.7±9.2%, p=0.01), actual FVC and inspiratory capacity were observed. Suboptimal PIF significantly predicted moderate (p=0.03) and severe (p=0.01) exacerbations, was associated with higher hospitalisation risks (p=0.05), and with greater use of short-acting beta agonist, oral corticosteroid, and triple therapy. Conclusions Suboptimal PIF is a stable, clinically meaningful marker of worse COPD outcomes and may guide more personalised inhaler selection.

ERJ Open Research
Hospital Sant Joan de Déu Barcelona (ES), University of Antwerp (BE), University of Sassari (IT), Singapore General Hospital (SG), Mater Dei Hospital (MT), Ljubljana University Medical Centre (SI), Changi General Hospital (SG), Hospital Universitario Virgen Macarena (ES), Konkuk University Medical Center (KR), Hospital de La Ribera (ES), Royal Brompton Hospital (GB), Antwerp University Hospital (BE), Vall d'Hebron Institut de Recerca (ES), Hospital Universitario Virgen de las Nieves (ES), Vall d'Hebron Hospital Universitari (ES), Ulsan University Hospital (KR), Group for Organizational Effectiveness (US)
Boehringer Ingelheim
Good health and well-being
Openalex Percentile: Top 7%
Chronic Obstructive Pulmonary Disease (COPD) Research
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