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Speech and language therapy for dysarthria in Parkinson's disease: a comparison of techniquesDeane K, Whurr R, Playford ED, Ben-Shlomo Y, Clarke CE SummaryMany people with Parkinson's disease suffer from disorders in their speech and voice. These disorders are typically characterised by speech and voice that is monotonous, quiet, hoarse and breathy. People with Parkinson's disease also tend to give fewer non-verbal cues, such as facial expressions and hand gestures. These disabilities tend to increase as the disease progresses and can lead to serious problems with communication.This review will compare the benefits of one form of speech and language therapy versus another for individuals with Parkinson's disease. Relevant trials were identified by electronic searches of 21 biomedical literature databases, various registers of clinical trials and an examination of the reference lists of the identified studies and other reviews. Only randomised controlled trials were included in this review. These were studies where two groups of patients were compared, each group of patients receiving a different form of S<. The patients were assigned to each of the two groups in a random fashion to reduce the potential for bias. Two trials were found comparing two forms of speech and language therapy in a total of 71 patients. Scott 83 examined the impact of adding visual feedback to prosodic exercises (See Glossary: Table 01). Ramig 95 compared the Lee Silverman Voice Therapy (LSVT), which emphasises increased vocal effort, with respiratory therapy which aimed to increase respiratory muscle activity. The methods varied so much that meta-analysis of the results was not possible. The methodological quality of the trials was variable, both of the studies failed in at least one critical area. Considering the small number of patients and the methodological flaws in these two studies, there is insufficient evidence to support the use of one form of speech and language therapy over another for the treatment of dysarthria in individuals with Parkinson's disease. Given the lack of evidence to support or refute the efficacy of speech and language therapy in Parkinson's disease at all (see Cochrane review, Speech and Language Therapy for Dysarthria in Patients with Parkinson's Disease) the consensus as to what is considered 'best-practice' speech and language therapy must be proved first through a large well designed placebo-controlled trial before examining variations in speech and language therapy methodology. 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.
This is a Cochrane review abstract and plain language summary, prepared and maintained by The Cochrane Collaboration, currently published in The Cochrane Database of Systematic Reviews 2010 Issue 1, Copyright © 2010 The Cochrane Collaboration. Published by John Wiley and Sons, Ltd.. The full text of the review is available in The Cochrane Library (ISSN 1464-780X).
This version first published online:
April 23. 2001 AbstractBackgroundDysarthria 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<), its aim being to improve the intelligibility of the patient's speech. ObjectivesTo compare the efficacy and effectiveness of novel S< techniques versus standard S< to treat dysarthria in patients with Parkinson's disease. Search strategyRelevant 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 criteriaOnly randomised controlled trials (RCT) were included. Data collection and analysisData was abstracted independently by KD and RW and differences settled by discussion. Main resultsOnly 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. Authors' conclusionsConsidering 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< over another to treat dysarthria in Parkinson's disease. Given the lack of evidence from RCTs to support or refute the efficacy of S< 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< must be proved first through a large well-designed placebo-controlled randomised trial before examining variations in S< 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. |