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1.
Artigo em Inglês | MEDLINE | ID: mdl-37149127

RESUMO

Approximately 40% of children with deafness have an additional developmental disorder or major medical problem, which may delay the age of diagnosis of hearing loss and/or require intervention by other professionals. This situation is referred to as "deafness with added disability" (AD+). The reason why the population of hearing-impaired children is more likely to have associated added disabilities is that the risk factors for hearing impairment overlap with those for many other disabilities. These factors can influence various aspects of development, including language acquisition. It is important to check that appropriate care is received, the effectiveness of hearing aids or implants, as well speech therapy intervention strategies, and family adherence to sessions and appointments. The challenge posed by AD+ is early detection, to allow early and appropriate intervention, and the need for fluid transdisciplinary collaboration between all professionals involved, together with the involvement of the family.


Assuntos
Surdez , Auxiliares de Audição , Perda Auditiva , Humanos , Criança , Surdez/complicações , Perda Auditiva/complicações , Auxiliares de Audição/efeitos adversos
2.
Artigo em Inglês | MEDLINE | ID: mdl-35872300

RESUMO

Ototoxicity is defined as the damage, reversible or irreversible, produced in the inner ear by various substances that are called ototoxic and that can cause hearing loss and/or an alteration of the vestibular system. Permanent hearing loss significantly affects quality of life and is especially important in children. The lack or delay in its detection is frequent, since it often progresses in an inconspicuous manner until it affects communication and overall development. This impact can be minimized by following a strategy of audiological monitoring of ototoxicity, which allows for its early detection and treatment. This document recommends that children who are going to be treated with cisplatin or aminoglycosides be monitored. This CODEPEH review and recommendation document focuses on the early detection, prophylaxis, otoprotection, monitoring and treatment of ototoxicity caused by aminoglycosides and platinum-based antineoplastics in the paediatric population.


Assuntos
Surdez , Perda Auditiva , Ototoxicidade , Aminoglicosídeos/efeitos adversos , Antibacterianos/efeitos adversos , Criança , Diagnóstico Precoce , Perda Auditiva/induzido quimicamente , Perda Auditiva/diagnóstico , Perda Auditiva/prevenção & controle , Humanos , Ototoxicidade/diagnóstico , Ototoxicidade/etiologia , Ototoxicidade/prevenção & controle , Qualidade de Vida
3.
Artigo em Inglês | MEDLINE | ID: mdl-34535222

RESUMO

Programmes for early detection of congenital hearing loss have been successfully implemented mainly in developed countries, after overcoming some conceptual errors argued against their implementation and some criticism of their efficacy. However, some difficulties and weaknesses are still identified in these programmes: the detection of late-onset hearing loss and the percentage of children who did not pass the screening and did not complete the process of diagnosis and treatment, these being cases that are lost in the process. The purpose of this Document is to analyse these problems to determine areas for improvement and to emphasize one of the basic principles for the success of the programmes: continuous training for the interdisciplinary team. The result of the review process carried out by CODEPEH has been drafted as Recommendations for updating the Programmes with the evidence of the last decade, including advances in screening technology, the impact of the present knowledge on congenital infection by cytomegalovirus, genetic hearing loss research and control systems of lost to follow-up cases, treatment and follow up.


Assuntos
Surdez , Perda Auditiva Neurossensorial , Perda Auditiva , Criança , Citomegalovirus , Audição , Perda Auditiva/diagnóstico , Humanos
4.
Artigo em Inglês, Espanhol | MEDLINE | ID: mdl-30579510

RESUMO

The aim of this document is to improve the management and the treatment of unilateral or asymmetrical hearing loss in children. One in one thousand newborn infants has unilateral hearing loss and this prevalence increases with age, due to cases of acquired and delayed-onset hearing loss. Although the impact on the development and learning processes of children of these kinds of hearing loss have usually been minimized, if they are not treated they will impact on language and speech development, as well as overall development, affecting the quality of life of the child and his/her family. The outcomes of the review are expressed as recommendations aimed at clinical diagnosis and therapeutic improvement for unilateral or asymmetrical hearing loss.


Assuntos
Perda Auditiva Bilateral/diagnóstico , Perda Auditiva Bilateral/terapia , Perda Auditiva Unilateral/diagnóstico , Perda Auditiva Unilateral/terapia , Prótese Ancorada no Osso , Encéfalo/diagnóstico por imagem , Encéfalo/fisiologia , Criança , Comportamento Infantil , Desenvolvimento Infantil , Implantes Cocleares , Cognição , Diagnóstico Precoce , Auxiliares de Audição , Transtornos da Audição/etiologia , Perda Auditiva Bilateral/etiologia , Perda Auditiva Unilateral/etiologia , Humanos , Relações Interpessoais , Aprendizagem , Qualidade de Vida , Localização de Som , Percepção da Fala/fisiologia
5.
Artigo em Inglês, Espanhol | MEDLINE | ID: mdl-29033123

