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1.
Codas ; 31(3): e20180135, 2019 Jun 27.
Article in Portuguese, English | MEDLINE | ID: mdl-31271581

ABSTRACT

PURPOSE: To verify the effect of the multiple exemplar instruction at the acquisition and integration of listening and speaking behaviors, with substantives and substantive-adjective combinations, in children with Auditory Neuropathy Spectrum Disorder (ANSD) and cochlear implant (CI). METHODS: Participants were two children with ANSD that were users of CI. We adopted dictated stimulus and pictures that corresponded to words (substantive) and substantive-adjective syntactic units. The study was arranged in teaching steps that were intercalated with listening and speaking behaviors probes, with all stimuli. The multiple exemplar instruction presented oral imitation (echoic), auditory recognition (listening) and pictures naming (touch) tasks, on a rotating way; the substantives were taught first and, after that, the substantive-adjective combinations. RESULTS: In the pre-test, the participants showed variability and discrepancy in the correct responses percentages of listening and speaking. All achieved firstly 100% correct responses in the listening task and the speaking performances were close to listening after the teaching. All extended substantive learning to substantive-adjective syntactic units. CONCLUSION: Children with ANSD and CI can learn and integrate listening and speaking behaviors by multiple exemplar instruction, from words to syntactic units.


OBJETIVO: Verificar o efeito do ensino por múltiplos exemplares na aquisição e integração dos comportamentos de ouvinte e falante, com substantivos e combinações substantivo-adjetivo, em crianças com Desordem do Espectro da Neuropatia Auditiva (DENA) e implante coclear (IC). MÉTODO: Participaram duas crianças com DENA que usavam IC. Foram adotados estímulos ditados e figuras que correspondiam a palavras (substantivo) e unidades sintáticas substantivo+adjetivo. O estudo foi organizado em passos de ensino que foram intercalados por avaliações dos comportamentos de ouvinte e falante, com todos os estímulos. O ensino por múltiplos exemplares apresentou tarefas de imitação oral (ecoico), reconhecimento auditivo (ouvinte) e nomeação de figuras (tato) de maneira rotativa; os substantivos foram ensinados primeiro e, em seguida, as combinações substantivo-adjetivo. RESULTADOS: No pré-teste, os participantes mostraram variabilidade e discrepância nas porcentagens de acertos de ouvinte e de falante. Todos alcançaram primeiro 100% de acertos nas tarefas de ouvinte e os desempenhos de falante ficaram próximos aos de ouvinte após o ensino. Todos estenderam a aprendizagem dos substantivos para as unidades sintáticas substantivo-adjetivo. CONCLUSÃO: Crianças com DENA e IC podem aprender e integrar comportamentos de ouvinte e de falante por meio do ensino por múltiplos exemplares, de palavras a unidades sintáticas.


Subject(s)
Cochlear Implants , Hearing Loss, Central/complications , Hearing Loss, Sensorineural/rehabilitation , Speech Perception , Verbal Learning , Child , Child Language , Female , Humans , Language Development , Male , Teaching Materials
2.
CoDAS ; 31(3): e20180135, 2019. tab, graf
Article in Portuguese | LILACS | ID: biblio-1011934

ABSTRACT

RESUMO Objetivo Verificar o efeito do ensino por múltiplos exemplares na aquisição e integração dos comportamentos de ouvinte e falante, com substantivos e combinações substantivo-adjetivo, em crianças com Desordem do Espectro da Neuropatia Auditiva (DENA) e implante coclear (IC). Método Participaram duas crianças com DENA que usavam IC. Foram adotados estímulos ditados e figuras que correspondiam a palavras (substantivo) e unidades sintáticas substantivo+adjetivo. O estudo foi organizado em passos de ensino que foram intercalados por avaliações dos comportamentos de ouvinte e falante, com todos os estímulos. O ensino por múltiplos exemplares apresentou tarefas de imitação oral (ecoico), reconhecimento auditivo (ouvinte) e nomeação de figuras (tato) de maneira rotativa; os substantivos foram ensinados primeiro e, em seguida, as combinações substantivo-adjetivo. Resultados No pré-teste, os participantes mostraram variabilidade e discrepância nas porcentagens de acertos de ouvinte e de falante. Todos alcançaram primeiro 100% de acertos nas tarefas de ouvinte e os desempenhos de falante ficaram próximos aos de ouvinte após o ensino. Todos estenderam a aprendizagem dos substantivos para as unidades sintáticas substantivo-adjetivo. Conclusão Crianças com DENA e IC podem aprender e integrar comportamentos de ouvinte e de falante por meio do ensino por múltiplos exemplares, de palavras a unidades sintáticas.


ABSTRACT Purpose To verify the effect of the multiple exemplar instruction at the acquisition and integration of listening and speaking behaviors, with substantives and substantive-adjective combinations, in children with Auditory Neuropathy Spectrum Disorder (ANSD) and cochlear implant (CI). Methods Participants were two children with ANSD that were users of CI. We adopted dictated stimulus and pictures that corresponded to words (substantive) and substantive-adjective syntactic units. The study was arranged in teaching steps that were intercalated with listening and speaking behaviors probes, with all stimuli. The multiple exemplar instruction presented oral imitation (echoic), auditory recognition (listening) and pictures naming (touch) tasks, on a rotating way; the substantives were taught first and, after that, the substantive-adjective combinations. Results In the pre-test, the participants showed variability and discrepancy in the correct responses percentages of listening and speaking. All achieved firstly 100% correct responses in the listening task and the speaking performances were close to listening after the teaching. All extended substantive learning to substantive-adjective syntactic units. Conclusion Children with ANSD and CI can learn and integrate listening and speaking behaviors by multiple exemplar instruction, from words to syntactic units.


Subject(s)
Humans , Male , Female , Child , Speech Perception , Verbal Learning , Cochlear Implants , Hearing Loss, Central/complications , Hearing Loss, Sensorineural/rehabilitation , Teaching Materials , Child Language , Language Development
3.
Arq Neuropsiquiatr ; 76(3): 170-176, 2018 Mar.
Article in English | MEDLINE | ID: mdl-29809238

ABSTRACT

Objective To assess central auditory function in Friedreich's ataxia. Methods A cross-sectional, retrospective study was carried out. Thirty patients underwent the anamnesis, otorhinolaryngology examination, pure tone audiometry, acoustic immittance measures and brainstem auditory evoked potential (BAEP) assessments. Results The observed alterations were: 43.3% in the pure tone audiometry, bilateral in 36.7%; 56.6% in the BAEP test, bilateral in 50%; and 46.6% in the acoustic immittance test. There was a significant difference (p < 0.05) in the comparison between the tests performed. Conclusion In the audiological screening, there was a prevalence of the descending audiometric configuration at the frequency of 4kHz, and absence of the acoustic reflex at the same frequency. In the BAEP test, there was a prevalence of an increase of the latencies in waves I, III and V, and in the intervals of interpeaks I-III, I-V and III-V. In 13.3% of the patients, wave V was absent, and all waves were absent in 3.3% of patients.


