The purpose of this study is to use the OXYFLEX® device in real care conditions during the hospital management of a population of patients from various hospital services. These services include patients from the severe trauma pathway, intensive care, the polyvalent intensive care unit, and the operating room. The objective is to assess the reliability of the data collected by the OXYFLEX® biosensor compared to those obtained from standard monitoring used in these different services and conditions.
Adult patient (≥ 18 years old);
in severe traum pathway in the emergency services department
or in the operating room for a general anesthesia procedur or locoregional anesthesia planned for a surgical duration grater than 2 hours
or admitted to intesive care/ general intensive care units.
Opposition from the patient or their family to participate in the research ;
Pregnant, parturient or breastfeeding woman ;
Patient under judical protection (guardianship, curatorship …) or legal safeguarding ;
Inability to wear the headband and the sensor (in particular : intracranial neurosurgery, othorhinolaryngology or maxillofacial surgery, debilitating trauma to the head or face …) ;