Five years of universal newborn hearing screening: an incidence study
Autor(a) principal: | |
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Data de Publicação: | 2023 |
Outros Autores: | , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | https://doi.org/10.25753/BirthGrowthMJ.v32.i3.28944 |
Resumo: | Introduction: Universal newborn hearing screening (UNHS) is an essential tool for early diagnosis and prognosis of hearing loss. The aims of this study were to estimate the incidence of sensorineural hearing loss (SNHL) in the Baixo Vouga region, to evaluate the importance of first-degree parental consanguinity (FDPC) as a risk factor for hearing loss in the UNHS program of Centro Hospitalar do Baixo Vouga (CHBV), and to determine the quality of hearing screening program and the main difficulties experienced in its implementation. Methods: Retrospective incidence study of all newborns born in a level II hospital between 2014 and 2018. According to the presence or absence of risk factors (RF) for early childhood hearing loss, each newborn was included in one of two groups: with RF and without RF. FDPC was included in addition to the recommended RF. All newborns underwent hearing screening. Those with abnormal screening or with RF also performed diagnostic audiologic evaluation. Results: Eight thousand seven hundred and twenty-seven newborns were evaluated, of whom 90.88% had no RF. The incidence rate of SNHL was 2.4/1000 infants without RF and 27.6/1000 infants with RF. Screening had an effectiveness of 99.86%, a false positive rate of 0.34%, and a referral rate to an otolaryngologist of 1.24%. FDPC was the third most common RF and the first in infants with SNHL. The missed diagnostic evaluation rate was 44.56%. Discussion: The reported incidence of SNHL is similar to that reported in the literature. The CHBV UNHS program meets national guidelines for quality screening. FDPC is an important RF in this population. The rate of missed diagnostic evaluations was identified as a priority area for improvement. |
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Five years of universal newborn hearing screening: an incidence studyCinco anos de rastreio auditivo neonatal universal: estudo de incidênciaOriginal ArticlesIntroduction: Universal newborn hearing screening (UNHS) is an essential tool for early diagnosis and prognosis of hearing loss. The aims of this study were to estimate the incidence of sensorineural hearing loss (SNHL) in the Baixo Vouga region, to evaluate the importance of first-degree parental consanguinity (FDPC) as a risk factor for hearing loss in the UNHS program of Centro Hospitalar do Baixo Vouga (CHBV), and to determine the quality of hearing screening program and the main difficulties experienced in its implementation. Methods: Retrospective incidence study of all newborns born in a level II hospital between 2014 and 2018. According to the presence or absence of risk factors (RF) for early childhood hearing loss, each newborn was included in one of two groups: with RF and without RF. FDPC was included in addition to the recommended RF. All newborns underwent hearing screening. Those with abnormal screening or with RF also performed diagnostic audiologic evaluation. Results: Eight thousand seven hundred and twenty-seven newborns were evaluated, of whom 90.88% had no RF. The incidence rate of SNHL was 2.4/1000 infants without RF and 27.6/1000 infants with RF. Screening had an effectiveness of 99.86%, a false positive rate of 0.34%, and a referral rate to an otolaryngologist of 1.24%. FDPC was the third most common RF and the first in infants with SNHL. The missed diagnostic evaluation rate was 44.56%. Discussion: The reported incidence of SNHL is similar to that reported in the literature. The CHBV UNHS program meets national guidelines for quality screening. FDPC is an important RF in this population. The rate of missed diagnostic evaluations was identified as a priority area for improvement.Introdução: O rastreio auditivo neonatal universal é uma ferramenta essencial no diagnóstico precoce e no prognóstico da surdez. Os objetivos deste estudo foram estimar a incidência de hipoacusia sensorioneural (HSN) na região do Baixo Vouga, avaliar a importância da consanguinidade parental em primeiro grau (CPPG) como fator de risco para surdez e verificar a qualidade do programa de rastreio e as principais dificuldades na sua implementação. Métodos: Estudo retrospetivo de incidência de todas as crianças nascidas num hospital de nível II entre 2014 e 2018. Cada recém-nascido foi incluído num de dois grupos em função da presença ou ausência de fatores de risco (FR) para surdez: com FR e sem FR. Para além dos FR recomendados foi incluída também a CPPG. Todos os recém-nascidos foram submetidos a rastreio; aqueles com rastreio anormal ou com FR, realizaram também avaliação audiológica diagnóstica. Resultados: Foram estudados 8,727 recém-nascidos, 90,88% dos quais sem FR. A taxa de incidência de HSN foi de 2,4/1000 crianças sem FR e 27,6/1000 crianças com FR. O rastreio apresentou uma efetividade de 99,86%, um índice de falsos positivos de 0,34% e uma taxa de referenciação