Ophthalmic complications of slit-ventricle syndrome in children

Abstract

ObjectiveTo present the ophthalmic features and visual prognosis of patients with slit-ventricle syndrome (SVS).Design:Observational case series. ParticipantsSix patients diagnosed and treated with SVS at the Montreal Children’s Hospital between 1985 and 1999. MethodsPatients were included in this study if they had an appropriate ophthalmologic follow-up and if they fulfilled the criteria for the diagnosis of SVS based on intracranial pressure monitoring and neuroimaging studies. Main outcome measuresFeatures studied included patients’ baseline ophthalmologic evaluation, visual outcome, and neurosurgical characteristics. ResultsThe follow-up ranged from 1 to 14 years. The average number of shunting procedures was 3.7. Ocular examination performed on the initial visit revealed a normal visual acuity in four patients, esotropia in three of six patients, and nystagmus in two of six patients. Cycloplegic refraction was normal in all the subjects. Initial funduscopic evaluation revealed optic atrophy in a 4-month-old infant, whereas two children developed optic atrophy later in the course of the disease. One child developed severe visual field defects. The two children with optic atrophy had moderate to severe loss of visual acuity associated with SVS. ConclusionsA prompt recognition of patients with SVS is crucial, because these individuals are at an increased risk for significant visual loss.