Subject(s)
Evoked Potentials, Auditory, Brain Stem/physiology , Friedreich Ataxia/physiopathology , Hearing Loss, Central/physiopathology , Adolescent , Adult , Age Factors , Aged , Audiometry, Pure-Tone/methods , Auditory Pathways/physiopathology , Child , Cross-Sectional Studies , Female , Friedreich Ataxia/complications , Hearing Loss, Central/etiology , Humans , Male , Middle Aged , Reference Values , Retrospective Studies , Severity of Illness Index , Time Factors , Young Adult
4.
Arq. neuropsiquiatr ; Arq. neuropsiquiatr;76(3): 170-176, Mar. 2018. tab
Article in English | LILACS | ID: biblio-888372

ABSTRACT

ABSTRACT Objective To assess central auditory function in Friedreich's ataxia. Methods A cross-sectional, retrospective study was carried out. Thirty patients underwent the anamnesis, otorhinolaryngology examination, pure tone audiometry, acoustic immittance measures and brainstem auditory evoked potential (BAEP) assessments. Results The observed alterations were: 43.3% in the pure tone audiometry, bilateral in 36.7%; 56.6% in the BAEP test, bilateral in 50%; and 46.6% in the acoustic immittance test. There was a significant difference (p < 0.05) in the comparison between the tests performed. Conclusion In the audiological screening, there was a prevalence of the descending audiometric configuration at the frequency of 4kHz, and absence of the acoustic reflex at the same frequency. In the BAEP test, there was a prevalence of an increase of the latencies in waves I, III and V, and in the intervals of interpeaks I-III, I-V and III-V. In 13.3% of the patients, wave V was absent, and all waves were absent in 3.3% of patients.


RESUMO Objetivo Avaliar a função auditiva central na ataxia de Friedreich (AFRD). Métodos Foi realizado um estudo retrospectivo de corte transversal. 30 pacientes realizaram anamnese, avaliações otorrinolaringológica, audiológica, imitanciométrica e do potencial evocado auditivo de tronco encefálico (PEATE). Resultados As alterações observadas foram: 43,3% no exame audiométrico sendo 36,7% dos casos, bilateralmente; 56,6% na avaliação do PEATE com 50% dos casos, bilateralmente e 46,6% no exame imitanciométrico. Houve diferença significativa (p < 0,05) na comparação entre os exames realizados. Conclusão No exame audiológico, ocorreu uma preponderância maior da configuração audiométrica descendente a partir da freqüência de 4kHz e ausência do reflexo acústico na mesma frequência. No exame do PEATE, houve prevalência do aumento das latências nas ondas I, III e V, e nos intervalos dos interpicos I-III, I-V e III-V. Em 13,3% dos casos, a onda V estava ausente, e em 3,3% dos casos, todas as ondas estavam ausentes.


Subject(s)
Humans , Male , Female , Child , Adolescent , Adult , Middle Aged , Aged , Young Adult , Friedreich Ataxia/physiopathology , Evoked Potentials, Auditory, Brain Stem/physiology , Hearing Loss, Central/physiopathology , Reference Values , Audiometry, Pure-Tone/methods , Auditory Pathways/physiopathology , Time Factors , Severity of Illness Index , Friedreich Ataxia/complications , Cross-Sectional Studies , Retrospective Studies , Age Factors , Hearing Loss, Central/etiology
5.
Braz. j. otorhinolaryngol. (Impr.) ; Braz. j. otorhinolaryngol. (Impr.);82(6): 722-736, Oct.-Dec. 2016. tab, graf
Article in English | LILACS | ID: biblio-828244

ABSTRACT

Abstract Introduction: Auditory Neuropathy/Dyssynchrony is a disorder characterized by the presence of Otoacoustic Emissions and Cochlear Microphonic Potentials, an absence or severe alteration of Brainstem Evoked Auditory Potential, auditory thresholds incompatible with speech thresholds and altered acoustic reflexes. The study of the Cochlear Microphonic Potential appears to be the most important tool for an accurate diagnosis of this pathology. Objective: Determine the characteristics of the Cochlear Microphonic in Auditory Neuropathy/Dyssynchrony using an integrative review. Methods: Bibliographic survey of Pubmed and Bireme platforms and MedLine, LILACS and SciELO data banks, with standardized searches up to July 2014, using keywords. Criteria were established for the selection and assessment of the scientific studies surveyed, considering the following aspects: author, year/place, degree of recommendation/level of scientific evidence, objective, sample, age range, mean age, tests, results and conclusion. Results: Of the 1959 articles found, 1914 were excluded for the title, 20 for the abstract, 9 for the text of the article, 2 for being repeated and 14 were selected for the study. Conclusion: The presence of the Cochlear Microphonic is a determining finding in the differential diagnosis of Auditory Neuropathy/Dyssynchrony. The protocol for the determination of Cochlear Microphonic must include the use of insert earphones, reverse polarity and blocking the stimulus tube to eliminate electrical artifact interference. The amplitude of the Cochlear Microphonic in Auditory Neuropathy/Dyssynchrony shows no significant difference from that of normal individuals. The duration of the Cochlear Microphonic is longer in individuals with Auditory Neuropathy/Dyssynchrony.


Resumo Introdução: A Neuropatia/Dessincronia Auditiva é uma doença caracterizada pela presença das Emissões Otoacústicas e do Microfonismo Coclear, com ausência ou grave alteração do Potencial Evocado Auditivo de Tronco Encefálico, limiares auditivos incompatíveis com limiares vocais e reflexos acústicos alterados. O estudo do Microfonismo Coclear parece ser a ferramenta mais importante para um diagnóstico preciso desta patologia. Objetivo: Verificar por meio de uma revisão integrativa as características do Microfonismo Coclear na Neuropatia/Dessincronia Auditiva. Método: Levantamento bibliográfico nas plataformas Pubmed e Bireme e nas bases de dados MedLine, LILACS e SciELO, com buscas padronizadas até julho de 2014, utilizando-se palavraschave. Para a seleção e avaliação dos estudos científicos levantados, foram estabelecidos critérios, contemplando os aspectos: autor, ano/local, grau de recomendação/nível de evidência científica, objetivo, amostra, faixa etária, média de idade em anos, testes, resultados e conclusão. Resultados: Dos 1959 artigos encontrados, 1914 foram excluídos pelo título, 20 pelo resumo, nove pela leitura do artigo, dois eram repetidos e 14 foram selecionados para o estudo. Conclusão: A presença do Microfonismo Coclear é um achado determinante no diagnóstico diferencial da Neuropatia/Dessincronia auditiva. O protocolo de registro do Microfonismo Coclear deve contar com o uso de fones de inserção, a inversão da polaridade e o bloqueio do tubo do estímulo para impedir a interferência de artefato elétrico. A amplitude do Microfonismo Coclear na Neuropatia/Dessincronia auditiva não apresenta diferença significante entre a amplitude do Microfonismo Coclear em ouvintes normais. A duração do Microfonismo Coclear é maior em indivíduos com Neuropatia/Dessincronia auditiva.


