Pediatric Bilateral Sensorineural Hearing Loss: Minimum Test Battery and Referral Criteria for Cochlear Implant Candidacy Evaluation

Author:

Anne Samantha1,Brown Kevin D.2,Goldberg Donald M.13,Adunka Oliver F.4,Kenna Margaret5,Chien Wade6,Teagle Holly7,Zwolan Teresa A.8,Sydlowski Sarah A.1,Roush Patricia2,Buchman Craig A.9

Affiliation:

1. Head and Neck Institute, Cleveland Clinic, Cleveland, Ohio, USA

2. School of Medicine, University of North Carolina, Chapel Hill, North Carolina, USA

3. College of Wooster, Wooster, Ohio, USA

4. Department of Otolaryngology–Head and Neck Surgery, The Ohio State University, Columbus, Ohio, USA

5. Department of Otolaryngology–Head and Neck Surgery, Boston Children’s Hospital and Harvard Medical School, Boston, Massachusetts, USA

6. Johns Hopkins School of Medicine, Baltimore, Maryland, USA

7. University of Auckland, Auckland, New Zealand

8. Department of Otolaryngology–Head and Neck Surgery, Michigan Medicine, Ann Arbor, Michigan, USA

9. Washington University School of Medicine, St Louis, Missouri, USA

Abstract

Among the various cochlear implant systems approved by the Food and Drug Administration, current labeling for pediatric usage encompasses (1) bilateral profound bilateral sensorineural hearing loss in children aged 9 to 24 months and bilateral severe to profound sensorineural hearing loss in children older than 2 years; (2) use of appropriately fitted hearing aids for 3 months (this can be waived if there is evidence of ossification); and (3) demonstration of limited progress with auditory, speech, and language development. Pediatric guidelines require children to have significantly worse speech understanding before qualifying for cochlear implantation. The early years of life have been shown to be critical for speech and language development, and auditory deprivation is especially detrimental during this crucial time. Level of evidence: 2.

Publisher

SAGE Publications

Subject

Otorhinolaryngology,Surgery

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