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Psychopharmacological Treatments for Mental Disorders in Patients with Neuromuscular Diseases: A Scoping Review

Mental disorders are observed in neuromuscular diseases, especially now that patients are living longer. Psychiatric symptoms may be severe and psychopharmacological treatments may be required. However, very little is known about pharmacotherapy in these conditions. We aimed to summarize the current...

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Autores principales: Brusa, Chiara, Gadaleta, Giulio, D’Alessandro, Rossella, Urbano, Guido, Vacchetti, Martina, Davico, Chiara, Vitiello, Benedetto, Ricci, Federica S., Mongini, Tiziana E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8870619/
https://www.ncbi.nlm.nih.gov/pubmed/35203936
http://dx.doi.org/10.3390/brainsci12020176
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author Brusa, Chiara
Gadaleta, Giulio
D’Alessandro, Rossella
Urbano, Guido
Vacchetti, Martina
Davico, Chiara
Vitiello, Benedetto
Ricci, Federica S.
Mongini, Tiziana E.
author_facet Brusa, Chiara
Gadaleta, Giulio
D’Alessandro, Rossella
Urbano, Guido
Vacchetti, Martina
Davico, Chiara
Vitiello, Benedetto
Ricci, Federica S.
Mongini, Tiziana E.
author_sort Brusa, Chiara
collection PubMed
description Mental disorders are observed in neuromuscular diseases, especially now that patients are living longer. Psychiatric symptoms may be severe and psychopharmacological treatments may be required. However, very little is known about pharmacotherapy in these conditions. We aimed to summarize the current knowledge on the use of psychopharmacological treatments for mental disorders in patients living with a neuromuscular disease. A scoping review was performed using the methodology of the Joanna Briggs Institute. Four databases were searched from January 2000 to July 2021. Articles were screened based on titles and abstracts. Full-text papers published in peer-reviewed journals in English were selected. Twenty-six articles met eligibility criteria, all being case reports/series focusing on the psychopharmacological control of psychiatric symptoms for the following conditions: myasthenia gravis (n = 11), Duchenne (n = 5) and Becker (n = 3) muscular dystrophy, mitochondrial disorders (n = 3), glycogen storage disease (n = 1), myotonic dystrophy (n = 1), hyperkalemic periodic paralysis (n = 1), and congenital myasthenic syndrome (n = 1). None of the articles provided details on the decision-making process to choose a specific drug/regimen or on follow-up strategies to monitor safety and efficacy. Larger studies showing real-world data would be required to guide consensus-based recommendations, thus improving current standards of care and, ultimately, the quality of life of patients and their families.
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spelling pubmed-88706192022-02-25 Psychopharmacological Treatments for Mental Disorders in Patients with Neuromuscular Diseases: A Scoping Review Brusa, Chiara Gadaleta, Giulio D’Alessandro, Rossella Urbano, Guido Vacchetti, Martina Davico, Chiara Vitiello, Benedetto Ricci, Federica S. Mongini, Tiziana E. Brain Sci Review Mental disorders are observed in neuromuscular diseases, especially now that patients are living longer. Psychiatric symptoms may be severe and psychopharmacological treatments may be required. However, very little is known about pharmacotherapy in these conditions. We aimed to summarize the current knowledge on the use of psychopharmacological treatments for mental disorders in patients living with a neuromuscular disease. A scoping review was performed using the methodology of the Joanna Briggs Institute. Four databases were searched from January 2000 to July 2021. Articles were screened based on titles and abstracts. Full-text papers published in peer-reviewed journals in English were selected. Twenty-six articles met eligibility criteria, all being case reports/series focusing on the psychopharmacological control of psychiatric symptoms for the following conditions: myasthenia gravis (n = 11), Duchenne (n = 5) and Becker (n = 3) muscular dystrophy, mitochondrial disorders (n = 3), glycogen storage disease (n = 1), myotonic dystrophy (n = 1), hyperkalemic periodic paralysis (n = 1), and congenital myasthenic syndrome (n = 1). None of the articles provided details on the decision-making process to choose a specific drug/regimen or on follow-up strategies to monitor safety and efficacy. Larger studies showing real-world data would be required to guide consensus-based recommendations, thus improving current standards of care and, ultimately, the quality of life of patients and their families. MDPI 2022-01-28 /pmc/articles/PMC8870619/ /pubmed/35203936 http://dx.doi.org/10.3390/brainsci12020176 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Brusa, Chiara
Gadaleta, Giulio
D’Alessandro, Rossella
Urbano, Guido
Vacchetti, Martina
Davico, Chiara
Vitiello, Benedetto
Ricci, Federica S.
Mongini, Tiziana E.
Psychopharmacological Treatments for Mental Disorders in Patients with Neuromuscular Diseases: A Scoping Review
title Psychopharmacological Treatments for Mental Disorders in Patients with Neuromuscular Diseases: A Scoping Review
title_full Psychopharmacological Treatments for Mental Disorders in Patients with Neuromuscular Diseases: A Scoping Review
title_fullStr Psychopharmacological Treatments for Mental Disorders in Patients with Neuromuscular Diseases: A Scoping Review
title_full_unstemmed Psychopharmacological Treatments for Mental Disorders in Patients with Neuromuscular Diseases: A Scoping Review
title_short Psychopharmacological Treatments for Mental Disorders in Patients with Neuromuscular Diseases: A Scoping Review
title_sort psychopharmacological treatments for mental disorders in patients with neuromuscular diseases: a scoping review
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8870619/
https://www.ncbi.nlm.nih.gov/pubmed/35203936
http://dx.doi.org/10.3390/brainsci12020176
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