Diagnóstico y tratamiento de la otitis media secretora infantil: recomendaciones CODEPEH 2016

• Faustino Núñez Batalla ^[1] ; Carmen Jáudenes Casaubón ^[2] ; José Miguel Sequí Canet ^[3] ; Ana Vivanco Allende ^[1] ; José Zubicaray Ugarteche ^[4]
  1. [1] Hospital Universitario Central de Asturias

     Hospital Universitario Central de Asturias

     Oviedo, España

     
  2. [2] Confederación Española de Familias de Personas Sordas (FIAPAS)
  3. [3] Hospital de Gandía-Valencia
  4. [4] Complejo Hospitalario de Navarra-Pamplona

  Mostrar afiliaciones +
• Localización: Revista Española de Discapacidad (REDIS), ISSN-e 2340-5104, Vol. 5, Nº. 1, 2017, págs. 169-193
• Idioma: español
• DOI: 10.5569/2340-5104.05.01.10
• Títulos paralelos:
  • Diagnosis and treatment of otitis media with effusion: 2016 CODEPEH recommendations
• Enlaces
  • Texto completo (pdf)
• Resumen

  • La otitis media secretora (OMS) se define por la presencia de un fluido en el oído medio, sin acompañarse de síntomas o signos de infección aguda (Stool et al., 1994; Antolí-Candela et al., 2013). Se pueden encontrar varios sinónimos en la literatura como “otitis media serosa” u “otitis media seromucosa”. Tras la revisión bibliográfica llevada a cabo, en el presente documento se ha optado por el término “otitis media secretora”, dado que es la terminología más frecuente en relación con esta entidad clínica. Este tipo de otitis es diferente de la otitis media aguda (OMA), cuyas manifestaciones se caracterizan por una historia de inicio agudo, acompañado habitualmente de dolor, fiebre y, en ocasiones, de supuración.

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