Effect of Driving Pressure Change During Extracorporeal Membrane Oxygenation in Adults With Acute Respiratory Distress Syndrome: A Randomized Crossover Physiologic Study*

医学 体外膜肺氧合 机械通风 麻醉 通风(建筑) 平均气道压 交叉研究 持续气道正压 充氧 呼吸窘迫 重症监护 吸入氧分数 重症监护医学 阻塞性睡眠呼吸暂停 替代医学 病理 工程类 机械工程 安慰剂
作者
Lorenzo Del Sorbo,Alberto Goffi,George Tomlinson,Tommaso Pettenuzzo,Francesca Facchin,Alice Vendramin,Ewan C. Goligher,Marcelo Cypel,Arthur S. Slutsky,Shaf Keshavjee,Niall D. Ferguson,Eddy Fan
出处
期刊:Critical Care Medicine [Ovid Technologies (Wolters Kluwer)]
卷期号:48 (12): 1771-1778 被引量:50
标识
DOI:10.1097/ccm.0000000000004637
摘要

Venovenous extracorporeal membrane oxygenation is an effective intervention to improve gas exchange in patients with severe acute respiratory distress syndrome. However, the mortality of patients with severe acute respiratory distress syndrome supported with venovenous extracorporeal membrane oxygenation remains high, and this may be due in part to a lack of standardized mechanical ventilation strategies aimed at further minimizing ventilator-induced lung injury. We tested whether a continuous positive airway pressure ventilation strategy mitigates ventilator-induced lung injury in patients with severe acute respiratory distress syndrome on venovenous extracorporeal membrane oxygenation, compared with current ventilation practice that employs tidal ventilation with limited driving pressure. We used plasma biomarkers as a surrogate outcome for ventilator-induced lung injury.Randomized crossover physiologic study.Single-center ICU.Ten patients with severe acute respiratory distress syndrome supported on venovenous extracorporeal membrane oxygenation.The study included four phases. After receiving pressure-controlled ventilation with driving pressure of 10 cm H2O for 1 hour (phase 1), patients were randomly assigned to receive first either pressure-controlled ventilation 20 cm H2O for 2 hours (phase 2) or continuous positive airway pressure for 2 hours (phase 3), and then crossover to the other phase for 2 hours; during phase 4 ventilation settings returned to baseline (pressure-controlled ventilation 10 cm H2O) for 4 hours.There was a linear relationship between the change in driving pressure and the plasma concentration of interleukin-6, soluble receptor for advanced glycation end products, interleukin-1ra, tumor necrosis factor alpha, surfactant protein D, and interleukin-10.Ventilator-induced lung injury may occur in acute respiratory distress syndrome patients on venovenous extracorporeal membrane oxygenation despite the delivery of volume- and pressure-limited mechanical ventilation. Reducing driving pressure to zero may provide more protective mechanical ventilation in acute respiratory distress syndrome patients supported with venovenous extracorporeal membrane oxygenation. However, the risks versus benefits of such an approach need to be confirmed in studies that are designed to test patient centered outcomes.
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