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Optic neuritis in paediatric patients: Experience over 27 years and a management protocol. / Neuritis óptica en pediatría: experiencia en 27 años y protocolo de actuación.
Monge Galindo, L; Martínez de Morentín, A L; Pueyo Royo, V; García Iñiguez, J P; Sánchez Marco, S; López-Pisón, J; Peña-Segura, J L.
Afiliación
  • Monge Galindo L; Sección de Neuropediatría, Hospital Infantil Universitario Miguel Servet, Zaragoza, España. Electronic address: pediatriazaragoza@hotmail.com.
  • Martínez de Morentín AL; Sección de Neuropediatría, Hospital Infantil Universitario Miguel Servet, Zaragoza, España.
  • Pueyo Royo V; Servicio de Oftalmología, Hospital Infantil Universitario Miguel Servet, Zaragoza, España.
  • García Iñiguez JP; Unidad de Cuidados Intensivos Pediátricos, Hospital Infantil Universitario Miguel Servet, Zaragoza, España.
  • Sánchez Marco S; Unidad de Cuidados Intensivos Pediátricos, Hospital Infantil Universitario Miguel Servet, Zaragoza, España.
  • López-Pisón J; Sección de Neuropediatría, Hospital Infantil Universitario Miguel Servet, Zaragoza, España.
  • Peña-Segura JL; Sección de Neuropediatría, Hospital Infantil Universitario Miguel Servet, Zaragoza, España.
Neurologia (Engl Ed) ; 36(4): 253-261, 2021 May.
Article en En, Es | MEDLINE | ID: mdl-29526320
INTRODUCTION AND OBJECTIVE: In this article, we present our experience on optic neuritis (ON) and provide a diagnostic/therapeutic protocol, intended to rule out other aetiologies (particularly infection), and a fact sheet for parents. MATERIAL AND METHODS: We conducted a descriptive, retrospective study of patients with ON over a 27-year period (1990-2017). A review of the available scientific evidence was performed in order to draft the protocol and fact sheet. RESULTS: Our neuropaediatrics department has assessed 20,744 patients in the last 27 years, of whom 14 were diagnosed with ON: 8 had isolated ON, 1 had multiple sclerosis (MS), 1 had clinically isolated syndrome (CIS), 3 had acute disseminated encephalomyelitis, and 1 had isolated ON and a history of acute disseminated encephalomyelitis one year previously. Patients' age range was 4-13 years; 50% were boys. Eight patients were aged over 10: 7 had isolated ON and 1 had MS. Nine patients had bilateral ON, and 3 had retrobulbar ON. MRI results were normal in 7 patients and showed involvement of the optic nerve only in 2 patients and optic nerve involvement + central nervous system demyelination in 5. Thirteen patients received corticosteroids. One patient had been vaccinated against meningococcus-C the previous month. Progression was favourable, except in the patient with MS. A management protocol and fact sheet are provided. CONCLUSIONS: ON usually has a favourable clinical course. In children aged older than 10 years with risk factors for MS or optic neuromyelitis (hyperintensity on brain MRI, oligoclonal bands, anti-NMO antibody positivity, ON recurrence), the initiation of immunomodulatory treatment should be agreed with the neurology department. The protocol is useful for diagnostic decision-making, follow-up, and treatment of this rare disease with potentially major repercussions. The use of protocols and fact sheets is important.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neuritis Óptica Tipo de estudio: Diagnostic_studies / Guideline / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Child / Child, preschool / Female / Humans / Male Idioma: En / Es Revista: Neurologia (Engl Ed) Año: 2021 Tipo del documento: Article Pais de publicación: España

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neuritis Óptica Tipo de estudio: Diagnostic_studies / Guideline / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Child / Child, preschool / Female / Humans / Male Idioma: En / Es Revista: Neurologia (Engl Ed) Año: 2021 Tipo del documento: Article Pais de publicación: España