Medication Augmentation after the Failure of SSRIs for Depression
The University of Texas Southwestern Medical Center · Massachusetts General Hospital · +3 more institutions
Abstract
Although clinicians frequently add a second medication to an initial, ineffective antidepressant drug, no randomized controlled trial has compared the efficacy of this approach.
We randomly assigned 565 adult outpatients who had nonpsychotic major depressive disorder without remission despite a mean of 11.9 weeks of citalopram therapy (mean final dose, 55 mg per day) to receive sustained-release bupropion (at a dose of up to 400 mg per day) as augmentation and 286 to receive buspirone (at a dose of up to 60 mg per day) as augmentation. The primary outcome of remission of symptoms was defined as a score of 7 or less on the 17-item Hamilton Rating Scale for Depression (HRSD-17) at the end of this study; scores were obtained over the telephone by raters blinded to treatment assignment. The 16-item Quick Inventory of Depressive Symptomatology--Self-Report (QIDS-SR-16) was used to determine the secondary outcomes of remission (defined as a score of less than 6 at the end of this study) and response (a reduction in baseline scores of 50 percent or more).
Citation impact
- FWCI
- 67.95
- Percentile
- 100%
- References
- 19
Authors
13Topics & keywords
- Medicine
- Depression (economics)
- Intensive care medicine
- Psychiatry
- MEDLINE
- Good health and well-being
Funding
- UDU.S. Department of Health and Human Services
- ALAbbott Laboratories
- BSBristol-Myers Squibb
- ELEli Lilly and Company
- PPfizer
- AAstraZeneca
- BBayer
- GGlaxoSmithKline
- SSanofi
- PPharmavite
- UOUniversity of Texas Southwestern Medical Center
- HLH. Lundbeck A/S
- NINational Institutes of HealthAward: N01MH90003
- NINational Institute of Mental HealthAward: N01MH90003