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Home » Major Depressive Disorder

Psychiatric Times. Vol. 29 No. 3
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PUTTING RESEARCH INTO PRACTICE 

Bupropion After Nonresponse or Partial Response to an SSRI or SNRI?

By Rajnish Mago, MD | March 1, 2012
Dr Mago is Director of the Mood Disorders Program at Thomas Jefferson University and Associate Professor of Psychiatry and Human Behavior at Jefferson Medical College in Philadelphia. Dr Mago reports that he has received research grants from Bristol-Myers Squibb, Eli Lilly and Company, Forest Research Institute, Otsuka Pharmaceuticals, GlaxoSmithKline, and AstraZeneca. He has been a speaker and consultant for Bristol-Myers Squibb.

The beneffits of adding Bupropion to SSRI or SNRIs in depression treatmentThis is the third in a series of occasional columns that aim to help clinicians interpret research related to a clinical question. Perhaps more important, the tips and discussion of the issues aim to improve clinicians’ understanding of research methodology and critical appraisal of the literature in general. Your questions, comments, and suggestions are eagerly solicited at rajnish.mago@jefferson.edu.

While SSRIs and SNRIs are valuable in the treatment of major depressive disorder (MDD), partial response or nonresponse occurs in many patients.1 In a survey of clinicians, the most frequently chosen agent for addition to an SSRI after inadequate response was bupropion (30%).2 In that survey, bupropion was chosen as the “augmenting” agent by more experienced clinicians; by US rather than Canadian clinicians; and by clinicians from community, individual practice, or group settings rather than from academic settings.

TIP: Many treatment strategies that are widely practiced are not based on scientific evidence. Make it a habit to question treatments that are routinely used. Some of these treatments may in fact turn out to be effective, but some others will be shown to be myths. The history of medicine is full of treatments that were widely used for years before being shown to be myths.

Is the strategy of adding bupropion to an SSRI or SNRI based on reliable scientific studies or mainly on the hypothesis that combining antidepressants with different mechanisms of action may result in greater efficacy than using either one of them alone?

Case reports and open-label studies3 have suggested that augmentation of SSRIs or SNRIs with bupropion may be efficacious.

TIP: When trying to determine whether a treatment is efficacious or not, look for only double-blind, randomized, controlled trials (RCTs). Case reports and uncontrolled studies can only suggest that a treatment may work, but such treatments are frequently disproved. Busy clinicians can save a lot of reading time and avoid confusion by focusing only on RCTs whenever possible.

Before looking for evidence, we should define our questions. Is ad­dition of bupropion to an SSRI or SNRI helpful in patients (1) with minimal or no response to the SSRI or SNRI? (2) with response to the SSRI or SNRI (greater than 50% improvement) but failure to achieve remission? or (3) who are just starting treatment with the SSRI or SNRI, ie, from the outset? (The possibility that bupropion may treat some of the adverse effects of serotonergic antidepressants is beyond the purview of this column.) Importantly, we must distinguish from switching from an SSRI to bupropion (ie, is any perceived benefit from the addition of bupropion to an SSRI better than simply switching to bupropion?).

A systematic search of the MEDLINE and Scopus databases was done (last on December 8, 2011). Many clinicians will be surprised to know that no RCT of the addition of bupropion to an SSRI or SNRI has ever been conducted. This includes a comparison to simply continuing the SSRI or SNRI, switching to bupropion, or other possible comparison strategies. There are, however, other types of studies that shed some tentative light on the issue and a discussion of their limitations may be of general educational value.

The STAR*D study included the addition of bupropion in patients with MDD who did not achieve remission after 12 weeks of treatment with citalopram(Drug information on citalopram).4 This strategy was compared with augmentation of ci­talopram with buspirone(Drug information on buspirone). However, in this large sample (N = 565), no statistically significant difference was found in remission (the primary outcome measure) between the two groups.

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by sharon A | July 16, 2012 7:11 PM EDT

I always have to wonder about misdiagnosis in the first place. How many "non-responders"are actually undiagnosed ADHD? [or the latest popular add on, Bipolar?] In fact, who knows how many suicides of SSRI treated were because of a whole other diagnosis that just wasn't quite evident or was mis-perceived at the time of diagnosis [e.g. treated for "OCD" with high dose SSRI's when the person is more ADHD with OCD tendencies; in which case, treating with an SSRI while not addressing the dopaminergic situation creates a real problem].

Be careful to watch closely whenever titrating from one to the other. I have personally had a very difficult experience, even with a very slow titration, from an SSRI to Buproprion....tolerated three weeks of significant depression. I find that I actually do BEST with some combination. The very small addition of an SSRI helps take the edge off anxiety that the Buproprion doesn't efficiently cover [while the Buproprion helps with so many other symptoms the SSRI doesn't fully address].






 
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