OBJECTIVE: To assess neurodevelopmental outcome after endovascular treatment of vein of Galen malformations (VOGM). METHODS: Outcome of patients who underwent endovascular treatment for VOGM between 1983 and 2002 was assessed by chart review and parental questionnaires. Development was classified as normal, minor delay (slow initial acquisition of milestones but no permanent disability), or significant delay (slow or incomplete acquisition of milestones with some permanent disability) using an adaptation of the Denver Developmental Questionnaire. RESULTS: Twenty-seven patients were identified: five presented prenatally (by ultrasound), 16 as neonates, and 6 after the neonatal period. The most common presenting features were congestive heart failure (CHF; 16/27) and hydrocephalus (8/27). The 16 patients with CHF all presented either prenatally or neonatally; 4 died acutely, 6 had significant delay, and 6 had no or minor developmental delay. Of those presenting in the perinatal period without CHF, all survived, two of five were significantly delayed, and three of five had no delay. Of those presenting after the neonatal period, all survived and only one of six had delay. By angiographic classification, outcome was worse for those with choroidal VOGM (3/13 died; 5/13 had significant delay) than for those with mural VOGM (2/10 had significant delay; none died). For the entire series, 52% of all cases (61% of survivors) had no or minor delay. CONCLUSIONS: Fourteen of 27 children who received treatment for VOGM had a favorable outcome. Features associated with worse outcome were perinatal presentation, presence of CHF, and choroidal angioarchitecture.
OBJECTIVE: To assess neurodevelopmental outcome after endovascular treatment of vein of Galen malformations (VOGM). METHODS: Outcome of patients who underwent endovascular treatment for VOGM between 1983 and 2002 was assessed by chart review and parental questionnaires. Development was classified as normal, minor delay (slow initial acquisition of milestones but no permanent disability), or significant delay (slow or incomplete acquisition of milestones with some permanent disability) using an adaptation of the Denver Developmental Questionnaire. RESULTS: Twenty-seven patients were identified: five presented prenatally (by ultrasound), 16 as neonates, and 6 after the neonatal period. The most common presenting features were congestive heart failure (CHF; 16/27) and hydrocephalus (8/27). The 16 patients with CHF all presented either prenatally or neonatally; 4 died acutely, 6 had significant delay, and 6 had no or minor developmental delay. Of those presenting in the perinatal period without CHF, all survived, two of five were significantly delayed, and three of five had no delay. Of those presenting after the neonatal period, all survived and only one of six had delay. By angiographic classification, outcome was worse for those with choroidal VOGM (3/13 died; 5/13 had significant delay) than for those with mural VOGM (2/10 had significant delay; none died). For the entire series, 52% of all cases (61% of survivors) had no or minor delay. CONCLUSIONS: Fourteen of 27 children who received treatment for VOGM had a favorable outcome. Features associated with worse outcome were perinatal presentation, presence of CHF, and choroidal angioarchitecture.
Authors: Sasikhan Geibprasert; Timo Krings; Derek Armstrong; Karel G Terbrugge; Charles A Raybaud Journal: Childs Nerv Syst Date: 2009-08-07 Impact factor: 1.475
Authors: Jason A Ellis; Lauren Orr; Paul C McCormick Ii; Richard Ce Anderson; Neil A Feldstein; Philip M Meyers Journal: World J Radiol Date: 2012-03-28
Authors: S W Hetts; K Keenan; H J Fullerton; W L Young; J D English; N Gupta; C F Dowd; R T Higashida; M T Lawton; V V Halbach Journal: AJNR Am J Neuroradiol Date: 2012-07-05 Impact factor: 3.825
Authors: Gregory G Heuer; Brandon Gabel; Lauren A Beslow; Michael F Stiefel; Erin S Schwartz; Phillip B Storm; Rebecca N Ichord; Robert W Hurst Journal: Childs Nerv Syst Date: 2010-01-05 Impact factor: 1.475