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Updated: Dec 25, 2025

A Microfluidic Model of Biomimetically Breathing Pulmonary Acinar Airways
Published on: May 9, 2016
A linearized expiration flow homogenizes the compartmental pressure distribution in a physical model of the
Christin Wenzel1, Carina Frey1, Johannes Schmidt1
1Department of Anesthesiology and Critical Care, Medical Center - University of Freiburg, Faculty of Medicine, Hugstetter Strasse 55, 79106 Freiburg, Germany.
Objective:
Flow-controlled expiration (FLEX) and flow-controlled ventilation (FCV) imply a linearized expiration, and were suggested as new approaches for lung-protective ventilation, especially in the case of an inhomogeneous lung. We hypothesized that a linearized expiration homogenizes the pressure distribution between compartments during expiration, compared to volume-controlled (VCV) and pressure-controlled (PCV) ventilation.
Approach:
We investigated the expiratory pressure decays in a physical model of an inhomogeneous respiratory system. The model contained four compartments of which two had a high (25 ml cmH2O-1) and two a low compliance (10 ml cmH2O-1). These were combined with either a high (6.5 cmH2O s l-1) or low resistance (2.8 cmH2O s l-1), respectively. The model was ventilated in all modes at various tidal volumes and peak pressures, and we determined in each compartment the expiratory time at which the pressure declined to 50% (t50) of the end-inspiratory pressure, and the maximal differences of t50 (Δt50) and pressure (Δpmax) between all compartments.
Main Results:
During FLEX and FCV, t50 was 6- to 7-fold higher compared to VCV and PCV (all P < 0.001). During VCV and PCV, Δt50 was higher (128 ± 18 ms) compared to FLEX and FCV (49 ± 19 ms; all P < 0.001). Δpmax reached up to 3.8 ± 0.2 cmH2O during VCV and PCV, but only 0.6 ± 0.1 cmH2O during FLEX and FCV (P < 0.001).
Significance:
FLEX and FCV provide a more homogeneous expiratory pressure distribution between compartments with different mechanical properties compared with VCV and PCV. This may reduce shear stress within inhomogeneous lung tissue.
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