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Four Days Exposure And Reprocessing Therapy For PTSD

INTRODUCTION: Post-traumatic stress disorder (PTSD) is a debilitating disorder affecting approximately 6% of the population. Current treatments have been shown to efficaciously reduce symptom burden between 30%-50%. However, due to the high intensity of treatment over a long period of time. drop-out...

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Autores principales: Duek, O., Levy, I., Harpaz-Rotem, I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cambridge University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10434592/
http://dx.doi.org/10.1192/j.eurpsy.2023.1019
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author Duek, O.
Levy, I.
Harpaz-Rotem, I.
author_facet Duek, O.
Levy, I.
Harpaz-Rotem, I.
author_sort Duek, O.
collection PubMed
description INTRODUCTION: Post-traumatic stress disorder (PTSD) is a debilitating disorder affecting approximately 6% of the population. Current treatments have been shown to efficaciously reduce symptom burden between 30%-50%. However, due to the high intensity of treatment over a long period of time. drop-out rates are as high as 50%. OBJECTIVES: Assess the effect of one-time ketamine infusion in subanasthetic dosage on PTSD psychotherapy Assess feasibility and effect of massed, four days, esposure focused psychotherapy for PTSd METHODS: Here, we tested the efficacy of a four-day exposure and processing-focused psychotherapy at reducing PTSD severity. Twenty-seven participants with chronic PTSD were randomized to two groups, one receiving a one-time infusion of ketamine in a subanesthetic dose (0.5mg/kg for 40 minutes), the other receiving midazolam. Both groups underwent four 90-120 minutes of daily psychotherapy sessions a day after infusion, followed by in-vivo exposure practice. The severity of PTSD was assessed with the PCL-5 before and at the end of treatment, and at 30 and 90 days follow-up. Brain reactivation to the trauma reminders was measured using fMRI RESULTS: PTSD severity in both treatment groups decreased by 13, 16, and 15 points on the PCL-5 at the end of treatment, 30 days follow-up, and 90 days respectively, surpassing the minimum clinical difference of 7.9 points. There was no significant difference in symptom reductions between the treatment groups. However, brain reactivation to trauma stories differed between the groups, with the ketamine group showing a decline in the amygdala and hippocampus reactivation compared to the midazolam group, at the end of treatment. Image: CONCLUSIONS: Our results imply comparable efficacy of this short-term intervention to standard trauma-focused psychotherapies, emphasizing its clinical usefulness as a short and effective intervention. DISCLOSURE OF INTEREST: None Declared
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spelling pubmed-104345922023-08-18 Four Days Exposure And Reprocessing Therapy For PTSD Duek, O. Levy, I. Harpaz-Rotem, I. Eur Psychiatry Abstract INTRODUCTION: Post-traumatic stress disorder (PTSD) is a debilitating disorder affecting approximately 6% of the population. Current treatments have been shown to efficaciously reduce symptom burden between 30%-50%. However, due to the high intensity of treatment over a long period of time. drop-out rates are as high as 50%. OBJECTIVES: Assess the effect of one-time ketamine infusion in subanasthetic dosage on PTSD psychotherapy Assess feasibility and effect of massed, four days, esposure focused psychotherapy for PTSd METHODS: Here, we tested the efficacy of a four-day exposure and processing-focused psychotherapy at reducing PTSD severity. Twenty-seven participants with chronic PTSD were randomized to two groups, one receiving a one-time infusion of ketamine in a subanesthetic dose (0.5mg/kg for 40 minutes), the other receiving midazolam. Both groups underwent four 90-120 minutes of daily psychotherapy sessions a day after infusion, followed by in-vivo exposure practice. The severity of PTSD was assessed with the PCL-5 before and at the end of treatment, and at 30 and 90 days follow-up. Brain reactivation to the trauma reminders was measured using fMRI RESULTS: PTSD severity in both treatment groups decreased by 13, 16, and 15 points on the PCL-5 at the end of treatment, 30 days follow-up, and 90 days respectively, surpassing the minimum clinical difference of 7.9 points. There was no significant difference in symptom reductions between the treatment groups. However, brain reactivation to trauma stories differed between the groups, with the ketamine group showing a decline in the amygdala and hippocampus reactivation compared to the midazolam group, at the end of treatment. Image: CONCLUSIONS: Our results imply comparable efficacy of this short-term intervention to standard trauma-focused psychotherapies, emphasizing its clinical usefulness as a short and effective intervention. DISCLOSURE OF INTEREST: None Declared Cambridge University Press 2023-07-19 /pmc/articles/PMC10434592/ http://dx.doi.org/10.1192/j.eurpsy.2023.1019 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
Duek, O.
Levy, I.
Harpaz-Rotem, I.
Four Days Exposure And Reprocessing Therapy For PTSD
title Four Days Exposure And Reprocessing Therapy For PTSD
title_full Four Days Exposure And Reprocessing Therapy For PTSD
title_fullStr Four Days Exposure And Reprocessing Therapy For PTSD
title_full_unstemmed Four Days Exposure And Reprocessing Therapy For PTSD
title_short Four Days Exposure And Reprocessing Therapy For PTSD
title_sort four days exposure and reprocessing therapy for ptsd
topic Abstract
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10434592/
http://dx.doi.org/10.1192/j.eurpsy.2023.1019
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