Evaluation of the coagulation system in children with two-ventricle congenital heart disease

Kirsten C Odegard1, David Zurakowski, Stephan Hornykewycz

  • 1Department of Anesthesiology, Children's Hospital Boston, Harvard Medical School, Boston, Massachusetts 02115, USA. kirsten.odegard@childrens.harvard.edu

Insights

Children with two-ventricle congenital heart disease (CHD) show reduced levels of key blood clotting factors. These abnormalities normalize by age four, similar to single-ventricle conditions.

Area of Science:

  • Pediatric Cardiology
  • Hematology
  • Congenital Heart Disease Research

Background:

  • Coagulation factor abnormalities are known in single-ventricle physiology.
  • This study investigates coagulation factors in two-ventricle congenital heart disease (CHD).

Purpose of the Study:

  • To evaluate coagulation factor levels in children with two-ventricle CHD.
  • To compare these levels with age-matched healthy controls.

Main Methods:

  • Assayed coagulation factors in 120 CHD patients across four age groups (0-3 months, 3-12 months, 12-48 months, >48 months).
  • Measured factors II, V, VII, VIII, IX, X, protein C, protein S, plasminogen, and antithrombin III.
  • Used healthy children as age-matched controls and empirical 95% confidence intervals for normal ranges.

Main Results:

  • Significantly reduced mean levels of procoagulant and anticoagulant factors in infants and young children (groups 1, 2, 3) compared to controls.
  • No significant differences observed in children older than 4 years (group 4).
  • Specific factor exceptions noted in each age group, with fibrinogen, factor VIII, factor IX, protein S, plasminogen, and antithrombin III showing less reduction or normal levels in certain groups.

Conclusions:

  • Neonates and infants with two-ventricle CHD exhibit lower procoagulant and anticoagulant factor levels.
  • These levels approach normal ranges in children over 4 years old.
  • The observed coagulation factor abnormalities in two-ventricle CHD are comparable to those in single-ventricle physiology.
Abstract

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