Clinical experience of an adhesive bone conduction hearing system in children with congenital single-sided deafness.

OBJECTIVES: This study aimed to investigate the effects of an adhesive bone conduction device (aBCD) in children with congenital single-sided deafness (SSD). Specifically, we examined whether the aBCD elicits improvement in the speech perception ability of children with congenital SSD and whether using this device would adversely affect the horizontal localisation abilities of these children. METHODS: Thirteen school-aged children with SSD and seven children with Normal Hearing (NH) were included in this study. Speech perception in noise was measured using the Mandarin Speech Test Materials and sound localisation performance was evaluated using broadband noise stimuli (0.5-20 kHz), randomly played from seven loudspeakers at different stimulus levels (65-, 70-, and 75-dB SPL). RESULTS: All children with SSD showed inferior speech perception and sound localisation performance compared with children with NH. The aBCD use remarkably improved the speech perception abilities of these children under quiet and noise conditions; however, their sound localisation abilities neither improved nor deteriorated. CONCLUSION: This study reveals the effectiveness and safety of a non-surgical aBCD in paediatric patients with SSD. Our results provide a theoretical basis for early hearing intervention with an aBCD in children with congenital SSD who are temporarily unable to undergo ear surgery. LEVEL OF EVIDENCE: Level 3.

Evaluation of surgery and surgical results of Baha® Attract system implantations - single centre experience of hundred twenty five cases / Avaliação da cirurgia e resultados cirúrgicos dos implantes do sistema Baha® Attract - experiência de um único centro com cento e vinte e cinco casos

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.

Evaluation of surgery and surgical results of Baha® Attract system implantations - single centre experience of hundred twenty five cases.

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 42min. 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.

Extended high-frequency hearing loss following the first episode of otitis media.

OBJECTIVES/HYPOTHESIS: Otitis media has been associated with several auditory and developmental sequelae. Here, the results of auditory tests were evaluated in patients who had a first episode of unilateral otitis media and compared with the contralateral healthy ear. STUDY DESIGN: Cohort study. METHODS: This study was undertaken from 2015 to 2016, with a follow-up period of 6 months. RESULTS: A total of 41 patients who had been diagnosed with unilateral acute otitis media were selected. Standard (250 Hz-8 kHz) and extended high-frequency (8 kHz-16 kHz) audiometry was performed within 5 days of the beginning of the clinical symptoms, and then in defined time frames for a period of 6 months. The results of the contralateral healthy ears were used as individual controls. After closure of the initial air-bone gap, the results of the standard audiometry did not demonstrate significant differences in the thresholds of diseased ears compared with controls. A significant elevation of the mean extended high-frequency thresholds in the ears affected by otitis media was observed at the first and subsequent appointments within the 6-month follow-up period. Diseased ears from patients who experienced tinnitus during the 6-month follow-up period had significantly higher thresholds in the extended high frequencies than diseased ears from patients without residual tinnitus. CONCLUSIONS: These results suggest that the first episode of otitis media may lead to persistent elevation of the mean thresholds of extended high-frequencies, whereas persistent tinnitus after 6 months of the acute infection is associated with more severe hearing loss. LEVEL OF EVIDENCE: 2b Laryngoscope, 128:2879-2884, 2018.

Erosion of the long process of the incus with incomplete ossicular discontinuity in simple chronic otitis media: Should we reconstruct or leave it be?

