Division of Epidemiology and Clinical Research, Department of Pediatrics, University of Minnesota, Minneapolis, Minnesota.
Department of Pediatrics, Oregon Health and Science University, Portland, Oregon.
Cancer Epidemiol Biomarkers Prev. 2024 Sep 3;33(9):1177-1184. doi: 10.1158/1055-9965.EPI-24-0203.
Childhood cancer survivors treated with platinum-based chemotherapy are at risk of treatment-induced hearing loss. Accurate evaluation of hearing thresholds has historically been limited to clinical audiometry, which is logistically challenging and expensive to include in epidemiologic studies. We evaluated the feasibility of using a remote, tablet-based hearing assessment in a cohort of pediatric germ cell tumor survivors treated with platinum-based chemotherapy.
Survivors from the GCT Outcomes and Late effects Data (GOLD) study were recruited to the pilot study (n = 100). Study personnel conducted remote hearing assessments of standard and extended high frequency thresholds using validated tablet-based audiometry (SHOEBOX, Inc.). T tests and Wilcoxon rank-sum tests evaluated differences in assessment characteristics between children and adults. Agreement between self-reported and measured hearing loss was calculated using Cohen κ.
We were able to reach 136/168 (81%) eligible participants, of which 100 (74%) agreed to participate. Successful completion of the remote hearing assessment was high [97%; 20 children (ages 7-17), 77 adults (ages 18-31)]. The mean assessment length was 37.6 minutes, and the mean turnaround time was 8.3 days. We observed hearing loss at standard frequencies in 21% of participants. Agreement between self-reported and measured hearing loss was significant (P value = 1.41 × 10-7), with 83.5% concordance.
Hearing loss measured using the remote assessment aligns with self-reporting and rates of hearing loss reported in the literature for this population.
Remote application of tablet-based audiometry is a feasible and efficacious method for measuring hearing in epidemiologic studies with participants spread across large geographic areas.
接受含铂类化疗的儿童癌症幸存者有发生治疗诱导性听力损失的风险。听力阈值的准确评估在历史上仅限于临床听力测试,但在流行病学研究中,该方法在后勤上具有挑战性且昂贵。我们评估了在接受含铂类化疗的儿科生殖细胞肿瘤幸存者队列中使用远程、基于平板电脑的听力评估的可行性。
GCT 结局和晚期效应数据(GOLD)研究的幸存者被招募到该试点研究中(n=100)。研究人员使用经过验证的基于平板电脑的听力计(SHOEBOX,Inc.)对标准和扩展高频阈值进行远程听力评估。T 检验和 Wilcoxon 秩和检验评估了儿童和成人评估特征之间的差异。采用 Cohen κ 计算自我报告和测量的听力损失之间的一致性。
我们能够联系到 168 名符合条件的参与者中的 136 名(81%),其中 100 名(74%)同意参与。远程听力评估的成功率很高[97%;20 名儿童(7-17 岁),77 名成人(18-31 岁)]。平均评估时间为 37.6 分钟,平均周转时间为 8.3 天。我们观察到标准频率下有 21%的参与者存在听力损失。自我报告和测量的听力损失之间的一致性显著(P 值=1.41×10-7),一致性为 83.5%。
使用远程评估测量的听力损失与该人群文献中报告的自我报告和听力损失率一致。
基于平板电脑的听力计的远程应用是一种在地理区域广泛的参与者的流行病学研究中测量听力的可行且有效的方法。