Prütz, M.
Bozkurt, A.
Löser, B.
Haas, S. A.
Tschopp, D.
Rieder, P.
Trachsel, S.
Vorderwülbecke, G.
Menk, M.
Balzer, F.
Treskatsch, S.
Reuter, D. A.
Zitzmann, A.
Funding for this research was provided by:
Universitätsmedizin Rostock
Article History
Received: 17 October 2023
Revised: 13 May 2024
Accepted: 26 May 2024
First Online: 28 June 2024
Declarations
:
: G. Vorderwülbecke reports support for attending “Norddeutsches Kolloquium Perioperatives Gerinnungsmanagement” from CSL Behring. F. Balzer reports grants from German Federal Ministry of Education & Research, German Federal Ministry of Health, Hans Böckler Foundation, Berlin Institute of Health, Einstein Foundation and Berlin University Alliance, consulting fees from Medtronic, honoraria for lectures from GE HealthCare and Pfizer, travel support from Robert Koch Institute and Deutsche Gesellschaft für Anästhesiologie und Intensivmedizin (DGAI) and licenses from Elsevier Publishing outside the submitted work. S. Treskatsch reports research grants from Orionpharma, Cytosorbents and BD and honoraria for lectures or workshops from Philips, Orionpharma, Edwards LifeSciences, Anomed and Chiesi. D.A. Reuter reports institutional research grants from Edwards Lifesciences, Getinge and Sentec AG, honoraria for educational lectures for Edwards Lifesciences, Baxter, TEVA Ratiopharm GmbH and Philips and travel support for expert meetings by Philips Germany outside the submitted work. He participates on the Medical Evaluation Board for Edwards Lifesciences and is national coordinator for the European Society of Anaesthesiology and Intensive Care and chairman of Mecklenburg-Western Pomerania for Deutsche Gesellschaft für Anästhesiologie und Intensivmedizin (DGAI). A. Zitzmann reports institutional research grants and honoraria for educational lectures from Edwards Lifesciences. M. Prütz, A. Bozkurt, B. Löser, S.A. Haas, D. Tschopp, P. Rieder, S. Trachsel and M. Menk declare that they have no competing interests.
: All procedures performed in studies involving human participants or on human tissue were in accordance with the ethical standards of the institutional and/or national research committee and with the 1975 Helsinki declaration and its later amendments or comparable ethical standards. Written patient consent was not required for this study due to the process that only routine data were collected and all data analyses were performed in a pseudonymized way.