RESUMO
The incidence of single-sided deafness(SSD) is increasing year by year. Due to the hearing defects of one ear, the ability of sound localization, speech recognition in noise, and quality of life of patients with single-sided deafness will be affected to varying degrees. This article reviews the intervention effects of different types of bone conduction hearing aids in patients with single-sided deafness and asymmetric hearing loss, and the differences of intervention effects between bone conduction hearing aids, contralateral routing of signal(CROS) aids, and cochlea implant(CI), to provide a reference for the auditory intervention and clinical treatment of single-sided deafness and asymmetric hearing loss.
Assuntos
Humanos , Qualidade de Vida , Condução Óssea , Perda Auditiva Unilateral/terapia , Percepção da Fala , Auxiliares de Audição , Perda Auditiva , Localização de Som , Surdez , Resultado do TratamentoRESUMO
Objective: To analyze the surgical efficacy of patients with mixed hearing loss and otosclerosis with different air bone gap (ABG) before surgery, and to provide reference for the prognosis evaluation of otosclerosis surgery. Methods: The clinical data of 108 cases(116 ears) of otosclerosis who had undergone stapes fenestration technique artificial stapes implantation in Xiangya Hospital of Central South University from November 2013 to May 2020 and had mixed hearing loss before surgery were collected, including 71 women(76 ears)and 37 men (40 ears), with an average age of 38.5 years. According to preoperative pure tone audiometry ABG, they were divided into three groups: group S, 15 dB≤ABG<31 dB, a total of 39 ears; group M, 31 dB≤ABG<46 dB, a total of 58 ears; and group L, ABG≥46 dB, 19 ears in total. The hearing outcomes of three groups of patients at 6-12 months after surgery were compared and analyzed using SPSS 24.0 statistical software. Results: A total of 3 patients (group S: 2 cases; group L: 1 case) experienced severe sensorineural hearing loss after surgery and were not included in the statistical analysis. After surgery, the pure tone hearing threshold of patients with otosclerosis in each group was significantly improved compared to before surgery, with an average air conduction threshold improvement of(21.6±13.4) dB. The difference between before and after surgery was statistically significant(t=17.13, P<0.01). The average bone conduction threshold improved by(3.7±7.6) dB, and the difference was statistically significant before and after surgery(t=5.20, P<0.01). The postoperative ABG was(18.3±9.3) dB, which was significantly reduced compared to preoperative(36.2±8.6)dB. Among the three groups of patients, the L group had the highest improvement in air conduction threshold[(29.9±10.8)dB], while the S group had the lowest improvement[(15.7±11.4)dB]. There was no statistically significant difference in post operative pure tone hearing thresholds between the three groups(P>0.05). The postoperative ABG in group S was the smallest[(16.5±9.0)dB], while in group L, the postoperative ABG was the largest[(20.5±10.0)dB]. Compared with group S, group M and group L still had a large residual ABG at 2 000 Hz after surgery. The bone conduction threshold of both S and M groups improved to some extent after surgery compared to before (P<0.01). Conclusions: Surgery can benefit patients with mixed hearing loss and otosclerosis with different preoperative ABG. Patients with small preoperative ABG have better surgical results and ideal ABG closure at all frequencies after surgery. Patients with large preoperative ABG can significantly increase the gas conduction threshold during surgery, but certain frequencies of ABG may still be left behind after surgery. The improvement effect of surgery on bone conduction threshold is not significant. Patients should be informed of treatment methods such as hearing aids based on their actual situation for selection.
Assuntos
Masculino , Humanos , Feminino , Adulto , Condução Óssea , Otosclerose/cirurgia , Perda Auditiva Condutiva-Neurossensorial Mista/cirurgia , Cirurgia do Estribo/métodos , Resultado do Tratamento , Limiar Auditivo , Audição , Audiometria de Tons Puros , Surdez , Estudos RetrospectivosRESUMO
Abstract Introduction The cortical auditory evoked potential allows the possibility of objectively evaluating the entire auditory system, which is desirable in the pediatric population. Bone conduction auditory stimulation is recommended in the differential diagnosis of conductive hearing loss. However, there are not many studies of cortical auditory evoked potential using bone conduction. Objective The aim of this study was to characterize the response of cortical auditory evoked potential through bone conduction in normal-hearing neonates using an automated response analysis equipment. Methods This study included 30 normal-hearing neonates, without risk factors for hearing loss. The equipment used was the HEARlab automated response analysis and the cortical responses were evaluated at the frequencies of 500-4000 Hz through bone conduction, at intensity ranging from 0 to 60 dBnHL. The latencies and amplitudes were manually marked by experienced judges. Results Cortical auditory evoked potential responses were detected in 100% of the evaluated subjects and there was no difference regarding the cortical response of the neonates in relation to the variables of gender, ear and masking use. At an intensity of 60 dBnHL for the frequencies of 500, 1000, 2000 and 4000 Hz the latencies were 234; 241; 239 and 253 ms and the amplitudes were 15.6; 8.4; 6.2; 6.3 µV. The mean thresholds were 23.6; 28; 31 and 33.1 dBnHL, respectively. Conclusion It was possible to measure the cortical auditory evoked potential response in the neonatal population using bone vibrator as sound transducer and to draw the profile of the cortical auditory evoked potential latencies and amplitudes by frequencies at the intensity of 60 dBnHL and at the threshold.