Subject(s)
Humans , Auditory Threshold/physiology , Evoked Potentials, Auditory, Brain Stem/physiology , Otoacoustic Emissions, Spontaneous/physiology , Cochlear Microphonic Potentials/physiology , Hearing Loss, Central/physiopathology
6.
Braz. j. otorhinolaryngol. (Impr.) ; Braz. j. otorhinolaryngol. (Impr.);82(5): 493-499, Sept.-Oct. 2016. graf
Article in English | LILACS | ID: biblio-828232

ABSTRACT

ABSTRACT INTRODUCTION: ANSD is a challenging problem. OBJECTIVE: To present our experience on management of the children with ANSD with respect to clinical data. METHODS: This retrospective study included all children younger than 16 years of age who applied to the department between 2005 and 2013 (with the exception of newborn hearing screening NHS referrals). The data were derived from pure tone, OAEs and ABR tests, and further medical risk factors of the subjects were evaluated. RESULTS: ANSD was recognized in 74 ears of 40 children (B/U: 34/6) among 1952 children with SNHL (2.04%) detected among 9520 applicants to the department (0.42%). The clinical tests revealed that hearing loss greater than 15 dB was present in both ears of 38 cases. The degree of hearing loss was profound in 48% children, severe in 12% children, moderate in 28% children, mild in 10% children and normal in 5% children. ABRs were absent/abnormal in 37/3 ears and CMs were detected in all. Acoustic reflexes were absent in all ears. Rehabilitation was managed by CI and hearing aids in 15 and 23 cases, respectively. FM system was given to two cases displaying normal hearing but poor speech discrimination in noisy environments. CONCLUSION: ANSD is a relatively challenging problem for the audiology departments because of its various clinical features and difficulties in management. Our patients with ANSD most commonly displayed profound hearing loss. The number of overlooked cases may be minimized by performing ABR and OAE in every case referred with the suspicion of hearing loss.


Resumo Introdução: Espectro da neuropatia auditiva ainda é uma condição clínica desafiadora. Objetivo: Apresentar nossa experiência no tratamento de crianças com espectro da neuropatia auditiva em relação aos dados clínicos. Método: Este estudo retrospectivo incluiu crianças menores de 16 anos de idade que deram entrada no departamento entre 2005 e 2013 (com exceção de encaminhamentos para triagem auditiva neonatal). Foram avaliados os dados obtidos a partir dos exames de audiometria tonal, emissões otoacústicas (EOA), potencial evocado auditivo de tronco encefálico (ABR) e outros fatores de risco. Resultados: Das 1.952 crianças com perda auditiva neurossensorial (2,04%) detectadas dentre os 9.520 candidatos que deram entrada no departamento (0,42%), espectro da neuropatia auditiva foi reconhecida em 74 orelhas de 40 crianças (B/U: 34/6). Os testes clínicos revelaram que uma perda auditiva superior a 15 dB estava presente em ambas as orelhas em 38 casos. O grau de perda auditiva das crianças era profundo em 48%, grave em 12%, moderado em 28%, leve em 10%, e normal em 5%. ABR estava ausente/anormal em 37/3 orelhas e microfonia coclear foi detectado em todas as crianças. Reflexos acústicos estavam ausentes em todas as orelhas. A reabilitação foi tratada com implante coclear e aparelhos auditivos em 15 e 23 casos, respectivamente. Um sistema FM foi utilizado em dois casos que apresentavam audição normal, mas discriminação deficiente da fala em ambientes ruidosos. Conclusão: Espectro da neuropatia auditiva é um problema desafiador para os departamentos de audiologia, devido às suas várias características clínicas e dificuldades no tratamento. Em nossos pacientes a perda auditiva profunda foi a mais frequente. O número de casos negligenciados pode ser diminuído com a realização dos exames ABR e EOA em todos os casos encaminhados com suspeita de perda auditiva.


Subject(s)
Humans , Male , Female , Infant , Child, Preschool , Child , Adolescent , Hearing Loss, Central/rehabilitation , Hearing Loss, Sensorineural/rehabilitation , Reflex, Acoustic , Audiometry, Pure-Tone , Severity of Illness Index , Retrospective Studies , Evoked Potentials, Auditory, Brain Stem , Otoacoustic Emissions, Spontaneous , Hearing Loss, Central/diagnosis , Hearing Loss, Sensorineural/diagnosis
7.
J Int Adv Otol ; 12(1): 8-15, 2016 Apr.
Article in English | MEDLINE | ID: mdl-27340976

ABSTRACT

OBJECTIVE: To describe the performance and results of CIs (cochlear implant) in patients with AN (auditory neuropathy) and to present a medical literature review. MATERIALS AND METHODS: Retrospective chart review of patients with AN who were treated with CI. The mesh terms used for the review in the Pubmed and Scopus databases were as follows: "hearing loss, cochlear implants, rehabilitation of persons with hearing impairment, auditory neuropathy". STATISTICAL ANALYSES: The Mann-Whitney test was performed. RESULTS: The sample consisted of 10 patients. The mean age at surgery was 4.3 years, range 2-16 years. The average length of CI use was 5.2 years. The comparison of hearing levels before and after CI use showed a significant improvement in all patients, with p<0.05. All of them also reported an increase in overall satisfaction 1 year after the procedure. A CI is the standard treatment for the hearing rehabilitation of patients with severe profound hearing loss who do not benefit from conventional hearing aids. There are diseases such as AN that also invoke a discussion in the literature regarding CI benefits. CONCLUSION: Individuals with an demonstrated a significant gain in hearing levels and language use with CI.


