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Transcript
Revised Mar 1, 2008
Obsessive Compulsive Disorder (OCD):
Medication Guide for Primary Care Physicians
Compiled by Michael Cheng, MD, FRCP(C)
Note that there is also an accompanying family handout:
“Obsessive Compulsive Disorder: Information for Families”
(available from http://www.drcheng.ca)
Disclaimer
The content of this document is for general information and education only. The accuracy, completeness, adequacy, or
currency of the content is not warranted or guaranteed. The content is not intended to be a substitute for professional
medical advice, diagnosis, or treatment. Users should always seek the advice of physicians or other qualified health
providers with any questions regarding a health condition. Any procedure or practice described here should be applied by
a health professional under appropriate supervision in accordance with professional standards of care used with regard to
the unique circumstances that apply in each practice situation. The authors disclaim any liability, loss, injury, or damage
incurred as a consequence, directly or indirectly, or the use and application of any of the contents of this document.
This work is “licensed” under a Creative Commons License (Attribution-Non Commercial-Sharelike 2.0,
http://creativecommons.org/licenses/by-nc-sa/2.0/) which means that you are free to copy, distribute, display and
perform the work, and make derivative works as long as you give the original author credit, the work is not used for
commercial purposes, and if you alter, transform, or build upon this work, you may distribute the resulting work only
under a license identical to this one.
Where to Get this Handout
This handout is available from http://www.drcheng.ca in the Mental Health Information section. Any
comments and suggestions are welcome and will help ensure this handout is helpful.
1 of 8
Table of Contents
Sequence of Treatment ...........................................................................................................2
Medication Treatment for OCD .................................................................................................2
Duration of Treatment .............................................................................................................5
Second-Generation Antidepressants: Dosing in Children and Adolescents ...................................3
If SSRI monotherapy is insufficient ..........................................................................................4
Addendum: PANDAS (Pediatric Autoimmune Neuropsychiatric Disorders Associated with
Streptococcal Infection) ...........................................................................................................5
Overview of Treatment Strategies for OCD ...............................................................................7
References .............................................................................................................................8
Treatment Guidelines ..............................................................................................................8
Sequence of Treatment
For mild to moderate OCD in children and youth, it is usually felt best to commence with nonmedication interventions:



Specific anti-OCD interventions such as Cognitive Behavioral Therapy (CBT)
General health interventions such as ensuring adequate sleep, adequate diet
General coping interventions such as stress management, i.e. identifying sources of stress
(e.g. with school, work, family, relationships), and using conflict resolution or problemsolving to deal with stresses
Medication Treatment for OCD
Medication can be helpful for OCD that is causing severe distress, or for OCD that has not
responded sufficiently to non-medication interventions:

Start with any single SSRI agent, which includes:
 Fluoxetine, Fluvoxamine, Sertraline, Paroxetin, Citalopram (Geller’s 2003 meta-analysis
suggested it doesn’t matter which SSRI one starts with)
 Due to controversy about self-harm, it might be simpler to not start a patient on
Paroxetine
 On the other hand, if you have a patient who is doing well on Paroxetine, do not
necessarily feel you have to automatically discontinue their medication. If they are doing
well, consider obtaining informed consent, and continuing them on the medication.
2
Second-Generation Antidepressants: Dosing in Children and
Adolescents
Many children and teenagers may require adult dosages of medications, due to their metabolism.
Note that (as with adult conditions), many psychiatric medications are prescribed ‘off-label’ as not
every medication use has been fully documented with clinical trials. (Note that in general, over
60% of all medications prescribed are felt to be used ‘off-label’).
Agent
Fluoxetine (Prozac)
Sertraline (Zoloft)
Fluvoxamine (Luvox)
Paroxetine (Paxil)
Citalopram (Celexa)
Comments
FDA approval: Major Depression, OCD (age 7-17)
Start at 5 mg daily for child; 10 mg daily for adolescent
Target dosage range 20-60 mg daily, aim for higher end dosage for
OCD
Maximum 80 mg daily
FDA approval: OCD (age 6-18)
Start at 25 mg daily for child; 50 mg daily for adolescent
Target dosage range 50-200 mg daily, aim for higher end dosage
for OCD
Maximum 200-300 mg daily
FDA approval: OCD (age 6-18)
Start at 25 mg daily for child; 25-50 mg daily for adolescent
Target dosage 25-200 mg daily, aim for higher end dosage for OCD
Maximum 300 mg daily
Note: although FDA is currently recommending against its use in
major depressive disorder in youth, note Geller’s recent positive
study in JACAAP Nov 2004 journal showing efficacy in OCD in youth
Start 5-10 mg q daily
Target dosage 20-40 mg daily, aim for higher dosage for OCD
Maximum 60 mg daily
FDA: FDA Approval for OCD
No official indication for children/adolescents, though used off-label
Start 10 mg q daily for child; 10 mg daily for adolescent
Target dosage 10-40 mg daily, aim for higher end dosage for OCD
Maximum 60 mg daily
Source: Adapted from Bostic et al, 2003. Retrieved Oct 3, 2003 from
http://www.psychiatrictimes.com/p030988.html
3
If SSRI monotherapy is insufficient

