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经颅磁刺激治疗耳鸣:在一项随机对照试验中使用耳鸣功能指数预测疗效

Transcranial magnetic stimulation for tinnitus: using the Tinnitus Functional Index to predict benefit in a randomized controlled trial.

作者信息

Theodoroff Sarah M, Griest Susan E, Folmer Robert L

机构信息

VA RR&D, National Center for Rehabilitative Auditory Research, VA Portland Health Care System, 3710 SW US Veterans Hospital Road (NCRAR - P5), Portland, OR, 97239, USA.

Department of Otolaryngology, Head-Neck-Surgery, Oregon Health and Science University, 3181 SW Sam Jackson Park Road, Portland, OR, 97239, USA.

出版信息

Trials. 2017 Feb 9;18(1):64. doi: 10.1186/s13063-017-1807-9.

DOI:10.1186/s13063-017-1807-9
PMID:28183355
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5301432/
Abstract

BACKGROUND

Identifying characteristics associated with transcranial magnetic stimulation (TMS) benefit would offer insight as to why some individuals experience tinnitus relief following TMS treatment, whereas others do not. The purpose of this study was to use the Tinnitus Functional Index (TFI) and its subscales to identify specific factors associated with TMS treatment responsiveness.

METHODS

Individuals with bothersome tinnitus underwent 2000 pulses of 1-Hz TMS for 10 consecutive business days. The primary outcome measure was the TFI which yields a total score and eight individual subscale scores. Analyses were performed on baseline data from the active arm (n = 35) of a prospective, double-blind, randomized placebo-controlled clinical trial of TMS for tinnitus.

RESULTS

Baseline total TFI score and three of the eight TFI subscales were useful in differentiating between responders and nonresponders to TMS intervention for tinnitus. These findings are not definitive, but suggest potential factors that contribute to perceived benefit following TMS.

CONCLUSIONS

Overall, the main factor associated with TMS benefit was a higher tinnitus severity score for responders at baseline. The TFI subscales helped to clarify the factors that contributed to a higher severity score at baseline. Large-scale prospective research using systematic approaches is needed to identify and describe additional factors associated with tinnitus benefit following TMS.

TRIAL REGISTRATION

ClinicalTrials.gov, ID: NCT01104207 . Registered on 13 April 2010.

摘要

背景

确定与经颅磁刺激(TMS)疗效相关的特征,将有助于深入了解为何有些人在接受TMS治疗后耳鸣得到缓解,而另一些人却没有。本研究的目的是使用耳鸣功能指数(TFI)及其子量表来确定与TMS治疗反应性相关的特定因素。

方法

患有困扰性耳鸣的个体连续10个工作日接受2000次1赫兹的TMS脉冲治疗。主要结局指标是TFI,它会产生一个总分和八个单独的子量表分数。对一项关于TMS治疗耳鸣的前瞻性、双盲、随机安慰剂对照临床试验的活性组(n = 35)的基线数据进行分析。

结果

基线TFI总分以及八个TFI子量表中的三个,有助于区分对TMS耳鸣干预有反应者和无反应者。这些发现并不确定,但提示了TMS后产生感知疗效的潜在因素。

结论

总体而言,与TMS疗效相关的主要因素是有反应者在基线时耳鸣严重程度得分较高。TFI子量表有助于阐明导致基线时严重程度得分较高的因素。需要采用系统方法进行大规模前瞻性研究,以识别和描述与TMS后耳鸣疗效相关的其他因素。

试验注册

ClinicalTrials.gov,标识符:NCT01104207。于2010年4月13日注册。

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本文引用的文献

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JAMA Otolaryngol Head Neck Surg. 2015 Aug;141(8):716-22. doi: 10.1001/jamaoto.2015.1219.
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Tinnitus and hearing survey: a screening tool to differentiate bothersome tinnitus from hearing difficulties.耳鸣与听力调查:一种区分困扰性耳鸣与听力障碍的筛查工具。
Am J Audiol. 2015 Mar;24(1):66-77. doi: 10.1044/2014_AJA-14-0042.
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Experimental, controversial, and futuristic treatments for chronic tinnitus.
耳鸣随机对照试验的方法学方面:系统评价以及决策支持系统如何克服障碍
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针对慢性耳鸣的实验性、有争议性及未来主义的治疗方法。
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