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帕金森病构音障碍的言语和语言治疗技术比较

A comparison of speech and language therapy techniques for dysarthria in Parkinson's disease.

作者信息

Deane K H, Whurr R, Playford E D, Ben-Shlomo Y, Clarke C E

机构信息

Department of Neurology, City Hospital NHS Trust, Dudley Road, Birmingham, West Midlands, UK, B18 7QH.

出版信息

Cochrane Database Syst Rev. 2001(2):CD002814. doi: 10.1002/14651858.CD002814.

Abstract

BACKGROUND

Dysarthria is a common manifestation of Parkinson's disease that increases in frequency and intensity with the progress of the disease (Streifler 1984). Up to 20% of Parkinsonian patients are referred for speech and language therapy (S & LT), its aim being to improve the intelligibility of the patient's speech.

OBJECTIVES

To compare the efficacy and effectiveness of novel S & LT techniques versus standard S & LT to treat dysarthria in patients with Parkinson's disease. To compare the efficacy and effectiveness of one S & LT technique versus a second form of S & LT to treat Parkinsonian dysarthria.

SEARCH STRATEGY

Relevant trials were identified by electronic searches of MEDLINE, EMBASE, CINAHL, ISI-SCI, AMED, MANTIS, REHABDATA, REHADAT, GEROLIT, Pascal, LILACS, MedCarib, JICST-EPlus, AIM, IMEMR, SIGLE, ISI-ISTP, DISSABS, Conference Papers Index, Aslib Index to Theses, the Cochrane Controlled Trials Register, the CentreWatch Clinical Trials listing service, the metaRegister of Controlled Trials, ClinicalTrials.gov, CRISP, PEDro, NIDRR and NRR; and examination of the reference lists of identified studies and other reviews.

SELECTION CRITERIA

Only randomised controlled trials (RCT) were included.

DATA COLLECTION AND ANALYSIS

Data was abstracted independently by KD and RW and differences settled by discussion.

MAIN RESULTS

Only two trials were identified with only 71 patients. The method of randomisation was good in only one trial and the concealment of allocation was inadequate in both trials. These methodological problems could potentially lead to bias from a number of sources. The methods used in the two studies varied so much that meta-analysis of the results was not possible. Scott 83 compared prosodic exercises with visual cues with prosodic exercises alone (See Glossary: Table 01). The authors examined prosody and intelligibility as outcome measures immediately after therapy. Ramig 95 compared the Lee Silverman Voice Therapy (LSVT) which emphasises increased vocal effort, with respiratory therapy which aimed to increase respiratory muscle activity. Ramig 95 examined a wide range of vocal characteristics, activities of daily living affected by speech, depression and the carer's impressions of the patient's speech quality. Some of these outcomes were measured up to 24 months after the end of the therapy. However, in neither study were changes in outcomes due to 'Therapy A' compared with the changes due to 'Therapy B' statistically. Therefore no comment on the comparative efficacy of these types of speech and language therapy can be made.

REVIEWER'S CONCLUSIONS: Considering the methodological flaws in both of these studies, the small number of patients examined, and the possibility of publication bias, there is insufficient evidence to support or refute the efficacy of any given form of S & LT over another to treat dysarthria in Parkinson's disease. Given the lack of evidence from RCTs to support or refute the efficacy of S & LT in Parkinson's disease (see Cochrane review 'Speech and Language therapy for Dysarthria in Patients with Parkinson's Disease'), the consensus as to what is considered 'best-practice' S & LT must be proved first through a large well-designed placebo-controlled randomised trial before examining variations in S & LT methodology. The design of these trials should minimise bias and be reported fully using CONSORT guidelines (CONSORT 1996). Outcome measures with particular relevance to patients, their carers, physicians and speech and language therapists should be chosen and the patients followed for at least 6 months to determine the duration of any improvement.

摘要

背景

构音障碍是帕金森病的常见表现,且随着疾病进展其发生频率和严重程度会增加(施特赖弗勒,1984年)。高达20%的帕金森病患者会接受言语和语言治疗(S&LT),其目的是提高患者言语的清晰度。

目的

比较新型S&LT技术与标准S&LT治疗帕金森病患者构音障碍的疗效和效果。比较一种S&LT技术与另一种S&LT形式治疗帕金森病构音障碍的疗效和效果。

检索策略

通过对MEDLINE、EMBASE、CINAHL、ISI-SCI、AMED、MANTIS、REHABDATA、REHADAT、GEROLIT、Pascal、LILACS、MedCarib、JICST-EPlus、AIM、IMEMR、SIGLE、ISI-ISTP、DISSABS、会议论文索引、阿思利布学位论文索引、Cochrane对照试验注册库、CenterWatch临床试验列表服务、对照试验元注册库、ClinicalTrials.gov、CRISP、PEDro、NIDRR和NRR进行电子检索,确定相关试验;并查阅已识别研究和其他综述的参考文献列表。

入选标准

仅纳入随机对照试验(RCT)。

数据收集与分析

KD和RW独立提取数据,通过讨论解决分歧。

主要结果

仅识别出两项试验,共71例患者。仅一项试验的随机化方法良好,两项试验的分配隐藏均不充分。这些方法学问题可能会导致多种来源的偏倚。两项研究中使用的方法差异很大,因此无法对结果进行荟萃分析。斯科特(1983年)将有视觉提示的韵律练习与单纯的韵律练习进行了比较(见术语表:表01)。作者在治疗后立即检查韵律和清晰度作为结果指标。拉米格(1995年)将强调增加发声努力的李·西尔弗曼嗓音疗法(LSVT)与旨在增加呼吸肌活动的呼吸疗法进行了比较。拉米格(1995年)检查了广泛的嗓音特征、受言语影响的日常生活活动、抑郁情况以及护理人员对患者言语质量的印象。其中一些结果在治疗结束后长达24个月进行了测量。然而,两项研究均未对“疗法A”导致的结果变化与“疗法B”导致的结果变化进行统计学比较。因此,无法对这些类型的言语和语言治疗的比较疗效发表评论。

综述作者结论

考虑到这两项研究存在方法学缺陷、所检查的患者数量较少以及存在发表偏倚的可能性,没有足够的证据支持或反驳任何一种特定形式的S&LT在治疗帕金森病构音障碍方面优于另一种。鉴于缺乏随机对照试验的证据来支持或反驳S&LT在帕金森病中的疗效(见Cochrane综述“帕金森病患者构音障碍的言语和语言治疗”),在研究S&LT方法的差异之前,必须首先通过一项大型精心设计的安慰剂对照随机试验来证明被视为“最佳实践”的S&LT是什么。这些试验的设计应尽量减少偏倚,并按照CONSORT指南(CONSORT,1996年)进行全面报告。应选择与患者、其护理人员、医生以及言语和语言治疗师特别相关的结果指标,并对患者进行至少6个月的随访,以确定任何改善的持续时间。

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