Mimosa Acoustics, Champaign, Illinois, USA.
Research Laboratory of Electronics, Massachusetts Institute of Technology, Cambridge, Massachusetts, USA.
Ear Hear. 2018 Sep/Oct;39(5):946-957. doi: 10.1097/AUD.0000000000000555.
Clinical pure-tone audiometry is conducted using stimuli delivered through supra-aural headphones or insert earphones. The stimuli are calibrated in an acoustic (average ear) coupler. Deviations in individual-ear acoustics from the coupler acoustics affect test validity, and variations in probe insertion and headphone placement affect both test validity and test-retest reliability. Using an insert earphone designed for otoacoustic emission testing, which contains a microphone and loudspeaker, an individualized in-the-ear calibration can be calculated from the ear-canal sound pressure measured at the microphone. However, the total sound pressure level (SPL) measured at the microphone may be affected by standing-wave nulls at higher frequencies, producing errors in stimulus level of up to 20 dB. An alternative is to calibrate using the forward pressure level (FPL) component, which is derived from the total SPL using a wideband acoustic immittance measurement, and represents the pressure wave incident on the eardrum. The objective of this study is to establish test-retest reliability for FPL calibration of pure-tone audiometry stimuli, compared with in-the-ear and coupler sound pressure calibrations.
The authors compared standard audiometry using a modern clinical audiometer with TDH-39P supra-aural headphones calibrated in a coupler to a prototype audiometer with an ER10C earphone calibrated three ways: (1) in-the-ear using the total SPL at the microphone, (2) in-the-ear using the FPL at the microphone, and (3) in a coupler (all three are derived from the same measurement). The test procedure was similar to that commonly used in hearing-conservation programs, using pulsed-tone test frequencies at 0.5, 1, 2, 3, 4, 6, and 8 kHz, and an automated modified Hughson-Westlake audiometric procedure. Fifteen adult human participants with normal to mildly-impaired hearing were selected, and one ear from each was tested. Participants completed 10 audiograms on each system, with test-order randomly varied and with headphones and earphones refitted by the tester between tests.
Fourteen of 15 ears had standing-wave nulls present between 4 and 8 kHz. The mean intrasubject SD at 6 and 8 kHz was lowest for the FPL calibration, and was comparable with the low-frequency reliability across calibration methods. This decrease in variability translates to statistically-derived significant threshold shift criteria indicating that 15 dB shifts in hearing can be reliably detected at 6 and 8 kHz using FPL-calibrated ER10C earphones, compared with 20 to 25 dB shifts using standard TDH-39P headphones with a coupler calibration.
These results indicate that reliability is better with insert earphones, especially with in-the-ear FPL calibration, compared with a standard clinical audiometer with supra-aural headphones. However, in-the-ear SPL calibration should not be used due to its sensitivity to standing waves. The improvement in reliability is clinically meaningful, potentially allowing hearing-conservation programs to more confidently determine significant threshold shifts at 6 kHz-a key frequency for the early detection of noise-induced hearing loss.
临床纯音测听使用通过耳罩式耳机或插入式耳机传递的刺激进行。刺激在声学(平均耳)耦合器中进行校准。个体耳的声学与耦合器声学的偏差会影响测试的有效性,而探头插入和耳机放置的变化会影响测试的有效性和复测的可靠性。使用专为耳声发射测试设计的插入式耳机,其中包含麦克风和扬声器,可以从麦克风测量的耳道声压中计算出个性化的耳内校准。然而,麦克风测量的总声压级(SPL)可能会受到高频驻波零的影响,导致刺激水平误差高达 20 dB。另一种方法是使用正向压力级(FPL)分量进行校准,该分量是通过宽带声导抗测量从总 SPL 中得出的,代表作用于鼓膜的压力波。本研究的目的是建立 FPL 校准纯音测听刺激的复测可靠性,与耳内和耦合器声压校准进行比较。
作者将使用现代临床听力计和 TDH-39P 耳罩式耳机对耦合器进行校准的标准听力测试与使用 ER10C 耳机进行校准的原型听力计进行了比较,该耳机有三种校准方式:(1)使用麦克风处的总 SPL 进行耳内校准,(2)使用麦克风处的 FPL 进行耳内校准,(3)在耦合器中校准(所有三种校准方式都来自于同一测量)。测试程序类似于听力保护计划中常用的程序,使用脉冲音测试频率为 0.5、1、2、3、4、6 和 8 kHz,并采用自动化修改后的 Hughson-Westlake 测听程序。选择了 15 名听力正常至轻度受损的成年参与者,每个参与者的一只耳朵进行了测试。参与者在每个系统上完成了 10 次听力测试,测试顺序随机变化,测试之间由测试者重新调整耳机和耳塞。
15 只耳朵中有 14 只耳朵在 4 到 8 kHz 之间存在驻波零点。6 和 8 kHz 时的个体内标准差最低的是 FPL 校准,与各校准方法的低频可靠性相当。这种变异性的降低转化为统计学上显著的阈值移位标准,表明使用 FPL 校准的 ER10C 耳机可以可靠地检测到 6 和 8 kHz 处 15 dB 的听力变化,而使用标准 TDH-39P 耳机和耦合器校准则需要 20 到 25 dB 的变化。
这些结果表明,与标准临床听力计与耳罩式耳机相比,插入式耳机,尤其是耳内 FPL 校准的可靠性更好。然而,由于其对驻波的敏感性,不应使用耳内 SPL 校准。可靠性的提高具有临床意义,有可能使听力保护计划更有信心地确定 6 kHz 处的显著阈值变化,6 kHz 是早期发现噪声性听力损失的关键频率。