Performance after cochlear implantation in DFNB1 patients
To evaluate the speech perception and language development with cochlear implants (CI) of DFNB1 children in comparison with non-DFNB1 deaf children. Retrospective case series. Academic tertiary center. Thirty-one congenitally deafened children, screened for GJB2 allele variants, were followed for an...
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Veröffentlicht in: | Otolaryngology-head and neck surgery 2007-10, Vol.137 (4), p.596-602 |
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container_title | Otolaryngology-head and neck surgery |
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creator | Connell, Sarah S. Angeli, Simon I. Suarez, Hamlet Hodges, Annelle V. Balkany, Thomas J. Liu, Xue Z. |
description | To evaluate the speech perception and language development with cochlear implants (CI) of DFNB1 children in comparison with non-DFNB1 deaf children.
Retrospective case series.
Academic tertiary center.
Thirty-one congenitally deafened children, screened for GJB2 allele variants, were followed for an average 32 months after CI. With the use of age-appropriate testing, 75% of DFNB1 and 53% of non-DFNB1 children achieved open set word recognition (speech perception category [SPC] level 6). Multivariate analysis showed that SPC was primarily dependent on duration of CI use, but not on the cause of hearing loss. In Reynell language tests, DFNB1 children showed more consistent and quicker gains than non-DFNB1 children.
Although children with CI with DFNB1 show faster gains in Reynell scores, duration of CI use appears to have a greater effect on speech perception than DFNB1 status.
Identification of DFNB1 children is useful in counseling of CI outcomes. |
doi_str_mv | 10.1016/j.otohns.2007.02.017 |
format | Article |
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Retrospective case series.
Academic tertiary center.
Thirty-one congenitally deafened children, screened for GJB2 allele variants, were followed for an average 32 months after CI. With the use of age-appropriate testing, 75% of DFNB1 and 53% of non-DFNB1 children achieved open set word recognition (speech perception category [SPC] level 6). Multivariate analysis showed that SPC was primarily dependent on duration of CI use, but not on the cause of hearing loss. In Reynell language tests, DFNB1 children showed more consistent and quicker gains than non-DFNB1 children.
Although children with CI with DFNB1 show faster gains in Reynell scores, duration of CI use appears to have a greater effect on speech perception than DFNB1 status.
Identification of DFNB1 children is useful in counseling of CI outcomes.</description><identifier>ISSN: 0194-5998</identifier><identifier>EISSN: 1097-6817</identifier><identifier>DOI: 10.1016/j.otohns.2007.02.017</identifier><identifier>PMID: 17903576</identifier><language>eng</language><publisher>Los Angeles, CA: Mosby, Inc</publisher><subject>Alleles ; Child ; Child Language ; Child, Preschool ; Cochlear Implantation ; Cochlear Implants ; Connexin 26 ; Connexins - genetics ; Deafness - congenital ; Deafness - genetics ; Deafness - surgery ; Female ; Follow-Up Studies ; Forecasting ; Genetic Variation - genetics ; Heterozygote ; Humans ; Infant ; Language Development ; Male ; Mutation - genetics ; Retrospective Studies ; Speech - physiology ; Speech Perception - physiology ; Time Factors ; Treatment Outcome</subject><ispartof>Otolaryngology-head and neck surgery, 2007-10, Vol.137 (4), p.596-602</ispartof><rights>2007 American Academy of Otolaryngology–Head and Neck Surgery Foundation</rights><rights>2007 SAGE Publications</rights><rights>2007 American Association of Otolaryngology‐Head and Neck Surgery Foundation (AAO‐HNSF)</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3701-b928db3bd1a7b3067be003a88231fee7da86f4f0dd4c15575d88d7659b9ae5243</citedby><cites>FETCH-LOGICAL-c3701-b928db3bd1a7b3067be003a88231fee7da86f4f0dd4c15575d88d7659b9ae5243</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.sagepub.com/doi/pdf/10.1016/j.otohns.2007.02.017$$EPDF$$P50$$Gsage$$H</linktopdf><linktohtml>$$Uhttps://journals.sagepub.com/doi/10.1016/j.otohns.2007.02.017$$EHTML$$P50$$Gsage$$H</linktohtml><link.rule.ids>314,776,780,1411,21798,27901,27902,43597,43598,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17903576$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Connell, Sarah S.</creatorcontrib><creatorcontrib>Angeli, Simon I.</creatorcontrib><creatorcontrib>Suarez, Hamlet</creatorcontrib><creatorcontrib>Hodges, Annelle V.</creatorcontrib><creatorcontrib>Balkany, Thomas J.</creatorcontrib><creatorcontrib>Liu, Xue Z.</creatorcontrib><title>Performance after cochlear implantation in DFNB1 patients</title><title>Otolaryngology-head and neck surgery</title><addtitle>Otolaryngol Head Neck Surg</addtitle><description>To evaluate the speech perception and language development with cochlear implants (CI) of DFNB1 children in comparison with non-DFNB1 deaf children.
