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Effects of Auditory Training on Cognition in Hearing Loss: A Systematic Review and Meta-analyses. 听力训练对听力损失患者认知的影响:系统回顾和meta分析。
IF 1.2 4区 医学 Q3 AUDIOLOGY & SPEECH-LANGUAGE PATHOLOGY Pub Date : 2025-01-01 Epub Date: 2025-02-28 DOI: 10.3766/jaaa.240049
Wenling Jiang, Qian Zhou, Jiahui Zhang, Qian He, Guoyu Cui, Rongkun Huang, Chen Liang, Zhiwu Huang

Purpose: The aim of this study was to examine the efficacy of auditory training to improve cognitive function in patients with age-related hearing loss (ARHL). Research Design: This is a systematic review and meta-analysis. Study Sample: Seven studies involving 443 participants met the inclusion criteria. Participants were typically older adults (mean age = 67.23 years, standard deviation = 7.14) with mild to severe hearing loss. Intervention: Auditory training includes speech perception training, phoneme discrimination training, and so on. Data Collection and Analysis: A literature search of academic databases (Cochrane Library, PubMed, Web of Science, Embase, Wanfang, Weipu, and China National Knowledge Infrastructure) identified relevant articles published up to December 2023. This review includes only randomized controlled trials. The primary outcome is cognition function, measured by Montreal Cognitive Assessment, Mini-Mental State Examination, and other cognition-related subtest indicators. Results: The overall effect of auditory training on overall cognition and executive function in ARHL is statistically significant (overall cognition: g = 0.79, 95 percent confidence interval [CI]: 0.57, 1.01; executive function: g = 3.84, 95 percent CI: 1.49, 6.19), but executive function domain has high heterogeneity (I² = 100 percent). The effect of auditory training on attention/processing speed and working memory is small and not significant (attention/processing speed: g = 1.47, 95 percent CI: -0.48, 3.42; working memory: g = 0.68, 95 percent CI: -2.22, 3.58), but both attention/processing speed (I² = 96 percent) and working memory domain (I² = 98 percent) have high heterogeneity. Conclusions: The overall impact of auditory training on overall cognition and executive function seems to be significant, but because of the low quality of the literature and certain biases, it is impossible to conclude that auditory training can improve the cognitive function of ARHL; therefore, more high-quality evidence is needed.

目的:本研究的目的是探讨听觉训练对改善年龄相关性听力损失(ARHL)患者认知功能的疗效。研究设计:这是一项系统综述和荟萃分析。研究样本:7项研究共443名受试者符合纳入标准。参与者是典型的老年人(平均年龄= 67.23岁,标准差= 7.14),患有轻度至重度听力损失。干预:听觉训练包括语音感知训练、音素辨别训练等。数据收集与分析:检索学术数据库(Cochrane Library,PubMed, Web of Science, Embase,万方,卫普,中国知识基础设施),确定截至2023年12月发表的相关文章。本综述仅包括随机对照试验。主要结果是认知功能,通过蒙特利尔认知评估、迷你精神状态检查和其他认知相关的子测试指标来测量。结果:听觉训练对ARHL患者整体认知和执行功能的总体影响具有统计学意义(整体认知:g = 0.79, 95%置信区间[CI]: 0.57, 1.01;执行功能:g = 3.84, 95% CI: 1.49, 6.19),但执行功能域具有高度异质性(I2 = 100%)。听觉训练对注意/加工速度和工作记忆的影响较小且不显著(注意/加工速度:g = 1.47, 95% CI: -0.48, 3.42;工作记忆:g = 0.68, 95% CI: -2.22, 3.58),但注意/加工速度(I2 = 96%)和工作记忆域(I2 = 98%)均具有较高的异质性。结论:听觉训练对整体认知和执行功能的影响似乎是显著的,但由于文献质量较低和存在一定的偏差,因此不能得出听觉训练可以改善ARHL认知功能的结论;因此,需要更多高质量的证据。
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引用次数: 0
Interrelations of Situational Vertigo, Smartphone Use, Sleep Duration, and Headache Among College Students: A Cross-Sectional Study. 大学生情境性眩晕、智能手机使用、睡眠时间和头痛的相互关系:一项横断面研究
IF 1.2 4区 医学 Q3 AUDIOLOGY & SPEECH-LANGUAGE PATHOLOGY Pub Date : 2025-01-01 Epub Date: 2025-02-27 DOI: 10.3766/jaaa.240075
Murad Al-Momani

