PMID- 33984868 OWN - NLM STAT- MEDLINE DCOM- 20220519 LR - 20230111 IS - 2567-689X (Electronic) IS - 0340-6245 (Linking) VI - 122 IP - 4 DP - 2022 Apr TI - Optimal Tests to Minimise Bleeding and Ischaemic Complications in Patients on Extracorporeal Membrane Oxygenation. PG - 480-491 LID - 10.1055/a-1508-8230 [doi] AB - Patients supported with extracorporeal membrane oxygenation (ECMO) experience a very high frequency of bleeding and ischaemic complications, including stroke and systemic embolism. These patients require systemic anticoagulation, mainly with unfractionated heparin (UFH) to prevent clotting of the circuit and reduce the risk of arterial or venous thrombosis. Monitoring of UFH can be very challenging. While most centres routinely monitor the activated clotting time and activated partial thromboplastin time (aPTT) to assess UFH, measurement of anti-factor Xa (anti-Xa) level best correlates with heparin dose, and appears to be predictive of circuit thrombosis, although aPTT may be a better predictor of bleeding. Although monitoring of prothrombin time, platelet count and fibrinogen is routinely undertaken to assess haemostasis, there is no clear guidance available regarding the optimal test.Additional tests, including antithrombin level and thromboelastography, can be used for risk stratification of patients to try and predict the risks of thrombosis and bleeding. Each has their specific role, strengths and limitations. Increased thrombin generation may have a role in predicting thrombosis. Acquired von Willebrand syndrome is frequent with ECMO, contributing to bleeding risk and can be detected by assessing the von Willebrand factor activity-to-antigen ratio, while the platelet function analyser can be used in urgent situations to detect this, with a high negative predictive value. Tests of platelet aggregation can aid in the prediction of bleeding.To personalise management, a selection of complementary tests to collectively assess heparin-effect, coagulation, platelet function and platelet aggregation is proposed, to optimise clinical outcomes in these high-risk patients. CI - Thieme. All rights reserved. FAU - Kanji, Rahim AU - Kanji R AD - Faculty of Medicine, National Heart and Lung Institute, Imperial College, London, United Kingdom. FAU - Vandenbriele, Christophe AU - Vandenbriele C AD - Department of Cardiovascular Diseases, University Hospitals Leuven, Leuven, Belgium. AD - Intensive Care Unit, Royal Brompton Hospital, London, United Kingdom. FAU - Arachchillage, Deepa R J AU - Arachchillage DRJ AD - Haematology Department, Royal Brompton Hospital, London, United Kingdom. AD - Centre for Haematology, Imperial College Healthcare NHS Trust & Imperial College, London, United Kingdom. FAU - Price, Susanna AU - Price S AD - Faculty of Medicine, National Heart and Lung Institute, Imperial College, London, United Kingdom. AD - Intensive Care Unit, Royal Brompton Hospital, London, United Kingdom. FAU - Gorog, Diana Adrienne AU - Gorog DA AUID- ORCID: 0000-0002-9286-1451 AD - Faculty of Medicine, National Heart and Lung Institute, Imperial College, London, United Kingdom. LA - eng PT - Journal Article DEP - 20210621 PL - Germany TA - Thromb Haemost JT - Thrombosis and haemostasis JID - 7608063 RN - 0 (Anticoagulants) RN - 9005-49-6 (Heparin) SB - IM MH - Anticoagulants/adverse effects MH - *Extracorporeal Membrane Oxygenation/adverse effects MH - Hemorrhage/diagnosis/etiology/prevention & control MH - Heparin/adverse effects MH - Humans MH - Partial Thromboplastin Time MH - *Thrombosis/diagnosis/etiology/prevention & control COIS- None declared. EDAT- 2021/05/14 06:00 MHDA- 2022/05/20 06:00 CRDT- 2021/05/13 20:31 PHST- 2021/05/13 00:00 [aheadofprint] PHST- 2021/05/14 06:00 [pubmed] PHST- 2022/05/20 06:00 [medline] PHST- 2021/05/13 20:31 [entrez] AID - 10.1055/a-1508-8230 [doi] PST - ppublish SO - Thromb Haemost. 2022 Apr;122(4):480-491. doi: 10.1055/a-1508-8230. Epub 2021 Jun 21.