Department of Otolaryngology, Head & Neck Surgery, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.
Department of Audiology, Norton Sound Health Corporation, Nome, Alaska, USA.
Ear Hear. 2023;44(4):877-893. doi: 10.1097/AUD.0000000000001336. Epub 2023 Mar 13.
Diagnostic accuracy was evaluated for various screening tools, including mobile health (mHealth) pure-tone screening, tympanometry, distortion product otoacoustic emissions (DPOAE), and inclusion of high frequencies to determine the most accurate screening protocol for identifying children with hearing loss in rural Alaska where the prevalence of middle ear disease is high.
Hearing screening data were collected as part of two cluster randomized trials conducted in 15 communities in rural northwest Alaska. All children enrolled in school from preschool to 12th grade were eligible. Analysis was limited to data collected 2018 to 2019 (n = 1449), when both trials were running and measurement of high frequencies were included in the protocols. Analyses included estimates of diagnostic accuracy for each screening tool, as well as exploring performance by age and grade. Multiple imputation was used to assess diagnostic accuracy in younger children, where missing data were more prevalent due to requirements for conditioned responses. The audiometric reference standard included otoscopy, tympanometry, and high frequencies to ensure detection of infection-related and noise-induced hearing loss.
Both the mHealth pure-tone screen and DPOAE screen performed better when tympanometry was added to the protocol (increase in sensitivity of 19.9%, 95% Confidence Interval (CI): 15.9 to 24.1 for mHealth screen, 17.9%, 95% CI: 14.0 to 21.8 for high-frequency mHealth screen, and 10.4%, 95% CI: 7.5 to 13.9 for DPOAE). The addition of 6 kHz to the mHealth pure-tone screen provided an 8.7 percentage point improvement in sensitivity (95% CI: 6.5 to 11.3). Completeness of data for both the reference standard and the mHealth screening tool differed substantially by age, due to difficulty with behavioral testing in young children. By age 7, children were able to complete behavioral testing, and data indicated that high-frequency mHealth pure-tone screen with tympanometry was the superior tool for children 7 years and older. For children 3 to 6 years of age, DPOAE plus tympanometry performed the best, both for complete data and multiply imputed data, which better approximates accuracy for children with missing data.
This study directly evaluated pure-tone, DPOAE, and tympanometry tools as part of school hearing screening in rural Alaskan children (3 to 18+ years). Results from this study indicate that tympanometry is a key component in the hearing screening protocol, particularly in environments with higher prevalence of infection-related hearing loss. DPOAE is the preferred hearing screening tool when evaluating children younger than 7 years of age (below 2nd grade in the United States) due to the frequency of missing data with behavioral testing in this age group. For children 7 years and older, the addition of high frequencies to pure-tone screening increased the accuracy of screening, likely due to improved identification of hearing loss from noise exposure. The lack of a consistent reference standard in the literature makes comparing across studies challenging. In our study with a reference standard inclusive of otoscopy, tympanometry, and high frequencies, less than ideal sensitivities were found even for the most sensitive screening protocols, suggesting more investigation is necessary to ensure screening programs are appropriately identifying noise- and infection-related hearing loss in rural, low-resource settings.
评估各种筛查工具的诊断准确性,包括移动医疗(mHealth)纯音筛查、鼓室图、畸变产物耳声发射(DPOAE),以及纳入高频来确定最准确的筛查方案,以识别阿拉斯加农村地区听力损失的儿童,该地区中耳疾病的患病率较高。
听力筛查数据是作为在阿拉斯加农村西北部的 15 个社区进行的两项集群随机试验的一部分收集的。所有从幼儿园到 12 年级的在校儿童都有资格参加。分析仅限于 2018 年至 2019 年(n=1449)收集的数据,当时两项试验都在进行,并且在方案中纳入了高频测量。分析包括对每种筛查工具的诊断准确性的估计,以及通过年龄和年级来探索性能。多重插补用于评估因需要条件反应而导致数据缺失更多的年幼儿童的诊断准确性。听力参考标准包括耳镜检查、鼓室图和高频,以确保检测到与感染和噪声有关的听力损失。
当在方案中添加鼓室图时,mHealth 纯音筛查和 DPOAE 筛查的性能都有所提高(mHealth 筛查的敏感性增加了 19.9%,95%置信区间[CI]:15.9 至 24.1;高频 mHealth 筛查为 17.9%,95%CI:14.0 至 21.8;DPOAE 为 10.4%,95%CI:7.5 至 13.9)。将 6kHz 添加到 mHealth 纯音筛查中,敏感性提高了 8.7 个百分点(95%CI:6.5 至 11.3)。由于年幼儿童的行为测试困难,mHealth 纯音筛查的参考标准和 mHealth 筛查工具的数据完整性在年龄上存在显著差异。到 7 岁时,儿童能够完成行为测试,数据表明高频 mHealth 纯音筛查联合鼓室图是 7 岁及以上儿童的最佳工具。对于 3 至 6 岁的儿童,DPOAE 联合鼓室图的表现最佳,无论是完整数据还是多重插补数据,都更接近缺失数据儿童的准确性。
本研究直接评估了纯音、DPOAE 和鼓室图工具作为阿拉斯加农村儿童(3 至 18+岁)学校听力筛查的一部分。本研究的结果表明,鼓室图是听力筛查方案的关键组成部分,特别是在感染相关听力损失患病率较高的环境中。当评估 7 岁以下(美国二年级以下)的儿童时,DPOAE 是首选的听力筛查工具,因为在该年龄段进行行为测试时数据缺失的频率较高。对于 7 岁及以上的儿童,在纯音筛查中加入高频可以提高筛查的准确性,这可能是由于对噪声暴露引起的听力损失的识别得到了改善。由于文献中缺乏一致的参考标准,使得比较研究具有挑战性。在我们的研究中,使用了包括耳镜检查、鼓室图和高频的参考标准,即使是最敏感的筛查方案,也发现了不太理想的敏感性,这表明需要进一步研究,以确保听力筛查计划能够在农村、资源匮乏的环境中适当识别噪声和感染相关的听力损失。