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Gender differences in response and remission rates among patients receiving esketamine

INTRODUCTION: Depressive disorders are among the leading causes of disability. The lifetime risk for developing clinically significant depression is estimated around 15%. Multiple studies have found female-male ratio of 2:1 across nations and cultures. The reason for this marked difference is still...

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Autores principales: Guterman, A. T., Feffer, K., Gershi, A. Z.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cambridge University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10596366/
http://dx.doi.org/10.1192/j.eurpsy.2023.385
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author Guterman, A. T.
Feffer, K.
Gershi, A. Z.
author_facet Guterman, A. T.
Feffer, K.
Gershi, A. Z.
author_sort Guterman, A. T.
collection PubMed
description INTRODUCTION: Depressive disorders are among the leading causes of disability. The lifetime risk for developing clinically significant depression is estimated around 15%. Multiple studies have found female-male ratio of 2:1 across nations and cultures. The reason for this marked difference is still not clear, although several theories addressing social, biological, and environmental contributors have been suggested. Respond to anti-depressant treatment is considerably similar in both genders. However, several studies have shown worse outcomes among women during menopause. In 2019, the US Food and Drug Administration (FDA) approved a nasal spray formulation of esketamine for the treatment of resistant depression (TRD) in adults, and the treatment has been approved to use by the ministry of health in Israel since 2020 . Recent studies found more than 50% response and 35% remission rates, when nasal esketamine was given as an add-on therapy. OBJECTIVES: to assess gender differences in response and remission rates among patients receiving esketamine as an add-on therapy for TRD in a real-world setting METHODS: 23 female and 22 males received at least 12 weeks of esketamine treatment in a day-care setting. Data collected included depression, dissociation and quality of life scales. RESULTS: Females tend to experience more severe dissociation during treatment. Average response and remission rates were similar in both groups (48% and 32% respectively), however females were less favorable to show rapid response (during the first 4 weeks). among responders no major differences in time to response has been found. CONCLUSIONS: no major gender differences in response or remission rates have been found among patients receiving esketamine treatment for TRD aside from lower rates of rapid response. Additionally, Females report more severe dissociation during treatment. DISCLOSURE OF INTEREST: None Declared
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spelling pubmed-105963662023-10-25 Gender differences in response and remission rates among patients receiving esketamine Guterman, A. T. Feffer, K. Gershi, A. Z. Eur Psychiatry Abstract INTRODUCTION: Depressive disorders are among the leading causes of disability. The lifetime risk for developing clinically significant depression is estimated around 15%. Multiple studies have found female-male ratio of 2:1 across nations and cultures. The reason for this marked difference is still not clear, although several theories addressing social, biological, and environmental contributors have been suggested. Respond to anti-depressant treatment is considerably similar in both genders. However, several studies have shown worse outcomes among women during menopause. In 2019, the US Food and Drug Administration (FDA) approved a nasal spray formulation of esketamine for the treatment of resistant depression (TRD) in adults, and the treatment has been approved to use by the ministry of health in Israel since 2020 . Recent studies found more than 50% response and 35% remission rates, when nasal esketamine was given as an add-on therapy. OBJECTIVES: to assess gender differences in response and remission rates among patients receiving esketamine as an add-on therapy for TRD in a real-world setting METHODS: 23 female and 22 males received at least 12 weeks of esketamine treatment in a day-care setting. Data collected included depression, dissociation and quality of life scales. RESULTS: Females tend to experience more severe dissociation during treatment. Average response and remission rates were similar in both groups (48% and 32% respectively), however females were less favorable to show rapid response (during the first 4 weeks). among responders no major differences in time to response has been found. CONCLUSIONS: no major gender differences in response or remission rates have been found among patients receiving esketamine treatment for TRD aside from lower rates of rapid response. Additionally, Females report more severe dissociation during treatment. DISCLOSURE OF INTEREST: None Declared Cambridge University Press 2023-07-19 /pmc/articles/PMC10596366/ http://dx.doi.org/10.1192/j.eurpsy.2023.385 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Abstract
Guterman, A. T.
Feffer, K.
Gershi, A. Z.
Gender differences in response and remission rates among patients receiving esketamine
title Gender differences in response and remission rates among patients receiving esketamine
title_full Gender differences in response and remission rates among patients receiving esketamine
title_fullStr Gender differences in response and remission rates among patients receiving esketamine
title_full_unstemmed Gender differences in response and remission rates among patients receiving esketamine
title_short Gender differences in response and remission rates among patients receiving esketamine
title_sort gender differences in response and remission rates among patients receiving esketamine
topic Abstract
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10596366/
http://dx.doi.org/10.1192/j.eurpsy.2023.385
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