Expert perspectives on ECCO(2)R for acute hypoxemic respiratory failure: consensus of a 2022 European roundtable meeting

关于ECCO(2)R治疗急性低氧性呼吸衰竭的专家观点:2022年欧洲圆桌会议共识

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Abstract

BACKGROUND: By controlling hypercapnia, respiratory acidosis, and associated consequences, extracorporeal CO(2) removal (ECCO(2)R) has the potential to facilitate ultra-protective lung ventilation (UPLV) strategies and to decrease injury from mechanical ventilation. We convened a meeting of European intensivists and nephrologists and used a modified Delphi process to provide updated insights into the role of ECCO(2)R in acute respiratory distress syndrome (ARDS) and to identify recommendations for a future randomized controlled trial. RESULTS: The group agreed that lung protective ventilation and UPLV should have distinct definitions, with UPLV primarily defined by a tidal volume (V(T)) of 4-6 mL/kg predicted body weight with a driving pressure (ΔP) ≤ 14-15 cmH(2)O. Fourteen (93%) participants agreed that ECCO(2)R would be needed in the majority of patients to implement UPLV. Furthermore, 10 participants (majority, 63%) would select patients with PaO(2):FiO(2) > 100 mmHg (> 13.3 kPa) and 14 (consensus, 88%) would select patients with a ventilatory ratio of > 2.5-3. A minimum CO(2) removal rate of 80 mL/min delivered by continuous renal support machines was suggested (11/14 participants, 79%) for this objective, using a short, double-lumen catheter inserted into the right internal jugular vein as the preferred vascular access. Of the participants, 14/15 (93%, consensus) stated that a new randomized trial of ECCO(2)R is needed in patients with ARDS. A ΔP of ≥ 14-15 cmH(2)O was suggested by 12/14 participants (86%) as the primary inclusion criterion. CONCLUSIONS: ECCO(2)R may facilitate UPLV with lower volume and pressures provided by the ventilator, while controlling respiratory acidosis. Since recent European Society of Intensive Care Medicine guidelines on ARDS recommended against the use of ECCO(2)R for the treatment of ARDS outside of randomized controlled trials, new trials of ECCO(2)R are urgently needed, with a ΔP of ≥ 14-15 cmH(2)O suggested as the primary inclusion criterion.

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