No registrations found.
ID
Source
Brief title
Health condition
ECMO
Coagulation
Stolling
child
kind
Sponsors and support
Intervention
Outcome measures
Primary outcome
1.Bleeding complications in the first 14 days of ECMO therapy
2.Clotting complications in the first 14 days of ECMO therapy
Secondary outcome
None
Background summary
Bleeding and clotting complications occur in about 50% of the pediatric extracorporeal membrane oxygenation (ECMO) patients, causing a decrease in survival of about 40%.(1-3) The interaction between blood and the ECMO circuit generates a hypercoagulable state, and unfractionated heparin is used to maintain patency of the circuit as well as to reduce thrombotic events while minimizing bleedings. Worldwide, no consensus exists about how to monitor this precarious hemostatic balance.
Current conventional tests (APTT, ACT and anti-FXa assay) assess only isolated parts of the coagulation cascade, while alternative tests (thromboelastography [TEG/ROTEM] and thrombin generation assay [TGA]) assess the complete coagulation cascade. Therefore, we hypothese that the alternative coagulation tests better reflect the thrombotic or haemorrhagic phenotype than the conventional tests, and as a consequence will improve coagulation monitoring in ECMO patients, leading to less hemostatic complications and improved survival. In this pilot study we will prospectively investigate the ability of both conventional and alternative coagulation tests to predict bleeding and clotting complications in 160 ECMO children in 8 established ECMO centers worldwide. We expect to find one or a combination of coagulation tests with a good association with the bleeding and/or clotting complications. In a future project, the test(s) can be incorporated in a new anticoagulation protocol, that will be studied in a randomized controlled trial.
Study objective
Addition of alternative tests (TEG/ROTEMĀ® and/or TGA) which reflect the whole hemostatic status of a patient might help recognizing the level of thrombin formation and fibrinolysis and improve care in ECMO patients and potentially reduce the risk of hemostatic complications.
Study design
Before start of ECMO, the first 14 days of ECMO therapy and within 24 hrs after stop of ECMO.
Intervention
Collecting data about all coagulation tests during the first 14 days of ECMO, including conventional tests such as APTT, PT/INR, ACT, platelets, anti-Xa level, D-dimer, antithrombin and alternative tests, including ROTEM/TEG and TGA.
ErasmusMC Sophia Children's Hospital
Rotterdam 3015CN
The Netherlands
010 7036691
c.vanommen@erasmusmc.nl
ErasmusMC Sophia Children's Hospital
Rotterdam 3015CN
The Netherlands
010 7036691
c.vanommen@erasmusmc.nl
Inclusion criteria
Children from 0 to 18 years old treated with ECMO therapy can be included in this study within 48 hours after start of ECMO and after obtained informed consent.
Exclusion criteria
1. Patients without informed consent
2. Patients after 48 hours of start of ECMO
Design
Recruitment
Followed up by the following (possibly more current) registration
No registrations found.
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
Register | ID |
---|---|
NTR-new | NL6977 |
NTR-old | NTR7165 |
Other | na : Project S18-33 (Vrienden van Sophia) |