Literature DB >> 9305249

Cochlear implants in children with congenital inner ear malformations.

M Luntz1, T Balkany, A V Hodges, F F Telischi.   

Abstract

OBJECTIVE: To describe clinical experiences with multichannel cochlear implantation in children with inner ear malformations, including surgical indications and techniques, imaging findings, and outcomes.
DESIGN: A retrospective review of a series of 10 consecutive cases with a mean follow-up of 29 months, as well as a review of the literature.
SETTING: Academic referral center.
SUBJECTS: Ten children who underwent multichannel cochlear implantation for inner ear malformations. High-resolution computed tomographic scans demonstrated a common cavity deformity in 3, an incomplete cochlear partition in 4, and an enlarged vestibule in 1. Two had membranous anomalies as indicated by cerebrospinal fluid gushers at surgery, but the results of imaging were normal. INTERVENTION: All subjects received multichannel cochlear implants. Two subjects underwent mastoid obliteration at the time of implantation owing to preoperative recurrent meningitis or chronic otitis media with episodes of clinical mastoiditis. MAIN OUTCOME MEASURES: The 10 subjects were evaluated for electrode insertion and stability and auditory function for up to 7 years.
RESULTS: All 22 electrodes are functional in each child with an incomplete partition, an enlarged vestibule, or a membranous anomaly. Of 3 subjects with common cavities, 2 had full insertion of electrodes and 1 had 16 electrodes inserted. All subjects had speech awareness thresholds detected at 25 dB or better. Three (75%) of the 4 subjects with at least 30 months of experience, including 1 subject with a common cavity, have developed open-set word recognition.
CONCLUSIONS: Electrode insertion and hearing results in children with an incomplete partition, an enlarged vestibule, or a membranous anomaly are similar to those in children with normal cochleas. Specific surgical techniques are effective for children with a common cavity, and the results are less certain. Cerebrospinal fluid gushers were encountered frequently but were not difficult to control.

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Mesh:

Year:  1997        PMID: 9305249     DOI: 10.1001/archotol.1997.01900090090013

Source DB:  PubMed          Journal:  Arch Otolaryngol Head Neck Surg        ISSN: 0886-4470


  10 in total

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2.  Towards an etiologic diagnosis: assessing the patient with hearing loss.

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3.  A Study of Complications and Morbidity Profile in Cochlear Implantation: The MERF Experience.

Authors:  S Raghunandhan; Mohan Kameswaran; R S Anand Kumar; Anoop Kumar Agarwal; Mohammod Delwar Hossain
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4.  Cochlear Implantation in Children with Anomalous Cochleovestibular Anatomy: Our Experience.

Authors:  Mohnish Grover; Shitanshu Sharma; Shruti Bhargava; Shashank Nath Singh; Gaurav Gupta; Man Prakash Sharma
Journal:  Indian J Otolaryngol Head Neck Surg       Date:  2017-09-23

5.  Radiological diagnosis of incomplete partition type I versus type II: significance for cochlear implantation.

Authors:  Georgios Kontorinis; Friedrich Goetz; Alexandros Giourgas; Thomas Lenarz; Heinrich Lanfermann; Anja M Giesemann
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6.  Auditory maturity and hearing performance in inner ear malformations: a histological and electrical stimulation approach.

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Review 7.  Congenital hearing impairment.

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8.  Speech and language development after cochlear implantation in children with bony labyrinth malformations: long-term results.

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Journal:  Eur Arch Otorhinolaryngol       Date:  2014-10-05       Impact factor: 2.503

9.  Effect of inner ear malformations on intraoperative ECAP thresholds and postoperative auditory performance.

Authors:  Jeong-Seo Kim; Sung Hwa Hong; Il Joon Moon
Journal:  Laryngoscope Investig Otolaryngol       Date:  2022-06-15

10.  Communication outcomes following cochlear implantation in a child with cystic cochleovestibular anomaly.

Authors:  N Banumathy; Naresh K Panda
Journal:  J Otol       Date:  2016-04-05
  10 in total

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