耳声发射检测识别ICU听力损失的可行性研究。

Q4 Medicine
Critical care explorations Pub Date : 2025-03-03 eCollection Date: 2025-03-01 DOI:10.1097/CCE.0000000000001223
Ramya Kaushik, Nicholas Reed, Lauren E Ferrante
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引用次数: 0

摘要

目的:听力障碍与ICU患者谵妄和老年ICU幸存者缺乏功能恢复相关。我们评估了使用耳声发射(oae)测试来筛查ICU患者先前存在的听力损失的可行性。设计:初步研究。环境:三级医疗中心重症监护室。患者:所有在2021年11月29日至2021年12月3日期间入住内科ICU的成年人(年龄≥18岁)均符合研究条件。干预措施:OAE是一种非侵入性、非参与性的工具,通过检测耳蜗内运动对听觉刺激的反应来筛查听力损失。在6个频率(1k、1.5 k、2k、3k、4k赫兹)下测试OAE的存在或不存在。测量和主要结果:可行性的主要结果被先验地定义为完成大于或等于70%的尝试测试。测试完成的平均时间和障碍或促进因素也被衡量为结果。如果在至少一只耳朵中检测到六个频率中的至少两个,则患者通过了OAE测试,这表明他们没有中度或重度听力障碍(这需要放大器)。还收集了人口统计学、谵妄、通气、镇静、疾病严重程度和环境噪音方面的数据。在31例患者中,23例(74.2%)接受了检测。8名患者(25.8%)无法检测,最常见的原因是环境噪声升高。在18例数据完整的患者中,6例听力损失筛查阳性。每耳完成OAE测试的平均时间为152.6秒(sd = 97.6 s)。结论:OAE检测是筛查ICU患者听力损失的一种可行方法,包括非参与性患者。识别听力损失将有助于通过扩音器和辅助设施等干预措施改善沟通。未来的研究应评估在ICU中识别和治疗听力损失是否可以减少谵妄并改善ICU后的恢复。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Otoacoustic Emissions Testing to Identify Hearing Loss in the ICU: A Feasibility Study.

Objectives: Hearing impairment is associated with delirium among ICU patients and a lack of functional recovery among older ICU survivors. We assessed the feasibility of using otoacoustic emissions (OAEs) testing to screen for preexisting hearing loss in the ICU.

Design: Pilot study.

Setting: Medical ICU at a tertiary medical center.

Patients: All adults (age ≥ 18) and admitted to the medical ICU between November 29, 2021, and December 03, 2021, were eligible for the study.

Interventions: OAE is a noninvasive, nonparticipatory tool that is used to screen for hearing loss by detecting intracochlear motion in response to auditory stimulation. The presence or absence of OAE was tested at six frequencies (1 k, 1.5 k, 2 k, 3 k, 4 k hertz).

Measurements and main results: The primary outcome of feasibility was defined a priori as completion of greater than or equal to 70% of attempted tests. Average time of test completion and barriers or facilitators were also measured as outcomes. A patient passed OAE testing if at least two of six frequencies were detected in at least one ear, suggesting they did not have moderate or severe hearing impairment (that would require an amplifier). Data were also gathered on demographics, delirium, ventilation, sedation, illness severity, and ambient noise. Of 31 patients approached, 23 (74.2%) underwent testing. Eight patients (25.8%) were unable to be tested, most commonly due to elevated ambient noise. Among the 18 patients with complete data, six patients screened positive for hearing loss. The average time for OAE test completion per ear was 152.6 seconds (sd = 97.6 s).

Conclusions: OAE testing is a feasible method to screen for hearing loss in the ICU, including in nonparticipatory patients. Identification of hearing loss would facilitate improved communication through interventions such as amplifiers and accommodations. Future studies should evaluate whether identification and treatment of hearing loss in the ICU may reduce delirium and improve post-ICU recovery.

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CiteScore
5.70
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