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Disclaimer: Nothing on this site is meant to be construed as medical advice.
Any information on this site is the opinion of the author. You should discuss
treatment options with your doctor. By reading this site you are agreeing that
www.tourettestreatment.com is not liable for any medical decisions you make.
What follows are my notes that I took while researching treatment options
for tic disorders. Some fields are black because I was either unable
to find the correct information, or because they are irrelevant. Medications
are groups according to class (neuroleptic, SSRI, etc.) Where applicable,
notes about the entire class of medication have been added beneath the
class name. For each class of medication, information is divided into
the following sections:
Name - name of the medication
Tradename - tradename of the medication
Method - the method of action, or how the medication works
Notes - notes I found about the medication or results from trials
Side-effects - documented side-effects for the medication
All medications listed below were found somewhere in medical journal(s)
with reference to the treatment of Tourette's Syndrome and/or tic disorders.
Studies and references are cited where I still have the reference,
but since this information comes from casual notes that I took while
reading various source, I don't always have the reference information
available. I will make an attempt to find the sources and post it after
the study in the appropriate tables as I update this list.
Again, this information represents my collection of notes and is not
guaranteed to be accurate or complete. It is not meant to be a diagnostic
tool, a recommendation, or any form of advice. This is for informational
purposes only. Please do your own research and discuss your own situations
with your doctor.
Anti-psychotics/Neuroleptic
(- All neuroleptic medications may cause tardive dyskinesia, a potentially
irreversible movement disorder
- Not to be discontinued abruptly - may cause tardive dyskenesia
- May begin to work in a few days or weeks
- May cause sleepiness, depressed mood, weight gain
- May cause other movement disorders including bradykinesia, akathisia,
and acute dystonic reactions
- Antipsychotics may worsen tics - http://www.aafp.org/afp/990415ap/2263.html
)
Name |
Tradename |
Method |
Notes |
Side-effects |
Pimozide |
Orap |
|
Only FDA-approved antipsychotic for the treatment of tics |
- Cardiac changes (in the QT interval)- One double-blind study
found Pimozide superior to Haloperidol with respect to efficacy
and side effects
- muscular rigity, drooling, tremor, lack of facial expression,
slow movement, and restlessness |
Haloperidol |
Haldol |
|
|
- 4% per year risk of tardive dyskinesia in younger patients,
higher in those over 45
- depression resulting in suicide is common during long-term
treatment
- musular rigity, drooling, tremor, lack of facial expression,
slow movement, and restlessness |
Fluphenazine |
Prolixin |
|
- Seemingly less common side effects than other neuroleptics |
|
Sulpiride |
Not approved in US and Canada |
Dopamine blocker |
Anti-psychotic |
- fewer extrapyramidal side effects than many of the older
antipsychotic medications |
Thioridazine |
-Mellaril
-Novorizadine
-Thioril |
|
|
- Can prolong QT interval (lead to sudden death) |
Atypical Neuroleptic
(- All atypical neuroleptic medications may cause tardive dyskinesia,
a potentially irreversible movement disorder, although the risk with
atypical neuroleptics is thought to be lower than with neuroleptics
- Not to be discontinued abruptly - may cause tardive dyskinesia
- May begin to work in a few days or weeks
- May cause Neuroleptic Malignant Syndrome
- Increased risk of diabetes mellitus and hyperglycemia
- May cause sleepiness, depressed mood, and weight gain
- Atypical antipsychotics share a relatively greater affinity for the
5-HT2 and D2 receptors than traditional antipsychotic agents and cause
a lower incidence of extrapyramidal effects (such as tardive dyskinesia
- http://www.wipo.int/pctdb/en/wo.jsp?IA=US2002033628&DISPLAY=DESC)
Name |
Tradename |
Method |
Notes |
Side-effects |
Risperidone |
Risperdal |
-Dopamine and serotonin blocking properties |
-effective compared to placebo
-at least as effective as Clonidine
-Some reports say it can help OCD, others say it exacerbates
symptoms
-Shown to be effective in reducing tic frequency and intensity
in most, but not all, studies |
- Can prolong QT interval (lead to sudden death)
- Tardive Dyskinesia |
Olanzapine |
Zyprexa |
Dopamine-2 and serotonin-2A and -2C antagonism |
