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Comparison of efficacy of haloperidol and olanzapine in the treatment of delirium

OBJECTIVE: Till date, typical antipsychotic haloperidol is the treatment of choice for delirium. But, due to higher side effects with haloperidol, newer atypical antipsychotics (e.g., olanzapine) are increasingly being used in the treatment of delirious patients. The aim of the current research was...

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Autores principales: Jain, Rajan, Arun, Priti, Sidana, Ajeet, Sachdev, Atul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5806324/
https://www.ncbi.nlm.nih.gov/pubmed/29497187
http://dx.doi.org/10.4103/psychiatry.IndianJPsychiatry_59_17
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author Jain, Rajan
Arun, Priti
Sidana, Ajeet
Sachdev, Atul
author_facet Jain, Rajan
Arun, Priti
Sidana, Ajeet
Sachdev, Atul
author_sort Jain, Rajan
collection PubMed
description OBJECTIVE: Till date, typical antipsychotic haloperidol is the treatment of choice for delirium. But, due to higher side effects with haloperidol, newer atypical antipsychotics (e.g., olanzapine) are increasingly being used in the treatment of delirious patients. The aim of the current research was to study the efficacy and tolerability of haloperidol and olanzapine in the treatment of delirium. MATERIALS AND METHODS: This was an open-label, randomized controlled study carried out in a tertiary care hospital at Chandigarh, India. A total of 100 patients admitted in medicine, surgery, and orthopedic wards and diagnosed as having delirium on Confusion Assessment Method scale were included in the study. Patients were given either haloperidol (1–4 mg/day either orally or by nasogastric tube) or olanzapine (2.5–10 mg/day either orally or by nasogastric tube). Severity of delirium and pattern of symptom improvement were assessed by Memorial Delirium Assessment Scale (MDAS). Extrapyramidal side effects were assessed by Simpson–Angus Scale. RESULTS: There was an improvement in delirium severity in both groups with treatment. Mean daily dose of haloperidol and olanzapine used per patient was 2.10 and 5.49 mg, respectively, and the mean duration of treatment in olanzapine group and haloperidol group was 3.57 days and 3.37 days, respectively. There was no significant difference in the mean duration of treatment in both groups. At the end of study period, the MDAS scores in olanzapine and haloperidol groups were 8.43 and 8.00, respectively, and the difference was not significant statistically with P = 0.765. Five patients experienced drug-related mild side effects. CONCLUSION: Low-dose haloperidol and olanzapine were equally efficacious and well tolerated in delirium.
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spelling pubmed-58063242018-03-01 Comparison of efficacy of haloperidol and olanzapine in the treatment of delirium Jain, Rajan Arun, Priti Sidana, Ajeet Sachdev, Atul Indian J Psychiatry Original Article OBJECTIVE: Till date, typical antipsychotic haloperidol is the treatment of choice for delirium. But, due to higher side effects with haloperidol, newer atypical antipsychotics (e.g., olanzapine) are increasingly being used in the treatment of delirious patients. The aim of the current research was to study the efficacy and tolerability of haloperidol and olanzapine in the treatment of delirium. MATERIALS AND METHODS: This was an open-label, randomized controlled study carried out in a tertiary care hospital at Chandigarh, India. A total of 100 patients admitted in medicine, surgery, and orthopedic wards and diagnosed as having delirium on Confusion Assessment Method scale were included in the study. Patients were given either haloperidol (1–4 mg/day either orally or by nasogastric tube) or olanzapine (2.5–10 mg/day either orally or by nasogastric tube). Severity of delirium and pattern of symptom improvement were assessed by Memorial Delirium Assessment Scale (MDAS). Extrapyramidal side effects were assessed by Simpson–Angus Scale. RESULTS: There was an improvement in delirium severity in both groups with treatment. Mean daily dose of haloperidol and olanzapine used per patient was 2.10 and 5.49 mg, respectively, and the mean duration of treatment in olanzapine group and haloperidol group was 3.57 days and 3.37 days, respectively. There was no significant difference in the mean duration of treatment in both groups. At the end of study period, the MDAS scores in olanzapine and haloperidol groups were 8.43 and 8.00, respectively, and the difference was not significant statistically with P = 0.765. Five patients experienced drug-related mild side effects. CONCLUSION: Low-dose haloperidol and olanzapine were equally efficacious and well tolerated in delirium. Medknow Publications & Media Pvt Ltd 2017 /pmc/articles/PMC5806324/ /pubmed/29497187 http://dx.doi.org/10.4103/psychiatry.IndianJPsychiatry_59_17 Text en Copyright: © 2018 Indian Journal of Psychiatry http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Original Article
Jain, Rajan
Arun, Priti
Sidana, Ajeet
Sachdev, Atul
Comparison of efficacy of haloperidol and olanzapine in the treatment of delirium
title Comparison of efficacy of haloperidol and olanzapine in the treatment of delirium
title_full Comparison of efficacy of haloperidol and olanzapine in the treatment of delirium
title_fullStr Comparison of efficacy of haloperidol and olanzapine in the treatment of delirium
title_full_unstemmed Comparison of efficacy of haloperidol and olanzapine in the treatment of delirium
title_short Comparison of efficacy of haloperidol and olanzapine in the treatment of delirium
title_sort comparison of efficacy of haloperidol and olanzapine in the treatment of delirium
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5806324/
https://www.ncbi.nlm.nih.gov/pubmed/29497187
http://dx.doi.org/10.4103/psychiatry.IndianJPsychiatry_59_17
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