RESUMO

The incidence and the prevalence rates of otitis media with effusion (OME) are high. However, there is evidence that only a minority of professionals follow the recommendations provided in clinical practice guidelines. For the purpose of improving diagnosis and treatment of OME in children to prevent and/or reduce its impact on children's development, the Commission for the Early Detection of Deafness (CODEPEH) has deeply reviewed the scientific literature on this field and has drafted a document of recommendations for a correct clinical reaction to of OME, including diagnosis and medical and surgical treatment methodology. Among others, medication, in particular antibiotics and corticoids, should not be prescribed and 3 months of watchful waiting should be the first adopted measure. If OME persists, an ENT doctor should assess the possibility of sugical treatment. The impact of OME in cases of children with a comorbidity is higher, so it requires immediate reaction, without watchful waiting.


Assuntos
Otite Média com Derrame/diagnóstico , Otite Média com Derrame/terapia , Testes de Impedância Acústica , Adenoidectomia/estatística & dados numéricos , Corticosteroides/uso terapêutico , Antibacterianos/uso terapêutico , Audiometria , Criança , Transtornos do Comportamento Infantil/etiologia , Pré-Escolar , Fissura Palatina/epidemiologia , Comorbidade , Contraindicações de Medicamentos , Anormalidades Craniofaciais/epidemiologia , Deficiências do Desenvolvimento/etiologia , Síndrome de Down/epidemiologia , Perda Auditiva/diagnóstico , Perda Auditiva/epidemiologia , Perda Auditiva/etiologia , Perda Auditiva/prevenção & controle , Humanos , Lactente , Recém-Nascido , Transtornos da Linguagem/etiologia , Ventilação da Orelha Média/estatística & dados numéricos , Triagem Neonatal , Otite Média com Derrame/epidemiologia , Otoscopia/métodos , Fatores de Risco , Conduta Expectante
6.
Acta Otorrinolaringol Esp ; 68(1): 43-55, 2017.
Artigo em Inglês, Espanhol | MEDLINE | ID: mdl-27644946

RESUMO

Important progress in the fields of molecular genetics (principally) and diagnostic imaging, together with the lack of a consensus protocol for guiding the diagnostic process after confirming deafness by neonatal screening, have led to this new work document drafted by the Spanish Commission for the Early Detection of Child Deafness (Spanish acronym: CODEPEH). This 2015 Recommendations Document, which is based on the most recent scientific evidence, provides guidance to professionals to support them in making decisions regarding aetiological diagnosis. Such diagnosis should be performed without delay and without impeding early intervention. Early identification of the causes of deafness offers many advantages: it prevents unnecessary trouble for the families, reduces health system expenses caused by performing different tests, and provides prognostic information that may guide therapeutic actions.


Assuntos
Surdez/etiologia , Técnicas de Diagnóstico Otológico , Idade de Início , Criança , Pré-Escolar , Surdez/congênito , Surdez/epidemiologia , Surdez/genética , Técnicas de Diagnóstico Otológico/normas , Orelha/anormalidades , Diagnóstico Precoce , Feminino , Perda Auditiva/congênito , Perda Auditiva/epidemiologia , Perda Auditiva/etiologia , Perda Auditiva/genética , Testes Auditivos , Humanos , Lactente , Recém-Nascido , Exame Físico , Gravidez , Complicações Infecciosas na Gravidez , Viroses/complicações , Viroses/diagnóstico
7.
An Pediatr (Barc) ; 85(4): 215.e1-215.e6, 2016 Oct.
Artigo em Espanhol | MEDLINE | ID: mdl-26276692

RESUMO

The latest scientific literature considers early diagnosis of deafness as key element to define the educational prognosis and inclusion of the deaf child, as advantage can be taken in the critical period of development (0-4 years). Highly significant differences exist between those deaf persons who have been stimulated early and those who have received late or inappropriate intervention. Early identification of late-onset disorders requires special attention and knowledge of all childcare professionals. Programs and additional actions beyond neonatal screening should be designed and planned in order to ensure that every child with a significant hearing loss is detected early. For this purpose, the Committee for the Early Detection of Deafness (CODEPEH) would like to highlight the need for continuous monitoring on the hearing health of children. And, for this reason, CODEPEH drafts the recommendations included in the present document.


Assuntos
Perda Auditiva/diagnóstico , Pré-Escolar , Diagnóstico Precoce , Testes Auditivos , Humanos , Lactente
8.
Acta Otorrinolaringol Esp ; 67(1): 45-53, 2016.
Artigo em Inglês, Espanhol | MEDLINE | ID: mdl-26443498

RESUMO

The latest scientific literature considers early diagnosis of deafness as the key element to define the educational and inclusive prognosis of the deaf child, because it allows taking advantage of the critical period of development (0-4 years). Highly significant differences exist between deaf people who have been stimulated early and those who have received late or improper intervention. Early identification of late-onset disorders requires special attention and knowledge on the part of every childcare professional. Programs and additional actions beyond neonatal screening should be designed and planed to ensure that every child with a significant hearing loss is detected early. For this purpose, the CODEPEH would like to highlight the need for continuous monitoring of children's auditory health. Consequently, CODEPEH has drafted the recommendations included in the present document.


