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Pharmacological enhancement of exposure-based treatment in PTSD: a qualitative review

There is a good amount of evidence that exposure therapy is an effective treatment for posttraumatic stress disorder (PTSD). Notwithstanding its efficacy, there is room for improvement, since a large proportion of patients does not benefit from treatment. Recently, an interesting new direction in th...

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Detalles Bibliográficos
Autores principales: de Kleine, Rianne A., Rothbaum, Barbara O., van Minnen, Agnes
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Co-Action Publishing 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3800126/
https://www.ncbi.nlm.nih.gov/pubmed/24147208
http://dx.doi.org/10.3402/ejpt.v4i0.21626
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author de Kleine, Rianne A.
Rothbaum, Barbara O.
van Minnen, Agnes
author_facet de Kleine, Rianne A.
Rothbaum, Barbara O.
van Minnen, Agnes
author_sort de Kleine, Rianne A.
collection PubMed
description There is a good amount of evidence that exposure therapy is an effective treatment for posttraumatic stress disorder (PTSD). Notwithstanding its efficacy, there is room for improvement, since a large proportion of patients does not benefit from treatment. Recently, an interesting new direction in the improvement of exposure therapy efficacy for PTSD emerged. Basic research found evidence of the pharmacological enhancement of the underlying learning and memory processes of exposure therapy. The current review aims to give an overview of clinical studies on pharmacological enhancement of exposure-based treatment for PTSD. The working mechanisms, efficacy studies in PTSD patients, and clinical utility of four different pharmacological enhancers will be discussed: d-cycloserine, MDMA, hydrocortisone, and propranolol.
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spelling pubmed-38001262013-10-21 Pharmacological enhancement of exposure-based treatment in PTSD: a qualitative review de Kleine, Rianne A. Rothbaum, Barbara O. van Minnen, Agnes Eur J Psychotraumatol Review Article There is a good amount of evidence that exposure therapy is an effective treatment for posttraumatic stress disorder (PTSD). Notwithstanding its efficacy, there is room for improvement, since a large proportion of patients does not benefit from treatment. Recently, an interesting new direction in the improvement of exposure therapy efficacy for PTSD emerged. Basic research found evidence of the pharmacological enhancement of the underlying learning and memory processes of exposure therapy. The current review aims to give an overview of clinical studies on pharmacological enhancement of exposure-based treatment for PTSD. The working mechanisms, efficacy studies in PTSD patients, and clinical utility of four different pharmacological enhancers will be discussed: d-cycloserine, MDMA, hydrocortisone, and propranolol. Co-Action Publishing 2013-10-17 /pmc/articles/PMC3800126/ /pubmed/24147208 http://dx.doi.org/10.3402/ejpt.v4i0.21626 Text en © 2013 Rianne A. de Kleine et al. http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
de Kleine, Rianne A.
Rothbaum, Barbara O.
van Minnen, Agnes
Pharmacological enhancement of exposure-based treatment in PTSD: a qualitative review
title Pharmacological enhancement of exposure-based treatment in PTSD: a qualitative review
title_full Pharmacological enhancement of exposure-based treatment in PTSD: a qualitative review
title_fullStr Pharmacological enhancement of exposure-based treatment in PTSD: a qualitative review
title_full_unstemmed Pharmacological enhancement of exposure-based treatment in PTSD: a qualitative review
title_short Pharmacological enhancement of exposure-based treatment in PTSD: a qualitative review
title_sort pharmacological enhancement of exposure-based treatment in ptsd: a qualitative review
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3800126/
https://www.ncbi.nlm.nih.gov/pubmed/24147208
http://dx.doi.org/10.3402/ejpt.v4i0.21626
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