| Home | Subscribe to the Journal | Sign up for E-Lerts to your inbox |
| This
entire article is available in PDF format to paid subscribers (certain restrictions apply). If you have not already registered for Full Text Access to The Journal, then visit our registration page. |
Serotonin-Norepinephrine Reuptake Inhibitors in the Treatment of Obsessive-Compulsive Disorder: A Critical ReviewBernardo Dell'Osso, M.D.; Gerald Nestadt, M.B., B.Ch., M.P.H.; Andrea Allen, Ph.D.; and Eric Hollander, M.D.Objective: To critically review the antiobsessional properties of serotonin-norepinephrine reuptake inhibitors (SNRIs) (venlafaxine and clomipramine) in the treatment of obsessive-compulsive disorder (OCD) as an alternative to selective serotonin reuptake inhibitors (SSRIs), which are currently considered the first-line treatment of OCD. Data Sources: A MEDLINE search was performed to identify clinical trials with the SNRIs venlafaxine and clomipramine published from 1996 to 2004 (keywords: SNRIs, venlafaxine, duloxetine, and clomipramine, each matched individually with the term OCD), focusing on the best-designed studies for inclusion. Data Synthesis: Much of the literature about SNRIs in OCD supports the efficacy of these compounds in the treatment of OCD. However, double-blind, placebo-controlled studies with venlafaxine are lacking, and the most relevant studies consist of active comparison trials between SNRIs and SSRIs. In these studies, SNRIs seem to be as effective as SSRIs in OCD; SNRIs might be preferred for patients with certain types of treatment-resistant OCD or those with particular comorbid conditions. A large number of placebo-controlled and active comparison trials with clomipramine document efficacy in OCD, and meta-analytic studies suggest a small superiority over SSRIs. Compared with clomipramine, the SNRI venlafaxine showed fewer side effects and better tolerability. Conclusion: The SNRIs may represent a valid alternative to the SSRIs, particularly in specific cases. Double-blind, placebo-controlled studies are, however, needed to confirm the positive findings reported by several studies with venlafaxine. (J Clin Psychiatry 2006;67:600-610) Received July 17, 2005; accepted Oct. 8, 2005. From the Department of Psychiatry, Compulsive, Impulsive and Anxiety Disorders Program, Mount Sinai School of Medicine, New York, N.Y. (Drs. Dell'Osso, Allen, and Hollander); and the Department of Psychiatry and Behavioral Sciences, School of Medicine, The Johns Hopkins University, Baltimore, Md. (Dr. Nestadt). Dr. Hollander has been a consultant for Wyeth, Ortho-McNeil, Pfizer, and Abbott and has received grant/research support from Abbott, Ortho-McNeil, and Pfizer. Drs. Dell'Osso, Nestadt, and Allen report no financial or other relationship relevant to the subject matter of this article. Corresponding author and reprints: Eric Hollander, M.D., Box 1230, Mount Sinai School of Medicine, Department of Psychiatry, Compulsive, Impulsive and Anxiety Disorders Program, One Gustave L. Levy Place, New York, NY 10029 (e-mail: eric.hollander@mssm.edu). |
| Home | Subscribe to the Journal | Sign up for E-Lerts to your inbox |