Asunto(s)
Anestésicos Locales/efectos adversos , Quemaduras Químicas/etiología , Ventilación del Oído Medio/métodos , Fenol/efectos adversos , Membrana Timpánica/efectos de los fármacos , Anestésicos Locales/administración & dosificación , Esquema de Medicación , Humanos , Fenol/administración & dosificación , Perforación de la Membrana Timpánica/inducido químicamenteRESUMEN
OBJECTIVES: To review our experience of cochlear implant failure and subsequent revision surgery, and to illustrate the experience we have gained by presenting a series of lessons learned. METHODS: A combined retrospective and prospective study of revision surgery in a UK regional cochlear implant centre. RESULTS: Of the 746 cochlear implantations undertaken, 33 (4.7 per cent of adults and 4.1 per cent of children) had a registered failure requiring re-implantation. The mean time to device failure was 60 months in adults and 35 months in children. Causes of cochlear implant failure were medical (n = 11), electrode displacement (n = 2), 'hard device failure' (n = 15) and 'soft device failure' (n = 5). Chronic suppurative otitis media and post-auricular mastoid abscess were the commonest causes of medical failure. There was one case of electrode array displacement as a direct result of skin flap revision surgery. In 80 per cent of cases, audiological performances were stable or improved following re-implantation. CONCLUSION: As the number of cochlear implants increase and patients outlive the lifespan of their devices, we will face a growing number of revision procedures. Audiologists and otologists should be competent in diagnosing and managing device failure and medical complications requiring cochlear re-implantation.