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Surgical placement possibilities, audiological benefit, and quality of life following Bonebridge implantation in children

Identifikátory výsledku

  • Kód výsledku v IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F65269705%3A_____%2F25%3A00082794" target="_blank" >RIV/65269705:_____/25:00082794 - isvavai.cz</a>

  • Výsledek na webu

    <a href="https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0332978" target="_blank" >https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0332978</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1371/journal.pone.0332978" target="_blank" >10.1371/journal.pone.0332978</a>

Alternativní jazyky

  • Jazyk výsledku

    angličtina

  • Název v původním jazyce

    Surgical placement possibilities, audiological benefit, and quality of life following Bonebridge implantation in children

  • Popis výsledku v původním jazyce

    This study’s primary goal was to evaluate how smaller size of the BCI602 transcutaneous bone conduction implant affects surgical placement possibilities in children compared to its precursor model, the BCI601. Additionally, audiological benefits, quality of life, and surgical safety of the implant system were investigated in a retrospective cohort of 21 patients. Computed tomography imaging data of the previously implanted patients were examined using a surgical planning software to determine which locations on the scull were feasible for placing the floating mass transducer of the respective implant version. Audiological outcomes in terms of sound field audiometry, speech recognition threshold, and speech recognition in noise were assessed. The Speech, Spatial, and Qualities of Hearing Scale (SSQ12) and the Assessment of Quality of Life 6 Dimensions (AQoL-6D) questionnaires were used to assess subjective benefit in terms of hearing and quality of life. Evaluation of placement options revealed that placement of the BCI602 in the transmastoid plane was possible in 100% of the children, as well as in 89.5% of the cases with the BCI601 variant when using lifts. Likewise, it would be possible to place the BCI602 in 100% of patients superior to the temporal line. For the older BCI601 version, this would be possible only in 58% of cases. With the implant, audiological performance as well as subjective benefit scores improved significantly in the study population. The pediatric cohort reports significant audiological benefit, significantly improved quality of life, and low complication rates. Its combination of high safety, significant audiological benefits, and easy placement of the BCI602 makes the Bonebridge a comfortable and effective option for hearing rehabilitation in children.

  • Název v anglickém jazyce

    Surgical placement possibilities, audiological benefit, and quality of life following Bonebridge implantation in children

  • Popis výsledku anglicky

    This study’s primary goal was to evaluate how smaller size of the BCI602 transcutaneous bone conduction implant affects surgical placement possibilities in children compared to its precursor model, the BCI601. Additionally, audiological benefits, quality of life, and surgical safety of the implant system were investigated in a retrospective cohort of 21 patients. Computed tomography imaging data of the previously implanted patients were examined using a surgical planning software to determine which locations on the scull were feasible for placing the floating mass transducer of the respective implant version. Audiological outcomes in terms of sound field audiometry, speech recognition threshold, and speech recognition in noise were assessed. The Speech, Spatial, and Qualities of Hearing Scale (SSQ12) and the Assessment of Quality of Life 6 Dimensions (AQoL-6D) questionnaires were used to assess subjective benefit in terms of hearing and quality of life. Evaluation of placement options revealed that placement of the BCI602 in the transmastoid plane was possible in 100% of the children, as well as in 89.5% of the cases with the BCI601 variant when using lifts. Likewise, it would be possible to place the BCI602 in 100% of patients superior to the temporal line. For the older BCI601 version, this would be possible only in 58% of cases. With the implant, audiological performance as well as subjective benefit scores improved significantly in the study population. The pediatric cohort reports significant audiological benefit, significantly improved quality of life, and low complication rates. Its combination of high safety, significant audiological benefits, and easy placement of the BCI602 makes the Bonebridge a comfortable and effective option for hearing rehabilitation in children.

Klasifikace

  • Druh

    J<sub>imp</sub> - Článek v periodiku v databázi Web of Science

  • CEP obor

  • OECD FORD obor

    10700 - Other natural sciences

Návaznosti výsledku

  • Projekt

  • Návaznosti

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Ostatní

  • Rok uplatnění

    2025

  • Kód důvěrnosti údajů

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Údaje specifické pro druh výsledku

  • Název periodika

    PLoS ONE

  • ISSN

    1932-6203

  • e-ISSN

    1932-6203

  • Svazek periodika

    20

  • Číslo periodika v rámci svazku

    10

  • Stát vydavatele periodika

    US - Spojené státy americké

  • Počet stran výsledku

    13

  • Strana od-do

    "e0332978"

  • Kód UT WoS článku

    001590337100033

  • EID výsledku v databázi Scopus

    2-s2.0-105018238772