Anesthesia, Anesthesia; Shock, Blood Coagulation Disorder, Blood Loss, Fresh Blood Stool, Side Effect, Transfusion Reaction, Transfusion Related Complication
Conditions
Keywords
transfusion, monitoring, emergency situation, shock, fresh frozen plasma
Brief summary
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.
Detailed 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.
Interventions
Transfusion of an hemostatic product
Sponsors
Study design
Eligibility
Inclusion criteria
* all patients who have received an hemostasis product
Exclusion criteria
* patient who refused to consent to data analysis and study participation
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Hemostatic evolution through transfusion event | 12 hours | evolution of APTT (seconds) |
| ROTEM measures evolution through transfusion event | 12 hours | evolution of APTEMCT (seconds) |
| Haematologic measures evolution through transfusion event | 12 hours | evolution of hemoglobin (g/dL) |
| ionic measures evolution through transfusion event | 12 hours | evolution of lactate (mmol/L) |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Mortality at one month | one month | Mortality at one month |
Countries
Belgium