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Mandatory Fields
Goligher, EC;Combes, A;Brodie, D;Ferguson, ND;Pesenti, AM;Ranieri, VM;Slutsky, AS;Beale, R;Brochard, L;Chiche, JD;Fan, E;de Backer, D;Francois, G;Laffey, J;Mercat, A;McAuley, DF;Muller, T;Quintel, M;Vincent, JL;Taccone, FS;Peperstraete, H;Morimont, P;Schmidt, M;Levy, B;Diehl, JL;Guervilly, C;Capelier, G;Vieillard-Baron, A;Messika, J;Karagiannidis, C;Moerer, O;Urbino, R;Antonelli, M;Mojoli, F;Alessandri, F;Grasselli, G;Donker, D;Ferrer, R;Mancebo, J;Fanelli, V;Pham, T
Intensive Care Medicine
Determinants of the effect of extracorporeal carbon dioxide removal in the SUPERNOVA trial: implications for trial design
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Purpose To describe the variability and determinants of the effect of extracorporeal CO2 removal (ECCO2R) on tidal volume (V-t), driving pressure (Delta P), and mechanical power (Power(RS)) and to determine whether highly responsive patients can be identified for the purpose of predictive enrichment in ECCO2R trial design. Methods Using data from the SUPERNOVA trial (95 patients with early moderate acute respiratory distress syndrome), the independent effects of alveolar dead space fraction (ADF), respiratory system compliance (Crs), hypoxemia (PaO2/FiO(2)), and device performance (higher vs lower CO2 extraction) on the magnitude of reduction in V-t, Delta P, and Power(RS) permitted by ECCO2R were assessed by linear regression. Predicted and observed changes in Delta P were compared by Bland-Altman analysis. Hypothetical trials of ECCO2R, incorporating predictive enrichment and different target CO2 removal rates, were simulated in the SUPERNOVA study population. Results Changes in V-t permitted by ECCO2R were independently associated with ADF and device performance but not PaO2/FiO(2). Changes in Delta P and Power(RS) were independently associated with ADF, Crs, and device performance but not PaO2/FiO(2). The change in Delta P predicted from ADF and Crs was moderately correlated with observed change in Delta P (R-2 0.32, p < 0.001); limits of agreement between observed and predicted changes in Delta P were +/- 3.9 cmH(2)O. In simulated trials, restricting enrollment to patients with a larger predicted decrease in Delta P enhanced the average reduction in Delta P, increased predicted mortality benefit, and reduced sample size and screening size requirements. The increase in statistical power obtained by restricting enrollment based on predicted Delta P response varied according to device performance as specified by the target CO2 removal rate. Conclusions The lung-protective benefits of ECCO2R increase with higher alveolar dead space fraction, lower respiratory system compliance, and higher device performance. ADF and Crs, rather than severity of hypoxemia, should be the primary factors determining whether to enroll patients in clinical trials of ECCO2R.
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