OBJECTIVE: To determine whether patients with simple chronic otitis media and incomplete ossicular discontinuity should undergo ossicular reconstruction. DESIGN: Prospective, randomised surgical trial comparing no intervention with incus interposition over a 5-year period. SETTING: Tertiary referral hospital. PARTICIPANTS: Seventy-six participants with simple chronic otitis media and erosion of the long process of the incus but apparent good transmission throughout the ossicular chain as tested intra-operatively. Forty-four patients had partial erosion of the incus but still bony contact with the stapes head (Group A-Type I), and 32 had mainly connective tissue binding the incus and stapes (Group B-Type II). Each of these groups was randomised to either leaving the ossicular chain as it was (A1 and B1) or performing an incus interposition (A2 and B2). MAIN OUTCOME MEASURES: Average postoperative air-bone gap and the degree of ABG closure. A postoperative air-bone gap under 20 dB was considered a successful result. RESULTS: In group A, there was no significant difference between no intervention and incus interposition. In group B, patients in the no reconstruction subgroup had a significantly worse hearing result than the incus interposition subgroup (postoperative air-bone gap of 27.5 dB and 31% closure within 20 dB vs 15 dB and 75% closure). CONCLUSIONS: For Type I patients, the postoperative hearing results were similar for the reconstruction and no reconstruction groups. For Type II patients, the results clearly favour reconstruction.

Active Bone Conduction Prosthesis: BonebridgeTM

Introduction Bone conduction implants are indicated for patients with conductive and mixed hearing loss, as well as for patients with single-sided deafness (SSD). The transcutaneous technology avoids several complications of the percutaneous bone conduction implants including skin reaction, skin growth over the abutment, and wound infection. The Bonebridge (MED-EL, Austria) prosthesis is a semi-implantable hearing system: the BCI (Bone Conduction Implant) is the implantable part that contains the Bone Conduction-Floating Mass Transducer (BC-FMT), which applies the vibrations directly to the bone; the external component is the audio processor Amadé BB (MED-EL, Austria), which digitally processes the sound and sends the information through the coil to the internal part. Bonebridge may be implanted through three different approaches: the transmastoid, the retrosigmoid, or the middle fossa approach. Objective This systematic review aims to describe the world́ s first active bone conduction implant system, Bonebridge, as well as describe the surgical techniques in the three possible approaches, showing results from implant centers in the world in terms of functional gain, speech reception thresholds and word recognition scores. Data Synthesis The authors searched the MEDLINE database using the key term Bonebridge. They selected only five publications to include in this systematic review. The review analyzes 20 patients that received Bonebridge implants with different approaches and pathologies. Conclusion Bonebridge is a solution for patients with conductive/mixed hearing loss and SSD with different surgical approaches, depending on their anatomy. The system imparts fewer complications than percutaneous bone conduction implants and shows proven benefits in speech discrimination and functional gain.(AU)

Amplification by bone conduction in congenital malformations: patient benefits and satisfaction.

UNLABELLED: Hearing loss is one of the most common clinical findings in subjects with malformations of the ear. Treatment consists of surgery and/or adapt a hearing aid amplification by bone (HA VO). Early intervention is critical to auditory stimulation and development of speech and language. OBJECTIVE: To characterize the audiological profile of subjects with congenital malformation of the external ear and/or middle and evaluate the benefit and satisfaction of using HA VO. METHOD: A descriptive study, subjects with bilateral congenital malformations of the external ear and/or middle, conductive or mixed hearing loss, moderate or severe and HA VO users. Evaluation of the benefit test using sentence recognition in noise and measures of functional gain and satisfaction assessment questionnaire using international IQ - HA. RESULTS: 13 subjects were evaluated, 61% were male and 80% with moderate conductive hearing loss or severe. There was better performance in the evaluation proposal, provided with HA when compared to the condition without HA. CONCLUSION: HA VO showed advantages for the population studied and should be considered as an option for intervention. Satisfaction was confirmed by elevated scores obtained in IQ - HA.

