LAUSR

Background Flow-controlled ventilation is a novel ventilation method which allows to individualize ventilation according to dynamic lung mechanic limits based on direct tracheal pressure measurement at a stable constant gas flow during inspiration and expiration. The aim of this porcine study was to compare individualized flow-controlled ventilation (FCV) and current guideline-conform pressure-controlled ventilation (PCV) in long-term ventilation. Methods Anesthetized pigs were ventilated with either FCV or PCV over a period of 10 h with a fixed FiO 2 of 0.3. FCV settings were individualized by compliance-guided positive end-expiratory pressure (PEEP) and peak pressure ( P peak ) titration. Flow was adjusted to maintain normocapnia and the inspiration to expiration ratio (I:E ratio) was set at 1:1. PCV was performed with a PEEP of 5 cm H 2 O and P peak was set to achieve a tidal volume ( V T ) of 7 ml/kg. The respiratory rate was adjusted to maintain normocapnia and the I:E ratio was set at 1:1.5. Repeated measurements during observation period were assessed by linear mixed-effects model. Results In FCV ( n  = 6), respiratory minute volume was significantly reduced (6.0 vs 12.7, MD − 6.8 (− 8.2 to − 5.4) l/min; p  < 0.001) as compared to PCV ( n  = 6). Oxygenation was improved in the FCV group (paO 2 119.8 vs 96.6, MD 23.2 (9.0 to 37.5) Torr; 15.97 vs 12.87, MD 3.10 (1.19 to 5.00) kPa; p  = 0.010) and CO 2 removal was more efficient (paCO 2 40.1 vs 44.9, MD − 4.7 (− 7.4 to − 2.0) Torr; 5.35 vs 5.98, MD − 0.63 (− 0.99 to − 0.27) kPa; p  = 0.006). P peak and driving pressure were comparable in both groups, whereas PEEP was significantly lower in FCV ( p  = 0.002). Computed tomography revealed a significant reduction in non-aerated lung tissue in individualized FCV ( p  = 0.026) and no significant difference in overdistended lung tissue, although a significantly higher V T was applied (8.2 vs 7.6, MD 0.7 (0.2 to 1.2) ml/kg; p  = 0.025). Conclusion Our long-term ventilation study demonstrates the applicability of a compliance-guided individualization of FCV settings, which resulted in significantly improved gas exchange and lung tissue aeration without signs of overinflation as compared to best clinical practice PCV.