Improving the Accuracy of Baha(R) Fittings through Measures of Direct Bone Conduction

OBJECTIVES: Variability in Baha(R) sound processor fittings may arise from the nature of the implant-to-bone transmission as well as transcranial attenuation for patients with single-sided sensorineural deafness (SSD). One method of improving the predictability of Baha fittings is to measure the individual patient's actual bone conduction thresholds, thereby removing the influences of skin thickness and/or the implant location site. METHODS: Twenty adult wearers of the Baha bone conduction implant system participated in the study. Direct bone conduction thresholds were obtained through the BC Direct function of the Baha Fitting Software combined with the Cochlear Baha BP100 sound processor. For comparison, the masked and unmasked bone conduction responses of the patients were collected through standard audiometric testing techniques. Test-retest reliability measurement was performed for all participants. Data for each frequency and frequency range were analyzed separately. RESULTS: The results confirm the improved transmission of sound through the implant rather than transcutaneously through the skin. On average, the BC Direct thresholds were closer to the patient's unmasked thresholds than the masked values. In subjects with SSD, BC Direct results were poorer than contra-lateral bone conduction thresholds, most likely due to transcranial attenuation. The test-retest reliability for the BC Direct measurements was within +/-5 dB. The comparison of preferred amplification, based on direct bone conduction or bone conduction audiometry, found higher agreement for fittings based on direct bone conduction measurements. CONCLUSION: While the transfer function between the implant and the skin can be predicted on average, there are a number of patients for whom measurement is essential to determine the required amplification. These were patients with: 1) SSD, 2) asymmetrical hearing loss, 3) unusual implant location or skull formation, and 4) users of Testband or Softband. The result for the clinician is that a fitting can take place with less fine-tuning and a greater understanding of the variability of bone conducted sound transmission.

Hearing Performance Benefits of a Programmable Power Baha(R) Sound Processor with a Directional Microphone for Patients with a Mixed Hearing Loss

OBJECTIVES: New signal processing technologies have recently become available for Baha(R) sound processors. These technologies have led to an increase in power and to the implementation of directional microphones. For any new technology, it is important to evaluate the degree of benefit under different listening situations. METHODS: Twenty wearers of the Baha osseointegrated hearing system participated in the investigation. The control sound processor was the Baha Intenso and the test sound processor was the Cochlear(TM) Baha(R) BP110power. Performance was evaluated in terms of free-field audibility with narrow band noise stimuli. Speech recognition of monosyllabic phonetically balanced (PB) words in quiet was performed at three intensity settings (50, 65, and 80 dB sound pressure level [SPL]) with materials presented at 0 degrees azimuth. Speech recognition of sentences in noise using the Hearing in Noise Test (HINT) in an adaptive framework was performed with speech from 0 degrees and noise held constant at 65 dB SPL from 180 degrees. Testing was performed in both the omni and directional microphone settings. Loudness growth was assessed in randomly presented 10 dB steps between 30 and 90 dB SPL to narrow band noise stimuli at 500 Hz and 3,000 Hz. RESULTS: The test sound processor had significantly improved high frequency audibility (3,000-8,000 Hz). Speech recognition of PB words in quiet at three different intensity levels (50, 65, and 80 dB SPL) indicated a significant difference in terms of level (P0.05). Speech recognition of sentences in noise demonstrated a 2.5 dB signal-to-noise ratio (SNR) improvement in performance for the test sound processor. The directional microphone provided an additional 2.3 dB SNR improvement in speech recognition (P<0.0001). Loudness growth functions demonstrated similar performance, indicating that both sound processors had sufficient headroom and amplification for the required hearing loss. CONCLUSION: The test sound processor demonstrated significant improvements in the most challenging listening situation (speech recognition in noise). The implementation of a directional microphone demonstrated a further potential improvement in hearing performance. Both the control and test sound processors demonstrated good performance in terms of audibility, word recognition in quiet and loudness growth.

Avaliação de pacientes utilizando equipamento inovador de auxílio à visão subnormal / Evaluation of patients using an innovative low-vision aid

OBJETIVO: Avaliação preliminar na Clínica Oftalmológica do Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo (USP) de equipamento inovador para baixa visão desenvolvido na USP que consiste em prancha de leitura acoplada a lente de aumento que mantém fixos o foco e a linha de leitura. MÉTODOS: Foram avaliados 9 pacientes com visão subnormal usando o supracitado equipamento prancha de leitura acoplada a lente para auxílio em visão subnormal desenvolvida na USP em comparação com uso de uma lupa teste manual de dioptria semelhante, considerando-se os seguintes parâmetros de avaliação: causa da doença, acuidade visual corrigida no melhor olho para longe, impressão pessoal do paciente comparando prancha de leitura e lupa teste, impressão dos autores observando o uso dos 2 auxílios acima citados. RESULTADOS: A preferência pelos recursos foi: prancha de leitura acoplada a lupa - 5 pacientes; lupa manual - 2 pacientes; sem preferência por nenhum dos recursos - 1 paciente; inadequados para avaliação dos recursos preferidos - 1 paciente. CONCLUSÃO: Neste estudo preliminar, a maioria dos pacientes avaliados preferiu o recurso prancha de leitura acoplada à lupa, o que mostra que este produto inovador facilita a leitura; o médico avaliador interpreta a opinião do paciente como um especialista e contribui para o aprimoramento do produto para que ele possa ser futuramente submetido a novas avaliações.

ABSTRACT PURPOSE: To perform a preliminary evaluation at the "Clínica Oftalmológica do Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo (USP)" of an innovative equipment for low-vision developed at USP containing a reading stand and a magnifier that maintains in a stable position the reading line and focus. METHODS: 9 low-vision patients were evaluated using the above mentioned reading stand and a magnifier developed at USP comparing it with a hand magnifier of similar power taking into account the following evaluation parameters: etiology of low-vision, best corrected visual acuity for distance, patient's opinion comparing both low-vision aid resources, authors' opinion observing the patient using both low-vision aids. RESULTS: The numerical preference for the low-vision aids was: 5 patients for the reading stand and a magnifier that maintains at a stable position the reading line and focus; 2 patients for the hand magnifier; 1 patient indifferent regarding any of the resources; 1 patient inadequate for the evaluation of the low-vision aids. CONCLUSION: This preliminary study shows the preference of the majority of the patients for the reading stand and a magnifier that maintains at a stable position the reading line and focus showing that this innovative product makes reading easier; the evaluator doctor translates the patient's opinion as an expert and contributes to the improvement of the product so that it can be evaluated again in the future.