Amplificação por condução óssea em malformações congênitas: benefício e satisfação / Amplification by bone conduction in congenital malformations: patient benefits and satisfaction

A deficiência auditiva é um dos achados clínicos mais comuns em sujeitos com malformações de orelha. O tratamento consiste em realizar a cirurgia e/ou adaptar o aparelho de amplificação sonora por via óssea (AASI VO). A intervenção precoce é fundamental para favorecer a estimulação auditiva e desenvolvimento da fala e linguagem. OBJETIVO: Caracterizar o perfil audiológico de sujeitos com malformação congênita de orelha externa e/ou média e avaliar o benefício e a satisfação destes com o uso de AASI VO. MÉTODO: Estudo descritivo, sujeitos com malformações congênitas bilaterais de orelha externa e/ou média, deficiência auditiva condutiva ou mista, moderada ou grave e usuários de AASI VO. Avaliação do benefício utilizando teste de reconhecimento de sentenças com ruído competitivo e medidas de ganho funcional e avaliação da satisfação utilizando questionário internacional QI - AASI. RESULTADOS: Foram avaliados 13 sujeitos, sendo 61% do sexo masculino e 80% com deficiência auditiva condutiva moderada ou grave. Houve melhor desempenho na avaliação proposta na condição com AASI, quando comparada à condição sem AASI. CONCLUSÃO: Os AASI VO retroauriculares apresentaram vantagens para a população estudada e devem ser considerados como uma opção para intervenção. A satisfação foi confirmada pelos escores elevados obtidos no QI - AASI.

Hearing loss is one of the most common clinical findings in subjects with malformations of the ear. Treatment consists of surgery and/or adapt a hearing aid amplification by bone (HA VO). Early intervention is critical to auditory stimulation and development of speech and language. OBJECTIVE: To characterize the audiological profile of subjects with congenital malformation of the external ear and/or middle and evaluate the benefit and satisfaction of using HA VO. METHOD: A descriptive study, subjects with bilateral congenital malformations of the external ear and/or middle, conductive or mixed hearing loss, moderate or severe and HA VO users. Evaluation of the benefit test using sentence recognition in noise and measures of functional gain and satisfaction assessment questionnaire using international IQ - HA. RESULTS: 13 subjects were evaluated, 61% were male and 80% with moderate conductive hearing loss or severe. There was better performance in the evaluation proposal, provided with HA when compared to the condition without HA. CONCLUSION: HA VO showed advantages for the population studied and should be considered as an option for intervention. Satisfaction was confirmed by elevated scores obtained in IQ - HA.

Acoustic radiation effects on bone conduction threshold measurement.

UNLABELLED: Acoustic radiation is the sound energy escape from a bone vibrator that may be detected by air conduction mechanisms. The presence of acoustic radiation may result in an unreal bone conduction threshold, promoting an unreal air/bone gap in the high frequencies. AIM: aim to analyze the acoustic radiation effect on the extension of air/bone gap at 2,000, 3,000 and 4,000 Hz. MATERIALS AND METHOD: our clinical and experimental study had a sample of 101 individuals, who matched inclusion criteria: to have an air/bone gap higher than 10 dB in the frequencies of 2,000; 3,000 and 4,000 Hz. All of them had their bone conduction threshold measured in two conditions: open ear canal and closed ear canal. RESULTS: we found that major differences between the two conditions evaluated occurred at the 4,000 Hz; data analysis showed significant difference in the extension for the air/bone gap; analysis of the number of cases of mixed hearing loss that changed to sensorineural was significant too. CONCLUSION: These studies concluded that when the MAE is occluded, the acoustic radiation phenomenon is controlled or avoided, enabling bone measures at the frequencies of 3,000 and 4,000Hz to be more accurate.

Efeitos da radiação acústica na obtenção dos limiares ósseos / Acoustic radiation effects on bone conduction threshold measurement

