Published January 4, 2022 | Version v1
Dataset Restricted

Adjunctive vortioxetine for SSRI-resistant major depressive disorder: a ''real-world'' chart review study

  • 1. Department of Mental Health, Psychiatric Service of Diagnosis and Treatment, Hospital ''G. Mazzini,'' National Health Service (NHS), ASL 4 Teramo, Italy AND Department of Neurosciences and Imaging, University ''G. D'Annunzio'' Chieti, Italy
  • 2. Department of Psychiatry, Federico II University, Naples, Italy AND Polyedra, Teramo, Italy.

Description

Adjunctive vortioxetine for SSRI-resistant major
depressive disorder: a ‘‘real-world’’ chart review study

Objective: 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.
Methods: 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 p 7 were considered as remission.
Additional outcome measures included the Snaith-Hamilton Pleasure Scale (SHAPS) and the Scale
for Suicide Ideation (SSI).
Results: 32 patients completed the 8 weeks of treatment. At 8 weeks, a significant reduction in HAM-D
score was observed (p 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 p 0.001 for both scales).
Conclusions: 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.

Files

Restricted

The record is publicly accessible, but files are restricted. Log in to check if you have access.

Additional details

Related works

Is supplement to
10.1590/1516-4446-2019-0690 (DOI)