TY - JOUR
T1 - Multi-site diagnosis and management of 260 patients with auditory neuropathy/dys-synchrony (auditory neuropathy spectrum disorder
AU - Berlin, Charles I.
AU - Hood, Linda J.
AU - Morlet, Thierry
AU - Wilensky, Diane
AU - Li, Li
AU - Mattingly, Kelly Rose
AU - Taylor-Jeanfreau, Jennifer
AU - Keats, Bronya J.B.
AU - John, Patti St
AU - Montgomery, Elizabeth
AU - Shallop, Jon K.
AU - Russell, Benjamin A.
AU - Frisch, Stefan A.
PY - 2010
Y1 - 2010
N2 - Test results and management data are summarized for 260 patients with diagnoses of Auditory Neuropathy Spectrum Disorder (ANSD). Hearing aids were tried in 85 of these patients, and 49 patients tried cochlear implants. Approximately 15% reported some benefit from hearing aids for language learning, while improvement in speech comprehension and language acquisition was reported in 85% of patients who were implanted. Approximately 5% (13/260) of the total population developed normal speech and language without intervention. Patients were diagnosed at our laboratory (n=66) or referred from other sites (n=194), and all showed absent/grossly abnormal auditory brainstem responses (ABR), often 'ringing' cochlear microphonics, and the presence or history of otoacoustic emissions. Etiologies and co-existing conditions included genetic (n=41), peripheral neuropathies (n=20), perinatal jaundice and/or anoxia and/or prematurity (n=74). These patients comprise 10% or more of hearing impaired patients; their language acquisition trajectories are generally unpredictable from their audiograms.
AB - Test results and management data are summarized for 260 patients with diagnoses of Auditory Neuropathy Spectrum Disorder (ANSD). Hearing aids were tried in 85 of these patients, and 49 patients tried cochlear implants. Approximately 15% reported some benefit from hearing aids for language learning, while improvement in speech comprehension and language acquisition was reported in 85% of patients who were implanted. Approximately 5% (13/260) of the total population developed normal speech and language without intervention. Patients were diagnosed at our laboratory (n=66) or referred from other sites (n=194), and all showed absent/grossly abnormal auditory brainstem responses (ABR), often 'ringing' cochlear microphonics, and the presence or history of otoacoustic emissions. Etiologies and co-existing conditions included genetic (n=41), peripheral neuropathies (n=20), perinatal jaundice and/or anoxia and/or prematurity (n=74). These patients comprise 10% or more of hearing impaired patients; their language acquisition trajectories are generally unpredictable from their audiograms.
KW - Auditory brainstem response
KW - Auditory dys-synchrony
KW - Auditory neuropathy
KW - Cochlear microphonics
KW - Cued speech
KW - Diagnosis
KW - Hearing aidsCochlear implants
KW - Management
KW - Middle-ear muscle refl exes
KW - Otoacoustic emissions
KW - Spectrum disorder
UR - http://www.scopus.com/inward/record.url?scp=75149151905&partnerID=8YFLogxK
U2 - 10.3109/14992020903160892
DO - 10.3109/14992020903160892
M3 - Article
SN - 1499-2027
VL - 49
SP - 30
EP - 43
JO - International Journal of Audiology
JF - International Journal of Audiology
IS - 1
ER -