Radiação acústica é uma fuga da energia sonora do vibrador ósseo que pode ser detectada pela via aérea. A presença da radiação acústica poderia resultar em um limiar ósseo falso, um gap aéreo-ósseo irreal, nas frequências altas. Esse achado poderia ocorrer em pacientes sem comprometimento de orelha média e com história de doença de orelha interna, onde esse gap não é esperado. OBJETIVO: Verificar os efeitos da radiação acústica no tamanho do gap aéreo-ósseo nas frequências de 2.000, 3.000 e 4.000 Hz. MATERIAL E MÉTODO: Realizou-se estudo clínico e experimental em 101 indivíduos, com presença de gap aéreo-ósseo maior que 10 dB nas frequências de 2.000, 3.000 e/ou 4.000 Hz. Em todos participantes o limiar ósseo foi obtido nas condições: MAE aberto e fechado. RESULTADOS: Constatou-se que o gap aéreo/ósseo que mais sofreu mudança foi da frequência 4.000 Hz. Houve diferença significativa na frequência de mudança de status (misto x neurossensorial); na presença e ausência de diferenças entre via óssea fechada e aberta. CONCLUSÃO: Este estudo comprovou que quando o MAE é ocluído, o fenômeno da radiação acústica é controlado ou evitado, permitindo que as medidas ósseas para as frequências de 3.000 e 4.000 Hz sejam mais precisas.

Acoustic radiation is the sound energy escape from a bone vibrator that may be detected by air conduction mechanisms. The presence of acoustic radiation may result in an unreal bone conduction threshold, promoting an unreal air/bone gap in the high frequencies. AIM: aim to analyze the acoustic radiation effect on the extension of air/bone gap at 2,000, 3,000 and 4,000 Hz. MATERIALS AND METHOD: our clinical and experimental study had a sample of 101 individuals, who matched inclusion criteria: to have an air/bone gap higher than 10 dB in the frequencies of 2,000; 3,000 and 4,000 Hz. All of them had their bone conduction threshold measured in two conditions: open ear canal and closed ear canal. RESULTS: we found that major differences between the two conditions evaluated occurred at the 4,000 Hz; data analysis showed significant difference in the extension for the air/bone gap; analysis of the number of cases of mixed hearing loss that changed to sensorineural was significant too. CONCLUSION: These studies concluded that when the MAE is occluded, the acoustic radiation phenomenon is controlled or avoided, enabling bone measures at the frequencies of 3,000 and 4,000Hz to be more accurate.

The impact of chronic suppurative otitis media on children's and teenagers' hearing.

OBJECTIVE: Otitis media is the most common otological condition during childhood which compromises sound conduction in the middle ear. In chronic cases, it is estimated that the degree to which hearing is compromised is directly proportional to the damage caused to the middle ear's structures. It means that hearing thresholds may be influenced by factors such as the size and location of the tympanic perforation, the presence of ossicular chain erosion or disarticulation as well as the presence of cholesteatoma and its growth patterns. The goals of this study were to compare air conduction, bone conduction thresholds and air-bone gaps of children and teenagers between those with chronic suppurative otitis media with cholesteatoma and those without cholesteatoma. To compare air-bone gap values for different cholesteatoma growth patterns. To verify the relationship between the number of perforated quadrants and the size of the air-bone gap. To compare air-bone gap values between tympanic perforations in posterior quadrants with those in anterior quadrants. METHODS: A transversal study involving 202 children and teenagers (287 ears), aged between 6 and 18, with chronic suppurative otitis media with and without cholesteatoma, submitted to digital videotoscopy and pure tone audiometry (PTA) was conducted. RESULTS AND CONCLUSIONS: Air conduction, bone conduction thresholds and air-bone gaps in children and teenagers with CCOM are significantly greater. There were no significative differences between air-bone gaps in epitympanic and posterior mesotympanic cholesteatomas. In NCCOM, the gap value is positively correlated with the number of quadrants with tympanic perforation. There was no significative difference between the air-bone gaps in tympanic perforations affecting the posterior and anterior quadrants.

Influence of the type of transducer in profound hearing loss.

