Vortioxetine as adjunctive therapy in the treatment of schizophrenia

Author:

Redaelli Sofia1,Porffy Lilla1,Oloyede Ebenezer12,Dzahini Olubanke23ORCID,Lewis Gabriella12,Lobo Maria12,Whiskey Eromona43ORCID,Shergill Sukhi S.156

Affiliation:

1. Institute of Psychiatry, Psychology & Neuroscience, King’s College London, London, UK

2. South London and Maudsley NHS Foundation Trust, London, UK

3. Institute of Pharmaceutical Science, King’s College London, London, UK

4. Pharmacy Department, South London and Maudsley NHS Foundation Trust, London SE5 8AZ, UK

5. Kent and Medway NHS and Social Care Partnership Trust, Maidstone, UK

6. Kent and Medway Medical School, Canterbury, UK

Abstract

Background: The evidence for safe and effective interventions to treat the negative and cognitive symptoms of schizophrenia is lacking. Objectives: Vortioxetine is a novel antidepressant that has been used as adjunctive therapy for the treatment of psychosis; however, its effectiveness in clinical practice is relatively unknown. In this study, we aimed to determine the potential clinical effectiveness and safety and tolerability of vortioxetine in psychosis. Design: This is a non-interventional, retrospective study on the add-on use of vortioxetine in a group of people with schizophrenia-spectrum disorders in a large UK NHS mental health trust. Methods: Clinical effectiveness of vortioxetine was retrospectively assessed through the Clinical Global Impression – Severity (CGI-S) scale at 3 months. Safety and tolerability were evaluated through treatment discontinuation rates at 3, 6, and 12 months, and clinical reasons were evaluated at the primary endpoint of 3 months. Results: Data were available for 40 subjects with a diagnosis of schizophrenia or schizoaffective disorder–prescribed vortioxetine treatment; 30 (75%) remained on treatment at 3 months. At CGI-S assessment, 15 of the 35 evaluated subjects reported at least a 1-point improvement, from 5 at baseline to 4 after 3 months of treatment. Twenty-six (65%) remained on treatment at 1-year follow-up. The main reasons for those discontinuing treatment were inadequate response (10%) and manic switch (7.5%), while one subject refused treatment. Tolerability to treatment was good, and 36 subjects (90%) reported no adverse events specific to vortioxetine treatment. Conclusion: Schizophrenia is a complex illness, and there is insufficient treatment response in many individuals. A significant proportion of whom may require adjunctive treatments depending on the nature of the residual symptoms. Vortioxetine could be a potentially safe and effective option in such people, but further controlled studies are required.

Funder

king’s college london

Publisher

SAGE Publications

Subject

Pharmacology, Toxicology and Pharmaceutics (miscellaneous),Psychology (miscellaneous)

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