Resumo Introdução O potencial evocado auditivo cortical traz a possibilidade de avaliar de forma objetiva todo o sistema auditivo, o que é desejável na população infantil. A estimulação auditiva por condução óssea é recomendada no diagnóstico diferencial da perda auditiva condutiva. Entretanto, não há muitos estudos de potencial evocado auditivo cortical com o uso do vibrador ósseo. Objetivo Caracterizar a resposta do potencial evocado auditivo cortical por vibrador ósseo em neonatos normo-ouvintes com equipamento de análise automática de resposta. Metodologia A pesquisa incluiu 30 neonatos normo-ouvintes e sem fator de risco para deficiência auditiva. Foi usado o equipamento de análise automática de resposta HEARlab e foram avaliadas as repostas corticais na frequências de 500 a 4000 Hz por vibrador ósseo, na intensidade de 0 a 60 dBnNA. As latências e amplitudes foram marcadas manualmente por juízes experientes. Resultados Foram detectadas respostas de potencial evocado auditivo cortical em 100% dos sujeitos avaliados. Não houve diferença na resposta cortical dos neonatos para as variáveis: sexo, orelha e uso do mascaramento. Para as frequências de 500, 1000, 2000 e 4000 Hz foram observadas as latências de 234; 241; 239 e 253 ms, as amplitudes de 15,6; 8,4; 6,2; 6,3 µV, na intensidade de 60 dBnNA, e os limiares médios de 23,6; 28; 31 e 33,1 dBnNA, respectivamente. Conclusão Foi possível obter a resposta do potencial evocado auditivo cortical na população neonatal com vibrador ósseo como transdutor de som e traçar o perfil das latências e amplitudes dos potencial evocado auditivo cortical por frequência nas intensidades de 60 dBnNA e no limiar.
Assuntos
Humanos , Recém-Nascido , Criança , Condução Óssea , Potenciais Evocados Auditivos , Limiar Auditivo , Estimulação Acústica , Potenciais Evocados Auditivos do Tronco Encefálico , AudiçãoRESUMO
Objective: To investigate the feasibility and safety of auricle reconstruction combined with Bonebridge implantation for bilateral aural atresia patients. Methods: A retrospective analysis was conducted for 36 cases(72 ears) who underwent Bonebridge implantation combined with bilateral auricle reconstruction from February 1, 2017 to January 15, 2020. All cases were bilateral congenital aural atresia and underwent Nagata auricle reconstruction for both sides simultaneously. Bonebridge implantations were performed during the second stage of auricle reconstruction. Results: All 36 patients healed well and had no surgical complications when discharged. The preoperative average bone conduction threshold of the patients was(8.5±5.8) dB HL and postoperative bone conduction threshold was (8.4±5.2) dB HL. There was no significant change after the implantation (P=0.724). The preoperative average air conduction threshold of was(64.9±7.4)dB HL and postoperative air conduction threshold was (24.0±5.3) dB HL, which had a significant change after the implantation (P<0.001). The hearing threshold with Bonebridge significantly decreased by 40.9 dB HL compared with the preoperative air conduction threshold(P<0.001). The speech recognition rate of monosyllable words, disyllabic words and short sentences in quiet environment increased by 62.5%, 63.5% and 72.2% respectively. The differences were statistically significant (P<0.001). The speech recognition rate of monosyllabic words, disyllabic words and short sentences in noise environment were significantly increased by 55.9%, 58.9% and 69.9% respectively (P<0.001). After a follow-up of 18.3 months in average, the hearing results were stable and the aesthetic outcomes were satisfied. One patient had implant rupture and healed after revision surgery. Conclusions: With an integrated surgical procedure, patients with bilateral congenital aural atresia can complete bilateral auricle reconstruction and hearing implantation within six months. This integrated surgical procedure is safe and efficient, with a stable hearing improvement and good appearance.
Assuntos
Humanos , Condução Óssea , Orelha Externa , Auxiliares de Audição , Perda Auditiva Condutiva , Estudos Retrospectivos , Resultado do TratamentoRESUMO
Objectives: To evaluate the therapeutic effects of unilateral/bilateral bone conduction hearing rehabilitation in patients with bilateral microtia accompanied with severe conductive hearing loss following staged auricle reconstruction and bonebridge implantation. Methods: Thirty-two patients, including 20 males and 12 females, with an average age of 11.8, who received surgical treatment in Peking Union Medical College Hospital (PUMCH) from March, 2016 to January, 2020 with bilateral microtia-atresia were included. Hearing thresholds, speech perception and high-resolution CT of the temporal bone were evaluated prior to surgery and individualized surgery plans (staged auricle reconstruction and bonebridge implantation) were made. Hearing thresholds and speech perception in quiet and noise (SNR = 5 dB) using unilateral Bonebridge were tested two weeks after the implantation surgery when the Bonebridge was activated and at 3th, 6th, 12th month after activation. Hearing thresholds and speech perception were also tested at least three months after the activation of the Bonebridge under three conditions: unaided, unilateral Bonebridge, and bilateral bone conduction hearing devices (Bonebridge plus contralateral ADHEAR). The international hearing aid assessment questionnaire (IOI-HA) and Glasgow children's benefit questionnaire were used to evaluate the subjective benefits of the patients. SPSS 21.0 software was used for statistical analysis. Results: Among these 32 patients, nine were conducted Bonebridge implantation surgery before auricle reconstruction, six were simultaneously with auricle reconstruction and 17 were implanted after auricle reconstruction surgery. Compared with unaided, the mean hearing thresholds (0.5, 1, 2, and 4 kHz) and speech perception following unilateral BCHD and bilateral BCHD attachment were improved significantly (P<0.05 each). The speech perceptin in noise of bilateral BCHD was better than unilateral (P<0.05 each). The modified questionnaire revealed high levels of patient satisfaction following use of both unilateral and bilateral devices. Conclusions: Individulized surgical procedures involving auricle reconstruction and Bonebridge implantation are safe and effective for patients with bilateral microtia-atresia, solving both appearance and hearing problems. Speech perception in noise is better following bilateral BCHD than unilateral BCHD attachment.
