Rehabilitation of human hearing with a totally implantable cochlear implant: a feasibility study.

IF 5.4 Q1 MEDICINE, RESEARCH & EXPERIMENTAL
Philippe Pierre Lefebvre, Joachim Müller, Gerhard Mark, Florian Schwarze, Ingeborg Hochmair
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Abstract

Background: Cochlear implants (CIs) are neuroprosthetic devices which restore hearing in severe-to-profound hearing loss through electrical stimulation of the auditory nerve. Current CIs use an externally worn audio processor. A long-term goal in the field has been to develop a device in which all components are contained within a single implant. Here, we present initial clinical results with the totally implantable cochlear implant (TICI). The primary objective of this study was to assess the safety of the device in adults who suffer from bilateral severe-to-profound sensorineural hearing loss.

Methods: This study used a design with non-randomized single group assignment (trial registration: NCT04571333). Six implantations took place beginning in September 2020. Data collection took place at the two participating CI centers. Adverse events (the primary outcome), speech perception, patient reported outcomes, and device usage statistics were collected over the subsequent 52 weeks. A within-subjects comparison was used in which each participant was evaluated both with the TICI and with an external SONNET audio processor.

Results: One anticipated serious adverse device effect (ASADE) occurred. After treatment the event resolved without sequelae. No unanticipated serious adverse device effects (USADE) occurred. Speech perception in quiet and in noise scores were comparable between the TICI and the SONNET audio processor. Scores on the validated patient reported outcome instruments HUI3, SSQ-12, and HISQUI-19 all increased over the duration of the study. User satisfaction scores as reported in their daily diary also increased over the duration of the study. Based on device usage metrics, all but one user used the TICI without an external processor the majority of the time.

Conclusions: The primary outcome of assessing the safety of the device was achieved. The TICI provides high levels of hearing performance, comparable to those of a conventional CI. The development of the TICI expands the range of options for treatment of hearing loss.

用完全植入式人工耳蜗恢复人类听力的可行性研究。
背景:人工耳蜗是一种神经修复装置,通过电刺激听神经来恢复重度至重度听力损失患者的听力。目前的ci使用外接式音频处理器。该领域的长期目标是开发一种设备,其中所有组件都包含在单个植入物中。在这里,我们介绍了完全植入式人工耳蜗(TICI)的初步临床结果。本研究的主要目的是评估该装置在患有双侧重度到深度感音神经性听力损失的成年人中的安全性。方法:本研究采用非随机单组设计(试验注册号:NCT04571333)。从2020年9月开始,进行了六次植入。数据收集在两个参与的CI中心进行。在随后的52周内收集不良事件(主要结局)、语音感知、患者报告的结局和设备使用统计数据。使用受试者内部比较,其中每个参与者都使用TICI和外部SONNET音频处理器进行评估。结果:发生1例预期严重器械不良反应(ASADE)。治疗后,症状消失,无后遗症。未发生意外的严重器械不良反应(USADE)。TICI和SONNET音频处理器在安静和噪音方面的语音感知得分相当。在研究期间,经过验证的患者报告结果工具HUI3、SSQ-12和hiski -19的评分均有所增加。在研究期间,用户在日常日记中报告的满意度得分也有所增加。根据设备使用指标,除了一个用户之外,大多数时间都在使用没有外部处理器的TICI。结论:达到了评估该装置安全性的主要结果。TICI提供了高水平的听力表现,可与传统CI相媲美。TICI的发展扩大了治疗听力损失的选择范围。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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