Venous thromboembolism in neonates and children - Update 2013

Ulrike Nowak-Göttl*, Verena Janssen, Daniela Manner, Gili Kenet

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

39 Scopus citations

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.

Original languageEnglish
Pages (from-to)S39-S41
JournalThrombosis Research
Volume131
Issue numberSUPPL.1
DOIs
StatePublished - Jan 2013

Keywords

  • Pediatric thrombosis
  • Prothrombotic risk factors
  • Therapy
  • Thrombophilia screening
  • Underlying diseases

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