[Idiopathic intracranial hypertension: Experience over 25 years and a management protocol].

Abstract Introduction We present our experience on idiopathic intracranial hypertension (IIH), before and after the introduction of a specific diagnosis and management protocol. Method A descriptive retrospective study was conducted on patients with IIH over a 25 year period (1990–2015), comparing the last 7 years (after introduction of the protocol) with the previous 18 years. Results Among the 18,865 patients evaluated, there were 54 cases of IIH (29 infants and 25 children). A comparison was made between the two time periods: 32 cases in 1990–2008—published in An Pediatr (Barc). 2009;71:400-6—, and 23 cases in 2008–2015. In post-protocol period, there were 13 patients aged between 3–10 months (62% males) with transient bulging fontanelle, and 10 aged between 2 and 14 years (50% males), with papilloedema. A total of 54% of infants had recently finished corticosteroid treatment for bronchitis. In the older children, there was one case associated with venous thrombosis caused by otomastoiditis, one case on corticosteroid treatment for angioma, and another case treated with growth hormone. Transfontanelle ultrasound was performed on all infants, and CT, MRI and angio-MRI was performed on every child. Lumbar puncture was performed on 2 infants in whom meningitis was suspected, and in all children. All patients progressed favourably, with treatment being started in 3 of them. One patient relapsed. Discussion Characteristics and outcomes of patients overlap every year. IIH usually has a favourable outcome, although it may be longer in children than in infants. It can cause serious visual disturbances, so close ophthalmological control is necessary. The protocol is useful to ease diagnostic decisions, monitoring, and treatment.