Gaudry, Stéphane
Grolleau, François
Barbar, Saber
Martin-Lefevre, Laurent
Pons, Bertrand
Boulet, Éric
Boyer, Alexandre
Chevrel, Guillaume
Montini, Florent
Bohe, Julien
Badie, Julio
Rigaud, Jean-Philippe
Vinsonneau, Christophe
Porcher, Raphaël
Quenot, Jean-Pierre
Dreyfuss, Didier
Funding for this research was provided by:
Ministry of health, France (AOM12456, A00519-34)
Article History
Received: 10 February 2022
Accepted: 3 March 2022
First Online: 4 April 2022
Declarations
:
: The AKIKI trial and the IDEAL-ICU trial received approval for all participating centers from competent French legal authority (Comité de Protection des Personnes d’Ile de France VI, ID RCB 2013-A00765-40, NCT01932190 for AKIKI and Comité de Protection des Personnes Est I ID RCB 2012-A00519-34 for IDEAL-ICU), and consent of patient or relatives was obtained before inclusion (except in emergencies where deferred consent was allowed by the Institutional Review Board).
: Patients or their surrogates were informed both verbally and with a written document by the investigators. They could refuse to participate at any time, and their decision was recorded in patient files.
: None of the authors have competing interests in the manuscript.