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Published Online: 1 July 2014

Venlafaxine in Treatment Resistant Obsessive-Compulsive Disorder

Publication: The Journal of Neuropsychiatry and Clinical Neurosciences
To the Editor: Selective serotonin reuptake inhibitors (SSRIs) are the first line treatment option for obsessive compulsive disorder (OCD). However, nearly 40% to 60% of patients do not respond satisfactorily to SSRIs.1 There is evidence to suggest that venlafaxine, a serotonin norepinephrine reuptake inhibitor, is useful in the treatment of OCD. However, only one study has examined its effectiveness in patients who have not responded to multiple SSRI trials.2 Hence, we report a series of five patients who responded to venlafaxine and maintained sustained improvement over an extended period following failure to respond to multiple SSRI trials.
The patients were being treated at the OCD clinic of the National Institute of Mental Health and Neurosciences (NIMHANS), Bangalore, India. They met DSM-IV criteria for OCD and were evaluated with the Yale-Brown obsessive compulsive scale (YBOCS),3 the Mini International Neuropsychiatric Interview plus4 and the Clinical Global Impression scale (CGI).5 Clinical characteristics and treatment details are given in Table 1. Treatment resistance was defined as nonresponse (<25% YBOCS improvement and CGI-Improvement score ≥3) to adequate trial (12 weeks) of at least two SSRIs.1
TABLE 1. Clinical Characteristics and Treatment Details
 Patient 1Patient 2Patient 3Patient 4Patient 5
Age2530443334
GenderMaleFemaleMaleFemaleMale
Age of onset1515142617
DiagnosisOCDOCDOCDOCDOCD predominatly obsessions
Comorbid conditionsNilDysthymiaTic disorder, anxious avoidant and anankastic personality disordersDepressionDepression
Principal obsessions• Contamination• Aggressive• Sexual• Contamination• Aggression
• Religious• Pathological doubts• Pathological doubt• Pathological doubts• Pathological doubts
Principal compulsions• Washing• Washing• Checking• Washing 
• Repeating• Repeating• Checking
Previous failed trials (adequate dosage and duration)• Citalopram• Fluoxetine• FluoxetineClomipramine• Fluoxetine
• Fluoxetine• Escitalopram• Sertraline• Paroxetine• Sertraline
• Fluoxamine  • Fluvoxamine• Escitalopram
• Paroxetine  • Citalopram 
• Sertaline  • Fluoxetine 
   Sertraline 
Failed cognitive behavior TherapyYesYesNoNoYes
Augmentation strategiesRisperidoneRisperidone, MemantineRisperidoneRisperidone, Lithium, Buspirone, ClonazepamMirtazepine, Clonazepam,
Failed cognitive behavior TherapyYesYesNoNoYes
Dose of venlafaxine225 mg150 mg225 mg225 mg150 mg
At the time of initiation of Venlafaxine     
YBOCS score1719233912
CGI severityModerately illModerately illModerately illSeverely illModerately ill
Post venlafaxine trial
First follow-up6 months4 months3 months6 months5 months
YBOCS score71013154
CGI severityBorderline illMildly illMildly illMildly illMildly ill
CGI improvementMuch improvedMuch improvedMuch improvedVery much improvedVery much improved
Last follow-up
Time since initiation of Venlafaxine75 months6 months26 months45 months26 months
YBOCS score10094
CGI severityNormal, not illNormal, not illNormal, not illBorderline illBorderline ill
CGI improvementVery much improvedMuch improvedVery much improvedVery much improvedVery much improved
OCD: obsessive-compulsive disorder; YBOCS: Yale Brown Obsessive Compulsive Scale; CGI: clinical global impression.
It is evident from the table that all the patients had failed to show response to multiple trials of SSRIs and augmentation strategies. Three of them had not shown response to even addition of cognitive-behavior therapy (CBT). At the end of treatment, all the five patients showed significant improvement with symptom reduction of ≥35% over the pretreatment YBOCS scores, which is considered as a significant treatment response in the treatment trials of OCD with a CGI-I score of 1 or 2.1 Moreover, they maintained improvement over long periods of follow-up without any relapses. Only one patient reported gastritis, which required treatment with proton pump inhibitor. Other four patients did not report any untoward side effects and seemed to tolerate venlafaxine well.
Our case series adds to the existing literature that venlafaxine may be beneficial in individuals with OCD who have not responded to multiple SSRIs. A previous open label study also found venlafaxine to be beneficial in up to 76% of the patients who did not respond to at least one SSRI trial.2 That three of our patients who responded to venlafaxine had not responded previously to even CBT underscores the need to examine the efficacy of venlafaxine systematically in treatment resistant OCD. The findings of our report must be interpreted with caution because of the retrospective nature of the study, small sample size, and absence of a comparison group.

References

1.
Shetti CN, Reddy YC, Kandavel T, et al.: Clinical predictors of drug nonresponse in obsessive-compulsive disorder. J Clin Psychiatry 2005; 66:1517–1523
2.
Hollander E, Friedberg J, Wasserman S, et al.: Venlafaxine in treatment-resistant obsessive-compulsive disorder. J Clin Psychiatry 2003; 64:546–550
3.
Goodman WK, Price LH, Rasmussen SA, et al.: The Yale-Brown Obsessive Compulsive Scale. I. Development, use, and reliability. Arch Gen Psychiatry 1989; 46:1006–1011
4.
Sheehan DV, Lecrubier Y, Sheehan KH, et al.: The Mini-International Neuropsychiatric Interview (M.I.N.I.): the development and validation of a structured diagnostic psychiatric interview for DSM-IV and ICD-10. J Clin Psychiatry 1998; 59(Suppl 20):22–33, quiz 34–57
5.
Guy W: ECDEU Assessment Manual for Psychopharmacology, in US Department Health, Education and Welfare Publication (ADM) 76-338. Rockville, MD, National Institute of Mental Health, 1976, pp 218‒222.

Information & Authors

Information

Published In

Go to The Journal of Neuropsychiatry and Clinical Neurosciences
Go to The Journal of Neuropsychiatry and Clinical Neurosciences
The Journal of Neuropsychiatry and Clinical Neurosciences
Pages: E44 - E45
PubMed: 25093787

History

Published online: 1 July 2014
Published in print: Summer 2014

Authors

Affiliations

Janardhanan C. Narayanaswamy, M.D.
OCD Clinic, Dept. of Psychiatry, National Institute of Mental Health and Neurosciences (NIMHANS), Bangalore, India
Biju Viswanath, M.D.
OCD Clinic, Department of Psychiatry, National Institute of Mental Health and Neurosciences (NIMHANS), Bangalore, India
Anish V. Cherian, Ph.D.
K.S. Hegde Medical Academy, Mangalore, India
Suresh Bada Math, M.D., D.N.B.
OCD Clinic, Department of Psychiatry, National Institute of Mental Health and Neurosciences (NIMHANS), Bangalore, India
Y. C. Janardhan Reddy, M.D.
OCD Clinic, Dept. of Psychiatry, National Institute of Mental Health and Neurosciences (NIMHANS), Bangalore, India

Notes

Send correspondence to Dr. Viswanath; e-mail: [email protected]

Competing Interests

The authors report no financial relationships with commercial interests.

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