Subject(s)
Cochlear Implants , Hearing Loss, Central/rehabilitation , Adolescent , Child , Child, Preschool , Cross-Sectional Studies , Female , Follow-Up Studies , Hearing Loss, Central/diagnosis , Hearing Loss, Central/genetics , Hearing Tests , Humans , Language Development Disorders/diagnosis , Language Development Disorders/rehabilitation , Male , Retrospective Studies
8.
Braz J Otorhinolaryngol ; 82(6): 722-736, 2016.
Article in English | MEDLINE | ID: mdl-27177976

ABSTRACT

INTRODUCTION: Auditory Neuropathy/Dyssynchrony is a disorder characterized by the presence of Otoacoustic Emissions and Cochlear Microphonic Potentials, an absence or severe alteration of Brainstem Evoked Auditory Potential, auditory thresholds incompatible with speech thresholds and altered acoustic reflexes. The study of the Cochlear Microphonic Potential appears to be the most important tool for an accurate diagnosis of this pathology. OBJECTIVE: Determine the characteristics of the Cochlear Microphonic in Auditory Neuropathy/Dyssynchrony using an integrative review. METHODS: Bibliographic survey of Pubmed and Bireme platforms and MedLine, LILACS and SciELO data banks, with standardized searches up to July 2014, using keywords. Criteria were established for the selection and assessment of the scientific studies surveyed, considering the following aspects: author, year/place, degree of recommendation/level of scientific evidence, objective, sample, age range, mean age, tests, results and conclusion. RESULTS: Of the 1959 articles found, 1914 were excluded for the title, 20 for the abstract, 9 for the text of the article, 2 for being repeated and 14 were selected for the study. CONCLUSION: The presence of the Cochlear Microphonic is a determining finding in the differential diagnosis of Auditory Neuropathy/Dyssynchrony. The protocol for the determination of Cochlear Microphonic must include the use of insert earphones, reverse polarity and blocking the stimulus tube to eliminate electrical artifact interference. The amplitude of the Cochlear Microphonic in Auditory Neuropathy/Dyssynchrony shows no significant difference from that of normal individuals. The duration of the Cochlear Microphonic is longer in individuals with Auditory Neuropathy/Dyssynchrony.


Subject(s)
Auditory Threshold/physiology , Cochlear Microphonic Potentials/physiology , Evoked Potentials, Auditory, Brain Stem/physiology , Hearing Loss, Central/physiopathology , Otoacoustic Emissions, Spontaneous/physiology , Humans
9.
Mol Med Rep ; 14(1): 481-90, 2016 Jul.
Article in English | MEDLINE | ID: mdl-27177047

ABSTRACT

Auditory neuropathy is a type of hearing loss that constitutes a change in the conduct of the auditory stimulus by the involvement of inner hair cells or auditory nerve synapses. It is characterized by the absence or alteration of waves in the examination of brainstem auditory evoked potentials, with otoacoustic and/or cochlear microphonic issues. At present, four loci associated with non­syndromic auditory neuropathy have been mapped: Autosomal recessive deafness­9 [DFNB9; the otoferlin (OTOF) gene] and autosomal recessive deafness­59 [DFNB59; the pejvakin (PJVK) gene], associated with autosomal recessive inheritance; the autosomal dominant auditory neuropathy gene [AUNA1; the diaphanous­3 (DIAPH3) gene]; and AUNX1, linked to chromosome X. Furthermore, mutations of connexin 26 [the gap junction ß2 (GJB2) gene] have also been associated with the disease. OTOF gene mutations exert a significant role in auditory neuropathy. In excess of 80 pathogenic mutations have been identified in individuals with non­syndromic deafness in populations of different origins, with an emphasis on the p.Q829X mutation, which was found in ~3% of cases of deafness in the Spanish population. The identification of genetic alterations responsible for auditory neuropathy is one of the challenges contributing to understand the molecular bases of the different phenotypes of hearing loss. Thus, the present study aimed to investigate molecular changes in the OTOF gene in patients with auditory neuropathy, and to develop a DNA chip for the molecular diagnosis of auditory neuropathy using mass spectrometry for genotyping. Genetic alterations were investigated in 47 patients with hearing loss and clinical diagnosis of auditory neuropathy, and the c.35delG mutation in the GJB2 gene was identified in three homozygous patients, and the heterozygous parents of one of these cases. Additionally, OTOF gene mutations were tracked by complete sequencing of 48 exons, although these results are still preliminary. Studying the genetic basis of auditory neuropathy is of utmost importance for obtaining a differential diagnosis, developing more specific treatments and more accurate genetic counseling.


Subject(s)
Hearing Loss, Central/genetics , Adolescent , Adult , Alleles , Child , Child, Preschool , Exons , Female , Genes, Mitochondrial , Genetic Association Studies , Genotype , Hearing Loss, Central/diagnosis , Hearing Loss, Central/metabolism , Humans , INDEL Mutation , Male , Membrane Proteins/genetics , Middle Aged , Mutation , Polymorphism, Single Nucleotide , Sequence Analysis, DNA , Young Adult
10.
Codas ; 28(1): 22-6, 2016.
Article in English, Portuguese | MEDLINE | ID: mdl-27074185

ABSTRACT

PURPOSE: To analyze speech perception in children with pre-lingual hearing loss with auditory neuropathy spectrum disorder users of bilateral hearing aid. METHODS: This is a descriptive and exploratory study carried out at the Research Center Audiological (HRAC/USP). The study included four children aged between 8 years and 3 months and 12 years and 2 months. Lists of monosyllabic words, two syllables, nonsense words and sentences, the Infant Toddler-Meaningful Auditory Integration Scale (IT-MAIS) and the Meaningful Use of Speech Scale (MUSS), hearing, and language categories were used. All lists were applied in acoustic booth, with speakers, in free field, in silence. RESULTS: The results showed an average 69.5% for the list of monosyllabic words, 87.75% for the list of two-syllable words, 89.92% for the list of nonsense syllables, and 92.5% for the list of sentences. CONCLUSION: The therapeutic process that includes the use of bilateral hearing aid was extremely satisfactory, since it allowed the maximum development of auditory skills.


