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Updated: Sep 29, 2026

Conducting Respiratory Oscillometry in an Outpatient Setting
Published on: April 8, 2022
Elevated AbsΔX5 Identifies a Distinct COPD Phenotype with Peripheral Airway Dysfunction and Longitudinal Improvement
1Department of Allergy, Pulmonary and Critical Care Medicine, Gachon University College of Medicine, Incheon, Republic of Korea. jwpark@gilhospital.com.
Background:
Impulse oscillometry (IOS) is increasingly used to assess small airway dysfunction (SAD) in chronic obstructive pulmonary disease (COPD). However, the physiological significance of the absolute inspiratory-expiratory reactance difference (AbsΔX5) remains unclear. We investigated whether elevated AbsΔX5 identifies a distinct COPD phenotype associated with baseline physiological abnormalities and longitudinal physiological changes.
Methods:
We retrospectively analyzed patients with COPD who underwent serial IOS and spirometry between January 2023 and February 2025. COPD was defined as a post-bronchodilator FEV₁/FVC <0.70, and SAD as R5-R20 >0.07 kPa/L/s and/or AX >0.33 kPa/L. Patients were classified into COPD without SAD, SAD+/AbsΔX5 <0.10, and SAD+/AbsΔX5 ≥0.10. The 0.10 cutoff was determined by an exploratory threshold analysis. Baseline characteristics and longitudinal changes in IOS and post-bronchodilator spirometric parameters were compared.
Results:
Among 710 patients who underwent both IOS and spirometry, 112 met the diagnostic criteria for COPD. Patients were classified into COPD without SAD (n=36), SAD+/AbsΔX5 <0.10 (n=46), and SAD+/AbsΔX5 ≥0.10 (n=30). Baseline IOS abnormalities progressively worsened across the groups. Patients with SAD+/AbsΔX5 ≥0.10 had significantly higher R5-R20, AX, and Fres values and more negative X5 than the other groups. During follow-up, they showed greater improvements in R5, R5-R20, and AX, whereas spirometric changes were modest, except for a greater increase in FVC than in COPD without SAD.
Conclusions:
Elevated AbsΔX5 was most clinically informative in patients with IOS-defined SAD, identifying a distinct COPD phenotype characterized by more severe baseline peripheral airway dysfunction and greater longitudinal improvement in IOS parameters.
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