Retrospective case series.
Academic tertiary center.
Thirty-one congenitally deafened children, screened for GJB2 allele variants, were followed for an average 32 months after CI. With the use of age-appropriate testing, 75% of DFNB1 and 53% of non-DFNB1 children achieved open set word recognition (speech perception category [SPC] level 6). Multivariate analysis showed that SPC was primarily dependent on duration of CI use, but not on the cause of hearing loss. In Reynell language tests, DFNB1 children showed more consistent and quicker gains than non-DFNB1 children.
Although children with CI with DFNB1 show faster gains in Reynell scores, duration of CI use appears to have a greater effect on speech perception than DFNB1 status.
Identification of DFNB1 children is useful in counseling of CI outcomes.</description><subject>Alleles</subject><subject>Child</subject><subject>Child Language</subject><subject>Child, Preschool</subject><subject>Cochlear Implantation</subject><subject>Cochlear Implants</subject><subject>Connexin 26</subject><subject>Connexins - genetics</subject><subject>Deafness - congenital</subject><subject>Deafness - genetics</subject><subject>Deafness - surgery</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Forecasting</subject><subject>Genetic Variation - genetics</subject><subject>Heterozygote</subject><subject>Humans</subject><subject>Infant</subject><subject>Language Development</subject><subject>Male</subject><subject>Mutation - genetics</subject><subject>Retrospective Studies</subject><subject>Speech - physiology</subject><subject>Speech Perception - physiology</subject><subject>Time Factors</subject><subject>Treatment Outcome</subject><issn>0194-5998</issn><issn>1097-6817</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkE1rFTEUhoMo9tr6D0Rm5W7Gk8nkC0Sw1WuF0nah65BJzthcZibXZK6l_96UueBOuzoceJ-Xl4eQNxQaClS83zVxiXdzbloA2UDbAJXPyIaClrVQVD4nG6C6q7nW6oS8ynkHAEJI-ZKcUKmBcSk2RN9iGmKa7OywssOCqXLR3Y1oUxWm_WjnxS4hzlWYq8_b63Na7cuP85LPyIvBjhlfH-8p-bH98v3isr66-frt4tNV7ZgEWve6Vb5nvadW9gyE7BGAWaVaRgdE6a0SQzeA952jnEvulfJScN1ri7zt2Cl5t_buU_x1wLyYKWSHY5mG8ZCNUKwDzngJdmvQpZhzwsHsU5hsejAUzKMyszOrMvOozEBrirKCvT32H_oJ_V_o6KgEPqyB-zDiw5NKzc3l9fm2Ba1pwemKZ_sTzS4e0lx0_W_Tx5XBIvZ3wGSyK9Id-pDQLcbH8O-CP5PNoTg</recordid><startdate>200710</startdate><enddate>200710</enddate><creator>Connell, Sarah S.</creator><creator>Angeli, Simon I.</creator><creator>Suarez, Hamlet</creator><creator>Hodges, Annelle V.</creator><creator>Balkany, Thomas J.</creator><creator>Liu, Xue Z.</creator><general>Mosby, Inc</general><general>SAGE Publications</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>8BM</scope></search><sort><creationdate>200710</creationdate><title>Performance after cochlear implantation in DFNB1 patients</title><author>Connell, Sarah S. ; Angeli, Simon I. ; Suarez, Hamlet ; Hodges, Annelle V. ; Balkany, Thomas J. ; Liu, Xue Z.