Literature DB >> 28663124

Comparative evaluation of vortioxetine as a switch therapy in patients with major depressive disorder.

Michael E Thase1, Natalya Danchenko2, Melanie Brignone2, Ioana Florea3, Francoise Diamand2, Paula L Jacobsen4, Eduard Vieta5.   

Abstract

Switching antidepressant therapy is a recommended strategy for depressed patients who neither respond to nor tolerate an initial pharmacotherapy course. This paper reviews the efficacy and tolerability of switching to vortioxetine. All three published studies of patients with major depressive disorder (MDD) switched from SSRI/SNRI therapy to vortioxetine due to lack of efficacy or tolerability were selected. Vortioxetine was evaluated versus agomelatine directly (REVIVE) and versus sertraline, venlafaxine, bupropion, and citalopram in an indirect treatment comparison (ITC) from switch studies retrieved in a literature review. Vortioxetine׳s impact on SSRI-induced treatment-emergent sexual dysfunction (TESD) was assessed directly versus escitalopram (NCT01364649) in stable patients with MDD. Vortioxetine׳s tolerability in the switch population was compared to the overall MDD population. Vortioxetine showed significant benefits over agomelatine on efficacy, functioning, and quality-of-life outcomes, with fewer withdrawals due to adverse events (AEs) (REVIVE). Vortioxetine had numerically higher remission rates versus all therapies included (ITC). Withdrawal rates due to AEs were significantly lower for vortioxetine versus sertraline, venlafaxine, and bupropion, and numerically lower versus citalopram. Switching to vortioxetine was statistically superior to escitalopram in improving TESD (NCT01364649). Tolerability was similar in the switch and overall MDD populations. These findings suggest that vortioxetine is an effective switch therapy for patients with MDD whose response to SSRI/SNRI therapy is inadequate. Vortioxetine was well tolerated and, for patients with a history of TESD, showed significant advantages versus escitalopram. Vortioxetine appears to be a valid option for patients with MDD who have not been effectively treated with first-line pharmacotherapies.
Copyright © 2017 The Authors. Published by Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Comparative effectiveness research; Drug switching; Drug-related side effects and adverse reactions; Major depressive disorder; Vortioxetine

Mesh:

Substances:

Year:  2017        PMID: 28663124     DOI: 10.1016/j.euroneuro.2017.05.009

Source DB:  PubMed          Journal:  Eur Neuropsychopharmacol        ISSN: 0924-977X            Impact factor:   4.600


  4 in total

1.  Paroxetine versus Vortioxetine for Depressive Symptoms in Postmenopausal Transition: A Preliminary Study.

Authors:  Camilla Callegari; Marta Ielmini; Ivano Caselli; Giulia Lucca; Celeste Isella; Marcello Diurni; Fabiana Pettenon; Nicola Poloni
Journal:  Psychopharmacol Bull       Date:  2019-02-15

2.  Vortioxetine liposomes as a novel alternative to improve drug stability under stress conditions: toxicity studies and evaluation of antidepressant-like effect.

Authors:  Caroline Hermann Nodari; Natália Dalanhol De Quadros; Raquel Chiarentin; Francini Pereira Da Silva; Fernando Dal Pont Morisso; Mariele Feiffer Charão; Juliane Deise Fleck; Cristiane Bastos De Mattos; Andresa Heemann Betti; Simone Gasparin Verza
Journal:  Pharmacol Rep       Date:  2022-09-09       Impact factor: 3.919

3.  Acute caffeine reverses the disruptive effects of chronic fluoxetine on the sexual behavior of female and male rats.

Authors:  Brunella V González Cautela; Gonzalo R Quintana; Jessica Akerman; James G Pfaus
Journal:  Psychopharmacology (Berl)       Date:  2020-11-26       Impact factor: 4.530

4.  Intravenous vortioxetine to accelerate onset of effect in major depressive disorder: a 7-day randomized, double-blind, placebo-controlled exploratory study.

Authors:  Elmars Rancans; Janos Zambori; Mads Dalsgaard; Corine Baayen; Johan Areberg; Anders Ettrup; Ioana Florea
Journal:  Int Clin Psychopharmacol       Date:  2020-11       Impact factor: 2.023

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.