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在同一患者中使用每日随机化和基于成像的拟合来评估人工耳蜗植入的听力表现-ELEPHANT 研究。

Evaluating hearing performance with cochlear implants within the same patient using daily randomization and imaging-based fitting - The ELEPHANT study.

机构信息

Department of ENT/Audiology, School for Mental Health and Neuroscience (MHeNs), Maastricht University Medical Center, Maastricht, The Netherlands.

Department of Methodology and Statistics, School for Public Health and Primary Care (CAPHRI), Maastricht University Medical Center, Maastricht, The Netherlands.

出版信息

Trials. 2020 Jun 23;21(1):564. doi: 10.1186/s13063-020-04469-x.

Abstract

BACKGROUND

Prospective research in the field of cochlear implants is hampered by methodological issues and small sample sizes. The ELEPHANT study presents an alternative clinical trial design with a daily randomized approach evaluating individualized tonotopical fitting of a cochlear implant (CI).

METHODS

A single-blinded, daily-randomized clinical trial will be implemented to evaluate a new imaging-based CI mapping strategy. A minimum of 20 participants will be included from the start of the rehabilitation process with a 1-year follow-up period. Based on a post-operative cone beam CT scan (CBCT), mapping of electrical input will be aligned to natural place-pitch arrangement in the individual cochlea. The CI's frequency allocation table will be adjusted to match the electrical stimulation of frequencies as closely as possible to corresponding acoustic locations in the cochlea. A randomization scheme will be implemented whereby the participant, blinded to the intervention allocation, crosses over between the experimental and standard fitting program on a daily basis, and thus effectively acts as his own control, followed by a period of free choice between both maps to incorporate patient preference. With this new approach the occurrence of a first-order carryover effect and a limited sample size is addressed.

DISCUSSION

The experimental fitting strategy is thought to give rise to a steeper learning curve, result in better performance in challenging listening situations, improve sound quality, better complement residual acoustic hearing in the contralateral ear and be preferred by recipients of a CI. Concurrently, the suitability of the novel trial design will be considered in investigating these hypotheses.

TRIAL REGISTRATION

ClinicalTrials.gov: NCT03892941. Registered 27 March 2019.

摘要

背景

耳蜗植入物领域的前瞻性研究受到方法学问题和样本量小的限制。ELEPHANT 研究提出了一种替代的临床试验设计,采用每日随机方法评估耳蜗植入物(CI)的个体化音调拟合。

方法

将实施一项单盲、每日随机临床试验,以评估一种新的基于成像的 CI 映射策略。从康复过程开始,至少纳入 20 名参与者,并进行为期 1 年的随访。根据术后锥形束 CT 扫描(CBCT),将电输入的映射与个体耳蜗中的自然音位排列对齐。CI 的频率分配表将进行调整,以尽可能匹配电刺激与耳蜗中相应声位的频率。将实施随机方案,参与者在实验和标准拟合方案之间每天交叉,从而有效地作为自己的对照,然后在两种图谱之间自由选择一段时间,以纳入患者的偏好。通过这种新方法,可以解决一阶延续效应和样本量有限的问题。

讨论

实验拟合策略被认为会导致更陡峭的学习曲线,在具有挑战性的听力环境中表现更好,提高音质,更好地补充对侧耳的残余听力,并受到 CI 接受者的青睐。同时,将考虑新试验设计的适用性,以调查这些假设。

试验注册

ClinicalTrials.gov:NCT03892941。注册于 2019 年 3 月 27 日。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/967a/7310427/70624bd17620/13063_2020_4469_Fig1_HTML.jpg

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