# Physiological and clinical effects of two ultraprotective ventilation strategies in patients with veno-venous extracorporeal membrane oxygenation: the ECMOVENT study

**Authors:** Yorick Rodriguez, Alexandre Thomachot, Guillaume Deniel, Mehdi Mezidi, Louis Chauvelot, Hodane Yonis, Jean-Christophe Richard, Laurent Bitker

PMC · DOI: 10.1186/s13613-025-01525-0 · Annals of Intensive Care · 2025-08-01

## TL;DR

This study compares two ventilation strategies for patients with ARDS on VV-ECMO, finding differences in mechanical parameters but no significant clinical outcome differences.

## Contribution

The study introduces a comparison of two ultra-protective ventilation strategies in ARDS patients on VV-ECMO, focusing on mechanical parameters and clinical outcomes.

## Key findings

- The ∆P8 strategy resulted in higher driving pressure and respiratory rate, lower PaCO2, and higher static elastic mechanical power.
- No significant difference in day-90 survival rate or time to successful ECMO weaning was observed between the two strategies.
- The adjusted subdistribution hazard ratio showed no significant association between the ∆P8 strategy and improved outcomes.

## Abstract

The optimal ventilation strategy in acute respiratory distress syndrome (ARDS) patients with veno-venous extracorporeal membrane oxygenation (VV-ECMO) remains unknown. We aimed to compare the effects of two ultra-protective ventilatory strategies applied to patients with ARDS and VV-ECMO.

Our study was an observational, retrospective, single-center study with a before-and-after design. All consecutive patients treated with VV-ECMO for severe ARDS between 2016 and 2023 were included. Before 2021, patients received a quasi-apneic ventilation strategy in assist-controlled volume mode with a tidal volume (VT) of 1 ml.kg−1 predicted body weight (PBW), a respiratory rate (RR) of 5 min−1 and a PEEP set to keep plateau pressure (PPLAT) between 20 and 25 cmH2O. From 2021 onwards, the protocolized ventilatory strategy consisted in pressure-controlled mode with a PEEP of 14 cmH2O, a driving pressure (∆P) of 8 cmH2O and a RR of 10 min−1. We evaluated the impact of strategies on longitudinal respiratory mechanics and on the time to successful ECMO weaning at day-90 after VV-ECMO canulation.

121 patients were enrolled, with 69 receiving the VT1 strategy, and 52 the ∆P8 strategy. Over the first 7 days of ECMO, the ∆P8 strategy was associated with significantly higher ∆P and RR, lower PaCO2, and higher static elastic mechanical power, compared with the VT1 strategy. The day-90 survival rate was 30% with the VT1 strategy, and 42% with the ∆P8 strategy (P = 0.19). Time to successful VV-ECMO weaning was 7 [4–13] days in day-90 survivors, with no significant difference between groups. The adjusted subdistribution hazard ratio associated with the ∆P8 strategy was 0.99 (95% confidence interval: 0.53–1.84), as compared to the VT1 strategy (P > 0.9).

In the context of our center, a ventilatory strategy targeting a PEEP of 14 cmH2O, a ∆P of 8 cmH2O and a RR of 10 min−1 led to the application of ∆P, RR and static elastic mechanical power and improved decarboxylation, compared to a strategy in volumetric mode with a VT of 1 ml.kg−1 PBW and a RR of 5 min−1, in patients with ARDS and VV-ECMO. No significant difference on clinical outcomes was observed between both strategies.

The online version contains supplementary material available at 10.1186/s13613-025-01525-0.

## Linked entities

- **Diseases:** acute respiratory distress syndrome (MONDO:0006502), ARDS (MONDO:0006502)

## Full-text entities

- **Diseases:** COVID-19 (MESH:D000086382), respiratory failure (MESH:D012131), cor pulmonale (MESH:D011660), NMB (MESH:D020879), hypoxemia (MESH:D000860), airway obstruction (MESH:D000402), barotrauma (MESH:D001469), organ failure (MESH:D009102), alveolar collapse (MESH:D001261), lung injuries (MESH:D055370), unilateral pneumonia (MESH:D011014), death (MESH:D003643), sepsis (MESH:D018805), hypothermia (MESH:D007035), lung parenchymal abnormalities (MESH:D017563), pneumomediastinum (MESH:D008478), hypercapnia (MESH:D006935), VILI (MESH:D055397), right ventricular failure (MESH:D051437), pneumothorax (MESH:D011030), ARDS (MESH:D012128)
- **Chemicals:** norepinephrine (MESH:D009638), oxygen (MESH:D010100), Biphasic (-), ACV (MESH:D000212), P (MESH:D010758), steroids (MESH:D013256), CO2 (MESH:D002245)
- **Species:** Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090]

## Full text

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Source: https://tomesphere.com/paper/PMC12316621