Objective: This study aimed to investigate the relationships between situational vertigo, smartphone use, sleep duration, and headaches among college students. Methods: A cross-sectional, descriptive correlational design and survey methodology were used. A total of approximately 55,000 students from three public and three private universities were considered for participation. A nonproportional stratified sampling method was used to target a sample size of 395 students per university. Data were collected using the Situational Vertigo Questionnaire (SVQ), which includes questions about sociodemographic factors, smoking habits, electronics usage, working hours, housekeeping activities, sleep duration, and headaches. The SVQ was translated to Arabic and validated. The statistical analysis included descriptive statistics, linear regression, and Pearson's correlation coefficient. Results: This study included 1,600 participants with a mean age of 26.58 years. Significant correlations between the SVQ score and older age, female sex, and smoking were found. The strongest correlation was between the SVQ score and sleep duration (r = -0.84), indicating that a shorter sleep duration is associated with a higher incidence of situational vertigo. Smartphone use was positively correlated with the SVQ score (r = 0.67) and negatively correlated with sleep duration (r = -0.74). Additionally, headaches were associated with higher SVQ scores (r = 0.24). Conclusion: We identified significant associations between situational vertigo and smartphone use, sleep duration, and headaches among college students. Female sex, older age, and smoking were also associated with higher susceptibility to vertigo. These findings suggest that excessive smartphone use may lead to sleep disturbances, which contribute to vertigo. Increased awareness of these relationships can inform the development of preventive measures and counseling strategies for students on college campuses and aid health care providers in managing patients with vertigo.

目的:探讨大学生情境性眩晕、智能手机使用、睡眠时间与头痛的关系。方法:采用横断面、描述性相关设计和调查方法。共有来自三所公立大学和三所私立大学的大约55 000名学生被考虑参加。采用非比例分层抽样方法,每所大学的样本规模为395名学生。数据是通过情景性眩晕问卷(SVQ)收集的,其中包括有关社会人口因素、吸烟习惯、电子产品使用、工作时间、家务活动、睡眠时间和头痛的问题。将SVQ翻译成阿拉伯语并进行验证。统计分析包括描述性统计、线性回归和Pearson相关系数。结果:这项研究包括1600名参与者,平均年龄26.58岁。SVQ得分与年龄、女性性别和吸烟之间存在显著相关性。SVQ评分与睡眠持续时间之间的相关性最强(r = -0.84),表明较短的睡眠持续时间与较高的情境性眩晕发生率相关。智能手机的使用与SVQ得分呈正相关(r = 0.67),与睡眠时间呈负相关(r = -0.74)。此外,头痛与较高的SVQ评分相关(r = 0.24)。结论:我们确定了大学生情境性眩晕与智能手机使用、睡眠时间和头痛之间的显著关联。女性、年龄较大和吸烟也与眩晕的易感性相关。这些发现表明,过度使用智能手机可能会导致睡眠障碍,从而导致眩晕。提高对这些关系的认识可以为大学校园学生提供预防措施和咨询策略的发展,并帮助卫生保健提供者管理眩晕患者。
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引用次数: 0
Usability and Performance of Self-Fitting Over-the-Counter Hearing Aids. 自配非处方助听器的可用性和性能。
IF 1.2 4区 医学 Q3 AUDIOLOGY & SPEECH-LANGUAGE PATHOLOGY Pub Date : 2025-01-01 Epub Date: 2025-02-03 DOI: 10.3766/jaaa.240037
Megan Knoetze, Vinaya Manchaiah, De Wet Swanepoel

Purpose: Over-the-counter (OTC) hearing aids can potentially improve access to hearing-health care and enable individuals with mild-to-moderate hearing loss to self-manage their condition. This study compared the usability and performance of a range of self-fitting over-the-counter (OTC-SF) hearing aids. Research Design: This cross-sectional study evaluated six OTC-SF hearing aids. Study Sample: Forty-three adults with self-perceived mild-to-moderate hearing difficulties participated in this study. Data Collection and Analysis: Participants were randomly assigned to two of six OTC-SF hearing aids and used the manufacturer-provided instructions and smartphone applications. These hearing aids included HP Hearing PRO, Jabra Enhance Plus, Lexie B2 Powered by Bose, Lexie Lumen, Soundwave Sontro, and Sony CRE-C10. Usability was assessed based on the fitting time, hearing aid skills and knowledge (HASK), self-reported ease of the SF process, and Post-Study System Usability Questionnaire (PSSUQ) results. Performance was evaluated using the judgment of sound quality (JSQ) test and speech-in-noise benefit using the digits-in-noise and quick speech-in-noise tests. Results: Fitting time ranged from 14.4 to 27.1 min, with Lexie Lumen requiring the longest time (27.1 min; standard deviation [SD], 5.9 min) and HP Hearing PRO requiring the shortest time (14.4 min; SD = 1.9 min). The HASK scores varied, with Soundwave Sontro achieving the highest score (8.9/10) and HP Hearing PRO achieving the lowest score (6.8/10). Self-reported ease of SF and PSSUQ scores did not differ significantly between the OTC-SF hearing aids. Overall sound quality and clarity ratings significantly differed, with Lexie B2 receiving the highest rating (8.1/10 and 7.5/10) and HP Hearing PRO receiving the lowest rating (6.3/10 and 5.1/10). Speech-in-noise benefit did not differ significantly between devices. A thematic analysis identified seven themes of the participants' SF experiences and six themes of the researcher's field notes. Participants generally considered OTC-SF hearing aids user-friendly, although issues with Bluetooth connectivity, handling and insertion, and sound quality were noted by the researcher as common challenges. Conclusions: Usability and performance of OTC-SF hearing aids were similar across devices in terms of usability and speech-in-noise benefits. However, the devices exhibited variations in fitting time, HASK, and sound quality, including the overall impression and clarity. These findings can support the decisions of consumers and recommendations of health-care professionals. Further research of the long-term usability and selection processes of OTC-SF hearing aids is necessary.

