Auditory neuropathy spectrum disorder (ANSD) and cochlear implantation

作者：Harrison Robert V^*; Gordon Karen A; Papsin Blake C; Negandhi Jaina; James Adrian L

来源：International Journal of Pediatric Otorhinolaryngology, 2015, 79(12): 1980-1987.

DOI：10.1016/j.ijporl.2015.10.006

• Neonatal hearing screening
• High-risk infant
• Cochlear nerve aplasia
• Cochlear hypoxia
• Cl candidacy protocol
• Auditory dys-synchrony

We discuss issues related to cochlear implantation in children with auditory neuropathy spectrum disorder (ANSD). We describe the varied nature of this disease category including the numerous potential causes of auditory neuropathy. The most prevalent etiology for infants with ANSD is associated with prolonged neonatal intensive care unit (NICU) stay. We discuss the potential contribution of cochlear hypoxia to this etiology. The second part of this review describes in detail our own experience at the Hospital for Sick Children in Toronto, with cochlear implantation of children diagnosed with ANSD. We outline the detection, diagnosis, and referral routes for our patients. We provide an overview of our "standard operation procedures" regarding candidacy, and discuss some of the special considerations that need to be applied to children with ANSD. This includes decisions to implant children with better audiometric thresholds that are standard in non-ANSD patients, concerns about the possibility of spontaneous remission and the appropriate timing of implantation. Finally we review an extensive published literature in outcomes after cochlear implantation (CI) in ANSD. This is not a systematic review but rather an exercise to distill out some important reoccurring themes and the general consensus of opinion to date. Our conclusion is that the hearing loss category ANSD, together with its numerous comorbidities, is far too heterogeneous to make definitive statements about prognosis with Cl.

• 出版日期2015-12