Prevalence of various etiologies of hearing loss among cochlear implant recipients: Systematic review and meta-analysis

References

• Acke F.R., Dhooge I.J., Malfait F. & De Leenheer E.M. 2012. Hearing impairment in Stickler syndrome: A systematic review. Orphanet J Rare Dis, 7, 84.
   PubMed Web of Science ®Google Scholar
• Arnoldner C., Baumgartner W.D., Gstoettner W. & Hamzavi J. 2005. Surgical considerations in cochlear implantation in children and adults: A review of 342 cases in Vienna. Acta Otolaryngol, 125, 228–234.
   PubMed Web of Science ®Google Scholar
• Atas B., Altunhan H., Eryilmaz M.A. & Atas E. 2011. Frequency of congenital hearing loss in 43 503 healthy newborn infants in Konya, Turkey. J Pak Med Assoc, 61, 727–728.
   PubMed Web of Science ®Google Scholar
• Black J., Hickson L., Black B. & Perry C. 2011. Prognostic indicators in paediatric cochlear implant surgery: a systematic literature review. Cochlear Implants Int, 12, 67–93.
   PubMedGoogle Scholar
• Calhau C.M., Lima Junior L.R., Reis A.M., Capistrano A.K., Lima Ddo V. et al. 2011. Etiology profile of the patients implanted in the cochlear implant program. Braz J Otorhinolaryngol, 77, 13–18.
   PubMed Web of Science ®Google Scholar
• Chang D.T., Ko A.B., Murray G.S., Arnold J.E. & Megerian C.A. 2010. Lack of financial barriers to pediatric cochlear implantation: Impact of socioeconomic status on access and outcomes. Arch Otolaryngol Head Neck Surg, 136, 648–657.
   PubMed Web of Science ®Google Scholar
• Chen D., Chen X., Cao K., Zuo J., Jin X. et al. 2009. High prevalence of the connexin 26 (GJB2) mutation in Chinese cochlear implant recipients. ORL J Otorhinolaryngol Relat Spec, 71, 212–215.
   PubMed Web of Science ®Google Scholar
• Cosetti M.K. & Waltzman S.B. 2011. Cochlear implants: Current status and future potential. Expert Rev Med Devices, 8, 389–401.
   PubMed Web of Science ®Google Scholar
• Denoyelle F. 1999. Clinical features of the prevalent form of childhood deafness, DFNB1, due to a connexin-26 gene defect: Implications for genetic counselling. The Lancet (British edition), 353, 1298–1303.
   PubMed Web of Science ®Google Scholar
• Ding X., Tian H., Wang W. & Zhang D. 2009. Cochlear implantation in China: Review of 1237 cases with an emphasis on complications. ORL J Otorhinolaryngol Relat Spec, 71, 192–195.
   PubMed Web of Science ®Google Scholar
• Dror A.A. & Avraham K.B. 2009. Hearing loss: Mechanisms revealed by genetics and cell biology. Annu Rev Genet, 43, 411–437.
   PubMed Web of Science ®Google Scholar
• El-Hakim H., Levasseur J., Papsin B.C., Panesar J., Mount R.J. et al. 2001. Assessment of vocabulary development in children after cochlear implantation. Arch Otolaryngol Head Neck Surg, 127, 1053–1059.
   PubMed Web of Science ®Google Scholar
• Falzon K., Guerin M., Fulcher T. & Viani L. 2010. Ophthalmological screening of a paediatric cochlear implant population: A retrospective analysis and 12-year follow-up. Eye (Lond), 24, 1031–1036.
   PubMed Web of Science ®Google Scholar
• Fortnum H.M., Marshall D.H. & Summerfield A.Q. 2002. Epidemiology of the UK population of hearing-impaired children, including characteristics of those with and without cochlear implants: Audiology, aetiology, comorbidity, and affluence. Int J Audiol, 41, 170–179.
