Overview
the aim of this register is to collect exhaustively the different data available surrounding a transfusion act in the context of an active haemorrhage. The aim is to allow different modelling and analysis related to emergency transfusion.
Description
the aim of this register is to collect exhaustively the different data available surrounding a transfusion act in the context of an active haemorrhage. The aim is to allow different modelling and analysis related to emergency transfusion.
Patients will be informed at the time of the anaesthesia consultation about the inclusion in the registry.
The data will be collected from the patients' files by the investigators of the centre without modifying their management.
The data collection period will not exceed the period of acute management.
Eligibility
Inclusion Criteria:
- all patients who have received an hemostasis product
Exclusion Criteria:
- patient who refused to consent to data analysis and study participation