Subject(s)
Hearing Aids , Hearing Loss, Central/rehabilitation , Speech Perception , Auditory Perception , Child , Cochlear Implantation , Hearing Loss, Central/surgery , Humans , Language Development , Male , Surveys and Questionnaires
11.
J Pediatr ; 173: 84-9, 2016 Jun.
Article in English | MEDLINE | ID: mdl-26952116

ABSTRACT

OBJECTIVE: This study evaluates whether unbound bilirubin is a better predictor of auditory neuropathy spectrum disorder (ANSD) than total serum bilirubin (TSB) or the bilirubin:albumin molar ratio (BAMR) in late preterm and term neonates with severe jaundice (TSB ≥20 mg/dL or TSB that met exchange transfusion criteria). STUDY DESIGN: Infants ≥34 weeks' gestation with severe jaundice during the first 2 weeks of life were eligible for the prospective observational study. A comprehensive auditory evaluation was performed within 72 hours of peak TSB. ANSD was defined as absent or abnormal auditory brainstem evoked response waveform morphology at 80-decibel click intensity in the presence of normal outer hair cell function. TSB, serum albumin, and unbound bilirubin were measured using the colorimetric, bromocresol green, and modified peroxidase method, respectively. RESULTS: Five of 44 infants developed ANSD. By logistic regression, peak unbound bilirubin but not peak TSB or peak BAMR was associated with ANSD (OR, 4.6; 95% CI, 1.6-13.5; P = .002). On comparing receiver operating characteristic curves, the area under the curve for unbound bilirubin (0.92) was significantly greater (P = .04) compared with the area under the curve for TSB (0.50) or BAMR (0.62). CONCLUSIONS: Unbound bilirubin is a more sensitive and specific predictor of ANSD than TSB or BAMR in late preterm and term infants with severe jaundice.


Subject(s)
Bilirubin/blood , Hearing Loss, Central/diagnosis , Infant, Premature , Jaundice, Neonatal/blood , Jaundice, Neonatal/complications , Audiometry , Biomarkers/blood , Evoked Potentials, Auditory, Brain Stem , Female , Hearing Loss, Central/complications , Humans , Infant, Newborn , Male , Prospective Studies , Sensitivity and Specificity , Serum Albumin/analysis , Term Birth
12.
CoDAS ; 28(1): 22-26, jan.-fev. 2016. tab, graf
Article in Portuguese | LILACS | ID: lil-779122

ABSTRACT

RESUMO Objetivo: Analisar a percepção de fala em crianças portadoras de deficiência auditiva pré-lingual com desordem do espectro da neuropatia auditiva (DENA) usuárias de aparelho de amplificação sonora individual (AASI) bilateral. Métodos: Trata-se de um estudo descritivo e exploratório realizado no Centro de Pesquisas Audiológicas da Sessão de Implante Coclear do Hospital de Reabilitação de Anomalias Craniofaciais (HRAC/USP). Foram avaliadas 4 crianças com idade variando entre 8 anos e 3 meses e 12 anos e 2 meses. Foram utilizados: listas de palavras monossílabas, dissílabas, palavras sem sentido e sentenças, Escala de Integração Auditiva Significativa para Crianças Pequenas (IT-MAIS) e Questionário de Avaliação da Linguagem Oral (MUSS), categorias de linguagem e audição. Todas as listas foram aplicadas em cabine acústica, à viva-voz, em campo livre, no silêncio. Resultados: Os resultados apresentaram média de 69,5% para a lista de palavras monossílabas, 87,75% para a lista de palavras dissílabas, 89,92% para a lista de sílabas sem sentido e 92,5% para a lista de sentenças. Conclusão: O processo terapêutico aplicado, que incluiu o uso do AASI bilateral, foi extremamente satisfatório, uma vez que possibilitou o desenvolvimento máximo das habilidades auditivas.


ABSTRACT Purpose: To analyze speech perception in children with pre-lingual hearing loss with auditory neuropathy spectrum disorder users of bilateral hearing aid. Methods: This is a descriptive and exploratory study carried out at the Research Center Audiological (HRAC/USP). The study included four children aged between 8 years and 3 months and 12 years and 2 months. Lists of monosyllabic words, two syllables, nonsense words and sentences, the Infant Toddler-Meaningful Auditory Integration Scale (IT-MAIS) and the Meaningful Use of Speech Scale (MUSS), hearing, and language categories were used. All lists were applied in acoustic booth, with speakers, in free field, in silence. Results: The results showed an average 69.5% for the list of monosyllabic words, 87.75% for the list of two-syllable words, 89.92% for the list of nonsense syllables, and 92.5% for the list of sentences. Conclusion: The therapeutic process that includes the use of bilateral hearing aid was extremely satisfactory, since it allowed the maximum development of auditory skills.


Subject(s)
Child , Humans , Male , Hearing Aids , Hearing Loss, Central/rehabilitation , Speech Perception , Auditory Perception , Cochlear Implantation , Hearing Loss, Central/surgery , Language Development , Surveys and Questionnaires
13.
Braz J Otorhinolaryngol ; 82(5): 493-9, 2016.
Article in English | MEDLINE | ID: mdl-26781981

ABSTRACT

INTRODUCTION: ANSD is a challenging problem. OBJECTIVE: To present our experience on management of the children with ANSD with respect to clinical data. METHODS: This retrospective study included all children younger than 16 years of age who applied to the department between 2005 and 2013 (with the exception of newborn hearing screening NHS referrals). The data were derived from pure tone, OAEs and ABR tests, and further medical risk factors of the subjects were evaluated. RESULTS: ANSD was recognized in 74 ears of 40 children (B/U: 34/6) among 1952 children with SNHL (2.04%) detected among 9520 applicants to the department (0.42%). The clinical tests revealed that hearing loss greater than 15dB was present in both ears of 38 cases. The degree of hearing loss was profound in 48% children, severe in 12% children, moderate in 28% children, mild in 10% children and normal in 5% children. ABRs were absent/abnormal in 37/3 ears and CMs were detected in all. Acoustic reflexes were absent in all ears. Rehabilitation was managed by CI and hearing aids in 15 and 23 cases, respectively. FM system was given to two cases displaying normal hearing but poor speech discrimination in noisy environments. CONCLUSION: ANSD is a relatively challenging problem for the audiology departments because of its various clinical features and difficulties in management. Our patients with ANSD most commonly displayed profound hearing loss. The number of overlooked cases may be minimized by performing ABR and OAE in every case referred with the suspicion of hearing loss.