   PubMed Web of Science ®Google Scholar
• Heman-Ackah S.E., Roland J.T. Jr, Haynes D.S. & Waltzman S.B. 2012. Pediatric cochlear implantation: Candidacy evaluation, medical and surgical considerations, and expanding criteria. Otolaryngol Clin North Am, 45, 41–67.
   PubMed Web of Science ®Google Scholar
• Janeschik S., Teschendorf M., Arweiler-Harbeck D. & Bagus H. 2010. Development of hearing and speech abilities in cochlear implant users in relation to cause of deafness. Cochlear Implants Int, 11(Suppl 1), 312–314.
   PubMedGoogle Scholar
• Johnston J.C., Smith A.D., Fitzpatrick E., O’Connor A., Angus D. et al. 2010. Estimation of risks associated with paediatric cochlear implantation. Cochlear Implants Int, 11, 146–169.
   PubMedGoogle Scholar
• Kandogan T., Levent O. & Gurol G. 2005. Complications of paediatric cochlear implantation: Experience in Izmir. J Laryngol Otol, 119, 606–610.
   PubMed Web of Science ®Google Scholar
• Kenneson A. and Cannon M.J. 2007. Review and meta-analysis of the epidemiology of congenital cytomegalovirus (CMV) infection. Rev Med Virol, 17, 253–276.
   PubMed Web of Science ®Google Scholar
• Liu X., Han D., Li J., Han B., Ouyang X. et al. 2010. Loss-of-function mutations in the PRPS1 gene cause a type of nonsyndromic X-linked sensorineural deafness, DFN2. Am J Hum Genet, 86, 65–71.
   PubMed Web of Science ®Google Scholar
• Loundon N., Marlin S., Busquet D., Denoyelle F., Roger G. et al. 2003. Usher syndrome and cochlear implantation. Otol Neurotol, 24, 216–221.
   PubMed Web of Science ®Google Scholar
• Manrique M., Cervera-Paz F.J., Huarte A. & Molina M. 2004. Advantages of cochlear implantation in prelingual deaf children before 2 years of age when compared with later implantation. Laryngoscope, 114, 1462–1469.
   PubMed Web of Science ®Google Scholar
• Mathur P. & Yang J. 2015. Usher syndrome: Hearing loss, retinal degeneration and associated abnormalities. Biochim Biophys Acta, 1852, 406–420.
   PubMed Web of Science ®Google Scholar
• Moga C., Guo B., Schopflocher D. & Harstall C. 2012. Development of a quality appraisal tool for case series studies using a modified Delphi technique. Edmonton, Canada: Institute of Health Economics.
   Google Scholar
• Morzaria S., Westerberg B.D. & Kozak F.K. 2004. Systematic review of the etiology of bilateral sensorineural hearing loss in children. Int J Pediatr Otorhinolaryngol, 68, 1193–1198.
   PubMed Web of Science ®Google Scholar
• Nikolopoulos T.T. 2010. Treating options for deaf children. Early Hum Dev, 86, 669–674.
   PubMed Web of Science ®Google Scholar
• Pagon R., Bird T. & Dolan C. (eds.) 2012. GeneReviews: Deafness and Hereditary Hearing Loss Overview. http://www-ncbi-nlm-nih-gov.ez.statsbiblioteket.dk:2048/books/NBK1434/:
   Google Scholar
• Parving A., Hauch A.M. & Christensen B. 2003. Hearing loss in children: Epidemiology, age at identification, and causes through 30 years. Ugeskr Laeger, 165, 574–9.
   PubMedGoogle Scholar
• Petersen M.B., Wang Q. & Willems P.J. 2008. Sex-linked deafness. Clin Genet, 73, 14–23.
   PubMed Web of Science ®Google Scholar
• Petit C., Levilliers J. & Hardelin J.P. 2001. Molecular genetics of hearing loss. Annu Rev Genet, 35, 589–646.
   PubMed Web of Science ®Google Scholar
• Propst E.J., Papsin B.C., Stockley T.L., Harrison R.V. & Gordon K.A. 2006. Auditory responses in cochlear implant users with and without GJB2 deafness. Laryngoscope, 116, 317–327.
