Bianchin Giovanni, Bonali Marco, Russo Melania, Tribi Lorenzo
Department of Otolaryngology and Audiology, S. Maria Nuova Hospital of Reggio Emilia, Reggio Emilia, Italy.
ORL J Otorhinolaryngol Relat Spec. 2015;77(1):17-26. doi: 10.1159/000371425. Epub 2015 Jan 30.
To describe our experience with positioning the Bonebridge (BB) device, a semi-implantable transcutaneous bone conduction implant for patients with conductive and mixed hearing loss as well as for those suffering from single-sided deafness.
The following is a retrospective case review of 4 adults suffering from conductive or mixed hearing loss and single-sided deafness. The BB device was implanted unilaterally via 2 different approaches selected case by case: the presigmoid transmastoid and the retrosigmoid approach. An audiological evaluation in the free field was conducted to observe the functional benefit with this device. The Glasgow Health Status Inventory (GHSI) and the Glasgow Benefit Inventory (GBI) questionnaires were filled out to evaluate patients' quality of life in relationship to the intervention.
No intra- or postoperative complications were observed. The performance in the speech test in all 4 cases reached 100% in the aided condition at 65 dB, while in the unaided condition at 65 dB, it was less than 10%. The GHSI and GBI questionnaires showed an improvement in quality of life after implantation.
The BB device is a safe and effective solution for individuals with pathologies such as chronic otitis media, atresia auris and otosclerosis with inadequate benefit from conventional surgery or bone conduction hearing aids.
描述我们为患有传导性和混合性听力损失以及单侧耳聋患者植入半植入式经皮骨传导植入装置Bonebridge(BB)的经验。
以下是对4例患有传导性或混合性听力损失及单侧耳聋的成人患者的回顾性病例分析。根据具体情况,通过两种不同的方法单侧植入BB装置:乙状窦前经乳突入路和乙状窦后入路。在自由声场进行听力评估,以观察该装置的功能效益。填写格拉斯哥健康状况量表(GHSI)和格拉斯哥效益量表(GBI)问卷,以评估患者与干预措施相关的生活质量。
未观察到术中或术后并发症。所有4例患者在65分贝助听条件下言语测试表现均达到100%,而在65分贝未助听条件下,该比例低于10%。GHSI和GBI问卷显示植入后生活质量有所改善。
对于患有慢性中耳炎、外耳道闭锁和耳硬化症等疾病且从传统手术或骨传导助听器中获益不足的个体,BB装置是一种安全有效的解决方案。