Assuntos
Criança , Feminino , Humanos , Masculino , Condução Óssea , Microtia Congênita/cirurgia , Orelha Externa , Auxiliares de Audição , Perda Auditiva Condutiva/cirurgia , Percepção da FalaRESUMO
Objective: The auditory deficits of single-sided deafness (SSD) can be treated with a novel intra-oral device, SoundBite, which delivers sound by applying vibratory signal to the teeth. The purpose of this study was to evaluate the efficacy and benefit of the bone conduction device for Chinese adults with SSD. Methods: Eighteen patients aged 19-66 yrs with acquired, permanent sensorineural SSD and no current treatment by any other devices for SSD, were recruited in a prospective controlled, nonrandomized, unblinded study. They were requested the continually daily wear of the new device over a 30-day free trial period. The intra-oral hearing device was placed around two maxillary teeth and was similar to a small partial denture or retainer. The audiological tests included pure tone air conduction thresholds, monosyllable word recognition score (WRS) in quiet and sentence reception thresholds in noise (via CMNmatrix test). The benefit was determined with the Abbreviated Profile of Hearing Aid Benefit (APHAB) and the Speech, Spatial and Qualities of Hearing Scale (SSQ) questionnaire. Results: The monosyllable WRS and the 50% threshold of signal-to-noise ratio (SNR50) were significantly better in all aided conditions. The head shadow effect, assessed by the SNR50 via CMNmatrix test improved an average of 2.6 dB after 30 days' wearing compared with unaided condition (P<0.001). The APHAB scores improved (P<0.05) for all subjects for the Global and Ease of Communication, Reverberation, Background Noise subscales. The SSQ scores improved (P<0.05) for all subjects for Speech, Spatial and Qualities of Hearing subscales. Conclusion: The SoundBite is a good alternative to the well-established implantable bone conduction devices in patients with SSD. An improvement in listening ability in noise and quiet as well as a decrease of the head shadow effect is validated as the expected.
Assuntos
Adulto , Idoso , Humanos , Pessoa de Meia-Idade , Adulto Jovem , Condução Óssea , Surdez , Auxiliares de Audição , Perda Auditiva Unilateral , Estudos Prospectivos , Percepção da Fala , Resultado do TratamentoRESUMO
Objective: To evaluate the auditory efficacy and subjective satisfaction of adhesive bone conduction hearing aid in children with unilateral congenital aural atresia (UCAA). Methods: Ten subjects (5 males and 5 females) diagnosed with UCAA with an average age of 8.3 years old (ranged from 5 to 15) were included in Beijing Tongren Hospital, Capital Medical University from January to August 2019. The free sound field hearing threshold, word recognition score in quiet, speech reception threshold in noise and sound localization ability (results were measured by RMS error) tests were performed in unaided and aided situation, respectively. Subjective satisfaction questionnaires were also distributed to subjects. Paired t test and Wilcoxon signed rank test were used as statistical analysis methods. Results: The average hearing threshold in aided condition was improved by (21.9±4.4) dB (t=15.8,P<0.05). Speech recognition abilities were generally improved both under quiet and noise (P<0.05);however, when the binaural summation, squelch and head shadow effects were analyzed respectively, the binaural squelch effect was not statistically improved (P>0.05), while the other effects were improved in aided condition (P<0.05). In sound localization test, there was no significant difference of the RMS error value between the unaided and aided situation (P>0.05). The subjects got high satisfaction rates in three subjective questionnaires. Conclusion: The adhesive bone conduction hearing aid can provide significant audiological benefit for children with UCAA as well as raising the quality of their life.
Assuntos
Adolescente , Criança , Pré-Escolar , Feminino , Humanos , Masculino , Adesivos , Condução Óssea , Auxiliares de Audição , Perda Auditiva Condutiva , Percepção da Fala , Resultado do TratamentoRESUMO
RESUMO Objetivo Elaborar uma ferramenta virtual, com fins didáticos, que possibilite a integração da tecnologia ao ensino da Audiometria Tonal Limiar (ATL) e logoaudiometria. Método O audiômetro da marca Interacoustics AD229b foi utilizado como modelo físico para a consecução da ferramenta virtual. Utilizou-se a linguagem de programação Visual Basic 6, de modo que as cores, os caracteres e as funções fossem similares ao audiômetro real. Além disso, acrescentou-se a possibilidade de simular a resposta do paciente, como também de registrar os limiares auditivos em um audiograma virtualizado. Para a logoaudiometria, implementou-se a possibilidade de ajuste do "VU meter" e o registro da quantidade de acertos e erros no exame. Resultados A ferramenta desenvolvida mostrou-se capaz de reproduzir as frequências de 125 a 8000 Hz, em intensidades que variam de -10 a 110 dB, sendo possível empregar diferentes formas de apresentação do estímulo, assim como o mascaramento clínico por condução aérea e óssea. A ativação da função "microfone" pode ser aplicada para facilitar o ensino da logoaudiometria. Conclusão A versão virtualizada do audiômetro mostrou-se semelhante ao equipamento modelo, tornando factível a integração da tecnologia ao ensino, com exemplificação da ATL e da logoaudiometria.
ABSTRACT Purpose To elaborate a virtual tool, with didactic purposes, that allows the integration of technology to the teaching of Pure Tone Audiometry (PTA) and speech audiometry. Methods The Interacoustics AD229b audiometer was used as a physical model to achieve the virtual tool. The Visual Basic 6 programming language was used, so that the colors, characters, and functions were similar to the real audiometer. In addition, the possibility of simulating the patient's response was added, as well as of recording the hearing thresholds in a virtual audiogram. For speech audiometry, the possibility of adjusting the VU meter and recording the number of correct and incorrect answers were implemented. Results The developed tool was able to reproduce frequencies from 125 Hz to 8000 Hz, in intensities ranging from -10 to 110 dB, being possible to use different stimulus, as well as clinical masking by air and bone conduction. The microphone button can be used to facilitate the teaching of speech audiometry. Conclusion The virtual version of the audiometer is similar to the model equipment, making the integration of technology into teaching feasible, with exemplify the PTA and speech audiometry.
