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High dose droperidol and QT prolongation: analysis of continuous 12-lead recordings
AIMS: To investigate the QT interval after high dose droperidol using continuous 12-lead Holter recordings. METHODS: This was a prospective study of patients given droperidol with a continuous Holter recording. Patients were recruited from the DORM II study which included patients with aggression pr...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4004408/ https://www.ncbi.nlm.nih.gov/pubmed/24168079 http://dx.doi.org/10.1111/bcp.12272 |
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author | Calver, Leonie Isbister, Geoffrey K |
author_facet | Calver, Leonie Isbister, Geoffrey K |
author_sort | Calver, Leonie |
collection | PubMed |
description | AIMS: To investigate the QT interval after high dose droperidol using continuous 12-lead Holter recordings. METHODS: This was a prospective study of patients given droperidol with a continuous Holter recording. Patients were recruited from the DORM II study which included patients with aggression presenting to the emergency department. Patients initially received 10 mg droperidol as part of a standardized sedation protocol. An additional 10 mg dose was given after 15 min if required and further doses at the clinical toxicologist's discretion. Continuous 12-lead Holter recordings were obtained for 2–24 h utilizing high resolution digital recordings with automated QT interval measurement. Electrocardiograms were extracted hourly from Holter recordings. The QT interval was plotted against heart rate (HR) on the QT nomogram to determine if it was abnormal. QT(c)F (Fridericia's HR correction) was calculated and >500 ms was defined as abnormal. RESULTS: Forty-six patients had Holter recordings after 10–40 mg droperidol and 316 QT–HR pairs were included. There were 32 abnormal QT measurements in four patients, three given 10 mg and one 20 mg. In three of the four patients QT(c)F >500 ms but only in one taking methadone was the timing of QT(c)F >500 ms consistent with droperidol dosing. Of the three other patients, one took amphetamines, one still had QT prolongation 24 h after droperidol and one took a lamotrigine overdose. No patient given >30 mg had a prolonged QT. There were no arrhythmias. CONCLUSION: QT prolongation was observed with high dose droperidol. However, there was little evidence supporting droperidol being the cause and QT prolongation was more likely due to pre-existing conditions or other drugs. |
format | Online Article Text |
id | pubmed-4004408 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-40044082014-06-02 High dose droperidol and QT prolongation: analysis of continuous 12-lead recordings Calver, Leonie Isbister, Geoffrey K Br J Clin Pharmacol Drug Safety AIMS: To investigate the QT interval after high dose droperidol using continuous 12-lead Holter recordings. METHODS: This was a prospective study of patients given droperidol with a continuous Holter recording. Patients were recruited from the DORM II study which included patients with aggression presenting to the emergency department. Patients initially received 10 mg droperidol as part of a standardized sedation protocol. An additional 10 mg dose was given after 15 min if required and further doses at the clinical toxicologist's discretion. Continuous 12-lead Holter recordings were obtained for 2–24 h utilizing high resolution digital recordings with automated QT interval measurement. Electrocardiograms were extracted hourly from Holter recordings. The QT interval was plotted against heart rate (HR) on the QT nomogram to determine if it was abnormal. QT(c)F (Fridericia's HR correction) was calculated and >500 ms was defined as abnormal. RESULTS: Forty-six patients had Holter recordings after 10–40 mg droperidol and 316 QT–HR pairs were included. There were 32 abnormal QT measurements in four patients, three given 10 mg and one 20 mg. In three of the four patients QT(c)F >500 ms but only in one taking methadone was the timing of QT(c)F >500 ms consistent with droperidol dosing. Of the three other patients, one took amphetamines, one still had QT prolongation 24 h after droperidol and one took a lamotrigine overdose. No patient given >30 mg had a prolonged QT. There were no arrhythmias. CONCLUSION: QT prolongation was observed with high dose droperidol. However, there was little evidence supporting droperidol being the cause and QT prolongation was more likely due to pre-existing conditions or other drugs. Blackwell Publishing Ltd 2014-05 2014-04-22 /pmc/articles/PMC4004408/ /pubmed/24168079 http://dx.doi.org/10.1111/bcp.12272 Text en © 2013 The Authors. British Journal of Clinical Pharmacology published by John Wiley & Sons Ltd on behalf of The British Pharmacological Society. http://creativecommons.org/licenses/by-nc/3.0/ This is an open access article under the terms of the Creative Commons Attribution-NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Drug Safety Calver, Leonie Isbister, Geoffrey K High dose droperidol and QT prolongation: analysis of continuous 12-lead recordings |
title | High dose droperidol and QT prolongation: analysis of continuous 12-lead recordings |
title_full | High dose droperidol and QT prolongation: analysis of continuous 12-lead recordings |
title_fullStr | High dose droperidol and QT prolongation: analysis of continuous 12-lead recordings |
title_full_unstemmed | High dose droperidol and QT prolongation: analysis of continuous 12-lead recordings |
title_short | High dose droperidol and QT prolongation: analysis of continuous 12-lead recordings |
title_sort | high dose droperidol and qt prolongation: analysis of continuous 12-lead recordings |
topic | Drug Safety |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4004408/ https://www.ncbi.nlm.nih.gov/pubmed/24168079 http://dx.doi.org/10.1111/bcp.12272 |
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