Tourette Syndrome
Study register · detail Open-Label-Studie (prospektiv) · Tourette Syndrome · 2022

Medical Cannabis for Gilles de la Tourette Syndrome: An Open-Label Prospective Study.

Clear benefit GRADE Low 26 citations
Samplen = 18 Pat.
Duration12 weeks
EndpointYGTSS-Total
Blindingoffen
DesignOpen-Label-Studie (prospektiv)
Cannabinoidvollspektrum
Routeinhalativ
Key finding

Medical cannabis significantly reduces tic severity and premonitory urge sensations in GTS patients.

Summary

n=18 adult GTS patients, open-label study over 12 weeks of medical cannabis (THC/CBD titration, mostly smoking 80%). YGTSS-Total (0-100) decreased by an average of 38% (p=0.002); Premonitory Urge for Tic Scale (PUTS) by 20% (p=0.043). Common side effects: dry mouth (66,7%), fatigue (53,3%), dizziness (46,7%); 40% cognitive side effects.

P
PopulationAdults with Gilles-de-la-Tourette syndrome (GTS), n=18
I
InterventionMedical cannabis (MC) with variable Δ9-THC and CBD content, titration individual, predominantly smoking (80%), over 12 weeks
O
OutcomeSignificant YGTSS-Total reduction of 38% after 12 weeks (p=0,002); PUTS reduction of 20% (p=0,043)
Confidence in the evidence
Low

The second of four GRADE levels, the effect estimate is of limited reliability.

Downgraded for
Risk of biasImprecision
Quality profile
Sample size
Blinding Open-label
Effect size Clear benefit
Citations / year
Authors
Anis S, Zalomek C, Korczyn AD, Rosenberg A, Giladi N, Gurevich T.
DOI 10.1155/2022/5141773
Design: Open-Label-Studie (prospektiv)
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Abstract
<h4>Objectives</h4>Assessing the effectiveness and tolerability of medical cannabis (MC) treatment on Gilles de la Tourette syndrome (GTS) patients.<h4>Methods</h4>We report on an open-label, prospective study on the effect of MC on adult GTS patients. MC mode of use was decided by the treating neurologist and the patient. <i>Δ</i>9-Tetrahydrocannabinol (<i>Δ</i>9-THC) and cannabidiol (CBD) content within MC product and monthly dose were titrated during the study. Following treatment initiation, patients were assessed after 4 and 12 weeks for efficacy, tolerability, and side effects.<h4>Results</h4>Eighteen patients entered the study. Baseline Yale Global Tic Severity Scale- (YGTSS) Total (range 0-100) was 60.3 ± 17.1. Three patients did not reach the end of follow-up period. The most common mode of administration was smoking (80%). Following twelve weeks of treatment, a significant 38% average reduction (<i>p</i> = 0.002) of YGTSS-Total and a 20% reduction (<i>p</i> = 0.043) of Premonitory Urge for Tic Scale (PUTS) were observed. Common side effects were dry mouth (66.7%), fatigue (53.3%), and dizziness (46.7%). Three patients suffered from psychiatric side effects including worsening of obsessive compulsive disorder (stopped treatment), panic attack, and anxiety (resolved with treatment modification). Six patients (40%) reported cognitive side effects regarding time perception, visuospatial disorientation, confusion, slow processing speed, and attention.<h4>Conclusions</h4>MC treatment demonstrates good efficacy and tolerability in adult GTS patients. Predilection for smoking rather than using oil drops requires further comparative studies to evaluate the efficacy of each. Cognitive and psychiatric side effects have to be monitored and addressed.

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