Assuntos
Humanos , Condução Óssea , Audição , Audiometria de Tons Puros , Limiar Auditivo , TecnologiaRESUMO
RESUMO Objetivo Descrever os benefícios nos limiares auditivos e no desempenho de reconhecimento de sentenças no silêncio e no ruído em indivíduos com a adaptação unilateral do Sistema Ponto®. Métodos Estudo observacional, retrospectivo, de seguimento longitudinal. A casuística foi composta por fontes de dados secundários de dez indivíduos com perda auditiva condutiva ou mista, que foram submetidos à cirurgia com o Sistema Ponto®. Os resultados foram analisados nas seguintes condições: a) pré-cirúrgicas: sem AASI; com AASI por condução aérea ou óssea e com o processador Ponto Pro® acoplado a uma banda elástica; b) pós-cirúrgicas: na ativação e após seis meses de uso. Resultados Os limiares da audiometria tonal por conduções aérea e óssea mantiveram-se estáveis após a cirurgia, enquanto os limiares auditivos em campo livre e o reconhecimento de fala no silêncio e no ruído foram estatisticamente melhores na ativação e após seis meses de uso do Sistema Ponto®. Não houve diferença nos resultados com os indivíduos utilizando o Sistema Ponto® com a banda elástica e após a cirurgia. Conclusão O Sistema Ponto® propiciou benefício nas habilidades auditivas de detecção em todas as frequências testadas, assim como no reconhecimento de sentenças no silêncio e no ruído.
ABSTRACT Purpose To describe the benefits in hearing thresholds and sentence recognition performance in silence and noise, in users of the unilateral Ponto® system. Methods An observational, retrospective, longitudinal study. The sample consisted of secondary data sources from 10 individuals with conductive or mixed hearing loss who underwent surgery with the Ponto® System. The results were analyzed in the following pre-surgical conditions (without hearing aids; with hearing aids by air or bone conduction; with the Ponto Pro® processor with a soft band) and post-surgical (on activation and after six months of use). Results The thresholds of pure tone audiometry by air and bone conductions remained stable after surgery, while the auditory thresholds in free field and speech recognition in silence and in noise were statistically better when using the Ponto® system. There was no difference between the results obtained with the individuals using Ponto® with soft band and post-surgically. Conclusion The Ponto® system provided benefits in hearing detection skills in all tested frequencies, as well as, in recognition of the sentence in silence and noise.
Assuntos
Humanos , Limiar Auditivo , Condução Óssea , Prótese Ossicular , Auxiliares de Audição , Perda Auditiva Condutiva , Audiometria da Fala , Percepção da Fala , Reconhecimento de VozRESUMO
Abstract Introduction: Acute otitis media is a disease with high global prevalence, that can lead to several acute complications and auditory sequelae. Data regarding the auditory evaluation in the acute phase of acute otitis media are scarce. Objective: To evaluate the main audiometric changes (air and bone conduction thresholds) in the initial phase of an acute otitis media episode. Methods: A case-control study was performed. Patients diagnosed with acute otitis media with less than 7 days of evolution in relation to the complaint onset were selected, and healthy volunteers were selected as controls. The acute otitis media and control groups were submitted to pure tone and vocal audiometry. Results: The acute otitis media group included a total of 27 patients (30 ears). Hearing loss was present in 90.0% of the ears with acute otitis media, with conductive loss in 14 (46.67%) and mixed loss in 13 (43.33%). Both the air and bone conduction thresholds obtained with the tonal audiometry in the acute otitis media group were significantly worse than the controls at all tested frequencies (p< 0.05). In patients with acute otitis media, we observed that the thresholds for frequency >1 kHz (bone conduction) and 3 kHz (air conduction) were significantly worse in patients with tinnitus compared to patients without tinnitus. Conclusion: During the first 7 days of evolution after the onset of an isolated episode of acute otitis media, we observed significant increases in bone and air thresholds at all frequencies, especially >2 kHz, compared to healthy ears.
Resumo Introdução: A otite média aguda é uma doença de elevada incidência global, que pode levar a diversas complicações agudas e sequelas auditivas. Dados referentes à avaliação auditiva na fase aguda da otite média aguda são escassos. Objetivo: Avaliar as principais alterações audiométricas (limiares em via aérea e óssea) na fase inicial de um episódio de otite média aguda. Método: Realizou-se estudo de caso-controle. Selecionamos pacientes com diagnóstico de otite média aguda, com menos de sete dias de evolução em relação ao início das queixas, e voluntários saudáveis foram selecionados como controles. Os grupos otite média aguda e controle foram submetidos a audiometria tonal, vocal e audiometria. Resultados: O grupo otite média aguda incluiu 27 pacientes (30 orelhas). Observou-se presença de perda auditiva em 90% das orelhas com otite média aguda, condutiva em 14 (46,67%) e mista em 13 (43,33%). Tanto os limiares auditivos por via aérea quanto os limiares por via óssea obtidos com audiometria tonal do grupo otite média aguda eram significativamente piores em relação aos controles, em todas as frequências testadas (p < 0,05). Em pacientes com otite média aguda, observamos que os limiares das frequências acima de 1 kHz (via óssea) e 3 kHz (via aérea) eram significantemente piores entre pacientes com zumbido em comparação a pacientes sem zumbido. Conclusão: Nos primeiros sete dias de evolução do quadro inicial de um episódio isolado de otite média aguda, observamos aumentos significativos dos limiares ósseos e aéreos em todas as frequências, principalmente nas acima de 2 kHz, em comparação a orelhas sadias.
