Koozi, Hazem https://orcid.org/0000-0002-5892-3524
Engström, Jonas
Zwawi, Ahmad
Spångfors, Martin
Didriksson, Ingrid
Larsson, Anders
Friberg, Hans
Frigyesi, Attila
Funding for this research was provided by:
Centralsjukhuset Kristianstad
Regional research support, Region Skåne (2022-1284)
Government funding of clinical research within the Swedish National Health Service (2022:YF0009 and 2022-0075)
Crafoordska Stiftelsen (2021-0833)
Lions Skåne research grants
Skånes universitetssjukhus
Hjärt-Lungfonden (2022-0352, 2022-0458)
Regional research support, Region Skåne
Government funding of clinical research within the Swedish National Health Service (2022-0226, 2021-10233)
Hans-Gabriel och Alice Trolle-Wachtmeisters stiftelse för medicinsk forskning
Lund University
Article History
Received: 19 December 2024
Accepted: 10 March 2025
First Online: 3 April 2025
Declarations
:
: The study protocol was approved by the Swedish Ethical Review Authority (Dnr 2020-011955). Written informed consent was obtained at ICU admission, or if the patient was too severely ill, the consent was obtained as soon as possible. If the patient died before consent could be obtained, consent was presumed. The Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) guidelines were followed []. The study was registered on ClinicalTrials.gov Identifier: NCT04974775.
: Not applicable.
: All authors declare no competing, financial, or other interests.