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Call center 93 253 21 00

Monday to Sunday, from 8 am to 8:30 pm

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Monday to Friday, from 8 am to 7 pm

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Monday to Friday, from 8 am to 7 pm

SJD Barcelona Children's Hospital

Passeig Sant Joan de Déu, 2, 08950 Esplugues de Llobregat

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Dr Carme Fons in a neurology consultation with a patient and their mother
International Patient Specialties

Epilepsy

We treat all types of childhood epilepsy. To ensure correct, early diagnosis, our Epilepsy Unit is completely integrated into the Neurology Area at the SJD Barcelona Children's Hospital.

Why treat childhood epilepsy at the SJD Barcelona Children’s Hospital?

A leading European center with more than 20 years of experience at the Childhood Epilepsy Unit.

We are one of the leading centres in Europe for the diagnosis and treatment of childhood epilepsy. We have coordinated the European Reference Network for Rare and Complex Epilepsies (ERN-EpiCARE) since 2023.

We have facilities dedicated to video-EEG monitoring, ensuring optimal study of all kinds of drug-resistant epilepsy, at all ages.

In-house access to all available tests and medical knowledge to provide an early diagnosis to all neurological diseases associated with epilepsy.

We are experts in using available medications, with a high level of competence in pre-surgical assessment and epilepsy surgery. We continually contribute to clinical trials to help develop new treatments, including gene therapies.

Accreditations

  • ERN-EpiCARE, the European Reference Network for Rare and Complex Epilepsies, alongside Hospital Clinic.
  • The Spanish Government's Ministry of Health (CSUR) for the diagnosis and treatment of drug-refractory epilepsy in children.
  • XUEC in rare pediatric heterogeneous epilepsy that responds poorly to treatment, with a consequent impact on the patient's quality of life.

What is childhood epilepsy?

Epilepsy is a group of heterogeneous disorders, meaning it is due to multiple causes (such as brain injuries or genetic, metabolic, infectious or immune diseases).

Epileptic seizures can appear at any age, manifesting in various ways, and they are the first, or often primary, symptom of a neurological disease.

Epilepsy can impact neurological development, quality of life, education and/or life expectancy.

It is estimated that there are more than 160 rare types of epilepsy, a figure that grows each year as more new genetic forms of epilepsy are discovered.

Adding to these are the extremely complex cases of focal epilepsy, which often benefit from a pre-surgical assessment and, when indicated, surgical treatment.

Early epilepsy diagnosis

Early diagnosis of the subjacent neurological disease that is causing the epilepsy is a crucial step. It will inform treatment options (surgical or non-surgical), serve as a baseline for genetic counselling, and will help establish a prognosis.

At the SJD Barcelona Children's Hospital, we have cutting-edge equipment and methods to render an epilepsy diagnosis:

  • Video EEG monitoring to study brain activity and to establish the location of epileptic foci.
  • Magnetic resonance imaging.
  • Functional neuroimaging (PET, SPECT, fMRI).
  • Genetic screening.

Magnetic resonance

Treatment

The Epilepsy Unit at the SJD Barcelona Children's Hospital has more than 20 years of experience treating childhood epilepsy under its belt.

We expertly manage and utilise all available medications, with a high level of competence in pre-surgical assessment and epilepsy surgery, as well as contributing to clinical trials to develop new treatments, including gene therapy.

Drug treatments

For the last two decades, many new antiepileptic medications have appeared that have much fewer side effects. As such, treatment options can be better adapted to the individual needs of each patient.

Every day, we better understand the mechanisms behind certain types of epilepsy, particularly those of genetic origin. Nowadays, when treating children with epilepsy, it is vital to have an in-depth understanding of treatment indications, interactions between antiepileptic drugs and other drugs being used, and which drugs should be avoided or encouraged, depending on the type of epilepsy diagnosed.

Multidisciplinary medical teams are also better informed with regards to when and for whom a pre-surgical assessment should be considered in the early stages of epilepsy.

Surgery for childhood epilepsy

It is recommended to conduct a pre-surgical assessment in the early phases of the disease for all patients with focal epilepsy, regardless of the presence of a detectable brain injury. In the case of other forms of epilepsy, these patients can benefit from palliative surgical treatments or neuromodulation treatments.

Assessments should be conducted by a multidisciplinary team of medical and neurosurgery experts.

Surgical techniques that may be appropriate, depending on the case:

  • Intracranial electrode implantation to study complex epilepsy.
  • Hemispherotomy or disconnection of the affected hemisphere (16% of cases).
  • Surgical removal of the epileptogenic region (50% of cases).
  • Neuromodulation (21% of cases).
  • Thermocoagulation (13% of cases).

Services for our patients

Our patients

‘Iker had part of his brain isolated so that he would not have epileptic seizures, and since then, we have gained peace of mind’
“They proposed the epilepsy surgery to us after Gara had more than 60 seizures in one day”

Activity

+
1.000

Follow-up consultations per year

+
170

Hospital admissions per year

300

Transition processes per year

60

Surgeries per year

+
3.500

Patients

600

Monitoring services

Team

We are a multidisciplinary team of experts in the diagnosis and treatment of epilepsy in children and adolescents.

