The aim of the present retrospective and prospective data collection is to estimate the incidence and degree of perioperative coagulation abnormalities, using thromboelastometry (with both ROTEM® Delta and ROTEM® Sigma), as well as transfusion and…
ID
Bron
Verkorte titel
Aandoening
Aortic dissection, both elective and emergency aortic surgery
Ondersteuning
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
Comparison of standard-of-care thromboelastometry with ROTEM® Delta and ROTEM® Sigma at different timepoints perioperatively, in patients undergoing elective and emergency aortic surgery
Achtergrond van het onderzoek
The aim of the present retrospective and prospective data collection is to estimate the incidence and degree of perioperative coagulation abnormalities using thromboelastometry (with both ROTEM® Delta and ROTEM® Sigma) as well as transfusion and coagulation factor requirements in patients undergoing aortic surgery (emergency and elective). We will collect data on patients scheduled for emergency surgery, due to acute type A aortic dissection and patients undergoing elective surgery of the aorta. Furthermore, we will compare the results from viscoelastic testing using ROTEM® Delta with ROTEM® Sigma.
The findings may help to optimize coagulation management in patients undergoing major aortic surgery, in order to minimize bleeding as well as thromboembolic complications, both of which can have devastating consequences in this high-risk patient population.
Doel van het onderzoek
The aim of the present retrospective and prospective data collection is to estimate the incidence and degree of perioperative coagulation abnormalities, using thromboelastometry (with both ROTEM® Delta and ROTEM® Sigma), as well as transfusion and coagulation factor requirements, in patients undergoing elective and emergency aortic surgery.
Onderzoeksopzet
All available perioperative timepoints: T0 = Baseline (before aortic cross-clamp), T1 = after aortic cross-clamp, T2 = admission to ICU, T3 = post-op day 1 ICU, T4,5= (optional) daily on ICU until discharge from ICU, T6 = 30 day follow-up for morbidity and mortality
Onderzoeksproduct en/of interventie
None
Publiek
Jennifer Breel
0610019257
j.s.breel@amsterdamumc.nl
Wetenschappelijk
Jennifer Breel
0610019257
j.s.breel@amsterdamumc.nl
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
• 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
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
• Previous history of manifest coagulation disorders
Opzet
Deelname
Voornemen beschikbaar stellen Individuele Patiënten Data (IPD)
Opgevolgd door onderstaande (mogelijk meer actuele) registratie
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Andere (mogelijk minder actuele) registraties in dit register
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In overige registers
Register | ID |
---|---|
NTR-new | NL9530 |
Ander register | METC AMC : W21_186#21.201 |