,
Flaatten, Hans http://orcid.org/0000-0001-9186-3482
Guidet, Bertrand
Andersen, Finn H.
Artigas, Antonio
Cecconi, Maurizio
Boumendil, Ariane
Elhadi, Muhammed
Fjølner, Jesper
Joannidis, Michael
Jung, Christian
Leaver, Susannah
Marsh, Brian
Moreno, Rui
Oeyen, Sandra
Nalapko, Yuriy
Schefold, Joerg C.
Szczeklik, Wojciech
Walther, Sten
Watson, Ximena
Zafeiridis, Tilemachos
de Lange, Dylan W.
Funding for this research was provided by:
Health Region West, Norway
Conseil Régional, Île-de-France
Article History
Received: 10 November 2020
Accepted: 27 January 2021
First Online: 3 February 2021
Ethics approval and consent to participate
: The VIP2 study that includes this cohort of patients received ethical approval from all participating countries, as revealed in the original publication []. Briefly this included informed consent at admission in some countries, and this was not necessary in others because of the observational nature of the study. Some countries did require informed consent from raters, since they were in fact considered as “test persons” and this was approved when necessary. Ethical approval from Norway (the country of the PI) had the number 2018/87/REK sør-øst D.
: Not applicable.
: JCS declares that the Dept. of Intensive Care Medicine Bern has/had research and/or development/consulting contracts with (full disclosure): Orion Corporation, Abbott Nutrition International, B. Braun Medical AG, CSEM SA, Edwards Lifesciences Services GmbH/SA, Kenta Biotech Ltd, Maquet Critical Care AB, Omnicare Clinical Research AG, and Nestlé. Educational grants were received from Fresenius Kabi; GSK; MSD; Lilly; Baxter; Astellas; AstraZeneca; B. Braun Medical AG, CSL Behring, Maquet, Novartis, Covidien, Nycomed, Pierre Fabre Pharma (Roba Pharma); Pfizer, Orion Pharma. The money went into departmental funds. No personal financial gain applies. All other authors do not have any conflict of interest to declare related to this manuscript.