Assuntos
Humanos , Otite Média/complicações , Perda Auditiva Neurossensorial/etiologia , Audiometria de Tons Puros , Limiar Auditivo , Condução Óssea , Estudos de Casos e ControlesRESUMO
Abstract Introduction: Bone-anchored hearing aids are currently well-established solutions for treatment of hearing-impaired patients. Objective: To evaluate the surgery of the Baha® Attract system, healing process and soft tissue condition after the processor activation. Methods: 125 patients implanted with the Baha® Attract system during a 3 year period in a single ENT department were analysed. Evaluated parameters comprised: details of surgery, healing process and soft tissue condition at the time of the processor activation and on subsequent follow-up visits. Results: The implantation was conducted under local anaesthesia in 96% of patients. The mean surgery time was 42 min. Soft tissue reduction was performed in 43.2% of cases; bone polishing in 23.2% and bipolar coagulation in all the cases. Healing was uneventful in 92.8%. 10 days after the surgery, pain was reported in 48% of cases. On subsequent follow-up visits, 1 month and 3 months after the surgery, pain was present in 18.4% and 2.4% of cases respectively. Similarly, numbness and paresthesia, initially reported in 84% and 15.2%, were present in 60% and 11.2% after a month, and in 17.6% and 1.6% after three months. After the processor attachment, no serious problems were observed in the analysed group during follow-up visits. However, mild redness and/or mild pain over the magnet were observed in 9.6% of patients. Conclusion: Implantation of the Baha® Attract system is an easy and safe procedure. It can be performed under local anaesthesia in adults. There are no major surgical problems or complications, and the healing process proceeds efficiently in most patients. Postoperative pain is usually mild and gradually decreases in the following months. Numbness in the operated area is frequent, but as reinnervation occurs in time, the numb patch decreases in size and finally completely disappears in most cases.
Resumo Introdução: Os processadores de implantes auditivos de ancoragem óssea são atualmente soluções bem estabelecidas para o tratamento de pacientes com deficiência auditiva. Objetivo: Avaliar a cirurgia de implante do sistema Baha® Attract, o processo de cicatrização e a condição dos tecidos moles após a ativação do processador. Método: Foram analisados 125 pacientes implantados com o sistema Baha® Attract durante um período de 3 anos em um único departamento de otorrinolaringologia. Os parâmetros avaliados compreenderam: detalhes da cirurgia, processo de cicatrização e condição dos tecidos moles no momento da ativação do processador e nas consultas de seguimento subsequentes. Resultados: O implante foi realizado sob anestesia local em 96% dos pacientes. O tempo médio de cirurgia foi de 42 minutos. A redução de tecido mole foi realizada em 43,2% dos casos; polimento ósseo em 23,2% e coagulação bipolar em todos os casos. A cicatrização transcorreu sem complicações em 92,8%. Dez dias após a cirurgia, dor foi relatada em 48% dos casos. Nas consultas de seguimento subsequentes, 1 mês e 3 meses após a cirurgia, a dor esteve presente em 18,4% e 2,4% dos casos, respectivamente. Da mesma forma, dormência e parestesia, inicialmente relatados em 84% e 15,2%, estavam presentes em 60% e 11,2% dos casos após um mês, e em 17,6% e 1,6% após três meses. Após a fixação do processador, nenhum problema grave foi observado no grupo analisado durante as consultas de seguimento. No entanto, vermelhidão leve e/ou dor leve sobre o ímã foram observados em 9,6% dos pacientes. Conclusão: O implante do sistema Baha® Attract é um procedimento fácil e seguro. Ele pode ser realizado sob anestesia local em adultos. Não há grandes problemas ou complicações cirúrgicas, e o processo de cicatrização é contínuo e eficaz na maioria dos pacientes. No pós-operatório, a dor é geralmente leve e diminui gradualmente nos meses seguintes. A dormência na área operada é freqüente, mas como a reinervação ocorre com o tempo, a área dormente diminui de tamanho e finalmente desaparece por completo na maioria dos casos.
