面向非处方助听器的新循证适配范式。
Toward a New Evidence-Based Fitting Paradigm for Over-the-Counter Hearing Aids.
机构信息
Department of Communication Sciences and Disorders, The University of Iowa, Iowa City.
Department of Biostatistics, The University of Iowa, Iowa City.
出版信息
Am J Audiol. 2021 Mar 10;30(1):43-66. doi: 10.1044/2020_AJA-20-00085. Epub 2020 Dec 1.
Purpose This dual-aim study was intended to develop and validate a new fitting paradigm for over-the-counter (OTC) hearing aids. Aim 1 was undertaken to create a limited set of evidence-based preconfigured gain-frequency responses ("presets") for use in OTC devices. Aim 2 tested the efficacy of the presets relative to best-practice verification and determined the best method(s) for older adults to self-select amplification from the set. Method In Aim 1, audiometry data from 267 older adults with mild-to-moderate sensorineural hearing loss were obtained from the National Health and Nutrition Examination Survey database. Using these data and the National Acoustic Laboratories-Non-Linear 2 (NAL-NL2) prescriptive formula, a set of four presets were created that can fit a large percentage of older Americans with presbycusis. In Aim 2, 37 older adults with hearing loss used five methods to select presets. The selection methods were select-by-audiogram, select-by-self-test, select-by-trying, select-by-questionnaire, and random assignment. Using a crossover design, each participant completed speech recognition testing and sound quality ratings in quiet and noise for all selection methods and a verified NAL-NL2 condition. Results The set of presets can fit 67.9% of older Americans with mild-to-moderate hearing loss (Aim 1). Controlling for hearing thresholds and sound quality ratings, liner mixed-effects models indicated that speech recognition scores for select-by-audiogram, select-by-self-test, and select-by-trying were not statistically different from the NAL-NL2 condition. Statistical analysis indicated that select-by-self-test produced outcomes most consistent with individual outcomes for the NAL-NL2 condition (Aim 2). Conclusion This newly developed fitting paradigm may provide efficacy comparable to best-practice verification and could be used in OTC hearing aids.
目的
本双目标研究旨在开发和验证一种新的非处方(OTC)助听器适配范式。目的 1 旨在创建一套有限的基于证据的预设增益-频率响应(“预设”),用于 OTC 设备。目的 2 测试预设相对于最佳实践验证的效果,并确定老年人从预设中自我选择放大的最佳方法。
方法
在目的 1 中,从国家健康和营养检查调查数据库中获取了 267 名轻度至中度感音神经性听力损失的老年人的听力测试数据。使用这些数据和国家声学实验室非线性 2(NAL-NL2)处方公式,创建了一组四个预设,可适配大部分患有老年性聋的美国老年人。在目的 2 中,37 名听力损失的老年人使用五种方法来选择预设。选择方法包括根据听力图选择、自我测试选择、尝试选择、问卷选择和随机分配。使用交叉设计,每个参与者完成了语音识别测试和在安静和噪声环境下的声音质量评分,所有选择方法和经过验证的 NAL-NL2 条件。
结果
预设集可适配 67.9%的轻度至中度听力损失的美国老年人(目的 1)。控制听力阈值和声音质量评分,线性混合效应模型表明,根据听力图选择、自我测试选择和尝试选择的语音识别分数与 NAL-NL2 条件没有统计学差异。统计分析表明,自我测试选择产生的结果与 NAL-NL2 条件的个体结果最一致(目的 2)。
结论
这种新开发的适配范式可能提供与最佳实践验证相当的效果,并可用于 OTC 助听器。