Literature DB >> 8977862

Cochlear implantation in a case of Wegener's granulomatosis.

K A Abou-Elhmd1, M R Hawthorne, L M Flood.   

Abstract

Cochlear implantation is now a routine clinical procedure for deaf patients in many countries (Gibson, 1987). It replaces the function of damaged cochlear hair cells and therefore, detects sound and by electrical stimulation produces an appropriate signal in the remaining cochlear nerve fibres (House and Berliner, 1991). Wegener's granulomatosis is an uncommon auto-immune disease. It has a peak incidence at the fifth decade with slight male predominance. Nasal problems are the predominant presentation with otological manifestations presenting rarely. We report a case of Wegener's granulomatosis presenting with total hearing loss and after right cochlear implantation a free field threshold of 40 dB and 20 per cent Bamford-Kowal-Bench (BKB) speech test. We conclude that Wegener's granulomatosis is not an absolute contraindication for cochlear implantation.

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Year:  1996        PMID: 8977862     DOI: 10.1017/s0022215100135455

Source DB:  PubMed          Journal:  J Laryngol Otol        ISSN: 0022-2151            Impact factor:   1.469


  2 in total

1.  Structured clinical assessment of the ear, nose and throat in patients with granulomatosis with polyangiitis (Wegener's).

Authors:  Marcos Martinez Del Pero; Niels Rasmussen; Afzal Chaudhry; Piyush Jani; David Jayne
Journal:  Eur Arch Otorhinolaryngol       Date:  2012-07-18       Impact factor: 2.503

Review 2.  Hearing loss in inner ear and systemic autoimmune disease: A systematic review of post-cochlear implantation outcomes.

Authors:  Jonathan Lee; Kirsty Biggs; Jameel Muzaffar; Manohar Bance; Peter Monksfield
Journal:  Laryngoscope Investig Otolaryngol       Date:  2021-05-04
  2 in total

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