- "Some improvement" (Budman, Gayer, Lesser, Qiuhu
Shi, Bruun) |
- Sedation
- Weight gain
- Increased appetite
- Dry mouth
- Transient asymptomatic hypoglycemia |
Thiothixene |
Navane |
|
|
|
Clozapine |
Clozaril |
|
- Patient developed invluntary movements during treatment with
clozapine and fluvoxamine |
|
Quetiapine |
Seroquel |
blocks D1 and D2 receptors, and 5-HT2A, 5-HT2C, 5-HT1A, 5-HT1D,
and alpha receptors |
Found to decrease tic severity by 35% compared with a 7% change
in placebo |
|
Ziprasidone |
Geodon |
|
Found to significantly reduce tic frequency and count over
placebo |
-Cardiac changes in the QT interval
-Prolonged QT interval can cause ventricular fibrillation and
sudden death
-Less likely to cause weight gain |
Aripiprazole |
Abilify |
|
|
Tardive dyskinesia |
SSRI (Selective Serotonin Reuptake Inhibitor)
("When used alone, antidepressant medications are not useful in
the treatment of tics" - http://www.coursework4you.co.uk/francis.htm)
(McDougle et al. found that "compared to patients with OCD but
no tics, patients with tic-related OCD showed less theraputic response
to monotherapy with an SSRI)
Name |
Tradename |
Method |
Notes |
Side-effects |
Sertraline |
Zoloft |
|
|
- Movement disorder side-effects (Lambtert, Trutia, Petty) |
Fluoxetine |
|
|
|
- Movement disorder side-effects (Lambtert, Trutia, Petty)
- Exacerbate tics in a patient with TS but was found to have
no effect on tics in a small, double blind, placebo-controlled
crossover trial |
Paroxetine |
|
|
|
- Movement disorder side-effects (Lambtert, Trutia, Petty)
- One case of Paroxetine worsening tics in a 12 year old boy
with TS |
Fluvoxamine |
Luvox |
|
- Most often used to treat OCD
- One of few SSRIs to have monocyclic structure
- Improvement in 21% of patients with OCD and chronic tics, 52%
response rate in patients with OCD and NO tics (source
) |
- Normal SSRI side effects
- Single case of this drug causing TS in a patient being treated
for OCD (source)
- Akathasia, dyskinesia
- Cases of Fluvoxamine worsening tics |
Citalopram |
Celexa |
|
- shows to "significantly reduce tics in TS in one small
study"
- No reports to date of this agent exacerbating tic symptoms
- No evidence directly impolicating Citalopram with teeth grinding
(bruxism) |
|
Escitalopram |
|
|
- Examined in depressed, but not OCD |
|
Non-SSRI Antidepressant
Name |
Tradename |
Method |
Notes |
Side-effects |
Nefazodone |
Serzone (Discontinued by Bristol-Myers Squibb in US and Canada
in 2004; generic formulations are still available) |
Blocks post-synaptic serotonin type-2A receptors and, to a
lesser extent, by inhibiting pre-synaptic serotonin and norepinephrine
(noradrenaline) reuptake. Also a relatively potent alpha-1 adrenoceptor
antagonist |
Unlike most SNRIs and SSRIs, Nefazodone has no negative effects
on libido or sexual functioning |
|
Bupropion |
Wellbutrin, Zyban |
Norepinephrine and dopamine reuptake inhibitor, and nicotinic
antagonist |
- found to exacerbate tics in four children with TS
- no reports of it improving tics |
|
Tricyclic Antidepressant
(Older than SSRIs, typically more side-effects)
Name |
Tradename |
Method |
Notes |
Side-effects |
Clomipramine |
Anafranil |
- Strong, but not completely selective serotonin reuptake inhibitor,
as the primary active metabolite desmethylclomipramine acts preferably
as a norepinephrine reuptake inhibitor
- Alpha blockage, beta receptor downregulation, and postsynaptic
antagonism on histamine H1 receptors and dopamine receptors have
also been noted
- downregulation of NMDA receptors |
Tricyclic antidepressant |
- higher incidence of seizures than seen with other tricyclic
antidepressants
- No benefit found for Clomipramine or desipramine for patients
with TS
- Reported to worsen motor tics in one case with OCD and schizoid
personality disorder |
Nortriptyline |
|
Inhibits reuptake of norepinephrine and to a lesser extent,
serotonin |
- shown to improve tic symptoms in a chart review of 12 cases
of children with tics and ADHD |
|
Imipramine |
-Antideprin
-Deprenil
-Deprimin
-Deprinol
-Depsonil
-Dynaprin
-Eupramin
-Imipramil
-Irmin
-Janimine
-Melipramin
-Surplix
-Tofranil |
-Norepinephrine reuptake inhibition (strong)
- Serotonin reuptake inhibition (moderate to strong)
- Acetylcholine antagonist at M2 muscarinic acetylcholine receptors
- Epinephrine - antagonizes adreno-receptors (II)
- Dopamine reuptake and release at D1 and D2 receptors ("similar
to but less potent than the psychostimulants, dopamine agonists
and atypical antidepressant buproprion on dopaminergic mechanisms
(increase in release and blockage of reuptake inhibition")***
- Opiates and Enkephalinase - low activity
