Health-related quality of life evaluation in children with cochlear implants

dc.authorid0000-0002-7219-4516
dc.authorid0000-0001-6783-2133
dc.authorid0000-0001-9104-2756
dc.authorid0000-0003-0325-5511
dc.contributor.authorTulacı, Kamil Gökçe
dc.contributor.authorTulacı, Tuğba
dc.contributor.authorCeylan, Banu Tijen
dc.contributor.authorMutlu, Murad
dc.contributor.authorAkın, İstemihan
dc.contributor.authorÖzdek, Ali
dc.date.accessioned2026-03-13T10:34:50Z
dc.date.issued2025
dc.departmentFakülteler, Tıp Fakültesi, Cerrahi Tıp Bilimleri Bölümü
dc.descriptionTulacı, Kamil Gökçe (Balikesir Author)
dc.description.abstractBACKGROUND: To compare the quality of life scores of children with monoaural cochlear implants (CIs) aged 4-16 with those of normally hearing (NH) children and parents’ reports. METHODS: The KINDL-R questionnaire that measures health-related quality of life (HRQoL) was delivered to 72 children aged 4-16 years and their parents. The children were divided into 3 subgroups of 4-7, 8-11, and 12-16 years and asked to report their quality of life from their own perspectives. The parents were divided into 2 subgroups for 4-7 aged and 8-16 aged children and were asked to report their child’s quality of life status from their perspectives. The QoL scores of children with CI in the 3 subgroups were compared with the scores of their parents and NH peers. RESULTS: The total scores of children with CIs in all subgroups were significantly worse than NH peers. The total scores of parents and children with CIs in all subgroups revealed no statistically significant differences. In the correlation analysis, the age of implantation was negatively correlated with the total score both in 8-11 (ρ: −0.777) and 12-16 year subgroups (ρ: −0.591). Similarly, the implant usage duration was positively correlated with the total score in all age groups. CONCLUSION: Children with CI experience worse QoL status than their NH peers. The possible causes of the lower QoL scores following cochlear implantation must be investigated. Reports from parents on their children’s QoL status are reliable.
dc.identifier.doi10.5152/iao.2025.241705
dc.identifier.endpage6
dc.identifier.issn1308-7649
dc.identifier.issn2148-3817
dc.identifier.issue4
dc.identifier.pmid40693836
dc.identifier.scopus2-s2.0-105011326998
dc.identifier.scopusqualityQ3
dc.identifier.startpage1
dc.identifier.urihttp://doi.org/10.5152/iao.2025.241705
dc.identifier.urihttps://hdl.handle.net/20.500.12462/23472
dc.identifier.volume21
dc.identifier.wosWOS:001578603100001
dc.identifier.wosqualityQ3
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherAves
dc.relation.ispartofJournal of International Advanced Otology
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectChildren With Cochlear Implants
dc.subjectParents
dc.subjectQuality of Life
dc.titleHealth-related quality of life evaluation in children with cochlear implants
dc.typeArticle

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