PMID- 17177199 OWN - NLM STAT- MEDLINE DCOM- 20080114 LR - 20221207 IS - 1091-4269 (Print) IS - 1091-4269 (Linking) VI - 24 IP - 7 DP - 2007 TI - Quetiapine adjunct to selective serotonin reuptake inhibitors or venlafaxine in patients with major depression, comorbid anxiety, and residual depressive symptoms: a randomized, placebo-controlled pilot study. PG - 487-94 AB - This double-blind, placebo-controlled study examined the efficacy and tolerability of quetiapine in combination with selective serotonin reuptake inhibitors (SSRIs)/venlafaxine in 58 patients with major depressive disorder, comorbid anxiety symptoms (HAM-A-14 score > or =14), and residual depressive symptoms (HAM-D-17 score > or =18, CGI-S score > or =4). Patients had received an SSRI/venlafaxine (at a predefined therapeutic dose) for > or =6 weeks. Overall, 62% (18/29) of quetiapine- and 55% (16/29) of placebo-treated patients completed the study. The mean change in HAM-D and HAM-A total scores from baseline to Week 8 (primary endpoint) was significantly greater with quetiapine (mean dose 182 mg/day) than placebo: -11.2 vs. -5.5 (P=.008) and -12.5 vs. -5.9 (P=.002), respectively. The onset of quetiapine efficacy (HAM-D/HAM-A/CGI-I) was rapid (by Week 1) and continued through to Week 8. Significant differences (P<.05) from baseline to Week 8 were observed between groups in 7/17 HAM-D (including feelings of guilt, suicide) and 6/14 HAM-A items (including tension, cardiovascular symptoms). Response (> or =50% decrease in total score) was higher for quetiapine than placebo: HAM-D, 48% vs. 28% (not significant, NS); HAM-A, 62% vs. 28% (P=.02). Remission (total score < or =7) was higher for quetiapine than placebo: HAM-D, 31% vs. 17% (NS); HAM-A, 41% vs. 17% (NS). CGI-S, CGI-I, and the Global Assessment Scale showed that quetiapine was significantly more effective than placebo. For quetiapine, adverse events (AEs) were similar to those previously observed; sedation/somnolence/lethargy was the most commonly reported. Here quetiapine was shown to be effective as augmentation of SSRI/venlafaxine therapy in patients with major depression, comorbid anxiety, and residual depressive symptoms, with no unexpected tolerability issues. Further studies are warranted. CI - 2006 Wiley-Liss, Inc FAU - McIntyre, Alexander AU - McIntyre A AD - Department of Psychiatry, Penticton Regional Hospital, Penticton, British Columbia, Canada. amcintyre@telus.net FAU - Gendron, Alain AU - Gendron A FAU - McIntyre, Amanda AU - McIntyre A LA - eng PT - Comparative Study PT - Journal Article PT - Randomized Controlled Trial PT - Research Support, Non-U.S. Gov't PL - United States TA - Depress Anxiety JT - Depression and anxiety JID - 9708816 RN - 0 (Antidepressive Agents, Second-Generation) RN - 0 (Antipsychotic Agents) RN - 0 (Cyclohexanols) RN - 0 (Dibenzothiazepines) RN - 0 (Serotonin Uptake Inhibitors) RN - 2S3PL1B6UJ (Quetiapine Fumarate) RN - 7D7RX5A8MO (Venlafaxine Hydrochloride) SB - IM MH - Adult MH - Antidepressive Agents, Second-Generation/*administration & dosage/adverse effects MH - Antipsychotic Agents/*administration & dosage/adverse effects MH - Anxiety Disorders/diagnosis/drug therapy/psychology MH - Comorbidity MH - Cyclohexanols/*administration & dosage/adverse effects MH - Depressive Disorder, Major/*drug therapy MH - Dibenzothiazepines/*administration & dosage/adverse effects MH - Double-Blind Method MH - Drug Therapy, Combination MH - Female MH - Humans MH - Male MH - Middle Aged MH - Personality Inventory MH - Quetiapine Fumarate MH - Selective Serotonin Reuptake Inhibitors/*administration & dosage/adverse effects MH - Venlafaxine Hydrochloride EDAT- 2006/12/21 09:00 MHDA- 2008/01/15 09:00 CRDT- 2006/12/21 09:00 PHST- 2006/12/21 09:00 [pubmed] PHST- 2008/01/15 09:00 [medline] PHST- 2006/12/21 09:00 [entrez] AID - 10.1002/da.20275 [doi] PST - ppublish SO - Depress Anxiety. 2007;24(7):487-94. doi: 10.1002/da.20275.