   PubMed Web of Science ®Google Scholar
• Radulescu L., Martu C., Birkenhager R., Cozma S., Ungureanu L. et al. 2012. Prevalence of mutations located at the dfnb1 locus in a population of cochlear implanted children in eastern Romania. Int J Pediatr Otorhinolaryngol, 76, 90–94.
   PubMed Web of Science ®Google Scholar
• Rajput K., Brown T. & Bamiou D.E. 2003. Aetiology of hearing loss and other related factors versus language outcome after cochlear implantation in children. Int J Pediatr Otorhinolaryngol, 67, 497–504.
   PubMed Web of Science ®Google Scholar
• Rosa F., Coutinho M.B., Ferreira J.P. & Sousa C.A. 2015. Ear malformations, hearing loss and hearing rehabilitation in children with Treacher Collins syndrome. Acta Otorrinolaryngol Esp. Epub ahead of print.
   Google Scholar
• Rost S., Bach E., Neuner C., Nanda I., Dysek S. et al. 2014. Novel form of X-linked nonsyndromic hearing loss with cochlear malformation caused by a mutation in the type IV collagen gene COL4A6. Eur J Hum Genet, 22, 208–215.
   PubMed Web of Science ®Google Scholar
• Schraders M., Haas S.A., Weegerink N.J., Oostrik J., Hu H. et al. 2011. Next-generation sequencing identifies mutations of SMPX, which encodes the small muscle protein, X-linked, as a cause of progressive hearing impairment. Am J Hum Genet, 88, 628–634.
   PubMed Web of Science ®Google Scholar
• Schwartz P.J., Spazzolini C., Crotti L., Bathen J., Amlie J.P. et al. 2006. The Jervell and Lange-Nielsen syndrome: Natural history, molecular basis, and clinical outcome. Circulation, 113, 783–790.
   PubMed Web of Science ®Google Scholar
• Senthil Vadivu A., Sampath R., Paramasivan V.K., Mohan M. & Kameswaran M. 2013. Cochlear implantation and cardiac associations. Int J Pediatr Otorhinolaryngol, 77, 1303–1307.
   PubMed Web of Science ®Google Scholar
• Shearer A.E., DeLuca A.P., Hildebrand M.S., Taylor K.R., Gurrola J. 2nd. et al. 2010. Comprehensive genetic testing for hereditary hearing loss using massively parallel sequencing. Proc Natl Acad Sci USA, 107, 21104–21109.
   PubMed Web of Science ®Google Scholar
• Siem G., Fagerheim T., Jonsrud C., Laurent C., Teig E. et al. 2010. Causes of hearing impairment in the Norwegian paediatric cochlear implant program. Int J Audiol, 49, 596–605.
   PubMed Web of Science ®Google Scholar
• Stern R.E., Yueh B., Lewis C., Norton S. & Sie K.C.Y. 2005. Recent epidemiology of pediatric cochlear implantation in the United States: Disparity among children of different ethnicity and socioeconomic status. Laryngoscope, 115, 125–131.
   PubMed Web of Science ®Google Scholar
• Thorsen A., Devantier L. & Ovesen T. 2009. Attitudes towards prenatal diagnosis of deafness among parents to children with cochlear implants. Ugeskr Laeger, 171, 1387–91.
   PubMedGoogle Scholar
• Young N.M., Reilly B.K. & Burke L. 2011. Limitations of universal newborn hearing screening in early identification of pediatric cochlear implant candidates. Arch Otolaryngol Head Neck Surg, 137, 230–234.
   PubMed Web of Science ®Google Scholar
• Zwolan T.A., Ashbaugh C.M., Alarfaj A., Kileny P.R., Arts H.A. et al. 2004. Pediatric cochlear implant patient performance as a function of age at implantation. Otol Neurotol, 25, 112–120.
   PubMed Web of Science ®Google Scholar