目的:非处方(OTC)助听器可以潜在地改善获得听力保健的机会,并使轻度至中度听力损失的个人能够自我管理他们的状况。本研究比较了一系列自配非处方助听器(OTC-SF)的可用性和性能。研究设计:本横断面研究评估了6种OTC-SF助听器。研究样本:43名自认为有轻度至中度听力障碍的成年人参加了这项研究。数据收集和分析:参与者被随机分配到六种OTC-SF助听器中的两种,并使用制造商提供的说明和智能手机应用程序。这些助听器包括HP Hearing PRO, Jabra Enhance Plus, Bose驱动的Lexie B2, Lexie Lumen,声波Sontro和索尼CRE-C10。可用性评估基于拟合时间、助听器技能和知识(HASK)、SF过程的自我报告易用性和研究后系统可用性问卷(PSSUQ)结果。使用音质判断(JSQ)测试对性能进行评估,使用数字噪声和快速语音噪声测试对语音噪声效益进行评估。结果:拟合时间14.4 ~ 27.1 min,其中Lexie Lumen拟合时间最长(27.1 min,标准差[SD]为5.9 min), HP Hearing PRO拟合时间最短(14.4 min;SD = 1.9 min)。HASK得分各不相同,声波Sontro得分最高(8.9/10),惠普听力PRO得分最低(6.8/10)。自我报告的SF和PSSUQ评分在OTC-SF助听器之间没有显着差异。整体音质和清晰度评分差异显著,Lexie B2的评分最高(8.1/10和7.5/10),HP Hearing pro的评分最低(6.3/10和5.1/10)。不同设备的噪音语音效果没有显著差异。主题分析确定了参与者SF体验的七个主题和研究人员实地笔记的六个主题。参与者普遍认为OTC-SF助听器对用户友好,尽管研究人员指出蓝牙连接、处理和插入以及音质等问题是常见的挑战。结论:OTC-SF助听器的可用性和性能在不同设备的可用性和噪音语音效益方面是相似的。然而,这些设备在装配时间、HASK和声音质量(包括整体印象和清晰度)方面表现出差异。这些发现可以支持消费者的决定和卫生保健专业人员的建议。对OTC-SF助听器的长期可用性和选择过程进行进一步的研究是必要的。
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引用次数: 0
Evaluation of Otolithic Function in Patients with Unilateral Ménière's Disease Using Video Ocular Counter-Roll Test. 用视像眼反滚试验评价单侧mims患者耳石功能。
IF 1.2 4区 医学 Q3 AUDIOLOGY & SPEECH-LANGUAGE PATHOLOGY Pub Date : 2025-01-01 DOI: 10.3766/jaaa.240005
Başak Mutlu, Aleyna Nimet Gökay, İbrahim Esad Güyen, Muhammet Sade, Mahmut Tayyar Kalcıoğlu

Background: There is a need for more laboratory tests in the diagnosis of Ménière's disease (MD). Purpose: The adequacy of the findings of the video ocular counter-roll reflex (OCR) test to support the diagnosis of patients with unilateral MD in the nonattack period was investigated. Research Design: Hearing tests, ocular and cervical vestibular evoked myogenic potential (VEMP), Dizziness Handicap Inventory, and video OCR tests were performed on 31 patients with unilateral MD and 30 healthy controls, and the findings were compared. Study Sample: There were 10 males and 21 females (51.22 ± 12.76 years) in the MD group and 12 males and 18 females (46.43 ± 9.98) in the control group. Data Collection and Analysis: The significance of the difference between groups was analyzed using the Mann-Whitney U test for continuous data and the chi-squared test for categorical data. OCR degrees in the MD group were analyzed using the Wilcoxon test. A correlation matrix and intraclass correlation coefficients were also calculated to analyze the test-retest reliability of OCR degrees with the participant's head tilted at 15, 30, and 40°. Results: In the ocular VEMP test, the N1-P1 amplitudes of both ipsilesional (p < 0.001) and contralesional ears (p = 0.015) were significantly lower in the MD group than in the control group. In the cervical VEMP test, the P1-N1 amplitudes of the ipsilesional (p < 0.001) and the contralesional sides (p = 0.006) were significantly lower in the MD group than in the control group. The OCR degrees did not show a significant difference between the MD and control groups, except for the 30th-second OCR degree of the right eye when the head was tilted 30° to the ipsilesional side (p = 0.031) and the 20th-second OCR degree of the right eye when the head was tilted 40° to the ipsilesional side (p = 0.036). Conclusions: The video OCR (vOCR) test did not discriminate between the pathological and nonpathological ears in patients with unilateral MD during a nonattack period. Furthermore, the vOCR results did not discriminate between the patients with unilateral MD and the healthy controls. To obtain consistent vOCR degrees a head tilt of at least 30° and a recording time of at least 40 seconds may be required.

