Anticoagulant Therapy in Head Injury-Associated Cerebral Sinovenous Thrombosis in Children

作者:Xavier Frederico; Komvilaisak Patcharee; Williams Suzan; Kulkarni Abhaya V; deVeber Gabrielle; Moharir Mahendranath D*
来源:Pediatric Blood and Cancer, 2014, 61(11): 2037-2042.
DOI:10.1002/pbc.25168

摘要

BackgroundHead injury is a risk factor for cerebral sinovenous thrombosis (CSVT) in children. Literature concerning head injury-associated CSVT (HIA-CSVT) is scarce. Data supporting safety and efficacy of anticoagulant therapy (ACT) in childhood CSVT is emerging. However, intracranial hemorrhage (ICH) occurs frequently in children with HIA-CSVT at diagnosis making initiation of ACT controversial due to the fear of worsening of ICH. ProcedureWe conducted a retrospective descriptive review of a consecutive cohort of children with HIA-CSVT from 1998 to 2012. ResultsTwenty patients (14 males, mean age 7 years) with HIA-CSVT were identified. Most (19/20 [95%]) had significant ICH at diagnosis. None received ACT at diagnosis. Fourteen (70%) were later (median 7 days post-trauma, range 2-48 days) treated with ACT due to CSVT persistence (nine) and propagation (five), despite ICH in 13. None of the treated patients, including the 13 with pre-existing ICH, had significant worsening of hemorrhage. Three (21%) treated patients had minor asymptomatic extension of their hemorrhage and further ACT was withheld. No patient died while on ACT. No patient experienced CSVT propagation on ACT. Clinical outcomes were normal (no neurologic deficits) in 5/20(25%), mild neurological deficits in 10/20(50%), and moderate-severe neurological deficits in 5/20(25%). Small sample size did not permit assessment of the effect of ACT on outcome. ConclusionsAnticoagulant therapy is safe in selected children with HIA-CSVT. ICH is not an absolute contraindication to ACT in children with HIA-CSVT. Pediatr Blood Cancer 2014;61:2037-2042.

  • 出版日期2014-11