Our team includes pediatric neurologists specialising in epilepsy, neuropsychologists, neurosurgeons, neurophysiologists, neuroradiologists, nuclear medicine specialists, nurses, dieticians and electroencephalogram technicians trained in epilepsy treatment.

Recognised by the European Commission, with membership in the European Reference Network for Rare and Complex Epilepsies, ERN-EpiCARE. We work closely with Europe’s best experts.

We also maintain a solid collaboration with Hospital Clinic Barcelona’s Epilepsy Unit for healthcare provision, education and research, ensuring a smooth transition for adolescent patients moving to adult-centered care, as well as the best possible monitoring and follow-up.

All of our professionals have trained at international reference centres for epilepsy.

Alexis Arzimanoglou
Paediatric and epileptological neurologist
Languages: English, Spanish, French, Greek
Maria Carme Fons Estupiñà
Pediatric neurologist
Languages: Spanish, Catalan and English
Javier Aparicio Calvo
Paediatric and epileptological neurologist
Languages: English, Spanish and Catalan
Jana Domínguez Carral
Pediatric Neurologist
Languages: English, Spanish and Catalan
Laia Nou, paediatric neurologist at SJD Barcelona Children's Hospital
Laia Nou Fontanet
Paediatric neurologist
Languages: Catalan, Spanish, English
Juan Dario Ortigoza Escobar
Paediatric neurologist
Languages: Castellano, inglés.
Alia Ramírez Camacho
Paediatric and epileptological neurologist
José Hinojosa Mena-Bernal
Pediatric Neurosurgeon
Languages: English and Spanish
Jordi Rumià Arboix
Paediatric Neurosurgeon
Languages: English, Spanish, Catalan, French
Àngels García Cazorla
Paediatric neurologist
Languages: Spanish, Catalan, English and French
Thaís Armangué Salvador
Paediatric neurologist
Languages: Spanish, Catalan, English and Italian
Andrés Nascimento Osorio
Paediatric neurologist
Federico José Ramos
Pediatric neurologist
Languages: English, Spanish and Catalan
Verónica González Álvarez
Paediatric neurologist
Languages: Spanish and English
Verónica Delgadillo Chilavert
Pediatric neurologist
Languages: English, Spanish and Catalan
Itziar Alonso Colmenero
Clinical neurophysiologist
Òscar Sans Capdevila, head of the Sleep Disorders Unit - SJD Barcelona Children's Hospital
Òscar Ramon Sans Capdevila
Clinical neurophysiologist
Languages: English, Spanish and Catalan
Jana Climent Perin
Clinical neurophysiologist
Languages: English, Spanish, Catalan
Cristina Cámara Ayala
Nurse
Languages: English, Spanish and Catalan
Andrea Palacio Navarro
Neuropsychologist
Languages: English, Spanish, Catalan, German and Italian
Anna López Sala
Neuropsychologist
Languages: Spanish, Catalan and English
Jordi Muchart López
Radiologist
Mónica Rebollo Polo
Radiologist
Marta Gómez Chiari
Radiologist
Languages: English, Spanish, Catalan
Natalia Egea Castillo
Paediatric dietician-nutritionist
Jon Izaguirre Eguren
Child and adolescent psychiatrist
Judith Armstrong Morón
Genetics biologist
Languages: Spanish, Catalan, English, French and Danish
Cristina Jou Muñoz
Pathologist doctor
SJD Logo
Juana Rodríguez Gómez
Neurophysiology
SJD Logo
Concepción Agustín Mata
Paediatric nurse
Languages: Spanish and Catalan

Research

Our main goals in epilepsy research are to encourage investigation to better understand its causes, the biological mechanisms that trigger it, to improve diagnostic processes and to discover new treatments, including repurposing of drugs and gene therapies.

In-progress research projects on childhood epilepsy at the SJD Barcelona Children's Hospital

  • A comparative study of research tools in neuroimaging: Comparing the added value of different types of neuroimaging examinations for optimal localisation of involved brain regions in the onset of epileptic seizures.
  • The EpilETRE and EpilETRE.net studies: Prospective and long-term follow-up study on the cognitive and emotional profiles of children with new onset epilepsy. In collaboration with other university hospitals in France and Italy. The studies focus on neuropsychological evolution, including neuroimaging investigations.
  • GRIN-related epilepsy: A study on the various effects that mutations in the GRIN gene have on NMDA receptors (a glutamate receptor located in the neuronal membrane) in children. Includes a natural history study in collaboration with the University of Lyon (France) and studies focusing on the best treatment options.
  • A study on KCNQ2-type channelopathy: Identifying specific biomarkers for KCNQ2-type channelopathy to obtain more information about symptoms and the progression of the disease, as well as analysing how various treatment options function in mutated channels.