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固定水平频率阈值测试用于耳毒性监测。

Fixed-Level Frequency Threshold Testing for Ototoxicity Monitoring.

机构信息

1Geisel School of Medicine at Dartmouth, Hanover, New Hampshire, USA; 2Creare, LLC, Hanover, New Hampshire, USA; and 3Walter Reed National Military Medical Center, Bethesda, Maryland, USA.

出版信息

Ear Hear. 2017 Nov/Dec;38(6):e369-e375. doi: 10.1097/AUD.0000000000000433.

DOI:10.1097/AUD.0000000000000433
PMID:28362673
Abstract

OBJECTIVES

Hearing loss from ototoxicity is often most pronounced at high frequencies. To improve patient monitoring and compliance, high-frequency testing methods should be short and easy to administer. We evaluated the repeatability and accuracy of a Békésy-like, fixed-level frequency threshold (FLFT) technique. This test takes less than a minute and could provide a rapid and effective way to determine the highest audible frequency. We hypothesized the FLFT test would be repeatable in normal-hearing subjects, and accurate when compared with Békésy fixed-frequency audiometry in the sensitive region for ototoxicity (SRO).

DESIGN

Twenty-nine normal-hearing subjects (20 females, 9 males) performed 2 different automated audiometry tests at least 4 times over a period of no less than 3 weeks. Ages ranged from 23 to 35 years (average = 28 years). Subjects completed testing under Sennheiser HDA-200 headsets. Initial fixed-frequency audiometry thresholds were obtained at frequencies ranging from 0.5 to 20 kHz to identify each subject's highest audible frequency, which was used to determine the SRO. The SRO was defined as the seven frequencies at and below the highest audible frequency in 1/6-octave steps. These frequencies were monitored with fixed-frequency audiometry. At each session, the FLFT test was administered at 80 dB SPL. Subjects used a Békésy-style tracking method to determine the frequency threshold. All testing was completed in a sound booth (single wall, Industrial Acoustics Company) using a computerized, laptop-based, system. FLFT repeatability was calculated as the root mean square difference from the first test session. FLFT accuracy was calculated as the difference from the highest audible frequency determined from fixed-frequency audiometry interpolated to 80 dB SPL level.

RESULTS

The FLFT average RMSD for intersession variability was 0.05 ± 0.05 octaves. The test showed no learning effect [F(3,78) = 0.7; p = 0.6]. The overall intersession variability for SRO fixed-frequency audiometry thresholds at all frequencies was within clinically acceptable test-retest variability (10 dB) at 5.8 dB (range 2.7 to 9.9 dB). The SRO fixed-frequency audiometry therefore served as a repeatable basis of comparison for accuracy of the FLFT test. The mean absolute difference between the fixed-frequency audiometry and FLFT-determined highest audible frequency was 0.03 octaves. The FLFT and the highest audible frequency via fixed-frequency audiometry at 80 dB SPL were not different statistically (p = 0.12). The FLFT took approximately 30 seconds to complete, compared with approximately 4.5 min for fixed-frequency audiometry SRO and 20 to 25 min for a traditional ototoxic audiometric assessment.

CONCLUSIONS

The Békésy-style FLFT was repeatable within 1/12 octave (1 step size in the testing procedure). The FLFT agreed well with the highest audible frequency determined via fixed-frequency audiometry at 80 dB SPL. The FLFT test is amenable to automatic and self-administration and may enable quick, accurate, noise-tolerant ototoxicity, and high-frequency hearing monitoring.

摘要

目的

耳毒性引起的听力损失在高频时最为明显。为了改善患者监测和依从性,应采用短时间且易于管理的高频测试方法。我们评估了类似贝克西的固定水平频率阈值(FLFT)技术的可重复性和准确性。该测试耗时不到一分钟,可提供一种快速有效的方法来确定可听的最高频率。我们假设 FLFT 测试在听力正常的受试者中是可重复的,并且与敏感区域的贝克西固定频率听力测试(SRO)相比是准确的。

设计

29 名听力正常的受试者(20 名女性,9 名男性)在至少 3 周的时间内至少进行了 2 次不同的自动听力测试,次数不少于 4 次。年龄范围为 23 至 35 岁(平均 28 岁)。受试者在森海塞尔 HDA-200 耳机下完成测试。最初的固定频率听力阈值在 0.5 至 20 kHz 的频率范围内获得,以确定每个受试者可听的最高频率,该频率用于确定 SRO。SRO 定义为在 1/6 倍频程步长中高于和低于最高可听频率的七个频率。这些频率通过固定频率听力测试进行监测。在每次测试中,FLFT 测试在 80 dB SPL 下进行。受试者使用贝克西式跟踪方法来确定频率阈值。所有测试均在隔音室内(单壁,工业声学公司)使用基于计算机的笔记本电脑系统完成。FLFT 重复性通过从第一次测试会话计算均方根差来计算。FLFT 准确性通过从固定频率听力测试确定的最高可听频率与 80 dB SPL 水平插值的差值来计算。

结果

各次测试之间的 FLFT 平均 RMSD 变异性为 0.05 ± 0.05 倍频程。该测试没有显示出学习效果[F(3,78)= 0.7;p = 0.6]。在所有频率下,SRO 固定频率听力测试阈值的各次测试之间的总体变异性均在临床可接受的测试-重测变异性(10 dB)范围内,为 5.8 dB(范围为 2.7 至 9.9 dB)。因此,SRO 固定频率听力测试是 FLFT 测试准确性的可重复比较基础。固定频率听力测试和 FLFT 确定的最高可听频率之间的平均绝对差值为 0.03 倍频程。FLFT 和在 80 dB SPL 下通过固定频率听力测试确定的最高可听频率在统计学上没有差异(p = 0.12)。FLFT 完成大约需要 30 秒,而固定频率听力测试 SRO 大约需要 4.5 分钟,传统的耳毒性听力评估大约需要 20 至 25 分钟。

结论

贝克西风格的 FLFT 在 1/12 倍频程(测试过程中的 1 个步长)内是可重复的。FLFT 与通过 80 dB SPL 固定频率听力测试确定的最高可听频率吻合良好。FLFT 测试适合自动和自我管理,可能能够快速、准确、耐受噪声地监测耳毒性和高频听力。

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