Austin Health

Title
Coagulation abnormalities, bleeding, thrombosis, and management of patients with acute liver failure in Australia and New Zealand.
Publication Date
2019-11-05
Author(s)
Warrillow, Stephen J
Fisher, Caleb
Tibballs, Heath
Bailey, Michael
McArthur, Colin
Lawson-Smith, Pia
Prasad, Bheemasenachar
Anstey, Matthew
Venkatesh, Bala
Dashwood, Gemma
Walsham, James
Holt, Andrew
Wiersema, Ubbo
Gattas, David
Zoeller, Matthew
Garcia Alvarez, Mercedes
Bellomo, Rinaldo
Subject
acute liver failure
bleeding
coagulopathy
encephalopathy emergency liver transplant
thrombosis
Type of document
Journal Article
OrcId
0000-0002-7240-4106
DOI
10.1111/jgh.14876
Abstract
To study the management of coagulation and hematological derangements among severe acute liver failure (ALF) patients in Australia and New Zealand liver transplant intensive care units (ICUs). Analysis of key baseline characteristics, etiology, coagulation and hematological tests, use of blood products, thrombotic complications, and clinical outcomes during the first ICU week. We studied 62 ALF patients. The first day median peak international normalized ratio was 5.5 (inter-quartile range [IQR] 3.8-8.7), median longest activated partial thromboplastin time was 62 s (IQR 44-87), and median lowest fibrinogen was 1.1 (IQR 0.8-1.6) g/L. Fibrinogen was only measured in 85% of patients, which was less than other tests (P < 0.0001). Median initial lowest platelet count was 83 (IQR 41-122) × 109 /L. Overall, 58% of patients received fresh frozen plasma, 40% cryoprecipitate, 35% platelets, and 15% prothrombin complex concentrate. Patients with bleeding complications (19%) had more severe overall hypofibrinogenemia and thrombocytopenia. Thrombotic complications were less common (10% of patients), were not associated with consistent patterns of abnormal hemostasis, and were not immediately preceded by clotting factor administration and half occurred only after liver transplantation surgery. In ALF patients admitted to dedicated Australia and New Zealand ICUs, fibrinogen was measured less frequently than other coagulation parameters but, together with platelets, appeared more relevant to bleeding risk. Blood products and procoagulant factors were administered to most patients at variable levels of hemostatic derangement, and bleeding complications were more common than thrombotic complications. This epidemiologic information and practice variability provide baseline data for the design and powering of interventional studies.
Link
Citation
Journal of Gastroenterology and Hepatology 2020; 35(5): 846-854
Jornal Title
Journal of Gastroenterology and Hepatology

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