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Abstract Details

CBIT response in clinical practice: The potential importance of comorbidities and tic location
Movement Disorders
P15 - Poster Session 15 (12:00 PM-1:00 PM)
3-016

1) To evaluate whether comorbidities influence Comprehensive Behavioral Intervention for Tics (CBIT) response.

2) To evaluate the response of tic phenotypes and location to CBIT.

CBIT has been shown in multiple randomized controlled trials to significantly improve motor and vocal tic control in patients with Tourette syndrome (TS). While attention problems are frequently hypothesized to impair tic suppression therapies, the results have been inconclusive. A differential response to CBIT by tic phenotype and location also has not been extensively investigated. These issues, if better understood, could help inform more optimal candidates for CBIT.

A retrospective real-world analysis of a single Tourette Association of America (TAA) Center of Excellence tertiary referral center was undertaken. Excluded were patients with two or less CBIT therapy visits. The patient and/or the parent completed a tic hierarchy questionnaire at the initial therapy visit and final visit (target was 10 therapies).

There were 48 patients (77.1% males) with a mean age of 16.3±10.8 years and a mean number of visits of 5.9±2.2. Twenty-eight patients (58.3%) responded completely (n=16) or partially (n=12) to CBIT, while 20 patients (41.7%) did not meet pre-established therapy goals. Baseline clinical characteristics and comorbidities were similar between groups with the exception of more attention deficit hyperactivity disorder (ADHD) in the partial response subgroup (p=0.048). Tic phenotypes were assessed. Darting eyes, facial grimace, head forward, throwing head back, shrugging shoulders, quick flexion/extension of arms and stimulus-dependent tics revealed statistically significant improvements with CBIT (p<0.05).

This single center experience suggests that ADHD and tic phenotype may influence CBIT outcome in clinical practice.  This small cohort revealed a more positive effect on tics including head and neck and/or proximal upper extremity involvement. Larger and prospective studies will be needed to fully characterize CBIT response in real-world conditions.

Authors/Disclosures
Shannon Y. Chiu, MD, MSc (Mayo Clinic Arizona)
PRESENTER
Dr. Chiu has received research support from NIH.
Wissam G. Deeb, MD, FÂé¶¹´«Ã½Ó³»­ (UMass Memorial) Dr. Deeb has a non-compensated relationship as a Board member with Davis Phinney Foundation that is relevant to Âé¶¹´«Ã½Ó³»­ interests or activities.
Leonardo Almeida (University of Florida College of Medicine - Neurology) No disclosure on file
No disclosure on file
Michael S. Okun, MD, FÂé¶¹´«Ã½Ó³»­ (University of Florida) Dr. Okun has received personal compensation in the range of $0-$499 for serving on a Scientific Advisory or Data Safety Monitoring board for NIH. Dr. Okun has received personal compensation in the range of $10,000-$49,999 for serving as an officer or member of the Board of Directors for Parkinson's Foundation. Dr. Okun has received personal compensation in the range of $5,000-$9,999 for serving as an Editor, Associate Editor, or Editorial Advisory Board Member for JAMA Neurology. Dr. Okun has received personal compensation in the range of $500-$4,999 for serving as an Editor, Associate Editor, or Editorial Advisory Board Member for NEJM Journal Watch. The institution of Dr. Okun has received research support from NIH. The institution of Dr. Okun has received research support from Parkinson's Foundation. The institution of Dr. Okun has received research support from Tourette Association of America. The institution of Dr. Okun has received research support from Michael J Fox. Dr. Okun has received publishing royalties from a publication relating to health care.
Irene Malaty, MD, FÂé¶¹´«Ã½Ó³»­ (University of Florida) Dr. Malaty has received personal compensation in the range of $10,000-$49,999 for serving as a Consultant for Abbvie. Dr. Malaty has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Aevum. The institution of Dr. Malaty has received research support from Abbvie. The institution of Dr. Malaty has received research support from Revance. The institution of Dr. Malaty has received research support from Parkinson Foundation. The institution of Dr. Malaty has received research support from SAGE. The institution of Dr. Malaty has received research support from Emalex. The institution of Dr. Malaty has received research support from Acadia. Dr. Malaty has received publishing royalties from a publication relating to health care. Dr. Malaty has received personal compensation in the range of $500-$4,999 for serving as a Speaker & Center of Excellence Director with Parkinson Foundation. Dr. Malaty has a non-compensated relationship as a MAB member & Center of Excellence Directory with Tourette Association of America that is relevant to Âé¶¹´«Ã½Ó³»­ interests or activities.