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首页> 外文期刊>Otology and neurotology: official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology >First clinical experiences with a direct acoustic cochlear stimulator in comparison to preoperative fitted conventional hearing aids
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First clinical experiences with a direct acoustic cochlear stimulator in comparison to preoperative fitted conventional hearing aids

机译:与术前安装的传统助听器相比,直接听觉人工耳蜗刺激器的首次临床经验

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Objective: Patients with moderate-to-severe mixed hearing losses (MHLs) are hard to provide sufficient benefit with currently available conventional hearing aids. Here, the long-term safety of a direct acoustic cochlear stimulator (DACS) and the effectiveness compared with conventional "high-performance" hearing aids were investigated. Study Design: Prospective, within patient reference, nonrandomized, interventional multicenter clinical study performed at these 3 centers: Medical University Hannover, University of Heidelberg, and Helios Hospital Krefeld. Patients and Intervention: Ten otosclerosis patients with severe-to-profound MHL were preoperatively fitted with state-of-the-art conventional hearing aids (HA). After 2 months of testing conventional HA, 9 of the patients decided to be implanted with a DACS. Main Outcome Measures: Air conduction (AC) and bone conduction (BC) aided and unaided thresholds, speech discrimination before and after implantation and at 3, 6, and 12 months after activation. The subjective benefit was assessed by the Abbreviated Profile of Hearing Aid Benefit (APHAB). Results: Preoperative hearing thresholds were preserved over the 12 month observation time after activation. Average functional gain (0.5-4 kHz) achieved with conventional HA was 47 dB compared with 56 dB with the DACS. Speech-in-noise tests revealed a lower SNR for DACS (3.1 dB) than for the HA (6.6 dB) and patients were more satisfied with the DACS. Conclusion: The DACS significantly improved hearing, speech intelligibility, and satisfaction in patients with a severe-to-profound mixed hearing loss and can be considered a safe and useful alternative to conventional hearing aids.
机译:目的:患有中度至重度混合性听力损失(MHL)的患者难以利用当前可用的常规助听器提供足够的益处。在这里,研究了直接声学耳蜗刺激器(DACS)的长期安全性以及与传统“高性能”助听器相比的有效性。研究设计:在患者参考范围内,在汉诺威医科大学,海德堡大学和克雷费尔德赫里奥斯医院这3个中心进行的非随机,干预性多中心临床研究均经过前瞻性研究。患者和干预措施:10例重度至严重MHL的耳硬化症患者在术前已配备了最先进的传统助听器(HA)。在对常规HA进行2个月的测试后,其中9例患者决定植入DACS。主要观察指标:空气传导(AC)和骨传导(BC)辅助阈值和无辅助阈值,植入前后,激活后3、6和12个月的语音识别。主观效益是通过“助听器缩写简档”(APHAB)进行评估的。结果:激活后的12个月观察时间内,保留了术前听力阈值。传统HA的平均功能增益(0.5-4 kHz)为47 dB,而DACS为56 dB。噪声测试表明,DACS(3.1 dB)的SNR比HA(6.6 dB)低,并且患者对DACS更加满意。结论:DACS可显着改善重度至深层混合性听力损失患者的听力,语音清晰度和满意度,可以被认为是传统助听器的安全有效替代方法。

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