BACKGROUND: individuals with profound hearing loss may present vibrotactile responses when tested with supra-aural earphones due to the large skull area exposed to vibration in these transducers. AIM: to verify the influence of the type of transducer when assessing air conducted pure tone thresholds in individuals with profound sensorineural hearing loss. METHOD: 50 individuals, ranging in age from 16 to 55 years, were submitted to a clinical history questionnaire, meatoscopy, and pure tone and speech audiometry, using both TDH-39 supra-aural earphones and ER-3A insert earphones. RESULTS: in both pure tone and speech testing, thresholds were higher when obtained using insert earphones, with statistical significant differences for 250Hz and 1000Hz. Considering right and left ear testing with the different transducers, this difference was greater for the right ear, with statistical significant differences only for 250 Hz. Regarding gender, it was observed that the difference between the transducers was greater in males, with statistical significant differences for 250 Hz. However, in the SDT (Speech Detection Threshold), the greatest difference was found in females. CONCLUSION: people with bilateral sensorineural profound hearing loss presented higher (worse) thresholds with insert earphones (ER-3A) than with supra aural earphones (TDH-39) for low frequencies (250Hz and 1000Hz), confirming the existence of vibrotactile responses with supra aural earphones.

Influência do tipo de transdutor na deficiência auditiva de grau profundo / Influence of the type of transducer in profound hearing loss

TEMA: indivíduos com deficiência auditiva de grau profundo podem apresentar respostas por vibração com os fones supra-aurais devido a grande área do crânio exposta à vibração nestes transdutores. OBJETIVO: verificar a influência do tipo de transdutor na obtenção dos limiares auditivos por via aérea em indivíduos com deficiência auditiva neurossensorial de grau profundo. MÉTODO: 50 indivíduos, com idades variando de 16 a 55 anos, foram submetidos a anamnese, meatoscopia, e posteriormente, a audiometria tonal liminar e limiar de detecção de voz (LDV). As audiometrias tonal e vocal foram realizadas tanto com fones supra-aurais TDH-39 quanto com os fones de inserção ER-3A. RESULTADOS: nas audiometrias tonal e vocal, notamos que, com o fone de inserção, foram obtidos limiares auditivos mais elevados do que os obtidos com o fone supra-aural, com significância estatística nas freqüências de 250Hz e 1000Hz. Ao observarmos a diferença entre os resultados obtidos com o transdutor TDH-39 e o ER-3A em cada orelha separadamente, notamos que a diferença foi maior na orelha direita com significância estatística somente na freqüência de 250 Hz. Em relação ao sexo, notamos que as diferenças entre os transdutores foram maiores no sexo masculino com significância estatística na freqüência de 250 Hz. No entanto, no LDV, a diferença maior foi encontrada no sexo feminino. CONCLUSÃO: deficientes auditivos neurossensorias de grau profundo bilateral apresentam limiares de audibilidade mais elevados (piores) com os fones de inserção do que com os fones supra-aurais nas freqüências baixas, evidenciando a existência das respostas por vibração com os fones supra-aurais.

BACKGROUND: individuals with profound hearing loss may present vibrotactile responses when tested with supra-aural earphones due to the large skull area exposed to vibration in these transducers. AIM: to verify the influence of the type of transducer when assessing air conducted pure tone thresholds in individuals with profound sensorineural hearing loss. METHOD: 50 individuals, ranging in age from 16 to 55 years, were submitted to a clinical history questionnaire, meatoscopy, and pure tone and speech audiometry, using both TDH-39 supra-aural earphones and ER-3A insert earphones. RESULTS: in both pure tone and speech testing, thresholds were higher when obtained using insert earphones, with statistical significant differences for 250Hz and 1000Hz. Considering right and left ear testing with the different transducers, this difference was greater for the right ear, with statistical significant differences only for 250 Hz. Regarding gender, it was observed that the difference between the transducers was greater in males, with statistical significant differences for 250 Hz. However, in the SDT (Speech Detection Threshold), the greatest difference was found in females. CONCLUSION: people with bilateral sensorineural profound hearing loss presented higher (worse) thresholds with insert earphones (ER-3A) than with supra aural earphones (TDH-39) for low frequencies (250Hz and 1000Hz), confirming the existence of vibrotactile responses with supra aural earphones.