背景:需要更多的实验室检查来诊断msamimni病(MD)。目的:探讨视频眼反滚反射(OCR)检查结果在单侧MD非发作期诊断的充分性。研究设计:对31例单侧MD患者和30例健康对照者进行听力测试、眼和颈前庭诱发肌电位(VEMP)、头晕障碍量表和视频OCR测试,并对结果进行比较。研究样本:MD组男性10例,女性21例(51.22±12.76岁);对照组男性12例,女性18例(46.43±9.98岁)。资料收集与分析:连续资料采用Mann-Whitney U检验,分类资料采用卡方检验,对组间差异的显著性进行分析。采用Wilcoxon检验分析MD组OCR程度。计算相关矩阵和类内相关系数,分析被试头部倾斜15°、30°和40°时OCR度的重测信度。结果:在眼部VEMP测试中,MD组同侧耳(p < 0.001)和对侧耳(p = 0.015)的N1-P1波幅均显著低于对照组。在颈部VEMP试验中,MD组同侧(p < 0.001)和对侧(p = 0.006)的P1-N1波幅均显著低于对照组。除头部向同侧倾斜30°时右眼第30秒OCR度(p = 0.031)和头部向同侧倾斜40°时右眼第20秒OCR度(p = 0.036)外,MD组与对照组之间OCR度无显著差异。结论:视频OCR (vOCR)测试对单侧MD患者非发作期的病理性和非病理性耳无明显区别。此外,vOCR结果在单侧MD患者和健康对照组之间没有区别。为了获得一致的vOCR度,可能需要至少30°的头部倾斜和至少40秒的记录时间。
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引用次数: 0
Pendular Nystagmus Presenting in Usher Syndrome Type I: A Case Report. 病例报告:乌谢尔综合征 I 型中出现的眼球震颤。
IF 1 4区 医学 Q3 AUDIOLOGY & SPEECH-LANGUAGE PATHOLOGY Pub Date : 2024-10-01 Epub Date: 2024-05-02 DOI: 10.1055/a-2318-1389
Jamie M Bogle, David A Zapala

Background:  We describe a 42-year-old patient with reported "shaking" vision referred due to concerns of possible vestibular system dysfunction. The patient has known history of Usher syndrome type I, bilateral cochlear implants, and severe vision impairment.

Purpose:  This case describes an unusual nystagmus previously only reported in individuals with central demyelinating disorders, significant light deprivation, or in congenital/early-onset visual pathway impairment.

Research design:  Case study.

Data collection and analysis:  Retrospective chart review of vestibular function.

Results:  Vestibular function was likely absent in this case. There was no evidence of vestibular (jerk) nystagmus for sinusoidal harmonic acceleration stimuli or repeatable responses for cervical vestibular evoked myogenic potentials. Significant pendular low-amplitude high-frequency oscillations of approximately 6 Hz were present for horizontal and vertical tracings throughout testing.

Conclusion:  Nystagmus may not always be associated with vestibular system impairment. In this case, the patient's reported "shaking" vision was attributed to pendular low-amplitude high-frequency nystagmus and hypothesized to relate to long-standing significant vision impairment. This presentation is unusual in adults and has historically been associated with individuals with significant central pathology or in those with long duration light deprivation.

背景:我们描述了一名 42 岁的患者,据报告其视力 "颤抖",因担心可能存在前庭系统功能障碍而转诊。目的:本病例描述了一种不寻常的眼球震颤,以前只有在患有中枢性脱髓鞘疾病、严重光剥夺或先天性/早发性视觉通路损伤的患者中才有报道:病例研究:数据收集与分析:前庭功能回顾性病历:该病例可能缺乏前庭功能。正弦谐波加速度刺激没有前庭(抽搐)眼震的证据,颈前庭诱发肌源性电位也没有可重复的反应。在整个测试过程中,水平和垂直描记均出现明显的下垂低幅高频振荡,频率约为 6 赫兹:结论:眼震不一定总是与前庭系统受损有关。在本病例中,患者报告的 "晃动 "视力归因于下垂性低振幅高频眼震,并推测与长期严重的视力损伤有关。这种表现在成人中并不常见,历来与中枢病变或长期光照不足有关。
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引用次数: 0
Development and Standardization of Modified Simultaneous Multifrequency Stimulus for Recording Ocular Vestibular-Evoked Myogenic Potential and Its Interaction with the Alternate Electrode Montages. 用于记录 oVEMP 的改良同步多频 (SiMFy) 刺激及其与替代电极蒙太奇的交互作用的开发和标准化。
IF 1 4区 医学 Q3 AUDIOLOGY & SPEECH-LANGUAGE PATHOLOGY Pub Date : 2024-10-01 Epub Date: 2024-06-26 DOI: 10.1055/a-2353-2797
Rajesh Kumar Raveendran, Niraj Kumar Singh

Background:  Simultaneous multifrequency (SiMFy) is a time-saving and reliable stimulus to determine the frequency tuning of ocular vestibular-evoked myogenic potential (oVEMP); however, the absence of 4000 Hz in SiMFy potentially makes it a less potent tool for the diagnosis of superior semicircular canal dehiscence, a pathology with an ever-increasing prevalence. Further, SiMFy was validated using only the infraorbital (IO) electrode montage. However, the recordings obtained using the IO montage might be susceptible to reference contamination introduced by a small separation between the recording electrodes and also susceptible to reflex impurity due to the spatially displaced reference electrode from the inferior oblique muscle, rendering it vulnerable to picking up responses from other muscles. Nonetheless, little is known about the similarities/differences between the SiMFy-induced oVEMPs using alternate montages (belly-tendon [BT], chin-reference [CR], and sternum-reference [SR]) and the nonsimultaneous multifrequency oVEMPs (NSM-oVEMPs) using the IO montage.

Purpose of the study:  To develop a modified SiMFy stimulus and investigate its effects on frequency tuning of oVEMP using various electrode montages.

Research design:  Within-subject experimental design.

Study sample:  Thirty-three healthy adults aged 20 to 30 years.

Data collection and analysis:  Tone bursts of octave and mid-octave frequencies from 250 to 4000 Hz were generated and concatenated to create the modified SiMFy stimulus. All participants underwent NSM oVEMPs and modified SiMFy oVEMPs using BT, CR, SR, and IO montages simultaneously. The response rate, peak-to-peak amplitude, and frequency tuning were compared between NSM-oVEMP and modified SiMFy oVEMP and also between the electrode montages.

Results:  BT montage recorded the largest amplitude among the montages in NSM stimulation and modified SiMFy stimulation. Although the response rates were comparable, the modified SiMFy produced significantly lower oVEMP amplitudes than the NSM stimulation within each electrode montage (p < 0.05). A moderate-to-strong agreement on frequency tuning existed between the NSM stimuli and modified SiMFy stimulus for all the montages, except for the SR montage.

Conclusions:  Although the modified SiMFy produces smaller amplitude oVEMPs than the NSM stimulation for the respective montages, its use in combination with the BT montage yields higher response rates and larger peak-to-peak amplitudes than the NSM recording using IO montage.

背景:同步多频(SiMFy)是确定眼前庭诱发肌源性电位(oVEMP)频率调谐的一种省时、可靠的刺激方法;然而,由于 SiMFy 中没有 4000 Hz 频率,可能会使其在诊断上半规管开裂(一种发病率日益增高的病理现象)时不那么有效。此外,SiMFy 仅使用眶下(IO)电极蒙太奇进行验证。然而,由于记录电极之间的间距较小,使用 IO 电极单体获得的记录可能会受到参考污染的影响,而且由于下斜肌(IOM)的参考电极在空间上发生位移,还可能会受到反射杂质的影响,使其容易接收到其他肌肉的反应。然而,人们对使用交替蒙太奇[腹腱(BT)、下巴参照(CR)和胸骨参照(SR)]的 SiMFy 诱导的 oVEMP 与使用 IO 蒙太奇的非同步多频 oVEMP(NSM-oVEMP)之间的相似性/差异性知之甚少:开发改良的 SiMFy 刺激,并研究其对使用各种电极蒙太奇的 oVEMP 频率调谐的影响:研究样本:研究样本:33 名 20-30 岁的健康成年人:数据收集和分析:产生倍频程和中倍频程频率从 250 Hz 到 4000 Hz 的音爆,并将其连接起来,以创建改进的 SiMFy 刺激。所有参与者同时接受非同步多频 oVEMPs 和使用 BT、CR、SR 和 IO 蒙太奇的改良 SiMFy oVEMPs。对 NSM-oVEMP 和改良 SiMFy oVEMP 以及不同电极单体之间的反应率、峰-峰振幅和频率调谐进行了比较:结果:在非同步多频刺激和改良 SiMFy 刺激中,BT 单体记录的振幅最大。虽然反应率相当,但在每个电极蒙太奇中,改良 SiMFy 产生的 oVEMP 振幅明显低于非同时多频刺激(p < 0.05)。除 SR 蒙太奇外,在所有蒙太奇中,非同时多频刺激和改良 SiMFy 刺激在频率调谐方面存在中等至较强的一致性:结论:虽然改良 SiMFy 与非同时多频刺激相比,在各自的蒙太奇中产生的 oVEMPs 振幅较小,但与使用 IO 蒙太奇的非同时多频记录相比,改良 SiMFy 与 BT 蒙太奇结合使用可产生更高的反应率和更大的峰-峰振幅。
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引用次数: 0
Evaluating the Clinical Reliability and Reference Values of the International Outcome Inventory for Cochlear Implants in the Department of Defense Population. 评估国际人工耳蜗植入成果量表在国防部人群中的临床可靠性和参考值。
IF 1 4区 医学 Q3 AUDIOLOGY & SPEECH-LANGUAGE PATHOLOGY Pub Date : 2024-10-01 Epub Date: 2024-07-18 DOI: 10.1055/a-2368-9008
Alyssa Davidson, Amy Boudin-George, Elicia Pillion, Nicole Larionova

Background:  Hearing loss significantly affects an individual's well-being, communication, social interaction, and quality of life. Cochlear implants serve as a viable management option. Given the variability in the impact of impairment, self-report measures are crucial for evaluating the perceived benefits of management options.

Purpose:  The study aims to assess the reliability of the International Outcome Inventory for Cochlear Implants (IOI-CI) and establish evaluative cutoffs. This questionnaire evaluates patient's satisfaction with cochlear implants and contributes to the understanding of their experiences, addressing the increasing interest among cochlear implant clinicians.

Research design:  The design relies on electronic medical databases within the Veterans Affairs and Department of Defense systems. After identification of eligibility, recruitment was based on participants responding to mailed study documents. This research adopts a descriptive approach of the analysis of questionnaire responses as well as quantitatively evaluating the reliability.

Study sample:  Forty-nine service members, Veterans, and their dependents, including 32 men and 17 women, participated in the study. The participants had a mean age of 68.0 years, with cochlear implants ranging from 6 months to 2 years postinitial stimulation. The majority had a unilateral cochlear implant with a hearing aid on the contralateral ear.

Data collection and analysis:  Data collected involved mailing baseline study packets, including the IOI-CI questionnaire, to potential participants identified through medical databases. Participants indicated consent by returning the study packet. Follow-up packets were sent at a later time. Intraclass correlation coefficients were utilized for test-retest reliability and generalized linear models (GLM) for exploring the impact of clinical and demographic factors. Data were analyzed using R.

Results:  The ICC revealed a good level of agreement (ICC = 0.84) between baseline and follow-up assessments for the IOI-CI total score. The GLM did not identify significant factors influencing IOI-CI scores. Evaluative values were established, indicating total scores between 18 and 35 as within the range of general satisfaction with a cochlear implant for this questionnaire.

Conclusion:  The study contributes valuable insights into the reliability of the IOI-CI and establishes evaluative cutoffs, aiding clinicians in assessing cochlear implant users' experiences and satisfaction.

背景:听力损失严重影响个人的福祉、沟通、社交和生活质量。人工耳蜗是一种可行的治疗方法。目的:本研究旨在评估国际人工耳蜗植入成果量表(IOI-CI)的可靠性,并确定标准临界值。该问卷可评估患者对人工耳蜗植入的满意度,有助于了解他们的经历,解决人工耳蜗植入临床医生日益关注的问题:研究设计:该设计依赖于退伍军人事务部(VA)和国防部(DOD)系统内的电子医疗数据库。在确定资格后,根据参与者对邮寄的研究文件的回复进行招募。本研究采用描述性方法对问卷答复进行分析,并对可靠性进行定量评估:49名现役军人、退伍军人及其家属(包括32名男性和17名女性)参加了研究。参与者的平均年龄为 68.0 岁,植入人工耳蜗的时间从首次刺激后 6 个月到 2 年不等。大多数人植入了单侧人工耳蜗,对侧耳朵佩戴了助听器:数据收集工作包括向通过医疗数据库确定的潜在参与者邮寄基线研究资料包,其中包括 IOI-CI 问卷。参与者通过寄回研究资料包表示同意。后续数据包将在晚些时候寄出。利用类内相关系数(ICC)来检验重复测试的可靠性,利用广义线性模型(GLM)来探讨临床和人口统计因素的影响。数据使用 R 进行分析:ICC显示,IOI-CI总分的基线评估和随访评估之间具有良好的一致性(ICC=0.84)。GLM没有发现影响IOI-CI得分的重要因素。正常值已经确定,表明总分在 18 分至 35 分之间属于该问卷的正常范围:本研究为 IOI-CI 的可靠性提供了有价值的见解,并确定了标准临界值,有助于临床医生评估人工耳蜗用户的体验和满意度。
{"title":"Evaluating the Clinical Reliability and Reference Values of the International Outcome Inventory for Cochlear Implants in the Department of Defense Population.","authors":"Alyssa Davidson, Amy Boudin-George, Elicia Pillion, Nicole Larionova","doi":"10.1055/a-2368-9008","DOIUrl":"10.1055/a-2368-9008","url":null,"abstract":"<p><strong>Background: </strong> Hearing loss significantly affects an individual's well-being, communication, social interaction, and quality of life. Cochlear implants serve as a viable management option. Given the variability in the impact of impairment, self-report measures are crucial for evaluating the perceived benefits of management options.</p><p><strong>Purpose: </strong> The study aims to assess the reliability of the International Outcome Inventory for Cochlear Implants (IOI-CI) and establish evaluative cutoffs. This questionnaire evaluates patient's satisfaction with cochlear implants and contributes to the understanding of their experiences, addressing the increasing interest among cochlear implant clinicians.</p><p><strong>Research design: </strong> The design relies on electronic medical databases within the Veterans Affairs and Department of Defense systems. After identification of eligibility, recruitment was based on participants responding to mailed study documents. This research adopts a descriptive approach of the analysis of questionnaire responses as well as quantitatively evaluating the reliability.</p><p><strong>Study sample: </strong> Forty-nine service members, Veterans, and their dependents, including 32 men and 17 women, participated in the study. The participants had a mean age of 68.0 years, with cochlear implants ranging from 6 months to 2 years postinitial stimulation. The majority had a unilateral cochlear implant with a hearing aid on the contralateral ear.</p><p><strong>Data collection and analysis: </strong> Data collected involved mailing baseline study packets, including the IOI-CI questionnaire, to potential participants identified through medical databases. Participants indicated consent by returning the study packet. Follow-up packets were sent at a later time. Intraclass correlation coefficients were utilized for test-retest reliability and generalized linear models (GLM) for exploring the impact of clinical and demographic factors. Data were analyzed using R.</p><p><strong>Results: </strong> The ICC revealed a good level of agreement (ICC = 0.84) between baseline and follow-up assessments for the IOI-CI total score. The GLM did not identify significant factors influencing IOI-CI scores. Evaluative values were established, indicating total scores between 18 and 35 as within the range of general satisfaction with a cochlear implant for this questionnaire.</p><p><strong>Conclusion: </strong> The study contributes valuable insights into the reliability of the IOI-CI and establishes evaluative cutoffs, aiding clinicians in assessing cochlear implant users' experiences and satisfaction.</p>","PeriodicalId":50021,"journal":{"name":"Journal of the American Academy of Audiology","volume":" ","pages":"256-262"},"PeriodicalIF":1.0,"publicationDate":"2024-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141724862","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
JAAA CEU Program.
IF 1 4区 医学 Q3 AUDIOLOGY & SPEECH-LANGUAGE PATHOLOGY Pub Date : 2024-10-01 Epub Date: 2025-01-07 DOI: 10.1055/s-0045-1801839
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引用次数: 0
Quality and Readability of Hearing Aid-Related Websites in English and Spanish. 英语和西班牙语助听器相关网站的质量和可读性。
IF 1 4区 医学 Q3 AUDIOLOGY & SPEECH-LANGUAGE PATHOLOGY Pub Date : 2024-10-01 Epub Date: 2024-12-18 DOI: 10.1055/s-0044-1791215
Abbigayle Willgruber, Brian Kinealy, David Adkins, Marissa Schuh, Jennifer B Shinn, Trey A Cline, Ryleigh Board, Zain Hassan, Matthew Bush

Objective:  To determine the readability and quality of both English and Spanish Web sites for the topic of hearing aids.

Study design:  Cross-sectional Web site analysis.

Setting:  Various online search engines.

Methods:  The term "hearing aid" was queried across four popular search engines. The first resulted 75 English Web sites and first resulted 75 Spanish Web sites were extracted for data collection. Web sites that met the inclusion criteria were stratified by the presence of a Health on the Net Code (HONCode) certificate. Articles were then compiled to be independently reviewed by experts on hearing aids, using the DISCERN criteria, which allowed assessment of the quality of the Web sites. Readability was assessed by calculating the Flesch Reading Ease Score in English and the Fernandez Huerta Formula in Spanish. Readability and quality were both analyzed, comparing scores to their respective language and cross-comparing.

Results:  There were 37 English Web sites and 30 Spanish Web sites that met inclusion criteria. When analyzing readability, English Web sites were determined to be significantly more difficult to read (average = 55.37, standard deviation [SD] = 7.73, 95% confidence interval [CI] = 52.9-57.9) than the Spanish Web site counterparts (average = 58.64, SD = 5.26, 95% CI = 56.8-60.5, p = 0.035). For quality, Spanish Web sites (average = 38, SD = 9.7, 95% CI = 34.5-41.5) were determined to be of significantly higher quality than English Web sites (average = 32.16, SD = 10.60, 95% CI = 29.7-34.6). Additionally, there was a significant difference between the non-HONCode English Web sites versus the non-HONCode Spanish Web sites (p = 0.0081), signifying that Spanish non-HONCode certified Web sites were less reliable than non-HONCode certified English Web sites.

Discussion:  The present study highlights the importance and necessity of providing quality, readable materials to patients seeking information regarding hearing aids. This study shows that both English and Spanish Web sites are written at a level that is much higher than the American Medical Association (AMA)-recommended sixth-grade reading level, and no Web site included in this study fell at or below the AMA-recommended sixth-grade reading level. English and Spanish Web sites also lacked consistency and quality, as evidenced by their wide variability in DISCERN scores. Specifically, Hispanic patients are more likely to suffer long-term consequences of their health care due to low levels of health literacy. It is important to bridge this gap by providing adequate reading materials. It is especially important to provide evidence-based claims that are directly supported by experts in the field.

目的:确定英语和西班牙语助听器主题网站的可读性和质量。研究设计:横断面网站分析。设置:各种在线搜索引擎。方法:在四个流行的搜索引擎上查询“助听器”一词。第一个结果是75个英文网站,第一个结果是75个西班牙语网站,用于数据收集。符合纳入标准的网站根据是否存在网络健康代码(HONCode)证书进行分层。然后,文章被整理出来,由助听器专家使用DISCERN标准进行独立审查,该标准允许对网站的质量进行评估。通过计算英语的Flesch阅读简易分数和西班牙语的Fernandez Huerta公式来评估可读性。对可读性和质量进行分析,将得分与各自的语言进行比较,并进行交叉比较。结果:符合纳入标准的英文网站37个,西班牙语网站30个。在分析可读性时,英语网站的阅读难度明显高于西班牙语网站(平均= 55.37,标准差[SD] = 7.73, 95%可信区间[CI] = 52.9-57.9)(平均= 58.64,SD = 5.26, 95% CI = 56.8-60.5, p = 0.035)。在质量方面,西班牙语网站(平均= 38,SD = 9.7, 95% CI = 34.5-41.5)的质量明显高于英语网站(平均= 32.16,SD = 10.60, 95% CI = 29.7-34.6)。此外,非honcode英语网站与非honcode西班牙语网站之间存在显著差异(p = 0.0081),这表明西班牙语非honcode认证的网站比非honcode认证的英语网站更不可靠。讨论:本研究强调了为寻求助听器信息的患者提供高质量、可读材料的重要性和必要性。这项研究表明,英语和西班牙语网站的写作水平都远远高于美国医学协会(AMA)推荐的六年级阅读水平,而且本研究中没有一个网站达到或低于AMA推荐的六年级阅读水平。英语和西班牙语网站也缺乏一致性和质量,这可以从它们在DISCERN分数上的巨大差异中看出。具体而言,由于卫生知识水平低,西班牙裔患者更有可能遭受医疗保健的长期后果。通过提供足够的阅读材料来弥合这种差距是很重要的。尤其重要的是提供有证据支持的声明,并得到该领域专家的直接支持。
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引用次数: 0
A Pilot Dashboard System to Track Cumulative Exposure to Sound Levels during Music Instruction: A Technical Report. 在音乐教学过程中跟踪累积暴露于声级的试点仪表板系统:一份技术报告。
IF 1 4区 医学 Q3 AUDIOLOGY & SPEECH-LANGUAGE PATHOLOGY Pub Date : 2024-10-01 Epub Date: 2024-12-19 DOI: 10.1055/s-0044-1791210
Akansha Goel, Eeshan Joshi, Ted Kwee-Bintoro, Kamakshi V Gopal, Kris Chesky, Sara Champlin, Mark V Albert

Background:  Music-induced hearing loss (MIHL) is a critical public health issue. During music instruction, students and teachers are at risk of developing hearing loss due to exposure to loud and unsafe sound levels that can exceed 100 dBA. Prevention of MIHL in music students must be a desired action of all music educators.

Purpose:  To promote deliberate changes in music instruction and encourage more moderate sound creation and exposure during music education, it is essential to equip the instructors with live dynamic tools to monitor the overall sound intensities during music instruction. Equally important data to convey to the instructors are information regarding the intensity and duration of sounds at specific frequency regions in the music they are generating. Unfortunately, there are no feasible techniques to track cumulative live music exposures at various frequencies nor are there any guidelines for safe music exposure.

Research design:  We created a visually appealing, user-friendly dashboard prototype system to display the accumulated time and intensity of sound exposure during live classes/rehearsals categorized into three frequency ranges. These visuals can be easily understood at a glance allowing musicians and instructors to make informed decisions about how to play music safely.

Experimental approach and results:  The dashboard included a collection of circular dial graphs that displayed in real time the accumulated sound exposure in the instructor's selected frequency range and showed the percentage of the maximum daily sound exposure based on the National Institute for Occupational Safety and Health Standards (NIOSH, 1998). Although NIOSH standards are not widely applied for music exposure, we propose that these standards can be used to provide initial guidelines to develop critical levels of music exposure. Additionally, the dashboard included a color-coded equalizer that displayed the instantaneous frequency distribution of sounds to indicate if sound levels at specific frequencies were too high even for short-term exposure.

Conclusion:  Less expensive than existing technology and more convenient to use, this dashboard will enable music instructors to make informed decisions on how to best adapt their teaching approaches to protect the hearing health of their students.

背景:音乐诱发性听力损失(MIHL)是一个重要的公共卫生问题。在音乐教学过程中,由于暴露在超过100 dBA的大声和不安全的声音中,学生和教师都有听力损失的风险。预防音乐学生的MIHL必须成为所有音乐教育者的一项理想行动。目的:为了促进音乐教学中有意识的变化,鼓励在音乐教育中更适度的声音创造和暴露,有必要为教师配备实时动态工具来监测音乐教学过程中的整体声强。向教师传达的同样重要的数据是关于他们所产生的音乐中特定频率区域的声音强度和持续时间的信息。不幸的是,目前还没有可行的技术来追踪不同频率的现场音乐暴露,也没有任何安全音乐暴露的指导方针。研究设计:我们创建了一个视觉上吸引人的,用户友好的仪表板原型系统,以显示现场课程/排练中声音暴露的累积时间和强度,分为三个频率范围。这些视觉效果很容易理解,让音乐家和教师做出明智的决定,如何安全地播放音乐。实验方法和结果:仪表板包括一组圆形刻度图,实时显示教师所选频率范围内累积的声音暴露,并显示基于国家职业安全与健康标准研究所(NIOSH, 1998)的最大每日声音暴露的百分比。虽然NIOSH标准并未广泛应用于音乐暴露,但我们建议这些标准可用于为制定音乐暴露的临界水平提供初步指导。此外,仪表板上还有一个颜色编码的均衡器,可以显示声音的瞬时频率分布,以指示特定频率的声音水平是否过高,即使是短期暴露。结论:比现有技术更便宜,使用更方便,这个仪表盘将使音乐教师能够做出明智的决定,如何最好地调整他们的教学方法,以保护学生的听力健康。
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引用次数: 0
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Journal of the American Academy of Audiology
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