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Tourette Syndrome and tics: What are they and what can we do?

Tourette Syndrome and tics: What are they and what can we do?. Hugh Rickards Dec 2016. M.Sc. In Clinical Neuropsychiatry. www.bham.ac.uk. Contents. Clinical characteristics What are tics? Clinical course of symtpoms What other symptoms are there? Co-morbidity Epidemiology

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Tourette Syndrome and tics: What are they and what can we do?

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  1. Tourette Syndrome and tics: What are they and what can we do? Hugh Rickards Dec 2016

  2. M.Sc. In Clinical Neuropsychiatry www.bham.ac.uk

  3. Contents • Clinical characteristics • What are tics? • Clinical course of symtpoms • What other symptoms are there? • Co-morbidity • Epidemiology • Basics of treatment

  4. DSM-IV 307.23 • Multiple motor plus one or more vocal tics • “Nearly every day” (no tic free period of longer than 3 months) • Impairment in function • Onset before 18 years • Not due to substance intoxication or general medical condition

  5. What is a tic? • Stereotyped • Occur in bouts • Usually sudden • Can be simple or complex • Semi-voluntary

  6. The fractal nature of tics

  7. Sensory/Cognitive symptoms. • Premonitory sensation. • Relief after movement. • Movement suppressible. • Rebound after suppression.

  8. Is it a tic/tics? No What is it? Stereotypy, chorea,dystonia, myoclonus, seizure, akathisia, compulsion yes Are there atypical symptoms? (progressive, cognitive impairment,focal signs, dysmorphism, signs of specific syndrome, late onset, impaired consciousness) Consider investigation MRI, EEG, urate, copper, caeruloplasmin, Fragile X, Acanthocytes, Organic and amino acids. yes No Transient tic disorder Chronic multiple tics Tic disorder NOS Tourette syndrome

  9. Natural history of TS • Mean onset around 6 years • “Fractal” occurrence of tic symptoms • Typically start simple and get more complex • Phonic tics start at 8-15 years • Worst between 12-14 years and then improve • Repertoire of tics gets more stable • Tic-free periods longer • Rarely go away completely

  10. Mean tic severity in TS (N=42) Leckman et al. Pediatrics 1998

  11. Tics often improve but rarely go completely.

  12. How common is Tourette Syndrome?

  13. DSM-IV 307.23 • Multiple motor plus one or more vocal tics • “Nearly every day” (no tic free period of longer than 3 months) • Impairment in function • Onset before 18 years • Not due to substance intoxication or general medical condition

  14. Epidemiology II

  15. Epidemiology II • More common in boys than girls (2-3:1) • Common in EBD schools • Seen in all cultures and countries • Found in all social classes • People with TS often have lower social class than their parents

  16. Associated and co-morbid conditions

  17. Associated symptoms • Echolalia/Echopraxia • Coprolalia/copropraxia • Palilalia/palipraxia • Self-injurious behaviours • Obsessive compulsive behaviours (OCB)

  18. Co-morbid disorders • Obsessive-compulsive disorder • Attention deficit hyperactivity disorder • Depression • Anxiety • “Oppositional Defiant Disorder”

  19. “he had another peculiarity.…...This was his anxious care to go out or in a door or passage, by a certain number of steps from a certain point, or at least so as that either his right or his left foot (I am not certain which), should constantly make the first actual movement when he came close to the door or passage”.

  20. Kurlan et al. J. Clin. Exp. Neuropsych. (1988) • TS children had more “Just right” perceptions Evening up Self harm • Pure OC children have more Handwashing, fear of dirt

  21. Tourette Syndrome and ADHD • Increased co-morbidity in community samples • Developmental disorders more common in boys • Different time courses • TS has a later onset and quicker offset • “A kind of disinhibition”…. • Pseudo-ADHD

  22. Models for TS aetiology • Need to be temporally dynamic • Worse with default • Fractal nature of tics • Need to understand the nature of volition • Need to be non-dualistic

  23. Management of GTS

  24. Principles of management • Holistic. Individual not symptom • Comprehensive assessment • Comorbidity • TS related • Other physical or mental disorder • Specific learning difficulty • Family/social factors • Mental state/physical examination • Strengths • Education • Developmental trajectory/what’s causing any disability? • Broad based management plan

  25. Management II • Education about TS • Patient / family / teachers • Collaboration with TSA • ?genetic counselling • Biological treatments • Psychological treatments • Counselling • Family therapy • Behaviour therapy • Social interventions • Schools/exams • Courts • Respite

  26. WHY AM I GIVING THIS PERSON MEDICATION??

  27. Therapeutic trials in GTS • “In any trial, if you do nothing, a third of people will get worse, a third will stay the same and a third get better”

  28. Medical treatments • Risperidone. Sulpiride. • Clonidine/guanfacine • Aripiprazole • Tetrabenazine • Nabilone • Botox for single tics/coprolalia • SSRI’s or CBT for OCD • ?methylphenidate for ADHD • Atomoxetine for ADHD

  29. Adverse effects of medical treatments • Sedation • Weight gain • Loss of volition • Depression • School refusal • Acute dystonias • Tardive dyskinesia • ? glucose intolerance

  30. CBIT/ERP • Behavioural technique • Teach tic awareness and triggers • Hold a competing posture until the urge diminishes. • 3 RCT’s support its use.

  31. DBS in GTS • 150 cases worldwide • Medial thalamus and Gpi • No convincing logic for either • Generally good results

  32. Conclusion • A neurodevelopmental syndrome which can lead to significant social disability • Accurate diagnosis through holistic assessment • Management focussing on causes of disability and fostering development.

  33. Tourette and “neurodiversity” • Differences in brain function compared to “normal” • Most of the disability is purely social • ? A pathologisation of a normal variant on human behaviour. • Treatment should be aimed at others’ intolerance.

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