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Intravenous Haloperidol versus Midazolam in Management of Conversion Disorder; a Randomized Clinical Trial

INTRODUCTION: Conversion disorder is a condition in which the patient shows psychological stress in physical ways. This study aimed to compare the effects of haloperidol versus midazolam in patients with conversion disorder. METHODS: This double-blind randomized clinical trial was conducted on patie...

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Autores principales: Jafari, Mohammadali, Biuki, Amir Aliheidari, Hajimaghsoudi, Majid, Bagherabadi, Mehdi, Zarepur, Ehsan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Shahid Beheshti University of Medical Sciences 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6289157/
https://www.ncbi.nlm.nih.gov/pubmed/30584559
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author Jafari, Mohammadali
Biuki, Amir Aliheidari
Hajimaghsoudi, Majid
Bagherabadi, Mehdi
Zarepur, Ehsan
author_facet Jafari, Mohammadali
Biuki, Amir Aliheidari
Hajimaghsoudi, Majid
Bagherabadi, Mehdi
Zarepur, Ehsan
author_sort Jafari, Mohammadali
collection PubMed
description INTRODUCTION: Conversion disorder is a condition in which the patient shows psychological stress in physical ways. This study aimed to compare the effects of haloperidol versus midazolam in patients with conversion disorder. METHODS: This double-blind randomized clinical trial was conducted on patients with conversion disorder who had presented to the emergency department, throughout 2015. Patients were randomly divided into two groups and were either treated with 2.5 mg of intravenous (IV) haloperidol or 2.5 mg of IV midazolam. Recovery rate, time to recovery, and side effects of both drugs 1 hour, 24 hours, and 1 week after treatment were compared using SPSS19. RESULTS: 140 patients were divided into two groups of 70. There were no significant differences between the groups regarding the baseline characteristics. 12 (17.1%) patients who were treated with IV haloperidol experienced drug side effects within 1 hour and 12 (17.1%) within 24 hours, while only 3 (4.3%) patients in IV midazolam experienced side-effects within 1 hour after drug administration (p = 0.026). The symptoms of the disease subsided in 45 (success rate: 64.3%) patients in midazolam and in 64 (success rate: 91.5%) participants in haloperidol group (P<0.001). Mean recovery time was 31.24 ± 7.03 minutes in IV midazolam and 30.53 ± 7.11 minutes in IV haloperidol group (p = 0.592). Absolute risk reduction (ARR) of treating patients with haloperidol compared to midazolam is about 27%. CONCLUSION: The response of patients to treatment with haloperidol is clearly better than midazolam. Although more transient and minor side-effects were observed in the group treated with haloperidol compared to midazolam group, serious side-effects were rare for both treatments.
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spelling pubmed-62891572018-12-24 Intravenous Haloperidol versus Midazolam in Management of Conversion Disorder; a Randomized Clinical Trial Jafari, Mohammadali Biuki, Amir Aliheidari Hajimaghsoudi, Majid Bagherabadi, Mehdi Zarepur, Ehsan Emerg (Tehran) Original Article INTRODUCTION: Conversion disorder is a condition in which the patient shows psychological stress in physical ways. This study aimed to compare the effects of haloperidol versus midazolam in patients with conversion disorder. METHODS: This double-blind randomized clinical trial was conducted on patients with conversion disorder who had presented to the emergency department, throughout 2015. Patients were randomly divided into two groups and were either treated with 2.5 mg of intravenous (IV) haloperidol or 2.5 mg of IV midazolam. Recovery rate, time to recovery, and side effects of both drugs 1 hour, 24 hours, and 1 week after treatment were compared using SPSS19. RESULTS: 140 patients were divided into two groups of 70. There were no significant differences between the groups regarding the baseline characteristics. 12 (17.1%) patients who were treated with IV haloperidol experienced drug side effects within 1 hour and 12 (17.1%) within 24 hours, while only 3 (4.3%) patients in IV midazolam experienced side-effects within 1 hour after drug administration (p = 0.026). The symptoms of the disease subsided in 45 (success rate: 64.3%) patients in midazolam and in 64 (success rate: 91.5%) participants in haloperidol group (P<0.001). Mean recovery time was 31.24 ± 7.03 minutes in IV midazolam and 30.53 ± 7.11 minutes in IV haloperidol group (p = 0.592). Absolute risk reduction (ARR) of treating patients with haloperidol compared to midazolam is about 27%. CONCLUSION: The response of patients to treatment with haloperidol is clearly better than midazolam. Although more transient and minor side-effects were observed in the group treated with haloperidol compared to midazolam group, serious side-effects were rare for both treatments. Shahid Beheshti University of Medical Sciences 2018 2018-07-14 /pmc/articles/PMC6289157/ /pubmed/30584559 Text en © Copyright (2018) Shahid Beheshti University ofMedical Sciences This open-access article distributed under the terms of the Creative Commons Attribution NonCommercial 3.0 License (CC BY-NC 3.0)(https://creativecommons.org/licenses/by-nc/3.0/).
spellingShingle Original Article
Jafari, Mohammadali
Biuki, Amir Aliheidari
Hajimaghsoudi, Majid
Bagherabadi, Mehdi
Zarepur, Ehsan
Intravenous Haloperidol versus Midazolam in Management of Conversion Disorder; a Randomized Clinical Trial
title Intravenous Haloperidol versus Midazolam in Management of Conversion Disorder; a Randomized Clinical Trial
title_full Intravenous Haloperidol versus Midazolam in Management of Conversion Disorder; a Randomized Clinical Trial
title_fullStr Intravenous Haloperidol versus Midazolam in Management of Conversion Disorder; a Randomized Clinical Trial
title_full_unstemmed Intravenous Haloperidol versus Midazolam in Management of Conversion Disorder; a Randomized Clinical Trial
title_short Intravenous Haloperidol versus Midazolam in Management of Conversion Disorder; a Randomized Clinical Trial
title_sort intravenous haloperidol versus midazolam in management of conversion disorder; a randomized clinical trial
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6289157/
https://www.ncbi.nlm.nih.gov/pubmed/30584559
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