A prognostic model for thrombotic complications after pediatric cardiac surgery

Background. Cardiac surgery performed on pediatric patients with the use of artificial blood circulation (ABC) is accompanied by hemodilution, hypothermia and blood contact with artificial surfaces, as well as surgical trauma. All the above lead to endothelial cell injury, platelet aggregation and degranulation, activation of innate immunity, development of systemic inflammation and consumption of clotting, anti-coagulation and fibrinolytic factors, which is ultimately associated with the occurrence of thrombotic complications.Objective. The study aimed at developing a mathematical model for the prognosis of thrombotic complications in children which had undergone the ABC, based on assessment of their clinical and laboratory parameters.Methods. We have assessed clinical and laboratory data obtained from 153 children (newborn to 11 months 29 days of age) which had undergone cardiac surgery under conditions of ABC due to congenital heart defects (CHD). For all patients the general clinical and laboratory parameters: complete blood count, comprehensive metabolic panel, parameters of screening coagulogram, D-dimer concentration, von Willebrand factor activity, levels of antithrombin III, plasminogen, protein C and protein S, alpha-2-antiplasmin, thrombin activatable fibrinolysis inhibitor (TAFI) and fibrin-monomer have been assessed.Results. In 43 patients (28.1%) post-operative thromboses have been diagnosed. Examination of children revealed the presence of thrombosis of various localization including the intracardiac thrombi, ischemic cerebrovascular events, limb ischemia, etc. Based on logistic regression analysis, a model of development of thrombotic complications has been built which included 4 parameters: activity of lactate dehydrogenase (LDH), TAFI activity, von Willebrand factor activity and protein C activity. Model sensitivity was 95.3%, and its specificity — 96.4%.

[1]  Александр Александрович Гончаров,et al.  Cлучай интраоперационного выявления дефицита протеина C у больного, оперированного по поводу цианотического порока сердца , 2020 .

[2]  A. A. Goncharov,et al.  A clinical case of protein C deficiency revealed in a patient during surgery for cyanotic heart defect , 2020, Russian journal of hematology and transfusiology.

[3]  П. А. Жарков,et al.  Применение концентрата протеина С у детей с приобретенным его дефицитом , 2019 .

[4]  J. Griffin,et al.  Activated protein C, protease activated receptor 1, and neuroprotection. , 2018, Blood.

[5]  B. Siegerink FVIII, Protein C and the Risk of Arterial Thrombosis: More than the Sum of Its Parts , 2018, Thrombosis and Haemostasis.

[6]  Suzy Abd El Mabood,et al.  Protein C and Anti-Thrombin-III Deficiency in Children With Beta-Thalassemia , 2018, Journal of hematology.

[7]  M. Hall,et al.  Increasing rates of thrombosis in children with congenital heart disease undergoing cardiac surgery. , 2018, Thrombosis research.

[8]  S. Emani,et al.  Elevated preoperative von Willebrand factor is associated with perioperative thrombosis in infants and neonates with congenital heart disease , 2017, Journal of thrombosis and haemostasis : JTH.

[9]  N. Guzzetta,et al.  Cyanotic congenital heart disease (CCHD): focus on hypoxemia, secondary erythrocytosis, and coagulation alterations , 2015, Paediatric anaesthesia.

[10]  S. Emani,et al.  Hypercoagulability markers predict thrombosis in single ventricle neonates undergoing cardiac surgery. , 2013, The Annals of thoracic surgery.

[11]  B. McCrindle,et al.  Risk, Clinical Features, and Outcomes of Thrombosis Associated With Pediatric Cardiac Surgery , 2011, Circulation.

[12]  Ş. Kirazlı,et al.  Thrombin activatable fibrinolysis inhibitor activity (TAFIa) levels in neonates with meconium-stained amniotic fluid , 2008, The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians.

[13]  N. B. Lerner,et al.  Elevated risk of thrombosis in neonates undergoing initial palliative cardiac surgery. , 2007, The Annals of thoracic surgery.

[14]  D. Zurakowski,et al.  EVALUATION OF THE COAGULATION SYSTEM IN CHILDREN WITH TWO-VENTRICLE CONGENITAL HEART DISEASE , 2006, The Annals of thoracic surgery.

[15]  D. Yousem,et al.  Watershed Strokes After Cardiac Surgery: Diagnosis, Etiology, and Outcome , 2006, Stroke.

[16]  P. D. del Nido,et al.  Procoagulant and anticoagulant factor abnormalities following the Fontan procedure: increased factor VIII may predispose to thrombosis. , 2003, The Journal of thoracic and cardiovascular surgery.

[17]  P. D. del Nido,et al.  Coagulation factor abnormalities in patients with single-ventricle physiology immediately prior to the Fontan procedure. , 2002, The Annals of thoracic surgery.

[18]  H. Horigome,et al.  Overproduction of platelet microparticles in cyanotic congenital heart disease with polycythemia. , 2002, Journal of the American College of Cardiology.

[19]  J. Meijers,et al.  Thrombin‐activatable fibrinolysis inhibitor (TAFI, plasma procarboxypeptidase B, procarboxypeptidase R, procarboxypeptidase U) , 2003, Journal of thrombosis and haemostasis : JTH.

[20]  K. Fujikawa,et al.  Structure of von Willebrand Factor-cleaving Protease (ADAMTS13), a Metalloprotease Involved in Thrombotic Thrombocytopenic Purpura* , 2001, The Journal of Biological Chemistry.

[21]  T. Foroud,et al.  Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura , 2001, Nature.

[22]  B. Lämmle,et al.  Partial amino acid sequence of purified von Willebrand factor-cleaving protease. , 2001, Blood.

[23]  K. Fujikawa,et al.  Purification of human von Willebrand factor-cleaving protease and its identification as a new member of the metalloproteinase family. , 2001, Blood.

[24]  J. Morser,et al.  Both Cellular and Soluble Forms of Thrombomodulin Inhibit Fibrinolysis by Potentiating the Activation of Thrombin-activable Fibrinolysis Inhibitor* , 1998, The Journal of Biological Chemistry.