Venous thromboembolism in neonates and children--update 2013.

Abstract

Thromboses (VTE) in children were associated with medical diseases with and without acquired or inherited thrombophilic risk factors (IT). Disease recurrence rates vary between 3% in children with a first event during the neonatal period and 21% in children with idiopathic VTE. Recently reported systematic reviews showed significant associations between VTE and factor V G1691A or factor II G20210A mutations, protein C, protein S and antithrombin deficiency, more pronounced when combined IT were involved. The factor II G20210A mutation, protein C, protein S, and antithrombin deficiency did also play an important role at VTE recurrence. Primarily asymptomatic family members of pediatric VTE index cases showed annual VTE incidence rates of 2.82% in carriers of antithrombin, protein C, or protein S deficiency, 0.42% and 0.25% in carriers of the factor II G202010A or V G1691A mutation, and 0.10% in relatives with no IT.

• Authors: Ulrike Nowak-Göttl, Verena Janssen, Daniela Manner, Gili Kenet
• Journal: Thrombosis research (Thromb Res) Vol. 131 Suppl 1 Pg. S39-41 (Jan 2013) ISSN: 1879-2472 [Electronic] United States
• PMID: 23452739 (Publication Type: Journal Article)
• Copyright: Copyright © 2013 Elsevier Ltd. All rights reserved.

Chemical References

• Anticoagulants
• Factor V
• Prothrombin

Topics

• Anticoagulants (therapeutic use)
• Blood Coagulation (physiology)
• Child
• Factor V (genetics)
• Humans
• Infant, Newborn
• Mass Screening
• Mutation
• Odds Ratio
• Prothrombin (genetics)
• Recurrence
• Risk Factors
• Thrombosis
• Venous Thromboembolism (diagnosis, physiopathology)