Subject(s)
Hearing Loss, Central/rehabilitation , Hearing Loss, Sensorineural/rehabilitation , Adolescent , Audiometry, Pure-Tone , Child , Child, Preschool , Evoked Potentials, Auditory, Brain Stem , Female , Hearing Loss, Central/diagnosis , Hearing Loss, Sensorineural/diagnosis , Humans , Infant , Male , Otoacoustic Emissions, Spontaneous , Reflex, Acoustic , Retrospective Studies , Severity of Illness Index
14.
Braz. j. otorhinolaryngol. (Impr.) ; Braz. j. otorhinolaryngol. (Impr.);81(3): 321-328, May-Jun/2015. tab
Article in English | LILACS | ID: lil-751902

ABSTRACT

INTRODUCTION: Mutations in the otoferlin gene are responsible for auditory neuropathy. OBJECTIVE: To investigate the prevalence of mutations in the mutations in the otoferlin gene in patients with and without auditory neuropathy. METHODS: This original cross-sectional case study evaluated 16 index cases with auditory neuropathy, 13 patients with sensorineural hearing loss, and 20 normal-hearing subjects. DNA was extracted from peripheral blood leukocytes, and the mutations in the otoferlin gene sites were amplified by polymerase chain reaction/restriction fragment length polymorphism. RESULTS: The 16 index cases included nine (56%) females and seven (44%) males. The 13 deaf patients comprised seven (54%) males and six (46%) females. Among the 20 normal-hearing subjects, 13 (65%) were males and seven were (35%) females. Thirteen (81%) index cases had wild-type genotype (AA) and three (19%) had the heterozygous AG genotype for IVS8-2A-G (intron 8) mutation. The 5473C-G (exon 44) mutation was found in a heterozygous state (CG) in seven (44%) index cases and nine (56%) had the wild-type allele (CC). Of these mutants, two (25%) were compound heterozygotes for the mutations found in intron 8 and exon 44. All patients with sensorineural hearing loss and normal-hearing individuals did not have mutations (100%). CONCLUSION: There are differences at the molecular level in patients with and without auditory neuropathy. .


INTRODUÇÃO: Mutações no gene da otoferlina (OTOF) são responsáveis pela neuropatia auditiva. OBJETIVO: Investigar a prevalência de mutações no gene OTOF em pacientes com e sem neuropatia auditiva. MÉTODO: Estudo de casos em corte transversal sendo avaliados 16 casos índice com neuropatia auditiva, 13 pacientes com deficiência auditiva sensorioneural (DASN) e 20 indivíduos ouvintes. DNA foi extraído de leucócitos do sangue periférico e regiões do gene OTOF foram analisadas pela técnica PCR-RFLP. RESULTADOS: Dos 16 casos índice, 9 (56%) são do gênero feminino e 7 (44%) do masculino. Dos 13 pacientes com DASN, 7 (54%) são masculinos e 6 (46%) femininos. Dos 20 ouvintes, 13 (65%) são masculinos e 7 (35%) femininos. Treze (81%) casos índice apresentam o genótipo selvagem (AA) e 3 (19%) o genótipo heterozigoto AG para a mutação IVS8-2A-G (intron 8). A mutação 5473C-G (exon 44) foi encontrada em heterozigose (CG) em 7 (44%) dos casos índice e 9 (56%) apresentam o genótipo selvagem (CC). Destes mutantes, dois (25%) são heterozigotos compostos para as mutações encontradas no intron 8 e exon 44. Os pacientes com DASN e os ouvintes não apresentam mutações (100%). CONCLUSÃO: Existem diferenças, ao nível molecular, em pacientes com e sem neuropatia audi tiva. .


Subject(s)
Humans , Male , Female , Child , Adolescent , Adult , Middle Aged , Aged , Young Adult , Hearing Loss, Central/genetics , Membrane Proteins/genetics , Mutation , Case-Control Studies , Cross-Sectional Studies , Diagnostic Techniques, Otological , DNA Mutational Analysis , Genotype , Hearing Loss, Sensorineural/genetics , Polymerase Chain Reaction , Polymorphism, Restriction Fragment Length
15.
Braz J Otorhinolaryngol ; 81(3): 321-8, 2015.
Article in English | MEDLINE | ID: mdl-25900720

ABSTRACT

INTRODUCTION: Mutations in the otoferlin gene are responsible for auditory neuropathy. OBJECTIVE: To investigate the prevalence of mutations in the mutations in the otoferlin gene in patients with and without auditory neuropathy. METHODS: This original cross-sectional case study evaluated 16 index cases with auditory neuropathy, 13 patients with sensorineural hearing loss, and 20 normal-hearing subjects. DNA was extracted from peripheral blood leukocytes, and the mutations in the otoferlin gene sites were amplified by polymerase chain reaction/restriction fragment length polymorphism. RESULTS: The 16 index cases included nine (56%) females and seven (44%) males. The 13 deaf patients comprised seven (54%) males and six (46%) females. Among the 20 normal-hearing subjects, 13 (65%) were males and seven were (35%) females. Thirteen (81%) index cases had wild-type genotype (AA) and three (19%) had the heterozygous AG genotype for IVS8-2A-G (intron 8) mutation. The 5473C-G (exon 44) mutation was found in a heterozygous state (CG) in seven (44%) index cases and nine (56%) had the wild-type allele (CC). Of these mutants, two (25%) were compound heterozygotes for the mutations found in intron 8 and exon 44. All patients with sensorineural hearing loss and normal-hearing individuals did not have mutations (100%). CONCLUSION: There are differences at the molecular level in patients with and without auditory neuropathy.


Subject(s)
Hearing Loss, Central/genetics , Membrane Proteins/genetics , Mutation , Adolescent , Adult , Aged , Case-Control Studies , Child , Cross-Sectional Studies , DNA Mutational Analysis , Diagnostic Techniques, Otological , Female , Genotype , Hearing Loss, Sensorineural/genetics , Humans , Male , Middle Aged , Polymerase Chain Reaction , Polymorphism, Restriction Fragment Length , Young Adult
16.
Braz. j. otorhinolaryngol. (Impr.) ; Braz. j. otorhinolaryngol. (Impr.);81(1): 85-96, Jan-Feb/2015. tab
Article in English | LILACS | ID: lil-741322

ABSTRACT

Introduction: Currently, there are no doubts about the benefits of cochlear implants for the development of children with severe or profound hearing loss. However, there is still no consensus among researchers and professionals regarding the benefits for the improvement of hearing skills in children with auditory neuropathy spectrum disorder using cochlear implants. Objective: Review the available evidence in the literature to answer the following: "What is the performance of hearing skills in children with auditory neuropathy spectrum disorder using cochlear implants?" Methods: Systematic review of the literature through electronic database consultation, considering publications in the period 2002-2013. Results: Twenty-two studies met the criteria and were included in the systematic review. Conclusion: The analyzed studies demonstrated that after cochlear implant surgery, individuals with auditory neuropathy spectrum disorder improved their performance of hearing skills and had similar performance to that of children with sensorineural hearing loss using cochlear implant. .