Assuntos
Surdez , Auxiliares de Audição , Surdez/diagnóstico , Intervenção Médica Precoce , Perda Auditiva , Humanos , Recém-Nascido , Triagem Neonatal
9.
Acta Otorrinolaringol Esp ; 63(5): 382-90, 2012.
Artigo em Inglês, Espanhol | MEDLINE | ID: mdl-21514545

RESUMO

In the last decade, tremendous progress has been made very rapidly in the development of Early Hearing Detection and Intervention (EHDI) systems as a major public health initiative. The percentage of infants screened annually in Spain has increased significantly since the EHDI systems have expanded to all autonomic regions. Historically, high risk indicators have been used for the identification of infants who should receive audiological evaluation but who live in geographic locations where universal hearing screening is not yet available, to help identify infants who pass neonatal screening but are at risk of developing delayed-onset hearing loss and to identify infants who may have passed neonatal screening but have mild forms of permanent hearing loss. In this review, the standard risk factors for hearing loss are analysed and the risk factors known to be associated with late onset or progressive hearing loss are identified. The recommendation for infants with a risk factor that may be considered as low risk is to perform at least one audiology assessment by 24-30 months. In contrast, for an infant with risk factors known to be associated with late onset or progressive hearing loss (such as cytomegalovirus infection or family history), early and more frequent assessment is appropriate. All infants should have an objective standardised screening of global development with a validated assessment tool at 9, 18 and 24-30 months of age or at any time if the health care professional or the family is concerned.


Assuntos
Perda Auditiva Neurossensorial/epidemiologia , Idade de Início , Agendamento de Consultas , Audiometria , Pré-Escolar , Traumatismos Craniocerebrais/epidemiologia , Anormalidades Craniofaciais/epidemiologia , Progressão da Doença , Efeitos Colaterais e Reações Adversas Relacionados a Medicamentos/epidemiologia , Diagnóstico Precoce , Feminino , Doenças Fetais/epidemiologia , Doenças Genéticas Inatas/epidemiologia , Perda Auditiva Neurossensorial/diagnóstico , Perda Auditiva Neurossensorial/etiologia , Humanos , Lactente , Recém-Nascido , Doenças do Recém-Nascido/epidemiologia , Masculino , Programas de Rastreamento/normas , Triagem Neonatal/normas , Doenças Neurodegenerativas/epidemiologia , Otite Média com Derrame/epidemiologia , Guias de Prática Clínica como Assunto , Fatores de Risco
10.
Acta Otorrinolaringol Esp ; 61(1): 69-77, 2010.
Artigo em Inglês, Espanhol | MEDLINE | ID: mdl-19962682

RESUMO

Newborn hearing screening is currently performed routinely in many regional health-care systems in Spain. Despite the remarkable expansion in newborn hearing screening since 2000, its feasibility and the benefits of early identification and intervention, many major challenges still remain. In this article, the Committee for the Early Detection of Hearing Loss (Comisión para la Detección Precoz de la Hipoacusia, CODEPEH) updates the recommendations that are considered important for the future development of early hearing detection and intervention (EDHI) systems in the following points: 1. Screening protocols: Separate protocols are recommended for NICU (Neonatal Intensive Care Units) and well-infant nurseries. 2. Diagnostic audiology evaluation. Professionals with skills and expertise in evaluating newborn and young infants should provide diagnosis, selection and fitting of amplification devices. 3. Medical evaluation. Risk factors for congenital and acquired hearing loss have been combined in a single list rather than grouped by time of onset. A stepwise diagnostic paradigm is diagnostically more efficient and cost-effective than a simultaneous testing approach. 4. Early intervention and surveillance. All individuals providing services to infants with hearing loss should have specialized training and expertise in the development of audition, speech and language. Regular surveillance should be performed on developmental milestones, auditory skills, parental concerns, and middle ear status. 5. Quality control. Data management as part of an integrated system is important to monitor and improve the quality of EDHI services.


Assuntos
Perda Auditiva/diagnóstico , Diagnóstico por Imagem , Diagnóstico Precoce , Intervenção Educacional Precoce/organização & administração , Intervenção Educacional Precoce/normas , Potenciais Evocados Auditivos , Auxiliares de Audição , Perda Auditiva/etiologia , Perda Auditiva/reabilitação , Testes Auditivos/economia , Testes Auditivos/métodos , Testes Auditivos/estatística & dados numéricos , Humanos , Recém-Nascido , Unidades de Terapia Intensiva Neonatal , Triagem Neonatal/economia , Triagem Neonatal/métodos , Triagem Neonatal/estatística & dados numéricos , Berçários Hospitalares , Emissões Otoacústicas Espontâneas , Avaliação de Programas e Projetos de Saúde , Garantia da Qualidade dos Cuidados de Saúde
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