Assuntos
Humanos , Masculino , Feminino , Criança , Adolescente , Adulto , Pessoa de Meia-Idade , Idoso , Idoso de 80 Anos ou mais , Adulto Jovem , Implante Coclear/métodos , Perda Auditiva/cirurgia , Condução Óssea/fisiologia , Resultado do Tratamento , Auxiliares de AudiçãoRESUMO
Abstract Introduction The bone-anchored hearing aid (BAHA) is a bone conduction system that transmits the sound directly to the inner ear by surpassing the skin impedance and the subcutaneous tissue. It is indicated for patients with mixed, conductive and unilateral sensorineural hearing loss who did not benefit from conventional hearing aids (HAs). Although the benefits from BAHA are well demonstrated internationally, this field still lacks studies in Brazil. Objective To assess the auditory rehabilitation process in BAHA users through audiological, speech perception and tinnitus aspects. Methods Individuals with hearing loss were assessed before and after the implantation. The participants were subjected to pure tone audiometry in free field, functional gain audiometry, speech perception tests, tinnitus handicap inventory (THI) in open format, and to the visual analog scale (VAS). Results It was found that the participants benefited from the use of BAHA. The difference in the performance of the participants before and after the BAHA surgery was significant in terms of hearing acuity. There was no statistically significant difference in the speech perception tests. The tinnitus assessment showed that 80% of the participants scored slight tinnitus severity in THI after using a BAHA. Eighty percent of the participants classified their tinnitus as absent tomild in the VAS after the surgery. Conclusion Based on the results of the current study, we can conclude that the participants improved both the auditory perception and the tinnitus handicap. (AU)
Assuntos
Humanos , Masculino , Feminino , Adulto , Pessoa de Meia-Idade , Condução Óssea , Perda Auditiva Condutiva-Neurossensorial Mista/reabilitação , Auxiliares de Audição , Audiometria da Fala , Percepção da Fala , Zumbido/diagnóstico , Escala Visual Analógica , Testes AuditivosRESUMO
BACKGROUND AND OBJECTIVES: We reviewed the selection processes of contralateral routing of signal (CROS) hearing aids (HAs) and bone-conduction (BC) Has, and compared aided and unaided hearing thresholds. SUBJECTS AND METHOD: Twenty-four patients with asymmetrical hearing loss who used BC HAs (n=12) and CROS HAs (n=12) were enrolled. The choice of two different HAs were compared with respect to the degree of hearing loss, the unaided hearing thresholds and functional gains. RESULTS: When the hearing thresholds of the better hearing ears were >30 dB HL, most (92%, 11 of 12) chose CROS rather than BC HAs, with significant difference (p=0.001). Both CROS and BC HAs groups showed significantly improved functional gains (46.6 dB and 53.4 dB, respectively). Aided air-conduction (AC) thresholds (40.2 dB HL) in the CROS group were similar to the AC thresholds (43.1 dB HL) of better hearing ears. However, the hearing threshold of Aided AC thresholds (35.8 dB HL) in BC HAs group were less than the BC thresholds (17.3 dB HL) of better hearing ears by 19 dB (p30 dB HL. The CROS group showed aided thresholds similar to the thresholds of better hearing ears, but the BC HAs group showed poorer aided thresholds than the thresholds of better hearing ears. For patients with asymmetric hearing loss, HAs should be selected based on the degree and types of hearing loss and the maximum output level of the selected device.
Assuntos
Humanos , Condução Óssea , Surdez , Orelha , Auxiliares de Audição , Perda Auditiva , Audição , MétodosRESUMO
Introducción: los dispositivos audiológicos de conducción ósea ampliaron las opciones de tratamiento de las hipoacusias neurosensoriales unilaterales (HNU) y demostraron su eficacia clínica. No obstante, la valoración de la calidad de vida permite determinar la mejoría en las actividades cotidianas y la satisfacción del paciente con su tratamiento. Objetivo: determinar la calidad de vida y la adherencia terapéutica en pacientes con HNU manejados con dispositivos audiológicos de conducción ósea en el Hospital Universitario Clínica San Rafael en Bogotá D.C., Colombia, durante el período 2012-2017. Diseño: estudio observacional de corte transversal. Metodología: luego de la revisión de la historia clínica de los pacientes elegibles que asistieron a la consulta de otología del hospital, se aplicó la escala de evaluación de calidad de vida Glasgow Benefit Inventory (GBI) y el cuestionario de adherencia terapéutica. El puntaje de calidad de vida y el porcentaje de adherencia fueron analizados por medio de pruebas no paramétricas en relación con variables sociodemográficas y clínicas. Resultados: un total de 38 pacientes se incluyeron en el estudio. La mediana de la puntuación total del GBI fue de +36,1 (rango 0 a +61) y la adherencia reportada fue del 68%. No se identificó una diferencia estadísticamente significativa entre estas variables y el tipo de dispositivo de conducción ósea. Conclusiones: el uso de dispositivos de conducción ósea se asocia con una mejoría en la calidad de vida, alta tasa de adherencia y baja prevalencia de complicaciones. No se encontraron diferencias estadísticamente significativas entre los tipos de dispositivos disponibles en el mercado.
Introduction: bone conduction hearing devices have expanded the treatment options for unilateral sensorineural hearing loss and demonstrated their clinical efficacy. Nevertheless, the assessment of quality of life (QoL) allows to establish the patient's improvement in daily activities and their satisfaction with the treatment. Objective: to determine the QoL and treatment adherence of patients with sensorineural hearing loss treated with bone conduction hearing devices at Hospital Universitario Clinica San Rafael in Bogotá D.C., Colombia, between 2012-2017. Study design: crosssectional study. Methods: after the review of the medical history from the eligible patients who attended the hospital's otology clinic, a validated QoL questionnaire Glasgow Benefit Inventory (GBI) and an adherence questionnaire were filled out. The score of QoL questionnaire and percentage of adherence were analyzed by nonparametric tests in relation to sociodemographic and clinical variables. Results: a total of 38 patients were included in the study. The median of the total GBI score was +36.1 (range 0 to +61) and the reported adherence was 68%. We did not identify a statistically significant difference between these variables and the type of bone conduction hearing device. Conclusions: the use of bone conduction hearing devices is associated with an improvement in QoL, high adherence rate and low prevalence of complications, without identifying statistically significant differences between those devices currently available in the market.
Assuntos
Humanos , Perda Auditiva , Qualidade de Vida , Condução Óssea , Osseointegração , Cooperação e Adesão ao TratamentoRESUMO
It is acknowledged that implantable bone conduction hearing aids such as a bone anchored hearing aid provide benefit and satisfaction to patients with unilateral hearing loss in terms of sound localization and speech perception under noise circumstances. This review paper introduces current models of the implantable bone conduction hearing aids, their candidacy, brief surgical procedures, and general audiological examinations. A table summary was used for nine published research papers which have very similar results by three points, i.e., no change in ability of sound localization, better performance of Hearing-In-Noise Test, and improved satisfaction of sound quality using questionnaires after the implantation. Unfortunately, systematic fitting strategy for users of the implantable bone conduction hearing aids has not been either studied or developed yet. Futhermore, there is no scientific based approach of reason why the implantation has no benefit in sound localization but still provides better performance for speech perception in noise. In conclusion, specific and effective fitting strategy of the current implantable bone conduction hearing aids should be developed and also support effect of the implantation with sensitivity and specificity for both clinicians and patients while accompanying their advanced technology.