para consulta de otorrinolaringologia de 1,24%. CPPG foi o terceiro FR mais comum e o mais prevalente entre as crianças com HSN. A taxa de não comparência à avaliação diagnóstica foi de 44,56%. Discussão: A incidência de HNS está de acordo com o descrito na literatura. O programa de rastreio cumpre as diretrizes nacionais para um rastreio de qualidade. A CPPG é um importante FR na população considerada. A taxa de não comparência à avaliação diagnóstica é um foco prioritário de otimização.Centro Hospitalar Universitário de Santo António2023-11-16info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttps://doi.org/10.25753/BirthGrowthMJ.v32.i3.28944eng2183-9417Leal, BárbaraLopes, Ana CristinaPeixoto, DanielaCorreia, LauraAlmiro, Maria MiguelVilar, JoãoAzevedo, LuísaBicho, Maria Adelaideinfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-11-16T17:28:54Zoai:ojs.revistas.rcaap.pt:article/28944Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T22:53:52.083592Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse |
dc.title.none.fl_str_mv |
Five years of universal newborn hearing screening: an incidence study Cinco anos de rastreio auditivo neonatal universal: estudo de incidência |
title |
Five years of universal newborn hearing screening: an incidence study |
spellingShingle |
Five years of universal newborn hearing screening: an incidence study Leal, Bárbara Original Articles |
title_short |
Five years of universal newborn hearing screening: an incidence study |
title_full |
Five years of universal newborn hearing screening: an incidence study |
title_fullStr |
Five years of universal newborn hearing screening: an incidence study |
title_full_unstemmed |
Five years of universal newborn hearing screening: an incidence study |
title_sort |
Five years of universal newborn hearing screening: an incidence study |
author |
Leal, Bárbara |
author_facet |
Leal, Bárbara Lopes, Ana Cristina Peixoto, Daniela Correia, Laura Almiro, Maria Miguel Vilar, João Azevedo, Luísa Bicho, Maria Adelaide |
author_role |
author |
author2 |
Lopes, Ana Cristina Peixoto, Daniela Correia, Laura Almiro, Maria Miguel Vilar, João Azevedo, Luísa Bicho, Maria Adelaide |
author2_role |
author author author author author author author |
dc.contributor.author.fl_str_mv |
Leal, Bárbara Lopes, Ana Cristina Peixoto, Daniela Correia, Laura Almiro, Maria Miguel Vilar, João Azevedo, Luísa Bicho, Maria Adelaide |
dc.subject.por.fl_str_mv |
Original Articles |
topic |
Original Articles |
description |
Introduction: Universal newborn hearing screening (UNHS) is an essential tool for early diagnosis and prognosis of hearing loss. The aims of this study were to estimate the incidence of sensorineural hearing loss (SNHL) in the Baixo Vouga region, to evaluate the importance of first-degree parental consanguinity (FDPC) as a risk factor for hearing loss in the UNHS program of Centro Hospitalar do Baixo Vouga (CHBV), and to determine the quality of hearing screening program and the main difficulties experienced in its implementation. Methods: Retrospective incidence study of all newborns born in a level II hospital between 2014 and 2018. According to the presence or absence of risk factors (RF) for early childhood hearing loss, each newborn was included in one of two groups: with RF and without RF. FDPC was included in addition to the recommended RF. All newborns underwent hearing screening. Those with abnormal screening or with RF also performed diagnostic audiologic evaluation. Results: Eight thousand seven hundred and twenty-seven newborns were evaluated, of whom 90.88% had no RF. The incidence rate of SNHL was 2.4/1000 infants without RF and 27.6/1000 infants with RF. Screening had an effectiveness of 99.86%, a false positive rate of 0.34%, and a referral rate to an otolaryngologist of 1.24%. FDPC was the third most common RF and the first in infants with SNHL. The missed diagnostic evaluation rate was 44.56%. Discussion: The reported incidence of SNHL is similar to that reported in the literature. The CHBV UNHS program meets national guidelines for quality screening. FDPC is an important RF in this population. The rate of missed diagnostic evaluations was identified as a priority area for improvement. |
publishDate |
2023 |
dc.date.none.fl_str_mv |
2023-11-16 |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://doi.org/10.25753/BirthGrowthMJ.v32.i3.28944 |
url |
https://doi.org/10.25753/BirthGrowthMJ.v32.i3.28944 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
2183-9417 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.publisher.none.fl_str_mv |
Centro Hospitalar Universitário de Santo António |
publisher.none.fl_str_mv |
Centro Hospitalar Universitário de Santo António |
dc.source.none.fl_str_mv |
reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação instacron:RCAAP |
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Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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RCAAP |
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RCAAP |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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