Bupropion for Major Depressive Disorder or Persistent Depressive Disorder (Dysthymia)
Author(s) -
Erika MacDonald,
Jennifer Horton
Publication year - 2021
Publication title -
canadian journal of health technologies
Language(s) - English
Resource type - Journals
ISSN - 2563-6596
DOI - 10.51731/cjht.2021.62
Subject(s) - bupropion , sertraline , venlafaxine , major depressive disorder , escitalopram , vortioxetine , paroxetine , citalopram , fluoxetine , psychiatry , adverse effect , sexual dysfunction , medicine , psychology , antidepressant , anxiety , mood , receptor , pathology , smoking cessation , serotonin
Direct and indirect evidence from 6 systematic reviews did not demonstrate a difference in treatment response or remission rates, or functional outcomes, with bupropion as compared to other antidepressants in adults with major depressive disorder.
Direct and indirect evidence from 5 systematic reviews did not demonstrate a difference in overall adverse events, overall withdrawals, or withdrawals due to adverse events apart from a possible decreased risk of withdrawal due to adverse events with vortioxetine in a single indirect comparison.
Direct and indirect evidence from 2 systematic reviews supports that the risk of sexual dysfunction may be lower with bupropion than other antidepressants (escitalopram, paroxetine, sertraline, and fluoxetine), while 1 systematic review showed no significant difference in sexual function scores between bupropion and venlafaxine.
There is limited evidence supporting the cost-effectiveness of bupropion to augment citalopram, and dominance of vortioxetine compared to bupropion, for major depressive disorder with inadequate response to initial therapy.
There is a lack evidence surrounding the comparative clinical or cost-effectiveness of bupropion in dysthymia.
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