TRAUMAINDIZIERTEKOAGULOPATHIE D65
Conditions
Interventions
Group 1: Trauma patients which are rescued by the crew of the HEMS Christoph 22 (German Armed Forces Hospital Ulm, Germany) are included into the survey.
At these patients two blood samples are taken
Sponsors
Bundeswehrkrankenhaus UlmKlinik für Anästhesie und IntensivmedizinSektion Notfallmedizin
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: patients with a sever mono trauma or a sever multi system trauma
Exclusion criteria
Exclusion criteria: - sever hypothermia (< 30°C) - pregnancy - all types of coagulation inhibitors in patient history expect low dose aspirin - hereditary or acquired coagulation deficits - application of tranexamic acid before the blood sample (T0) could be obtained - patient (or her / his custodian) do not agree to be part of this study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Do trauma patients with suspected / real blood loss and / or carciocirculatory instability have a TIC already in the prehospital setting (T0 = prehospital setting)? | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary Outcome: Do patients with a proven TIC at T0 (longer CFT CFT, lower Clot firmness at T0) need more blood and blood products during their first 24h of treatment (T2 = 24h after injury) Tertiary Outcome: Do patients with a proven TIC at T0 (longer CFT CFT, lower Clot firmness at T0) have a higher 28 day mortality (T3 = 28 days after trauma) | — |
Countries
Germany
Contacts
Public ContactIngeborg Bretschneider
Bundeswehrkrankenhaus Ulm
Outcome results
None listed