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Research Report Abstracts - Gesundheit

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eS714<br />

inapplicable because they included items involving the use<br />

of long leg braces for walking or standing, and some patients<br />

did not use long leg braces. In the Barthel Index, a ceiling<br />

effect was prominent for slowly progressive MD (58.9%),<br />

while a floor effect existed for DMD (17.9%). Among the<br />

slowly progressive MDs, FSHD patients had the best level<br />

of functioning; they had better leg function and their ADL<br />

were less affected than patients with other forms of slowly<br />

progressive MD.<br />

Conclusions: Brooke and Vignos scale were insufficient for<br />

accessing the upper and lower limbs functional status for<br />

slowly progressive MD. Some of the limitations of these<br />

measures as applied to MD should be carefully considered.<br />

Implications: We suggest these applications be used in<br />

combination with other measures, or that a complicated<br />

instrument capable of evaluating the various levels of functional<br />

status be used. For example, to assess the basic mobility<br />

abilities (sitting from lying, rolling and changing body position)<br />

for DMD, and to assess the arm functions (managing<br />

objects overhead and carrying objects) for BMD, LGMD and<br />

FSHD is needed.<br />

Keywords: Muscular dystrophy; Functional status; Barthel<br />

Index<br />

Funding acknowledgements: This study was supported by<br />

grants for the National Science Council (NSC89-2614-B-<br />

037-005-M47, 90-2614-B-037-004-M47, 91-2614-B-037-<br />

009-M47).<br />

Ethics approval: The study was approved by the hospital’s<br />

institutional review board.<br />

<strong>Research</strong> <strong>Report</strong> Platform Presentation<br />

Number: RR-PL-3210 Wednesday 22 June 16:00<br />

RAI: Elicium 2<br />

TRANSCRANIAL DIRECT CURRENT<br />

STIMULATION FOR THE REDUCTION OF<br />

CLINICAL AND EXPERIMENTALLY INDUCED<br />

PAIN: A SYSTEMATIC REVIEW AND<br />

META-ANALYSIS<br />

Luedtke K. 1,2,3 , Rushton A. 1 , Wright C. 1 , Geiss B. 2 ,<br />

Juergens T.P. 2 , May A. 2<br />

1University of Birmingham, School of Health and Population<br />

Sciences, College of Medical and Dental Sciences,<br />

Birmingham, United Kingdom, 2Institute of Systems Neurosciences,<br />

University Hospital Eppendorf, Hamburg,<br />

Germany, 3Backpain Clinic ‘Am Michel’, Hamburg,<br />

Germany<br />

Purpose: To evaluate the effectiveness of transcranial direct<br />

current stimulation (tDCS) on clinical and experimental pain,<br />

and to identify the most beneficial stimulation parameters.<br />

Relevance: Central processing presents a promising treatment<br />

target in chronic pain syndromes. Surgically implanted<br />

brain stimulation has demonstrated pain-reducing effects.<br />

tDCS is non-invasive, pain-free, easy to administer and does<br />

not have serious side effects. Hence, it can be employed in<br />

physiotherapy management. Recent evidence suggests that<br />

tDCS is a potentially effective intervention.<br />

Participants: Participants were adult healthy volunteers or<br />

chronic pain patients. A total of 11 trials including 106 participants<br />

were included.<br />

Methods: A systematic review and meta-analysis of evidence<br />

for tDCS for the reduction of pain (clinical and<br />

experimental). Searches using pre-defined key terms were<br />

conducted in MEDLINE, EMBASE, CAB <strong>Abstracts</strong>, Psych-<br />

INFO, Cochrane Register of Controlled Trials, CINAHL, and<br />

PeDRO databases. Reference lists of retrieved articles, journal<br />

contents and conference proceedings were also searched.<br />

Two reviewers independently searched and screened for study<br />

eligibility. Controlled trials, including crossover designs,<br />

employing tDCS for the reduction of clinical or experimental<br />

pain published in any language prior to 31/5/2010 were<br />

included. Studies using magnetic stimulation/pulsed currents<br />

were excluded. Two reviewers independently evaluated risk<br />

of bias for included trials.<br />

Analysis: Trials with an overall high risk of bias were<br />

included in the descriptive analysis but excluded from<br />

the meta-analysis. Trials without pain reduction data were<br />

excluded from the meta-analysis. A meta-analysis using a<br />

random effects model was conducted on mean differences<br />

and standard deviations in pain intensity.<br />

Results: Trials investigating experimental pain in healthy<br />

participants (5 trials, n = 81 participants) used a wide variety<br />

of stimulation and outcome parameters, not permitting<br />

a synthesis of results. The quality of trials was poor, with 2<br />

trials assessed as high and 3 as unclear risk of bias. All trials<br />

reported some pain reduction with the allocated stimulation<br />

paradigm (anodal or cathodal stimulation modes; primary<br />

sensory or primary motor cortex as stimulation sites). Trials<br />

investigating chronic clinical pain (6 trials, n = 106 participants)<br />

used anodal motor cortex stimulation of 1 mA or 2 mA<br />

intensity, either as a single dose or on a maximum of 5 consecutive<br />

days. A meta-analysis of 4 trials (2 with high risk<br />

of bias were excluded) found a pooled effect size of −0.975<br />

with a 95% confidence interval of −1.547 to −0.404.<br />

Conclusions: There was low level evidence to support tDCS<br />

for pain reduction in a chronic clinical pain population. Effect<br />

sizes were small. Heterogeneity and poor quality of trials on<br />

experimental pain did not allow a synthesis of the results.<br />

Implications: The number and quality of the current trial<br />

evidence is not sufficient to recommend tDCS as a treatment<br />

for chronic pain syndromes. A high quality and effectively<br />

powered trial is required.<br />

Keywords: Pain; Direct current stimulation; Brain<br />

Funding acknowledgements: None.<br />

Ethics approval: Not required.

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