If there is poor response despite monotherapy with an SSRI, then other options include:

Switching to Clomipramine (Anafranil)
Clomipramine (Anafranil),
supplied in 10, 25, 50 mg
tablets

In children aged 10 to 17 years, an initial dose of 25
mg/day is recommended. Dosage may be increased by 25
mg increments, as tolerated, at 3 to 4 day intervals. By the
end of 2 weeks, patients may be titrated up to 100 to 150
mg/day or 3 mg/kg, whichever is lower. Thereafter, the
dose may be gradually increased to 200 mg or 3 mg/kg
whichever is lower.
Maximum dosage 200 mg daily for children or adolescents.
Augmentation – evidence in adults supports adding a second agent (which by itself is
not felt to be a primarily anti-OCD agent) in order to provide a synergistic anti-OCD
effect. Typically, medication dosages for an augmenting agent tend to be on the lower
dosage range for that agent. Typical augmenting agents reported for OCD include:

Dopamine antagonists (i.e. antipsychotics), particular if patient has comorbid tics,
such as:

Risperidone (0.5-3 mg daily): double-blind, placebo controlled studies in adults
showing efficacy (Hollander et al., 2003).

Olanzapine (5-10 mg daily): double-blind, placebo controlled studies in adults
showing efficacy (Bystritsky et al., 2004).

Quetiapine (using up to 300 mg daily): double blind study in adults (Denys D et
al., 2004)

Psychostimulant: possible efficacy for Dextroamphetamine (but
Methylphenidate) suggested by Joffe et al., 1991; Insel et al., 1983.

Pindolol (7.5 mg/day): double-blind, placebo controlled studies showing efficacy
(Dannon et al., 2000).

Naltrexone (Revia) at 25-50 mg daily reported as anecdotally helpful.

Mood stabilizer: Lithium has been reported to augment imipramine, clomirpamine,
desipramine and doxepin, however double-blind studies have not shown
overwhelming success with lithium augmentation in OCD.

Buspirone (Buspar) reported as being helpful in open trials, but not in double-blind
studies.

Eicosapentaenoic acid (EPA) (an Omega 3 fatty acid) has been reported anecdotally
as being helpful, but of note, Fux failed to find any additional benefit using
adjunctive EPA (Fux et al., 2004)
not
for
4

Novel-agent strategies



Second-messenger systems: Inositol shown helpful in six-week, double-blind,
controlled crossover trial (Fux et al., Am. J. Psychiatry, 1996).
Topiramate (Topamax)
 Open study in 2004 by Dr. Michael Van Ameringen, n=16 adults, showed 70% of patients
had improvement with mean dosage of Topiramate 250 mg/day added for 14-16 weeks to
SSRI therapy (abstract, not yet published)
Dual therapy with two serotonin agents
Duration of Treatment for at least 1-year
Daniel Pine recommends that after at least 1-year of remission of symptoms, one can consider
stopping the medication during the first low stress period that occurs. (For students, this low
stress period usually means the summer, as opposed to during the school year).
When the decision has been made to stop, the medication should be tapered down gradually
(e.g. reduce by 25% of the dosage per week, so that a medication can thus be stopped over a
month or so) until completely stopped.
PANDAS (Pediatric Autoimmune Neuropsychiatric Disorders
Associated with Streptococcal Infection)
In about <5% of cases of OCD in children, it is felt that a contributory medical condition causing
OCD symptoms is PANDAS (pediatric autoimmune neuropsychiatric disorders associated with
streptococcal infection). It is characterized by sudden onset or exacerbation of OCD symptoms in
the presence of streptococcal upper respiratory tract infections. The mechanism is believed to be
caused by antineuronal antibodies formed against group, beta-hemolytic streptococcal cell wall
antigens, which cross-react with caudate neural tissue with the consequence of initiation of
obsessive-compulsive symptoms.
The official criteria for PANDAS, as established in 1998 by Dr. Susan Swedo1 from the NIMH are:





presence of obsessive-compulsive disorder, tic disorder, or both;
with prepubertal onset;
sudden, severe symptom onset and an episodic course characterized by remissions and
abrupt exacerbations;
a link in time between either the symptom onset or exacerbation and a GABHS infection;
adventitious movements or clumsiness.
The following suggestions have been cited for children who may appear to be vulnerable to
PANDAS:


