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. 2017 Feb 23:8:32.
doi: 10.3389/fneur.2017.00032. eCollection 2017.

The Efficacy and Tolerability of the Clonidine Transdermal Patch in the Treatment for Children with Tic Disorders: A Prospective, Open, Single-Group, Self-Controlled Study

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The Efficacy and Tolerability of the Clonidine Transdermal Patch in the Treatment for Children with Tic Disorders: A Prospective, Open, Single-Group, Self-Controlled Study

Pan-Pan Song et al. Front Neurol. .

Abstract

Background: To evaluate the efficacy and tolerability of a clonidine transdermal patch in the treatment of children with tic disorders (TD) and to establish a predictive model for patients.

Methods: Forty-one patients who met the inclusion criteria entered into 12 weeks of prospective, open, single-group, self-controlled treatment with a clonidine transdermal patch. The Yale Global Tic Severity Scale (YGTSS) was employed before therapy (baseline) and at 4, 8, and 12 weeks after therapy.

Results: (1) The total effect rates of treatment with a clonidine transdermal patch were 29.27, 53.66, and 63.41% at 4, 8, and 12 weeks, respectively. Compared with the baseline, the differences were significant at three different observation periods. (2) Compared to the level of 25% reduction, there were significant decreases in the score-reducing rate of motor tic and total tic severities at 12 weeks. (3) If the disease course was ≤24 months and the motor tic score was <16 at the baseline, there was an effective rate of 100% for treatment with the clonidine transdermal patch. If the disease course was ≤24 months and the motor tic score was >16, there was an effective rate of 57.1%. If the disease course was >24 months and the clinical classification was chronic TD, there was an effective rate of 62.5%. If the disease course was >24 months and the clinical classification was Tourette's syndrome, 90% of the patients were invalid. (4) The main adverse events were rash, slight dizziness, and headache.

Conclusion: (1) When patients were pretreated with a D2-dopamine receptor antagonist that was ineffective or not tolerated well, switching to a clonidine transdermal patch treatment was effective and safe. (2) A clonidine transdermal patch could be a first-line medication for mild and moderate TD cases that are characterized by motor tics.

Keywords: children; clonidine transdermal patch; efficacy; prediction model; tic disorders.

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Figures

Figure 1
Figure 1
Growing method of classification and regression tree.
Figure 2
Figure 2
The importance of independent variables affecting treatment.

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References

    1. Roessner V, Schoenefeld K, Buse J, Bender S, Ehrlich S, Münchau A. Pharmacological treatment of tic disorders and Tourette syndrome. Neuropharmacology (2013) 68:143–9.10.1016/j.neuropharm.2012.05.043 - DOI - PubMed
    1. Houeto JL, Giré P. Tics and Tourette syndrome: diagnosis, course and treatment principles. Presse Med (2008) 37:263–70.10.1016/j.lpm.2007.11.007 - DOI - PubMed
    1. Olson LL, Singer HS, Goodman WK, Maria BL. Tourette syndrome: diagnosis, strategies, therapies, pathogenesis, and future research directions. J Child Neurol (2006) 21:630–41.10.1177/08830738060210080601 - DOI - PubMed
    1. Stern J. Update on tic disorders and Tourette syndrome. Paediatr Child Health (2010) 20:411–5.10.1016/j.paed.2010.03.013 - DOI
    1. Weisman H, Qureshi IA, Leckman JF, Scahill L, Bloch MH. Systematic review: pharmacological treatment of tic disorders – efficacy of antipsychotic and alpha-2 adrenergic agonist agents. Neurosci Biobehav Rev (2013) 37:1162–71.10.1016/j.neubiorev.2012.09.008 - DOI - PMC - PubMed

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