Sensorineural hearing loss in patients with chronic otitis media.

UNLABELLED: Chronic otitis media is generally associated with some degree of hearing loss, which is often the patient's chief complaint. This hearing loss is usually conductive, resulting from tympanic membrane rupture and/or changes in the ossicular chain due to fixation or erosion caused by the chronic inflammatory process. When cholesteatoma or granulation tissue is present in the middle ear cleft, the degree of ossicular destruction is even greater. An issue that has recently gained attention is additional sensorineural hearing loss due to chronic otitis media. While the conductive loss can be minimized through surgery, sensorineural hearing loss constitutes a permanent after effect, attenuated only through the use of a hearing aid. However, a few groups have reported a decrease in sensorineural function in these patients as well. This survey study performed at a referral center evaluates the occurrence of sensorineural hearing loss in ambulatory patients with this disease. We reviewed the files of patients with unilateral chronic otitis media. One hundred and fifty patients met the inclusion criteria: normal otoscopy and normal hearing in the contralateral ear. MAIN OUTCOME MEASURE: bone-conduction threshold averages were calculated for frequencies of 500, 1,000, 2,000, 3,000 and 4,000 Hz, with comparison between the normal ear and the ear with chronic otitis media. Thresholds were examined separately for each frequency. The bone-conduction threshold averages for the normal side were lower than those for the ear with chronic otitis media. The threshold shift was statistically significant for each frequency (P<0.0001, Student's t test). There were differences between the groups when analyzed for age (500 and 1,000 Hz) or the presence of cholesteatoma (1,000 Hz). This study shows that chronic otitis media is associated with a decrease in cochlear function.

[First two years of experience with BAHA: results in 12 patients]. / Primeros 2 años de experiencia en BAHA: resultados en 12 pacientes.

OBJECTIVE: To describe our first 2 years' experience following implementation of the BAHA program at our hospitals with special emphasis on the benefits and complications of use in each patient. MATERIAL AND METHOD: Retrospective review since the beginning of the programme at two Teaching Hospitals in 2004. Twelve patients were implanted with BAHA, and their complications are described, along with hearing loss and their audiological gain with the hearing aid. RESULTS: Eleven patients with BAHA completed the follow-up. The average age was 31.6 +/- 18.9 years, and their average conductive hearing loss of was 45.5 dB with an audiological gain of 33.6 dB. We had one patient with a minor complication (mild infection of the skin flap) and another with a major one (loss of the titanium implant). CONCLUSIONS: The BAHA programme started in 2004 has generated good results in terms of positive audiological data, patient acceptance and low complication rates.

Electrophysiologic threshold study in air and bone conduction in children with 2 months or less age.

UNLABELLED: The differential diagnosis of hearing loss with air and bone Auditory Brainstem Response in small children has not been enough studied in Brazil. AIM: To compare air and bone Auditory Brainstem Response results in children under 2 months of age with normal hearing. STUDY DESIGN: clinical with transversal cohort. MATERIALS AND METHODS: 12 children who passed the hearing screening were evaluated using air and bone Auditory Brainstem Response. No contralateral masking was used in the bone conduction test. The responses were compared and analyzed by the McNemar test and repetitive measurements of the variance test. RESULTS: There were no statistic differences between air and bone conduction Auditory Brainstem Response thresholds (p>0.05). The bone conduction latency for wave V was statistically higher than air conduction latency (p=0.000). CONCLUSION: There was agreement on the results recorded for air and bone conduction Auditory Brainstem Response for threshold intensities; latency for bone conduction wave V was statistically higher than the air conduction latency.