Introdução: Atualmente não restam dúvidas quanto aos benefícios do uso do implante coclear no desenvolvimento da população infantil com perda auditiva de grau severo e/ou profundo. Entretanto, ainda não há um consenso entre pesquisadores e profissionais sobre os seus benefícios para a melhora das habilidades auditivas em crianças com o espectro da neuropatia auditiva usuárias de implante coclear. Objetivo: Revisar a evidência disponível na literatura para responder ao questionamento: "Quais os resultados do desempenho das habilidades auditivas em crianças com o espectro da neuropatia auditiva usuárias de implante coclear?" Método: Revisão sistemática da literatura, a partir da consulta de bases de dados eletrônicas, considerando publicações no período de 2002 a 2013. Resultados: Vinte e dois estudos contemplaram os critérios e foram incluídos na revisão sistemática. Conclusão: Os estudos analisados demonstraram que, após a cirurgia de IC, os indivíduos como espectro da neuropatia auditiva melhoraram o desempenho das habilidades auditivas e apresentaram desempenho semelhante ao de crianças com perda auditiva sensorioneural usuárias de implante coclear. .


Subject(s)
Child , Humans , Cochlear Implants , Hearing Loss, Central/rehabilitation , Hearing Loss, Central/complications , Hearing Loss, Central/etiology , Speech Perception
17.
Braz J Otorhinolaryngol ; 81(1): 85-96, 2015.
Article in English | MEDLINE | ID: mdl-25458263

ABSTRACT

INTRODUCTION: Currently, there are no doubts about the benefits of cochlear implants for the development of children with severe or profound hearing loss. However, there is still no consensus among researchers and professionals regarding the benefits for the improvement of hearing skills in children with auditory neuropathy spectrum disorder using cochlear implants. OBJECTIVE: Review the available evidence in the literature to answer the following: "What is the performance of hearing skills in children with auditory neuropathy spectrum disorder using cochlear implants?" METHODS: Systematic review of the literature through electronic database consultation, considering publications in the period 2002-2013. RESULTS: Twenty-two studies met the criteria and were included in the systematic review. CONCLUSION: The analyzed studies demonstrated that after cochlear implant surgery, individuals with auditory neuropathy spectrum disorder improved their performance of hearing skills and had similar performance to that of children with sensorineural hearing loss using cochlear implant.


Subject(s)
Cochlear Implants , Hearing Loss, Central/rehabilitation , Child , Hearing Loss, Central/complications , Hearing Loss, Central/etiology , Humans , Speech Perception
18.
J Int Adv Otol ; 11(3): 229-35, 2015 Dec.
Article in English | MEDLINE | ID: mdl-26915155

ABSTRACT

OBJECTIVE: In auditory neuropathy (AN) a dyssynchrony in the nerve conduction of the auditory nerve fibers is observed. Typically, patients with AN exhibit moderate to profound sensorineural hearing loss, and treatment using cochlear implants (CIs) or hearing aids should be performed as early as possible for a better hearing rehabilitation. The aim of this study is to evaluate the satisfaction level of patients with AN spectrum disorder treated using CIs. The Satisfaction with Amplification in Daily Life questionnaire was selected to evaluate 10 patients with AN treated using CIs. MATERIALS AND METHODS: Clinical study of patients with AN spectrum disorder submitted to CI. A retrospective data analysis, genetic and clinical evaluation in a tertiary referral center was done. RESULTS: The means of the subscales for positive effects, services and costs, negative factors, and personal image were 6.15, 4.6, 3.26, and 3.33, respectively. CONCLUSIONS: Patients with AN treated using CIs consider themselves satisfied.


Subject(s)
Cochlear Implants , Hearing Loss, Central/surgery , Patient Satisfaction , Activities of Daily Living , Child , Child, Preschool , Connexin 26 , Connexins/genetics , Female , Hearing Loss, Central/genetics , Hearing Loss, Central/physiopathology , Humans , Male , Mutation , Retrospective Studies , Surveys and Questionnaires
19.
Distúrb. comun ; 26(1)mar. 2014. graf
Article in Portuguese | LILACS | ID: lil-725932

ABSTRACT

Introdução: Uma vez confirmado o diagnóstico do Transtorno do Processamento Auditivo torna-se necessária realização do treinamento auditivo, para trabalhar as habilidades auditivas que se encontram alteradas. O fundamento chave para o treinamento auditivo está embasado na plasticidade neuronal e nas mudanças benéficas no comportamento auditivo e no sistema nervoso auditivo central. Tais mudanças podem ser monitoradas por meio de testes eletrofisiológicos, como o potencial cognitivo P300. Objetivo: Avaliar a efetividade do treinamento auditivo em crianças com o diagnóstico de transtorno do processamento auditivo, por meio do P300 com estímulo de fala. Métodos: Realizada a avaliação do P300 em 10 indivíduos, com idades entre sete e 14 anos, de ambos os gêneros, antes e após o treinamento auditivo. O programa de intervenção foi composto por nove sessões individuais. Todos os participantes foram submetidos ao P300 com estímulos acústicos binaurais (sílabas ? BA e GA) e intensidade de 75 dB NA. Foram utilizados 500 estímulos, dentre os quais 80% foram requentes (sílaba BA) e 20% foram raros (sílaba GA). Os estímulos raros e frequentes foram apresentados de forma aleatória (paradigma oddball). Resultados: Foi observada redução da latência e aumento da amplitude do P300 no instante pós-treinamento auditivo, de forma estatisticamente significante. Conclusão: Considerando as mudanças verificadas em relação à latência e amplitude do P300, eliciado com estímulo de fala após o programa terapêutico proposto, é possível concluir que este teste eletrofisiológico é uma ferramenta objetiva sensível para monitorar a efetividade do treinamento auditivo.


Introduction: Once confirmed the diagnosis of Auditory Processing Disorder, it is necessary to provide auditory training to improve the auditory skills. The basis for auditory training is based on neuronal plasticity and beneficial changes in auditory behavior and the central auditory pathways. These changes can be monitored by electrophysiological tests, as the the long latency auditory evoked potentials (P300). Objective: To assess the effectiveness of auditory training in children with auditory processing disorder through P300 with speech stimuli. Methods: The P300 was performed in 10 subjects, aged betweenseven and 14 years (both genders) of Clinical Speech Pathology, University of Guarulhos, before and after auditory training. The intervention program consisted of nine individual sessions. All participants underwent the P300. The test was performed with 500 binaural acoustic stimuli (syllables /BA/ for high- probability sounds and /GA/ for low-probability sounds), at 75 dB HL. The rare and frequent stimuli were presented in random order (oddball paradigm). Results: After the auditory training it was observed an improvement in the results of P300, by a statistically significant latency reduction and increased amplitude of the P300 at the instant post-auditory training. Conclusion: P300 elicited by speech was considered a sensitive tool to monitor the effectiveness of auditory training.


