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Critical Review of the Use of Second-Generation Antipsychotics in Obsessive–Compulsive and Related Disorders

Currently, all second-generation antipsychotics are approved for schizophrenia. Many are also approved for bipolar disorder, with some also approved as adjunctive treatment for depression and autism-related irritability. Second-generation antipsychotics are increasingly being prescribed for indicati...

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Autores principales: Kim, Dongmi, Ryba, Nicole L., Kalabalik, Julie, Westrich, Ligia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6131117/
https://www.ncbi.nlm.nih.gov/pubmed/30171515
http://dx.doi.org/10.1007/s40268-018-0246-8
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author Kim, Dongmi
Ryba, Nicole L.
Kalabalik, Julie
Westrich, Ligia
author_facet Kim, Dongmi
Ryba, Nicole L.
Kalabalik, Julie
Westrich, Ligia
author_sort Kim, Dongmi
collection PubMed
description Currently, all second-generation antipsychotics are approved for schizophrenia. Many are also approved for bipolar disorder, with some also approved as adjunctive treatment for depression and autism-related irritability. Second-generation antipsychotics are increasingly being prescribed for indications other than those approved by the Food and Drug Administration, such as in dementia, anxiety, and post-traumatic stress disorder to name a few. Obsessive–compulsive and related disorders are a group of disorders characterized by preoccupation and repetitive behaviors. According to the latest edition of the Diagnostic and Statistical Manual of Mental Disorders, obsessive–compulsive disorder, body dysmorphic disorder, trichotillomania, hoarding disorder, and excoriation, the latter two being newly designated disorders, fall under obsessive–compulsive and related disorders. Due to a lack of well designed clinical studies specifically addressing the use of second-generation antipsychotics in obsessive–compulsive and related disorders, it is unknown whether these agents are clinically beneficial. Current research describing the pathophysiology of these disorders shows the involvement of similar brain regions and neurotransmitters across the five obsessive–compulsive and related disorders. Despite differences in the receptor binding profiles, second-generation antipsychotics share many common pharmacodynamics properties. This review sought to examine all the published reports of second-generation antipsychotics being used in the management of symptoms of the aforementioned diseases and compile evidence for clinicians who encounter patients who are unresponsive to standard treatment.
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spelling pubmed-61311172018-09-12 Critical Review of the Use of Second-Generation Antipsychotics in Obsessive–Compulsive and Related Disorders Kim, Dongmi Ryba, Nicole L. Kalabalik, Julie Westrich, Ligia Drugs R D Review Article Currently, all second-generation antipsychotics are approved for schizophrenia. Many are also approved for bipolar disorder, with some also approved as adjunctive treatment for depression and autism-related irritability. Second-generation antipsychotics are increasingly being prescribed for indications other than those approved by the Food and Drug Administration, such as in dementia, anxiety, and post-traumatic stress disorder to name a few. Obsessive–compulsive and related disorders are a group of disorders characterized by preoccupation and repetitive behaviors. According to the latest edition of the Diagnostic and Statistical Manual of Mental Disorders, obsessive–compulsive disorder, body dysmorphic disorder, trichotillomania, hoarding disorder, and excoriation, the latter two being newly designated disorders, fall under obsessive–compulsive and related disorders. Due to a lack of well designed clinical studies specifically addressing the use of second-generation antipsychotics in obsessive–compulsive and related disorders, it is unknown whether these agents are clinically beneficial. Current research describing the pathophysiology of these disorders shows the involvement of similar brain regions and neurotransmitters across the five obsessive–compulsive and related disorders. Despite differences in the receptor binding profiles, second-generation antipsychotics share many common pharmacodynamics properties. This review sought to examine all the published reports of second-generation antipsychotics being used in the management of symptoms of the aforementioned diseases and compile evidence for clinicians who encounter patients who are unresponsive to standard treatment. Springer International Publishing 2018-08-31 2018-09 /pmc/articles/PMC6131117/ /pubmed/30171515 http://dx.doi.org/10.1007/s40268-018-0246-8 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/), which permits any noncommercial use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Review Article
Kim, Dongmi
Ryba, Nicole L.
Kalabalik, Julie
Westrich, Ligia
Critical Review of the Use of Second-Generation Antipsychotics in Obsessive–Compulsive and Related Disorders
title Critical Review of the Use of Second-Generation Antipsychotics in Obsessive–Compulsive and Related Disorders
title_full Critical Review of the Use of Second-Generation Antipsychotics in Obsessive–Compulsive and Related Disorders
title_fullStr Critical Review of the Use of Second-Generation Antipsychotics in Obsessive–Compulsive and Related Disorders
title_full_unstemmed Critical Review of the Use of Second-Generation Antipsychotics in Obsessive–Compulsive and Related Disorders
title_short Critical Review of the Use of Second-Generation Antipsychotics in Obsessive–Compulsive and Related Disorders
title_sort critical review of the use of second-generation antipsychotics in obsessive–compulsive and related disorders
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6131117/
https://www.ncbi.nlm.nih.gov/pubmed/30171515
http://dx.doi.org/10.1007/s40268-018-0246-8
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