- Histamine antagonist at H1 receptors. Acute sedative effects
(all data in this cell from wikipedia) |
- *** says it's similar on dopamine to Buproprion, which has
been known to exaverbate tics
- reported to decrease tics in one TS case and have no effect
on TS symptoms in another |
fever, chills, cough, weight loss, irregular heart rhythms,
weight gain (in contrast to weight loss, mentioned earlier), sexual
side effects, tremor has been frequently reported, headache, confusion,
aggressiveness, weakness, sudden muscle spasms |
Blood Pressure medication
Name |
Tradename |
Method |
Notes |
Side-effects |
Clonidine hydrochloride |
Catapres |
- Alpha 2-adrenergic agonist
- °62- agonist |
-may take time to build up in the system before it begins working
- also used to treat ADHD
- combined with Ritalin reduced the severity of a child's tics
with 75% showing improvement
- more effective in reducing motor tics than reducing vocal tics
(Nass & Bressman, 2002)
- 11% of patients had significant improvement, 14% had moderate
improvement, 67% of subjects had no improvement or worsening
- another study showed no statistical improvements in tic distribution,
frequency, or severity
- another placebo controlled double blind study confirmed that
Clonidine is effective in lessening tics |
-Dry mouth
-Drowsiness |
Guanfacine |
Tenex |
- Alpha 2-adrenergic agonist
- °62- agonist |
- a study found a significant decrease in the severity of motor
and phonic tics
- double bline study of guanfacine for tics and ADHD found a
31% decrease in tic severity compared to placebo |
-Dry mouth
-Drowsiness (less than Clonidine) |
Dopamine inhibitors/blockers
Name |
Tradename |
Method |
Notes |
Side-effects |
Tetrabenazine |
Not approved by the FDA as a treatment for tics
Approved by FDA for use in US on 8/15/08? |
- Blocks dopamine receptors
-Dopamine depleter
-Monoamine - depleting |
- Produced significant tic amelioration in over half the patients
followed for over two years (Jankovic and Beach, 1997)
- "Powerful anti-tic drug"
- Does not cause tardive dyskinesia
- Given to 5 patients, 2 had good results, 3 had no improvement
but experienced side effects
- 57.4% improvement in 47 patients with tics in an open label
study (Jankovic and Beach) |
-Parkinsonism, sedation, akathisia, depression |
Dopamine agonist
Name |
Tradename |
Method |
Notes |
Side-effects |
Pergolide |
withdrawn from US market on 3/30/2007 |
- on the premise that dopamine agonists in very low dosages
preferentially act on the presynaptic receptors and thereby decrease
dopamine release…
- success on a trial group that was unresponsive to neuroleptics
suggests that in these patients the improvement due to pergolide
is not linked to an effect on D2-receptors-carrying GABAergic
neurons, as usually assumed, because the patients did not respond
to neuroleptics acting in this way. In these 3 cases, unlike in
other TD patents, a prevalent action of pergolide by pre-synaptic
inhibition of dopamine release on D1-receptors-carrying GABAergic
neurons is suggested. (source)
|
- In an open-label study of 32 patients, there was a 50% reduction
in tics in 24 patients.
- In a randomized double-blind placebo-controlled crossover study
with 24 subjects, 19 completed. Statistically significant reductions
with few side effects
- this is an older Parkinson’s drug |
- in 2003, reported to be associated with a form of heart disease
called cardiac fibrosis |
Dopamine autoagonist
Name |
Tradename |
Method |
Notes |
Side-effects |
Talipexole |
|
-dopamine agonist
-also has alpha-adrenergic agonist activity |
- tested on 13 subjects with TS. 5 dropped out, 4 experienced
intolerable side effects
.- Blinded evaluation of videotapes failed to show any statistically
significant improvement in tic frequency or severity
- Not recommended for standard treatment for TS |
|
|
|
|
|
|
Norepinephrine Reuptake Inhibitor
Name |
Tradename |
Method |
Notes |
Side-effects |
Atomoxetine (formally known as Tomoxetine) |
Strattera |
|
- After 2-3 weeks of treatment, a patients mother reported
reduction in tics and vocal tics eliminated. AHDH improved (source)
- Two children with ADHD developed tics while on Atomoxetine
that did not fully resolve upon discontinuation (Parraga, Parraga,
Harris) |
- upset stomach, sporadic nausea, sudden vomiting
- sexual side effects |
Reboxetine |
|
Selective Norepinephrine Reuptake Inhibitor |
|
|
Desipramine |
-Norpramin
-Pertofrane |
|
|
Can prolong QT interval (lead to sudden death) |
Cannabis
Name |
Tradename |
Method |
Notes |
Side-effects |
Marijuana |
|
|
- significant reduction in tics in two studies (Mueller-Vahl,