Assuntos
Humanos , Condução Óssea , Auxiliares de Audição , Perda Auditiva Unilateral , Ruído , Sensibilidade e Especificidade , Localização de Som , Percepção da Fala , Âncoras de SuturaRESUMO
OBJECTIVES: The aim of this prospective clinical study was to measure the audiologic outcomes of the patients that underwent endoscopic transcanal cartilage tympanoplasty, and to investigate the effects on cochlear function. METHODS: Thirty-three patients (33 ears) who were diagnosed with noncomplicated chronic otitis media and underwent endoscopic transcanal cartilage tympanoplasty technique were included. Pre- and postoperative first month distortion product otoacoustic emission (DPOAE) signal-to-noise ratio (SNR), bone conduction hearing levels and air bone gap (ABG) values were measured and total endoscope usage time was noted. RESULTS: Preoperative median SNR measurements at 0.5, 1, 2, and 4 kHz were 6 dB (1–11; interquartile range [IQR], 1), 6 dB (4–20; IQR, 1), 7 dB (3–26; IQR, 5) and 5.50 dB (0–9; IQR, 3), respectively. Postoperative median SNR measurements at 0.5, 1, 2, and 4 kHz were 6 dB (3–9; IQR, 1), 6 dB (2–21; IQR, 3), 7 dB (2–20; IQR, 3), and 6 dB (0–10; IQR, 7), respectively. Regarding the DPOAE measurements, there was no statistically significant difference between the SNR values of all given frequencies (P>0.05). Regarding the pure tone audiometry (PTA) measurements, bone conduction was significantly better at 0.5 and 1 kHz, postoperatively (P 0.05). Additionally, no statistically significant correlation was found between the SNR and PTA measurements and the endoscope usage time (P>0.05). CONCLUSION: We suggested that cochlear functions and sensorineural hearing remained stable after endoscopic transcanal cartilage tympanoplasty and cold light source doesn’t cause significant adverse effects cochlear functions.
Assuntos
Humanos , Audiometria , Condução Óssea , Cartilagem , Estudo Clínico , Endoscópios , Audição , Otite Média , Estudos Prospectivos , Razão Sinal-Ruído , TimpanoplastiaRESUMO
OBJECTIVES: The aim of this study was to evaluate and report the long-term results of the butterfly cartilage tympanoplasty. Short-term and long-term hearing outcomes were compared according to age and perforation location as well. METHODS: Ninety-three patients who were diagnosed with noncomplicated chronic otitis media and underwent microscopic transcanal butterfly cartilage tympanoplasty due to anterior, posterior, and central tympanic membrane perforation were included. Age, gender, follow-up time, pre- and postoperative pure tone audiometry thresholds (both air and bone conduction), pre- and postoperative air-bone gaps (ABGs), if any residual perforation was noted. RESULTS: At the end of the follow-up period, successful closure occurred in 88 of 93 patients and success rate is 94.6%. In all patients, including those with residual perforations, the mean preoperative bone conduction threshold was 15.9 dB (range, 5 to 50 dB) among all groups whereas mean air conduction threshold was 36.4±15.1 dB (range, 10 to 90 dB) preoperatively and 28.8±14.3 dB in 6th month follow-up and 24.9±14.1 dB 24th month follow-up. Preoperative mean ABG was 22.1±7.1 dB (range, 5 to 40 dB) whereas 13.3±5.9 dB 6 months after surgery and 11.9±5.5 dB 24 months after surgery. There was a significant difference between pre- and postoperative ABG in both 6th and 24th month follow-up (P(6 mo-24 mo) < 0.05). Furthermore, preoperative mean air conduction differed significantly from postoperative 6th and 24th month follow-up mean air conduction thresholds (P < 0.05). CONCLUSION: We suggested that butterfly cartilage tympanoplasty can be safely performed in small, moderate, and even large perforations, as the hearing outcomes and successful closure rate are similar to those of other surgical methods. Moreover, it can be performed under local anaesthesia and it has low complication rates.
Assuntos
Humanos , Audiometria , Condução Óssea , Borboletas , Cartilagem , Seguimentos , Audição , Métodos , Otite Média , Perfuração da Membrana Timpânica , TimpanoplastiaRESUMO
Objetivo: Describir y comparar los resultados audiológicos pre y postquirúrgicos de los pacientes que fueron sometidos a implante de conducción ósea osteointegrado en el Hospital Universitario de la Samaritana, Bogotá D.C. Diseño: Estudio tipo Cohorte descriptiva. Métodos: Se evaluaron los resultados audiológicos pre y postquirúrgicos de 36 pacientes sometidos a Implante de audífono de conducción ósea osteointegrado. Resultados: Se observó una disminución estadísticamente significativa entre el valor de PTA pre y postquirúrgico (Diferencia = 36.94 dB; IC95% 35.2 a 38.7; p<0.001) Mejoría en la brecha Ósea Aérea con una diferencia entre el valor previo y posterior a la intervención de 35.93 dB (IC95% 33.23 a 38.63; p<0.001). La diferencia entre el porcentaje de discriminación verbal antes y después del procedimiento quirúrgico fue de 6.67% (IC95% 1.41 a 11.92; p=0.008), con una reducción en los niveles de intensidad de sonido en la discriminación que fue de 32.26 dB (IC95% 29.21 a 35.32; p<0.001). Conclusión: Los resultados audiológicos esperados en pacientes con hipoacusia conductiva, mixta o neurosensorial unilateral que fueron sometidos a implante de audífono de conducción ósea osteointegrado muestran que el sistema ofrece un alto porcentaje de éxito y bajas tasas de complicaciones.