Estudo dos limiares eletrofisiológicos das vias aérea e óssea em crianças com até 2 meses de idade / Electrophysiologic threshold study in air and bone conduction in children with 2 months or less age

O diagnóstico diferencial de perdas auditivas com potencial evocado auditivo de tronco encefálico por via aérea e por via óssea em crianças pequenas tem sido pouco estudado no Brasil. OBJETIVO: Comparar as respostas do potencial evocado auditivo de tronco encefálico por vias aérea e óssea em crianças de até 2 meses de idade sem perdas auditivas. FORMA DE ESTUDO: Clínico prospectivo com coorte transversal. MATERIAL E MÉTODO: Foram avaliadas 12 crianças que passaram na triagem auditiva, por meio do potencial evocado auditivo de tronco encefálico por via aérea e via óssea. A via óssea foi realizada sem mascaramento contralateral. As respostas foram comparadas e analisadas por meio do teste de McNemar e pela análise de variância com medidas repetidas. RESULTADOS: Não houve diferença estatística no limiar eletrofisiológico por via aérea e via óssea (p>0,05). O tempo de latência por via óssea foi estatisticamente maior do que o tempo de latência por via aérea (p=0,000). CONCLUSÃO: Houve concordância no registro do Potencial Evocado Auditivo de Tronco Encefálico captado por vias aérea e óssea nas intensidades próximas ao limiar auditivo; a latência da onda V registrada por via óssea foi estatisticamente maior que a registrada por via aérea.

The differential diagnosis of hearing loss with air and bone Auditory Brainstem Response in small children has not been enough studied in Brazil. AIM: To compare air and bone Auditory Brainstem Response results in children under 2 months of age with normal hearing. STUDY DESIGN: clinical with transversal cohort. MATERIALS AND METHODS: 12 children who passed the hearing screening were evaluated using air and bone Auditory Brainstem Response. No contralateral masking was used in the bone conduction test. The responses were compared and analyzed by the McNemar test and repetitive measurements of the variance test. RESULTS: There were no statistic differences between air and bone conduction Auditory Brainstem Response thresholds (p>0.05). The bone conduction latency for wave V was statistically higher than air conduction latency (p=0.000). CONCLUSION: There was agreement on the results recorded for air and bone conduction Auditory Brainstem Response for threshold intensities; latency for bone conduction wave V was statistically higher than the air conduction latency.

[Bone conduction auditory brainstem responses in normal hearing individuals]. / Potenciais evocados auditivos do tronco encefálico por condução óssea em indivíduos normais.

BACKGROUND: bone conduction auditory brainstem responses (ABR) in normal hearing individuals. AIM: to evaluate the clinical applicability of bone conduction ABR, characterizing normality and determining an assessment protocol. METHOD: participants of this study were 22 individuals with normal hearing (20dB NA), with ages between 20 and 30 years, 14 female and 8 male. All individuals were assessed using air and bone (vibrator positioned on the forehead and mastoid) conduction ABR. EP25 equipment, Interacoustic; 3A insertion phone; B-71 bone vibrator; click stimulus. RESULTS: it was possible to evaluate the bone conduction ABR in all individuals. The results demonstrate that the electrophysiological threshold obtained when the vibrator was positioned on the forehead (32.69+/-5.63 and 32.5+/-7.07dB nHL) was higher than that obtained when the vibrator was positioned on the mastoid (25.00+/-7.33 and 30.00+/-5.34dB nHL) for both genders respectively. For this reason the vibrator was positioned on the mastoid. The electrophysiological threshold obtained by bone conduction was higher than that obtained by air conduction for both genders and also when all individuals were grouped together. Thus it is necessary to use a correction factor, according to the results, of 10dB nHL. The latency-intensity values of the V wave in the ipsilateral and contralateral recordings differed statistically according to gender, and should be considered separately. The value of 26.81+/-6.99dB nHL was adopted as being the normal threshold for bone conduction ABR. CONCLUSION: it is possible to evaluate bone conduction ABR in the clinical environment. These results, when considered along with the air conduction ABR, increase the chances of a more precise diagnosis regarding the type of hearing loss.