scholarly journals Cochlear Implantation in Pediatric Patients: Comparison of Limited-Incision and Standard Cochlear Implantation

2014 ◽  
Vol 67 (3) ◽  
pp. 238-241 ◽  
Author(s):  
Mahmood Shishegar ◽  
Seyed Basir Hashemi
2016 ◽  
Vol 32 (1) ◽  
pp. 55-59 ◽  
Author(s):  
Mohamed Hafez El Saied ◽  
Nashwa Nabil Mohamed ◽  
Hossam Mohamed Mohamed ◽  
Mohamed Ibrahim Amin

2013 ◽  
Vol 149 (2_suppl) ◽  
pp. P119-P119
Author(s):  
Robert F. Labadie ◽  
Fitsum A. Reda ◽  
Jack H. Noble ◽  
Gregoire Blachon ◽  
Benoit M. Dawant ◽  
...  

2008 ◽  
Vol 139 (2_suppl) ◽  
pp. P53-P54
Author(s):  
Anita Jeyakumar ◽  
Randall A Clary

Objective Be able to retrospectively review the complications of pediatric patients undergoing cochlear implantation at a tertiary referral center. Methods IRB permission was obtained. Retrospective analysis of all children who underwent cochlear implantation from January 2001 to December 2005 at a major academic cochlear implantation center. The patients were reviewed for demographic information, type of hearing loss, cochlear implant device, and complications, including implant failure, meningitis, hematomas (intracranial and extracranial), implant extrusion, cerebrospinal fluid leaks, facial palsy, and wound infections. Results A total of 165 patients records were reviewed. 53.5% of the patients were male. The most common device used was the Freedom NucleusTM (60%). The most common etiology of hearing loss was non-syndromic, non-genetic, congenital sensorineural hearing loss (60.6%) All patients had a follow-up of at least 1 year. The most common complication seen was device failure (3.0%), followed by flap infections (2.6%), and immediate postoperative hematomas (1.9%). There was no difference between the kind of device which failed, statistically. There was only one case of Ps. aeruginosa meningitis in a child with a Mondini deformity, who had the implant removed. Conclusions Cochlear implantation in children continues to be reliable and safe, with a low percentage of severe complications, in experienced hands. The patients should have lifetime follow-up.


2021 ◽  
Author(s):  
Liliya Benchetrit ◽  
Nicolette Jabbour ◽  
Swathi Appachi ◽  
Yi‐Chun Liu ◽  
Michael S. Cohen ◽  
...  

2020 ◽  
Vol 58 (2) ◽  
pp. 118-121
Author(s):  
Berat Demir ◽  
◽  
Adem Binnetoglu ◽  
Caglar Batman ◽  
◽  
...  

2020 ◽  
pp. 1-7
Author(s):  
Samanta Gallo ◽  
Patrizia Trevisi ◽  
Chiara Rigon ◽  
Ezio Caserta ◽  
Dario Seif Ali ◽  
...  

<b><i>Introduction:</i></b> Non-syndromic hereditary hearing loss is characterized by extreme genetic heterogeneity. So far, more than 100 pathogenic or likely pathogenic variants in <i>TMC1</i> gene have been reported in patients with autosomal recessive hearing loss (HL) DFNB7/11. The prevailing auditory phenotype of individuals with DFNB7/11 is congenital, profound, bilateral HL, but the functional outcome after cochlear implantation (CI) described in the literature is variable. The objective of this work is to evaluate the auditory outcome after CI in pediatric patients with DFNB7/11, born to non-consanguineous parents. <b><i>Methods:</i></b> A retrospective analysis of genetic and audiological data of DFNB7/11 patients followed up in a single Italian otolaryngology clinic was performed. Cases with biallelic pathogenic variants in <i>TMC1</i> were selected from the cohort of children with non-syndromic hearing loss who had undergone CI and had been molecularly characterized by multigene panel testing. All patients underwent extensive audiological assessment, and the auditory outcome after CI was evaluated. <b><i>Results:</i></b> DFNB7/11 was diagnosed in a total of 3 patients from 2 non-consanguineous families; a novel disease-causing variant in <i>TMC1</i> was detected [c.962G&#x3e;A p.(Trp321*)]. All the affected children showed the typical DFNB7/11 phenotype characterized by prelingual, severe-to-profound HL. The patients showed an excellent functional outcome after CI; speech perception, nonverbal cognition, and speech performance were comparable to those of patients with DFNB1 deafness. <b><i>Discussion/Conclusion:</i></b> Our results do not support the variable auditory outcome reported in the literature, which may be affected by several social and environmental factors and by the genetic background.


Author(s):  
Renae D. Van Wyhe ◽  
Claudia V. Emery ◽  
Robert A. Williamson

2014 ◽  
Vol 150 (4) ◽  
pp. 631-637 ◽  
Author(s):  
Ramya Balachandran ◽  
Fitsum A. Reda ◽  
Jack H. Noble ◽  
Grégoire S. Blachon ◽  
Benoit M. Dawant ◽  
...  

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