Thromboelastometry-based Assessment of Coagulation In Aortic Dissectio
Recruiting
- Conditions
- Aortic dissection, both elective and emergency aortic surgery
- Registration Number
- NL-OMON26674
- Lead Sponsor
- Department of Anesthesia, Amsterdam UMC, location AMC
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 200
Inclusion Criteria
•Patients > 18 years
•Patients already operated on or scheduled for acute or elective aortic surgery in Amsterdam UMC, location AMC in period 01 January 2021 - 31 December 2021
•Willing and able to sign consent letter for the re-use of care data
Exclusion Criteria
•Previous history of manifest coagulation disorders
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Comparison of standard-of-care thromboelastometry with ROTEM® Delta and ROTEM® Sigma at different timepoints perioperatively, in patients undergoing elective and emergency aortic surgery
- Secondary Outcome Measures
Name Time Method Incidence and degree of perioperative coagulation abnormalities, transfusion and coagulation factor requirements, complications, mortality, and morbidity up to 30 days postoperatively, in patients undergoing elective and emergency aortic surgery