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Effect of intravenous midazolam on cardiac parameters in acute tricyclic antidepressants poisoning

BACKGROUND: Midazolam is commonly and safely used in poisoning management and intensive care for the control of agitated poisoned patients. Despite the introduction of newer and safer antidepressants, tricyclic antidepressants (TCAs) are still prescribed and used in many countries due to their cost-...

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Autores principales: Eizadi-Mood, Nastaran, Aboofazeli, Elham, Hajhashemi, Valiollah, Gheshlaghi, Farzad, Badri, Shirinsadat, Sabzghabaee, Ali Mohammad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Isfahan Cardiovascular Research Center, Isfahan University of Medical Sciences 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5266137/
https://www.ncbi.nlm.nih.gov/pubmed/28149316
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author Eizadi-Mood, Nastaran
Aboofazeli, Elham
Hajhashemi, Valiollah
Gheshlaghi, Farzad
Badri, Shirinsadat
Sabzghabaee, Ali Mohammad
author_facet Eizadi-Mood, Nastaran
Aboofazeli, Elham
Hajhashemi, Valiollah
Gheshlaghi, Farzad
Badri, Shirinsadat
Sabzghabaee, Ali Mohammad
author_sort Eizadi-Mood, Nastaran
collection PubMed
description BACKGROUND: Midazolam is commonly and safely used in poisoning management and intensive care for the control of agitated poisoned patients. Despite the introduction of newer and safer antidepressants, tricyclic antidepressants (TCAs) are still prescribed and used in many countries due to their cost-effectiveness. Severe morbidity and mortality associated with these drugs arises largely from their well-documented cardiovascular toxicity. In this study we aimed to investigate the probable effect of midazolam on some hemodynamic indices in TCAs-poisoned patients. METHODS: In this clinical trial, we have evaluated some cardiovascular and hemodynamic indices of 100 TCAs-poisoned patients whom were randomly allocated for receiving midazolam with a first loading dose of 0.1 mg/kg (2 mg/minute) followed by a 6-hour maintenance infusion of 0.1 mg/kg/h of the drug in dextrose-saline (3.33% of dextrose and 0.33% of NaCl) or placebo (dextrose-saline infusion without midazolam). Pulse rate, systolic/diastolic blood pressure, respiratory rate, neurologic status and the outcome of therapy for all patients were recorded at the time of admission and hourly for the next 6 hours. RESULTS: There was a statistically significant reduction in the heart rate of the midazolam treated group after the first hour of hospital admission. There were no significant differences in the respiratory rate, central nervous system manifestations and other indices between the two groups. CONCLUSION: Midazolam may reduce tachycardia (and its fatal consequences) in the first hour of admission in TCAs-poisoned patients.
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spelling pubmed-52661372017-02-01 Effect of intravenous midazolam on cardiac parameters in acute tricyclic antidepressants poisoning Eizadi-Mood, Nastaran Aboofazeli, Elham Hajhashemi, Valiollah Gheshlaghi, Farzad Badri, Shirinsadat Sabzghabaee, Ali Mohammad ARYA Atheroscler Short Communication BACKGROUND: Midazolam is commonly and safely used in poisoning management and intensive care for the control of agitated poisoned patients. Despite the introduction of newer and safer antidepressants, tricyclic antidepressants (TCAs) are still prescribed and used in many countries due to their cost-effectiveness. Severe morbidity and mortality associated with these drugs arises largely from their well-documented cardiovascular toxicity. In this study we aimed to investigate the probable effect of midazolam on some hemodynamic indices in TCAs-poisoned patients. METHODS: In this clinical trial, we have evaluated some cardiovascular and hemodynamic indices of 100 TCAs-poisoned patients whom were randomly allocated for receiving midazolam with a first loading dose of 0.1 mg/kg (2 mg/minute) followed by a 6-hour maintenance infusion of 0.1 mg/kg/h of the drug in dextrose-saline (3.33% of dextrose and 0.33% of NaCl) or placebo (dextrose-saline infusion without midazolam). Pulse rate, systolic/diastolic blood pressure, respiratory rate, neurologic status and the outcome of therapy for all patients were recorded at the time of admission and hourly for the next 6 hours. RESULTS: There was a statistically significant reduction in the heart rate of the midazolam treated group after the first hour of hospital admission. There were no significant differences in the respiratory rate, central nervous system manifestations and other indices between the two groups. CONCLUSION: Midazolam may reduce tachycardia (and its fatal consequences) in the first hour of admission in TCAs-poisoned patients. Isfahan Cardiovascular Research Center, Isfahan University of Medical Sciences 2016-07 /pmc/articles/PMC5266137/ /pubmed/28149316 Text en © 2016 Isfahan Cardiovascular Research Center & Isfahan University of Medical Sciences http://creativecommons.org/licenses/by-nc/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License which allows users to read, copy, distribute and make derivative works for non-commercial purposes from the material, as long as the author of the original work is cited properly.
spellingShingle Short Communication
Eizadi-Mood, Nastaran
Aboofazeli, Elham
Hajhashemi, Valiollah
Gheshlaghi, Farzad
Badri, Shirinsadat
Sabzghabaee, Ali Mohammad
Effect of intravenous midazolam on cardiac parameters in acute tricyclic antidepressants poisoning
title Effect of intravenous midazolam on cardiac parameters in acute tricyclic antidepressants poisoning
title_full Effect of intravenous midazolam on cardiac parameters in acute tricyclic antidepressants poisoning
title_fullStr Effect of intravenous midazolam on cardiac parameters in acute tricyclic antidepressants poisoning
title_full_unstemmed Effect of intravenous midazolam on cardiac parameters in acute tricyclic antidepressants poisoning
title_short Effect of intravenous midazolam on cardiac parameters in acute tricyclic antidepressants poisoning
title_sort effect of intravenous midazolam on cardiac parameters in acute tricyclic antidepressants poisoning
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5266137/
https://www.ncbi.nlm.nih.gov/pubmed/28149316
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