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3701-b928db3bd1a7b3067be003a88231fee7da86f4f0dd4c15575d88d7659b9ae5243</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Alleles</topic><topic>Child</topic><topic>Child Language</topic><topic>Child, Preschool</topic><topic>Cochlear Implantation</topic><topic>Cochlear Implants</topic><topic>Connexin 26</topic><topic>Connexins - genetics</topic><topic>Deafness - congenital</topic><topic>Deafness - genetics</topic><topic>Deafness - surgery</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Forecasting</topic><topic>Genetic Variation - genetics</topic><topic>Heterozygote</topic><topic>Humans</topic><topic>Infant</topic><topic>Language Development</topic><topic>Male</topic><topic>Mutation - genetics</topic><topic>Retrospective Studies</topic><topic>Speech - physiology</topic><topic>Speech Perception - physiology</topic><topic>Time Factors</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Connell, Sarah S.</creatorcontrib><creatorcontrib>Angeli, Simon I.</creatorcontrib><creatorcontrib>Suarez, Hamlet</creatorcontrib><creatorcontrib>Hodges, Annelle V.</creatorcontrib><creatorcontrib>Balkany, Thomas J.</creatorcontrib><creatorcontrib>Liu, Xue Z.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>ComDisDome</collection><jtitle>Otolaryngology-head and neck surgery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Connell, Sarah S.</au><au>Angeli, Simon I.</au><au>Suarez, Hamlet</au><au>Hodges, Annelle V.</au><au>Balkany, Thomas J.</au><au>Liu, Xue Z.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Performance after cochlear implantation in DFNB1 patients</atitle><jtitle>Otolaryngology-head and neck surgery</jtitle><addtitle>Otolaryngol Head Neck Surg</addtitle><date>2007-10</date><risdate>2007</risdate><volume>137</volume><issue>4</issue><spage>596</spage><epage>602</epage><pages>596-602</pages><issn>0194-5998</issn><eissn>1097-6817</eissn><abstract>To evaluate the speech perception and language development with cochlear implants (CI) of DFNB1 children in comparison with non-DFNB1 deaf children.
Retrospective case series.
Academic tertiary center.
Thirty-one congenitally deafened children, screened for GJB2 allele variants, were followed for an average 32 months after CI. With the use of age-appropriate testing, 75% of DFNB1 and 53% of non-DFNB1 children achieved open set word recognition (speech perception category [SPC] level 6). Multivariate analysis showed that SPC was primarily dependent on duration of CI use, but not on the cause of hearing loss. In Reynell language tests, DFNB1 children showed more consistent and quicker gains than non-DFNB1 children.
Although children with CI with DFNB1 show faster gains in Reynell scores, duration of CI use appears to have a greater effect on speech perception than DFNB1 status.
Identification of DFNB1 children is useful in counseling of CI outcomes.</abstract><cop>Los Angeles, CA</cop><pub>Mosby, Inc</pub><pmid>17903576</pmid><doi>10.1016/j.otohns.2007.02.017</doi><tpages>7</tpages></addata></record> |
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subjects | Alleles Child Child Language Child, Preschool Cochlear Implantation Cochlear Implants Connexin 26 Connexins - genetics Deafness - congenital Deafness - genetics Deafness - surgery Female Follow-Up Studies Forecasting Genetic Variation - genetics Heterozygote Humans Infant Language Development Male Mutation - genetics Retrospective Studies Speech - physiology Speech Perception - physiology Time Factors Treatment Outcome |
title | Performance after cochlear implantation in DFNB1 patients |
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