Purpose: To evaluate the efficacy, safety, and tolerability of lacosamide in adults with LGS in the clinical setting.
Method: The present report is a retrospective, open-label treatment study carried out from June 2013 to December 2014 at the National Institute of Colombia. Lacosamide was introduced as add-on therapy.
Objectives: We aimed to investigate the prevalence and risk of mortality in patients with refractory temporal lobe epilepsy.
Methods: Eligible patients included all adults referred to the National Institute of Neurology (NIN) in Havana, Cuba. All patients were followed up for 9 years.