Adjunctive vortioxetine for SSRI-resistant major depressive disorder: a "real-world" chart review study.
Adult
Analysis of Variance
Antidepressive Agents
/ administration & dosage
Depressive Disorder, Major
/ drug therapy
Depressive Disorder, Treatment-Resistant
/ drug therapy
Drug Therapy, Combination
Female
Humans
Male
Psychiatric Status Rating Scales
Reproducibility of Results
Retrospective Studies
Serotonin and Noradrenaline Reuptake Inhibitors
/ administration & dosage
Statistics, Nonparametric
Time Factors
Treatment Outcome
Vortioxetine
/ administration & dosage
Journal
Revista brasileira de psiquiatria (Sao Paulo, Brazil : 1999)
ISSN: 1809-452X
Titre abrégé: Braz J Psychiatry
Pays: Brazil
ID NLM: 100895975
Informations de publication
Date de publication:
2020
2020
Historique:
received:
30
08
2018
accepted:
09
11
2019
pubmed:
12
3
2020
medline:
23
6
2020
entrez:
12
3
2020
Statut:
ppublish
Résumé
Selective serotonin reuptake inhibitors (SSRIs) are the cornerstone of treatment of major depressive disorder (MDD). However, non-response is common, often necessitating combination strategies. The present study assessed the efficacy of vortioxetine as an add-on therapy in patients with SSRI-resistant MDD. The charts of 36 adult outpatients with DSM-IV-TR MDD who had not achieved a response after at least 8 weeks of treatment with an SSRI were reviewed retrospectively. Subjects were treated with vortioxetine (5-20 mg/day) for 8 weeks added to the current SSRI. The main outcome measures were change from baseline in total Hamilton Scale for Depression (HAM-D) score and the rate of response (a 50% or greater reduction in HAM-D score and a Clinical Global Impression - Improvement module [CGI-I] score of 1 or 2 at endpoint). HAM-D scores ≤ 7 were considered as remission. Additional outcome measures included the Snaith-Hamilton Pleasure Scale (SHAPS) and the Scale for Suicide Ideation (SSI). 32 patients completed the 8 weeks of treatment. At 8 weeks, a significant reduction in HAM-D score was observed (p ≤ 0.001), with response obtained by 41.7% and remission by 33.3% of patients. Significant reductions in SHAPS and SSI were also observed (p ≤ 0.001 for both scales). Adjunctive vortioxetine may be useful and well-tolerated in stage I treatment-resistant depression. However, the limitations of this study (such as small sample size, absence of randomization and control group, retrospective design, etc.) must be considered.
Identifiants
pubmed: 32159712
pii: S1516-44462020005005202
doi: 10.1590/1516-4446-2019-0690
pmc: PMC7236167
pii:
doi:
Substances chimiques
Antidepressive Agents
0
Serotonin and Noradrenaline Reuptake Inhibitors
0
Vortioxetine
3O2K1S3WQV
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
317-321Références
Can J Psychiatry. 2010 Mar;55(3):126-35
pubmed: 20370962
Front Psychiatry. 2019 Jan 31;10:17
pubmed: 30766492
World Psychiatry. 2017 Oct;16(3):317-318
pubmed: 28941085
CNS Neurol Disord Drug Targets. 2017;16(1):65-92
pubmed: 27781949
Clin Pharmacokinet. 2018 Jun;57(6):673-686
pubmed: 29189941
Curr Pharm Des. 2019;25(4):381-387
pubmed: 30864501
J Neurol Neurosurg Psychiatry. 1960 Feb;23:56-62
pubmed: 14399272
Hum Psychopharmacol. 2018 Jan;33(1):
pubmed: 29327372
J Consult Clin Psychol. 1979 Apr;47(2):343-52
pubmed: 469082
Expert Opin Drug Discov. 2019 Jan;14(1):81-89
pubmed: 30457395
Int J Mol Sci. 2018 Sep 23;19(10):
pubmed: 30249029
J Clin Psychiatry. 2015 Sep;76(9):e1147
pubmed: 26455685
Rev Psiquiatr Salud Ment. 2018 Jan - Mar;11(1):48-59
pubmed: 28800937
Depress Anxiety. 2020 Feb;37(2):134-145
pubmed: 31638723
Lancet. 2018 Apr 7;391(10128):1357-1366
pubmed: 29477251
Pharmacol Rep. 2017 Aug;69(4):595-601
pubmed: 28499187
Prog Neuropsychopharmacol Biol Psychiatry. 2019 Apr 20;91:20-27
pubmed: 29601896
J Affect Disord. 2016 May 15;196:225-33
pubmed: 26938965
Neurosci Biobehav Rev. 2018 Jan;84:272-288
pubmed: 28859997
Int J Risk Saf Med. 2017;29(1-2):101-106
pubmed: 28885220
Wien Klin Wochenschr. 2016 Apr;128(7-8):295-8
pubmed: 26404738
Expert Rev Neurother. 2016 May;16(5):483-95
pubmed: 27050932
Br J Psychiatry. 1995 Jul;167(1):99-103
pubmed: 7551619
Br J Psychiatry. 2019 Jan;214(1):42-51
pubmed: 30457075
Clin Pharmacol Drug Dev. 2018 Mar;7(3):319-331
pubmed: 28941196
J Clin Psychopharmacol. 2017 Dec;37(6):732-734
pubmed: 29040153
Clin Pharmacol Drug Dev. 2018 Nov;7(8):880-888
pubmed: 29920978
Int J Neuropsychopharmacol. 2019 Feb 1;22(2):83-84
pubmed: 30753655