Introducción: Una vez confirmado el diagnóstico de Trastorno del Procesamiento Auditivo se hace necesaria la realización del entrenamiento auditivo, para trabajar las habilidades auditivas que se encuentran alteradas. El fundamento llave para el entrenamiento auditivo está embasado en la plasticidad neuronal y en los cambios benéficos para el comportamiento auditivo y el sistema nervioso auditivo central. Tales cambios pueden ser monitoreados por medio de pruebas eletrofisiológicas, como el potencial cognitivo P300. Objetivo: Evaluar la efectividad del entrenamiento auditivo en niños con el diagnóstico de trastorno del procesamiento auditivo, por medio del lo P300 con estímulo de habla. Métodos: Realizar la evaluación del P300 en 10 individuos, con edades entre los siete y 14 años, de ambos géneros, antes y después del entrenamiento auditivo. El programa de intervención fue compuesto por nueve sesiones individuales. Todos los participantes fueron sometidos al P300 con estímulos acústicos binaurales (sílabas ? BA y GA), a una intensidad de 75 dBNA. Fueron utilizados 500 estímulos entre los cuales 80% fueron frecuentes (sílaba BA) y 20% fueron raros (sílaba GA). Los estímulos raros y frecuentes fueron presentados de forma aleatoria (paradigma oddball). Resultados: Fue observada reducción de la latencia y aumento de la amplitud del lo P300 en el instante post-entrenamiento auditivo, de forma estadísticamente significante. Conclusión: Considerando los cambios verificados en la latencia y amplitud del P300, suscitados con estímulo de habla después del programa terapéutico propuesto, es posible concluir que esta prueba eletrofisiológica es una herramienta objetiva sensible para monitorear la efectividad del entrenamiento auditivo.


Subject(s)
Humans , Central Nervous System , Delivery of Health Care , Evoked Potentials, Auditory , Hearing Loss, Central
20.
Distúrb. comun ; 26(1): 27-34, mar. 2014. graf
Article in Portuguese | Index Psychology - journals | ID: psi-62215

ABSTRACT

Introdução: Uma vez confirmado o diagnóstico do Transtorno do Processamento Auditivo torna-se necessária realização do treinamento auditivo, para trabalhar as habilidades auditivas que se encontram alteradas. O fundamento chave para o treinamento auditivo está embasado na plasticidade neuronal e nas mudanças benéficas no comportamento auditivo e no sistema nervoso auditivo central. Tais mudanças podem ser monitoradas por meio de testes eletrofisiológicos, como o potencial cognitivo P300. Objetivo: Avaliar a efetividade do treinamento auditivo em crianças com o diagnóstico de transtorno do processamento auditivo, por meio do P300 com estímulo de fala. Métodos: Realizada a avaliação do P300 em 10 indivíduos, com idades entre sete e 14 anos, de ambos os gêneros, antes e após o treinamento auditivo. O programa de intervenção foi composto por nove sessões individuais. Todos os participantes foram submetidos ao P300 com estímulos acústicos binaurais (sílabas ? BA e GA) e intensidade de 75 dB NA. Foram utilizados 500 estímulos, dentre os quais 80% foram requentes (sílaba BA) e 20% foram raros (sílaba GA). Os estímulos raros e frequentes foram apresentados de forma aleatória (paradigma oddball). Resultados: Foi observada redução da latência e aumento da amplitude do P300 no instante pós-treinamento auditivo, de forma estatisticamente significante. Conclusão: Considerando as mudanças verificadas em relação à latência e amplitude do P300, eliciado com estímulo de fala após o programa terapêutico proposto, é possível concluir que este teste eletrofisiológico é uma ferramenta objetiva sensível para monitorar a efetividade do treinamento auditivo.(AU)


Introduction: Once confirmed the diagnosis of Auditory Processing Disorder, it is necessary to provide auditory training to improve the auditory skills. The basis for auditory training is based on neuronal plasticity and beneficial changes in auditory behavior and the central auditory pathways. These changes can be monitored by electrophysiological tests, as the the long latency auditory evoked potentials (P300). Objective: To assess the effectiveness of auditory training in children with auditory processing disorder through P300 with speech stimuli. Methods: The P300 was performed in 10 subjects, aged betweenseven and 14 years (both genders) of Clinical Speech Pathology, University of Guarulhos, before and after auditory training. The intervention program consisted of nine individual sessions. All participants underwent the P300. The test was performed with 500 binaural acoustic stimuli (syllables /BA/ for high- probability sounds and /GA/ for low-probability sounds), at 75 dB HL. The rare and frequent stimuli were presented in random order (oddball paradigm). Results: After the auditory training it was observed an improvement in the results of P300, by a statistically significant latency reduction and increased amplitude of the P300 at the instant post-auditory training. Conclusion: P300 elicited by speech was considered a sensitive tool to monitor the effectiveness of auditory training.(AU)


Introducción: Una vez confirmado el diagnóstico de Trastorno del Procesamiento Auditivo se hace necesaria la realización del entrenamiento auditivo, para trabajar las habilidades auditivas que se encuentran alteradas. El fundamento llave para el entrenamiento auditivo está embasado en la plasticidad neuronal y en los cambios benéficos para el comportamiento auditivo y el sistema nervioso auditivo central. Tales cambios pueden ser monitoreados por medio de pruebas eletrofisiológicas, como el potencial cognitivo P300. Objetivo: Evaluar la efectividad del entrenamiento auditivo en niños con el diagnóstico de trastorno del procesamiento auditivo, por medio del lo P300 con estímulo de habla. Métodos: Realizar la evaluación del P300 en 10 individuos, con edades entre los siete y 14 años, de ambos géneros, antes y después del entrenamiento auditivo. El programa de intervención fue compuesto por nueve sesiones individuales. Todos los participantes fueron sometidos al P300 con estímulos acústicos binaurales (sílabas ? BA y GA), a una intensidad de 75 dBNA. Fueron utilizados 500 estímulos entre los cuales 80% fueron frecuentes (sílaba BA) y 20% fueron raros (sílaba GA). Los estímulos raros y frecuentes fueron presentados de forma aleatoria (paradigma oddball). Resultados: Fue observada reducción de la latencia y aumento de la amplitud del lo P300 en el instante post-entrenamiento auditivo, de forma estadísticamente significante. Conclusión: Considerando los cambios verificados en la latencia y amplitud del P300, suscitados con estímulo de habla después del programa terapéutico propuesto, es posible concluir que esta prueba eletrofisiológica es una herramienta objetiva sensible para monitorear la efectividad del entrenamiento auditivo. (AU)


Subject(s)
Humans , Central Nervous System , Hearing Loss, Central , Evoked Potentials, Auditory , Delivery of Health Care
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