1
Treat all streptococcal infections aggressively with antibiotics
Be sure to complete the course of antibiotic treatment to avoid development of resistant
strains of bacteria.
Retrieved Nov 4, 2006 from http://www.medscape.com/viewarticle/547096?rss
5



Make use of proven therapies such as cognitive/behavioral therapy and serotonin medication
(SSRI's) as are utilized to treat the more usual forms of OCD.
Diagnostic investigations recommended include throat culture for streptococcus, antistreptolysin O titer (ASOT) and anti-streptococcal DNase B titer.
Consult a neurologist if you suspect PANDAS
6
Overview of Treatment Strategies for OCD
Mild to Moderate OCD
Psychotherapy (e.g.
Cognitive-Behavioral
Therapy) or Psychosocial
Interventions
Moderate to Severe OCD
If unsatisfactory response
In addition to Psychotherapy, also
consider medications
Medication Strategies
Start with any of the following SSRIs for
children/youth (Fluoxetine, Fluvoxamine,
Sertraline, Paroxetine, Citalopram)
If unsatisfactory response
Consider Clomipramine
If unsatisfactory response
Consider

Augmentation with antipsychotic,
stimulant, pindolol, naltrexone,
lithium

Switching to alternate monotherapy

Dual therapy with two serotonin
agents
7
References








Bystritsky A, Ackerman DL, Rosen RM, Vapnik T, Gorbis E, Maidment KM, et al.:
Augmentation of serotonin reuptake inhibitors in refractory obsessive-compulsive disorder
using adjunctive olanzapine: a placebo-controlled trial. J Clin Psychiatry, 2004 Apr;65(4):5658.
Christopher M: Update on pharmacologic management of OCD: agents and augmentation, J.
Clin. Psychiatry 1997;58(suppl 12): 11-17.
Denys D, de Geus F, van Megan HJ, Westenberg, HG. A double-blind, randomized, placebocontrolled trial of quetiapine addition in patients with obsessive-compulsive disorder
refractory to serotonin reuptake inhibitors. J Clin Psychiatry 2004;65:1040-8.
Fux et al.: A placebo-controlled cross-over trial of adjunctive EPA in OCD. J Psychiatr Res.
2004 May-Jun;38(3):323-5.
Geller et al.: Which SSRI? A Meta-Analysis of Pharmacotherapy Trials in Pediatric ObsessiveCompulsive Disorder, Am J Psychiatry 160:1919-1928, November 2003
http://ajp.psychiatryonline.org/cgi/content/abstract/160/11/1919
Kaplan A, Hollander E: A review of pharmacologic treatments for obsessive-compulsive
disorder, Psychiatric Services, August 2003, 54(8): 1111-1118.
Soomro GM, et al "Selective serotonin re-uptake inhibitors (SSRIs) versus placebo for
obsessive compulsive disorder (OCD) (Review)" Cochrane Database of Systematic Reviews
2008; Issue 1: DOI: 10.1002/14651858.cd001765.pub 3.
Tynan WD: Obsessive Compulsive Disorder, last updated May 16, 2005, retrieved May 16,
2005 from http://www.emedicine.com/ped/topic2794.htm
Treatment Guidelines and Interesting Reviews



See http://www.psychguides.com for the Expert Consensus Guideline Series on the
Treatment of OCD
See http://www.aacap.org for the Practice Parameters of the Treatment of OCD in Children
and Youth. As of July 16, 2005, the direct link is at
http://www.aacap.org/clinical/parameters/summaries/Ocdsum.htm
Geller’s metanalysis, 2003
 For the four serotonin reuptake inhibitors (SSRIs) of paroxetine (Paxil), fluoxetine
(Prozac), fluvoxamine (Luvox) and sertraline (Zoloft), all these four SSRIs were
equivalent in efficacy
 In comparing efficacy of those four SSRIs to clomipramine (Anafranil), clomipramine was
superior – however, it still cannot be recommended as first-line due to a higher risk of
adverse effects with clomipramine
8