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Published on: October 20, 2017
Long-term prognosis of cerebral venous sinus thrombosis in childhood
Els L L M De Schryver1, Ingrid Blom, Kees P J Braun
1Department of Neurology, University Medical Center Utrecht, H.02.128, PO Box 85500, 3508 GA Utrecht, The Netherlands. e.deschryver@neuro.azu.nl
Insights
Cerebral venous sinus thrombosis (CVST) in children has a generally fair prognosis, with most survivors showing normal development. However, some may experience mild cognitive deficits or decreased well-being.
Area of Science:
- Pediatric Neurology
- Neuroscience
- Child Health
Background:
- Cerebral venous sinus thrombosis (CVST) is a rare pediatric condition.
- Long-term neuropsychological, emotional, and quality-of-life outcomes for pediatric CVST are largely unstudied.
Purpose of the Study:
- To investigate the long-term neuropsychological and emotional sequelae in children surviving CVST.
- To assess the implications of pediatric CVST on quality of life.
Main Methods:
- A cohort of 17 children diagnosed with CVST after the neonatal period was studied.
- Clinical follow-up assessments were conducted on 12 survivors, with a mean follow-up of 2 years 8 months.
Main Results:
- Most children had average or high intelligence scores and normal cognitive/physical development.
- Two children experienced mild cognitive deficits, including issues with written language and attention.
- Three children reported decreased physical well-being; one had physical sequelae impacting skilled movement.
Conclusions:
- Children surviving CVST generally have a fair prognosis with good cognitive and physical development.
- Potential long-term effects include mild cognitive deficits and reduced physical/psychosocial well-being.
Abstract:
Cerebral venous sinus thrombosis (CVST) is a rare but potentially serious disorder in children. There is no literature on the long-term neuropsychological and emotional sequelae and implications for quality of life. We studied 17 children who had CVST after the neonatal period, aged between 1 month and 16 years at the time of CVST (mean age at CVST was 6 years, median 4 years 8 months). Five children died during follow-up. The cause of death was related to CVST in one child. Twelve children participated in a clinical follow-up assessment. Mean follow-up was 2 years 8 months. One child had physical sequelae with impairment of skilled movement. All children had average or high intelligence scores. Two children with CVST due to an uncomplicated mastoiditis had mild cognitive deficits: one child had difficulty with written language; the other had diminished cognitive efficiency with concentration and attention problems associated with decreased psychosocial functioning. Decreased physical well-being was reported in three of 12 children. We conclude that children who had survived CVST had a fair prognosis. Most had normal cognitive and physical development, although mild cognitive deficits or decreased physical and psychosocial well-being can occur.
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