Peak Inspiratory Flows

Background

Peak inspiratory flow (PIF) has been proposed as a measure to assess a patient's ability to use dry powder inhalers (DPIs). However, robust quality criteria to determine a repeatability limit for measuring PIF are lacking.

Research Questions

What are the repeatability limits for measuring PIF? What is the relationship between PIF measured using the In-Check DIAL device at Diskus (GlaxoSmithKline; PIF_D) and HandiHaler (Boehringer Ingelheim; PIF_HH) resistances?

Study Design and Methods

Data from a randomized, controlled, phase 3 trial (study 0149; see Clinical Trial Registration data) were used to define repeatability limits for PIF. In addition, a model to characterize the relationship between PIF measured with the In-Check DIAL device at PIF_D and PIF_HH was defined using data from two randomized, controlled, phase 3 trials (studies 0128 and 0149).

Results

In study 0128, the mean values (SD) for PIF at zero resistance and PIF_HH were 84.6 (33.4) and 57.3 (26.1) L/min, respectively. In study 0149, the mean values (SD) for PIF_D and PIF_HH were 42.4 (11.2) and 29.0 (8.3) L/min, respectively. At the mean level, the mean difference between measurement attempts for PIF_D and PIF_HH was small, < 5 and < 3 L/min, respectively. The repeatability limit was determined as 10 and 5 L/min for PIF_D and PIF_HH, respectively. Modeling the relationship between PIF_D and PIF_HH, after controlling for significant covariates, demonstrated that a PIF_D value of 60 L/min was approximately equivalent to PIF_HH of 40 L/min.

Interpretations

This analysis demonstrated that the two highest values of PIF using the In-Check DIAL device among three inspiratory efforts, met the repeatability limit. Altogether, these data provide guidance for measuring PIF against the simulated resistance of a specific DPI in clinical practice and research studies.

Clinical Trial Registration

ClinicalTrials.gov; Nos.: NCT02518139 (study 0128) and NCT03095456 (study 0149); URL: www.clinicaltrials.gov.