2003) |
|
Marinol |
|
|
- some patients clearly benefit when taking Marinol at a doseage
of 2.5 to 10mg twice a day |
|
Calcium antagonists
Name |
Tradename |
Method |
Notes |
Side-effects |
Nifedipine |
ProcardiaXL |
Acts on slow calcium channels invascular smooth muscle and
myocardium, producing vasodilation |
decrease in tic symptoms. 10mg 3 times daily |
- dizziness, giddiness, headache, autonomic flushing, warmth,
sweating, nasal congestion, sore throat
- nausea, constipation, flatulence
- dyspnea, cough, hpotension, wheezing, tachycardia, arrhythmias,
fever, heart failure, muscle cramping |
Verapamil |
Isoptin |
inhibits calcium transport into myocardialand vascular smooth
muscle cells, resulting in inhibition of excitation contraction
coupling and subsequent contraction |
decrease in motor tics, improvement in mood, 20mg 3 times daily |
- dizziness, headache, fatigue, constipation, abdominal discomfort
- bradycardia, hypotension, edema, heart block, sinus arrest,
pulmonary edema |
Benzodiazepine derivative
Name |
Tradename |
Method |
Notes |
Side-effects |
Clonazepam |
Klonopin (USA), Rivotril, Ravotril, or RIvatril, elsewhere |
- GABA receptor antagonist |
-sometimes useful in managing tics "since some of the
premonitory sensations resemble obsessions and the tics may be
viewed as 'compulsive' movements, anti-OCD medications also may
be helpful" |
Sedation, weight gain, impaired academic performance, social
anxiety with school refusal in children and a worsening of attention
in children with comorbid ADHD |
Anticonvulsant
Name |
Tradename |
Method |
Notes |
Side-effects |
Levetiracetam |
Keppa |
"antiepileptic drug with atypical mechanisms of action" |
All 60 patients showed improvement (Awaad, Michon, Minarik) |
- hair loss
- pins and needles sensation
- psychiatric symptoms ranging from irritability to depression
- headache
- nausea |
Topiramate |
Topamax |
|
- the reduction in tics in some patients may be explained by
its potentiation of GABA activity
- can be used for OCD
- no reports of it exacerbating movement disorders |
- change in taste, pins and needles, cognitive deficiency,
difficulty understanding concepts
- loss of appetits
- somnolence
- nausea
- upper respiratory tract infection
- osteroporosis |
Lamotrigine |
|
|
occasionally reported to cause tics, but they resolved completely
within a month following cessation of the drug. Tics reappeared
with the introduction of lamotrigine |
|
Antiepileptic
Name |
Tradename |
Method |
Notes |
Side-effects |
Carbmazepine |
|
|
Reported to worsen tics in 8 patients while improving them
in 1 |
Associated with the development of other movement disorders |
Opiod
(http://grande.nal.usda.gov/ibids/index.php?mode2=detail&origin=ibids_references&therow=175030
Opiods may worsen tics - http://www.aafp.org/afp/990415ap/2263.html)
Name |
Tradename |
Method |
Notes |
Side-effects |
Propoxyphene |
|
|
|
|
Naltrexone |
Vivitrol (USA), Revia, Depade (elsewhere) |
|
-significant lessening of tics after treatment than with placebo
-reported to improve symptoms of TS, but also reports of it worsening
TS
|
|
Oxycodone |
|
|
|
|
Muscle Relaxant
Name |
Tradename |
Method |
Notes |
Side-effects |
Carisoprodol |
Soma |
Centrally-acting muscle relaxant whose active metabolite is
meprobamate |
|
|
Anti-hypertensive
Name |
Tradename |
Method |
Notes |
Side-effects |
Propranolol |
Inderal |
Non-selective beta blocker |
|
|
Drugs to be added to the list in the future:
Ondansteron, a selective 5-HT3 antagonist at 8-16mg/day for 3 weeks
has been associated with a decrease in severity of tics.
Baclofen, a GABA(B) autoreceptor agonist, has been found to markedly
decrease the severity of motor and phonic tics in 95% of 264 patients
with TS, however a double-blind, placebo-controlled, crossover trial
of 9 patients with TS showed that the beneficial response to baclefen
was due to improvement in overall impairment score rather than a reduction
of tic activity.
Donepezil, a noncompetitive inhibitor of acetylcholinesterase, has
been reported anecdotally to suppress tics.
Finasteride
http://ajp.psychiatryonline.org/cgi/content/short/164/12/1914?rss=1
Botox Injections
Also, the treatment is fairly downstream in the sense that it only
inhibits your ability to perform the tic -- not the neurology causing
the tic, the urge to engage in the tic, or the tic attempts themselves.
There is some evidence to suggest that the premonitory urge to tic decreases
following Botox, but I can see how it might feel like you have an 'unscratchable
itch" for those in whom it doesn't.
Deep Brain Stimulation
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