Objective: To describe and compare pre and postoperative audiological results in patients who received a bone conduction hearing aid implant and the Hospital Universitario de la Samaritana, Bogotá D.C. Design: A descriptive cohort study. Methods: A descriptive cohort study was conducted. We evaluated audiological results before and after the bone conduction hearing aid implant procedure in 36 patients. Results: A statistically significant decrease in the PTA value was observed after the implant procedure (difference= 36.94 dB; 95CI% 35.2 - 38.7; p<0.001) The bone-air gap also presented improvement after the intervention with a decrease of 35.93 dB (95%CI 33.23 - 38.63; p<0.001). The difference in verbal discrimination percentage after the surgical procedure was 6.67% (95%CI 1.41 - 11.92; p=0.008), with a decrease in sound intensity discrimination levels of 32.26 db (95%CI 29.21 - 35.32; p<0.001). Conclusion: The audiological results in patients with conductive, mixed or unilateral sensorineural hearing loss that received a bone conduction hearing aid implant show that this intervention offers a high success rate and low postoperative complications.
Assuntos
Humanos , Perda Auditiva , Condução Óssea , Auxiliares de AudiçãoRESUMO
Introducción: la implementación de nuevas técnicas quirúrgicas permitió la preservación de los restos auditivos; así la estimulación no solo sería eléctrica del implante, sino también acústica. La cirugía atraumática permite, al colocar el implante coclear, recuperar audición en las frecuencias agudas, que recibirían estimulación eléctrica y, al mismo tiempo, se conservarían las frecuencias graves, que recibirán estimulación acústica otorgada mediante un componente acústico. El objetivo es determinar la preservación auditiva en pacientes que fueron sometidos a implantación coclear. Materiales y métodos: Se realizó un estudio retrospectivo descriptivo mediante revisión de historias clínicas de pacientes consecutivos que se sometieron a una implantación coclear entre diciembre de 2015 y mayo de 2016, en la Clínica Universitaria Reina Fabiola, de Córdoba Capital. Se evaluaron los umbrales de audición previamente a la cirugía y al momento del encendido del implante. R esultados: El promedio de los umbrales auditivos preimplante fue de 56,5 dB HL para los 250 Hz; 67,5 dB HL para los 500 Hz y 85 dB HL para los 1kHz, con una media de 69 dB HL. Al momento del encendido,se obtuvo un promedio de 66,55 dB HL para los 250 Hz; 80 dB HL para los 500 Hz y 94 dB HL para los 1kHz, con una media de 80,1 dB HL. Mediante la comparación de la medias, previamente a la cirugía y al encendido no se mostraron cambios en los umbrales estadísticamente significativos (p>0.05). Conclusiones: La preservación de los restos auditivos con técnicas atraumáticas se pudo preservar en un 80% de los pacientes al momento del encendido.
Introduction: the implementation of new surgical techniques, allowed the preservation of of residual hearing, thus the stimulation would not only be electric by the implant, if not also acoustic. Atraumatic surgery allows the placement of the cochlear implant, recovering the hearing in the acute frequencies, which would receive electrical stimulation and, at the same time, the low frequencies would be conserved, which will receive acoustic stimulation by a hearing aid . The objective is to determine hearing preservation in patients who underwent cochlear implantation. Materials and methods: We performed a retrospective descriptive study by reviewing the medical records of consecutive patients who underwent a cochlear implantation between December 2015 and May 2016, at the Clinica Universitaria Reina Fabiola, Cordoba Capital. Hearing Thresholds prior to surgery and at the time of implantation were evaluated. Results: The pre-implant auditory thresholds averaged 56.5dB HL for the 250 Hz; 67.5 dB HL for the 500 Hz and 85 dB HL for the 1 kHz, with an average of 69 dB HL. At power-up we obtain an averaged 66.55dB HL for 250 Hz; 80 dB HL for the 500 Hz and 94 dB HL for the 1 kHz, with a mean of 80.1 dB HL. By comparing the means, between the time before implatation and activation there were no changes in the statistically significant thresholds (p> 0.05). Conclusions: The preservation of auditory debris with atraumatic techniques could be preserved in 80% of patients at the activation.
Introdução: a implementação de novas técnicas cirúrgicas, permitiu a preservação da audição residual, assim, não só graves implante estimulação elétrica, mas também acústica. cirurgia atraumática permite colocar o implante coclear, recuperar auditiva em altas freqüências, que recebem estimulação elétrica e, ao mesmo tempo, as baixas frequências, que recebem estimulação acústica fornecido através de um componente acústico é mantido. O objetivo é determinar preservação da audição em pacientes submetidos ao implante coclear. Materiais e métodos: Um estudo retrospectivo foi realizado pela revisão dos prontuários de pacientes consecutivos submetidos a implante coclear entre dezembro de 2015 e maio 2016, no Hospital Universitário Rainha Fabíola, Córdoba Capital. Foram avaliados os limiares antes da cirurgia e no momento de ouvir sobre o implante. Resultados: A média de audiência limiares implante foi de 56,5dB pré HL para 250 Hz; 67,5 dB a 500 Hz e 85 dB NA de 1 kHz, com uma média de 69 dB NA. Na energização, um 66,55dB HL média para 250 Hz foi obtido; 80 dB a 500 Hz e 94 dB NA de 1 kHz, com uma média de 80,1 dB NA. Ao comparar as médias antes da cirurgia e em nenhuma alteração estatisticamente significativa nos limiares (p> 0,05) eles mostraram. Conclusões: A preservação da audição residual com técnicas atraumáticas poderia preservar 80% dos pacientes no poder.