Coagulation abnormalities in patients with single-ventricle physiology precede the Fontan procedure
- PMID: 11882816
- DOI: 10.1067/mtc.2002.120010
Coagulation abnormalities in patients with single-ventricle physiology precede the Fontan procedure
Abstract
Objective: Thromboembolic events in patients who have undergone the Fontan operation have been reported to be as high as 20% to 33%. A hypercoagulable state with deficiencies in proteins C and S has been implicated. Using age-matched control subjects, we evaluated whether an altered coagulation state is present earlier in the course of staged single-ventricle repair.
Methods: After informed consent had been obtained, coagulation factors were assayed in 36 infants (mean age, 7.7 +/- 3.6 months) with single-ventricle cardiac defects immediately before undergoing the bidirectional Glenn procedure; 34 infants (mean age, 8.4 +/- 2.6 months) without cardiac disease were assayed as control subjects. Concentration of factors II, V, VII, VIII, IX, and X; antithrombin III; plasminogen; proteins C and S; fibrinogen; serum albumin; and liver enzymes were measured. Normal reference intervals on the basis of the control subjects were determined by using 95% confidence limits. Patient demographic and hemodynamic variables were evaluated as possible predictors of coagulation abnormalities.
Results: Concentrations of protein C; factors II, V, VII, IX, and X; plasminogen; fibrinogen; and antithrombin III were significantly lower in the pre-Glenn infants compared with the age-matched control subjects (all P <.001, Student t test). On the basis of multiple logistic regression, no specific hemodynamic variables were predictive of a procoagulant or anticoagulant deficiency. Ventricular dysfunction did predict the presence of multiple coagulation abnormalities (P <.001).
Conclusion: Procoagulant and anticoagulant factor abnormalities occur early in the course of single-ventricle repair and precede the cavopulmonary connection.
Similar articles
-
Coagulation factor abnormalities in patients with single-ventricle physiology immediately prior to the Fontan procedure.Ann Thorac Surg. 2002 Jun;73(6):1770-7. doi: 10.1016/s0003-4975(02)03580-4. Ann Thorac Surg. 2002. PMID: 12078768
-
Procoagulant and anticoagulant factor abnormalities following the Fontan procedure: increased factor VIII may predispose to thrombosis.J Thorac Cardiovasc Surg. 2003 Jun;125(6):1260-7. doi: 10.1016/s0022-5223(02)73605-2. J Thorac Cardiovasc Surg. 2003. PMID: 12830042
-
Coagulation abnormalities and liver function after hemi-Fontan and Fontan procedures - the importance of hemodynamics in the early postoperative period.Eur J Cardiothorac Surg. 2007 May;31(5):866-72. doi: 10.1016/j.ejcts.2007.01.033. Epub 2007 Feb 27. Eur J Cardiothorac Surg. 2007. PMID: 17329113
-
Cardiac catheterization is necessary before bidirectional Glenn and Fontan procedures in single ventricle physiology.Pediatr Cardiol. 2005 Mar-Apr;26(2):159-61. doi: 10.1007/s00246-004-0955-3. Pediatr Cardiol. 2005. PMID: 15868324 Review.
-
Coagulation abnormalities and their neuro-ophthalmologic manifestations.Curr Opin Ophthalmol. 1999 Dec;10(6):382-93. doi: 10.1097/00055735-199912000-00004. Curr Opin Ophthalmol. 1999. PMID: 10662242 Review.
Cited by
-
Connection of discontinuous pulmonary arteries in patients with a superior or total cavopulmonary circulation.Ann Thorac Surg. 2008 Dec;86(6):1948-54. doi: 10.1016/j.athoracsur.2008.07.072. Ann Thorac Surg. 2008. PMID: 19022015 Free PMC article.
-
The Miracle Baby Grows Up: Hypoplastic Left Heart Syndrome in the Adult.Curr Cardiol Rep. 2017 Aug;19(8):74. doi: 10.1007/s11886-017-0877-3. Curr Cardiol Rep. 2017. PMID: 28744764 Review.
-
Intracardiac thrombi in pediatric patients: presentation profiles and clinical outcomes.Pediatr Cardiol. 2007 May-Jun;28(3):213-20. doi: 10.1007/s00246-005-1068-3. Pediatr Cardiol. 2007. PMID: 17404682
-
Prophylactic anticoagulation following the Fontan operation.Heart. 2005 Jul;91(7):854-6. doi: 10.1136/hrt.2004.039073. Heart. 2005. PMID: 15958342 Free PMC article. No abstract available.
-
Abnormalities in the Von Willebrand-Angiopoietin Axis Contribute to Dysregulated Angiogenesis and Angiodysplasia in Children With a Glenn Circulation.JACC Basic Transl Sci. 2021 Mar 22;6(3):222-235. doi: 10.1016/j.jacbts.2020.12.014. eCollection 2021 Mar. JACC Basic Transl Sci. 2021. PMID: 33778210 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources