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为耳鸣合并听力损失患者使用助听器进行放大。

Amplification with hearing aids for patients with tinnitus and co-existing hearing loss.

作者信息

Hoare Derek J, Edmondson-Jones Mark, Sereda Magdalena, Akeroyd Michael A, Hall Deborah

机构信息

National Institute for Health Research (NIHR) Nottingham Hearing Biomedical Research Unit, University of Nottingham, Ropewalk House, 113 The Ropewalk, Nottingham, UK, NG1 5DU.

出版信息

Cochrane Database Syst Rev. 2014 Jan 31;2014(1):CD010151. doi: 10.1002/14651858.CD010151.pub2.

Abstract

BACKGROUND

Tinnitus is described as the perception of sound or noise in the absence of real acoustic stimulation. In the current absence of a cure for tinnitus, clinical management typically focuses on reducing the effects of co-morbid symptoms such as distress or hearing loss. Hearing loss is commonly co-morbid with tinnitus and so logic implies that amplification of external sounds by hearing aids will reduce perception of the tinnitus sound and the distress associated with it.

OBJECTIVES

To assess the effects of hearing aids specifically in terms of tinnitus benefit in patients with tinnitus and co-existing hearing loss.

SEARCH METHODS

We searched the Cochrane Ear, Nose and Throat Disorders Group Trials Register; the Cochrane Central Register of Controlled Trials (CENTRAL); PubMed; EMBASE; CINAHL; Web of Science; Cambridge Scientific Abstracts; ICTRP and additional sources for published and unpublished trials. The date of the search was 19 August 2013.

SELECTION CRITERIA

Randomised controlled trials and non-randomised controlled trials recruiting adults with subjective tinnitus and some degree of hearing loss, where the intervention involves amplification with hearing aids and this is compared to interventions involving other medical devices, other forms of standard or complementary therapy, or combinations of therapies, no intervention or placebo interventions.

DATA COLLECTION AND ANALYSIS

Three authors independently screened all selected abstracts. Two authors independently extracted data and assessed those potentially suitable studies for risk of bias. For studies meeting the inclusion criteria, we used the mean difference (MD) to compare hearing aids with other interventions and controls.

MAIN RESULTS

One randomised controlled trial (91 participants) was included in this review. We judged the trial to have a low risk of bias for method of randomisation and outcome reporting, and an unclear risk of bias for other criteria. No non-randomised controlled trials meeting our inclusion criteria were identified. The included study measured change in tinnitus severity (primary measure of interest) using a tinnitus questionnaire measure, and change in tinnitus loudness (secondary measure of interest) on a visual analogue scale. Other secondary outcome measures of interest, namely change in the psychoacoustic characteristics of tinnitus, change in self reported anxiety, depression and quality of life, and change in neurophysiological measures, were not investigated in this study. The included study compared hearing aid use to sound generator use. The estimated effect on change in tinnitus loudness or severity as measured by the Tinnitus Handicap Inventory score was compatible with benefits for both hearing aids or sound generators but no difference was found between the two alternative treatments (MD -0.90, 95% confidence interval (CI) -7.92 to 6.12) (100-point scale); moderate quality evidence. No negative or adverse events were reported.

AUTHORS' CONCLUSIONS: The current evidence base for hearing aid prescription for tinnitus is limited. To be useful, future studies should make appropriate use of blinding and be consistent in their use of outcome measures. Whilst hearing aids are sometimes prescribed as part of tinnitus management, there is currently no evidence to support or refute their use as a more routine intervention for tinnitus.

摘要

背景

耳鸣被描述为在没有真实声学刺激的情况下对声音或噪声的感知。在目前尚无治愈耳鸣的方法的情况下,临床管理通常侧重于减轻诸如痛苦或听力损失等共病症状的影响。听力损失通常与耳鸣共存,因此从逻辑上讲,助听器放大外部声音会减少对耳鸣声音的感知以及与之相关的痛苦。

目的

专门评估助听器对伴有听力损失的耳鸣患者的耳鸣益处。

检索方法

我们检索了Cochrane耳鼻喉疾病组试验注册库;Cochrane对照试验中央注册库(CENTRAL);PubMed;EMBASE;CINAHL;科学引文索引;剑桥科学文摘;ICTRP以及其他已发表和未发表试验的来源。检索日期为2013年8月19日。

选择标准

招募有主观性耳鸣和一定程度听力损失的成年人的随机对照试验和非随机对照试验,其中干预措施包括使用助听器放大声音,并将其与涉及其他医疗设备、其他形式的标准或补充疗法或疗法组合、无干预或安慰剂干预的措施进行比较。

数据收集与分析

三位作者独立筛选所有选定的摘要。两位作者独立提取数据并评估那些可能合适的研究的偏倚风险。对于符合纳入标准的研究,我们使用平均差(MD)来比较助听器与其他干预措施和对照。

主要结果

本综述纳入了一项随机对照试验(91名参与者)。我们判断该试验在随机化方法和结果报告方面偏倚风险较低,在其他标准方面偏倚风险不明确。未识别出符合我们纳入标准的非随机对照试验。纳入的研究使用耳鸣问卷测量法测量耳鸣严重程度(主要关注指标)的变化,并使用视觉模拟量表测量耳鸣响度(次要关注指标)的变化。其他感兴趣的次要结局指标,即耳鸣心理声学特征的变化、自我报告的焦虑、抑郁和生活质量的变化以及神经生理学测量的变化,在本研究中未进行调查。纳入的研究将使用助听器与使用声音发生器进行了比较。通过耳鸣障碍量表评分测量的对耳鸣响度或严重程度变化的估计效应与助听器或声音发生器的益处相符,但两种替代治疗之间未发现差异(MD -0.90,95%置信区间(CI)-7.92至6.12)(100分制);中等质量证据。未报告负面或不良事件。

作者结论

目前关于耳鸣助听器处方的证据基础有限。为了有用,未来的研究应适当使用盲法,并在结局指标的使用上保持一致。虽然助听器有时作为耳鸣管理的一部分被处方,但目前没有证据支持或反驳将其作为耳鸣的更常规干预措施使用。

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