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Congenital or Early Acquired Deafness: An Overview of the Portuguese Situation, from Diagnosis to Follow-Up

dc.contributor.authorOliveira, C
dc.contributor.authorMachado, M
dc.contributor.authorZenha, R
dc.contributor.authorAzevedo, L
dc.contributor.authorMonteiro, L
dc.contributor.authorBicho, A
dc.date.accessioned2020-03-03T21:14:49Z
dc.date.available2020-03-03T21:14:49Z
dc.date.issued2019-12-02
dc.description.abstractCongenital deafness or early acquired deafness affects 1 to 3 out of 1000 newborns without risk factors and 20 to 40 out of 1000 newborns with risk factors. The universal newborn hearing screening enables its early identification. Children with congenital deafness/early acquired deafness have a higher prevalence of other conditions, especially ophthalmologic and neurodevelopmental ones, and at least 30% to 40% have at least one associated comorbidity. MATERIAL AND METHODS: We carried out a cross-sectional, multicenter study in which 83% (n = 30) of the hospitals/maternity hospitals of the National Health Service participated. RESULTS: All surveyed hospitals/maternity hospitals routinely performed universal newborn hearing screening to all newborns before discharge; 63% referred children with risk factors for hearing loss to Otorhinolaryngology. All children with congenital deafness/early acquired deafness are referred to: Pediatrics in 23% hospitals/maternity hospitals. In 23 hospitals/maternity hospitals, all children with congenital deafness/early acquired deafness are referred to: Speech Therapy in 44% hospitals/ maternity hospitals; Ophthalmology in 17% hospitals/maternity hospitals; National System of Early Intervention in Childhood in 30% hospitals/maternity hospitals; 22% of hospitals/maternity hospitals refer all children with congenital deafness/early acquired deafness, with no identified cause, to Clinical Genetics clinics. The number of diagnoses of deafness in the years 2014 and 2015 was 2.5 and 1.5 per 1000 newborns, respectively, in 15 hospitals/maternity hospitals. DISCUSSION: Awareness of universal newborn hearing screening seems to be widely spread in the National Health Service. The number of children with SC / SPA, as well as the percentage of different types of deafness diagnosed, were identical to those found in other studies and shows its importance. The assessment / follow-up of these children by specialties other than the otolaryngology was heterogeneous in different health entities and revealed that not all children with risk factors for deafness follow up advised by existing standards. CONCLUSION: Results show that Portugal made an important path in the screening and follow-up of children with SC / SPA. It is important, with the ultimate aim of continually improving the care of these children, to reflect on the involvement of specialties other than otolaryngology, such as the National Early Childhood Intervention System in the follow-up of these children.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationActa Med Port. 2019 Dec 2;32(12):767-775.pt_PT
dc.identifier.doi10.20344/amp.11880pt_PT
dc.identifier.urihttp://hdl.handle.net/10400.26/31615
dc.language.isoporpt_PT
dc.peerreviewedyespt_PT
dc.subjectDeafness/congenitalpt_PT
dc.subjectDeafness/diagnosispt_PT
dc.subjectHearing Testspt_PT
dc.subjectNeonatal Screeningpt_PT
dc.subjectSurdez/congénitapt_PT
dc.subjectSurdez/diagnósticopt_PT
dc.subjectRastreio Neonatalpt_PT
dc.subjectTestes Auditivospt_PT
dc.titleCongenital or Early Acquired Deafness: An Overview of the Portuguese Situation, from Diagnosis to Follow-Uppt_PT
dc.title.alternativeSurdez Congenita ou Precocemente Adquirida: Do Rastreio ao Seguimento, um Retrato de Portugalpt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.issue12pt_PT
oaire.citation.startPage767-775pt_PT
oaire.citation.titleActa medica portuguesapt_PT
oaire.citation.volume32pt_PT
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT

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