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Drugs and life-threatening ventricular arrhythmia risk: results from the DARE study cohort

OBJECTIVES: To establish a unique sample of proarrhythmia cases, determine the characteristics of cases and estimate the contribution of individual drugs to the incidence of proarrhythmia within these cases. SETTING: Suspected proarrhythmia cases were referred by cardiologists across England between...

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Autores principales: Coughtrie, Abigail L, Behr, Elijah R, Layton, Deborah, Marshall, Vanessa, Camm, A John, Shakir, Saad A W
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5652462/
https://www.ncbi.nlm.nih.gov/pubmed/29042382
http://dx.doi.org/10.1136/bmjopen-2017-016627
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author Coughtrie, Abigail L
Behr, Elijah R
Layton, Deborah
Marshall, Vanessa
Camm, A John
Shakir, Saad A W
author_facet Coughtrie, Abigail L
Behr, Elijah R
Layton, Deborah
Marshall, Vanessa
Camm, A John
Shakir, Saad A W
author_sort Coughtrie, Abigail L
collection PubMed
description OBJECTIVES: To establish a unique sample of proarrhythmia cases, determine the characteristics of cases and estimate the contribution of individual drugs to the incidence of proarrhythmia within these cases. SETTING: Suspected proarrhythmia cases were referred by cardiologists across England between 2003 and 2011. Information on demography, symptoms, prior medical and drug histories and data from hospital notes were collected. PARTICIPANTS: Two expert cardiologists reviewed data for 293 referred cases: 130 were included. Inclusion criteria were new onset or exacerbation of pre-existing ventricular arrhythmias, QTc >500 ms, QTc >450 ms (men) or >470 ms (women) with cardiac syncope, all secondary to drug administration. Exclusion criteria were acute ischaemia and ischaemic polymorphic ventricular tachycardia at presentation, structural heart disease, consent withdrawn or deceased prior to study. Descriptive analysis of Caucasian cases (95% of included cases, n=124) and culpable drug exposures was performed. RESULTS: Of the 124 Caucasian cases, 95 (77%) were QTc interval prolongation-related; mean age was 62 years (SD 15), and 63% were female. Cardiovascular comorbidities included hypertension (53%) and patient-reported ‘heart rhythm problems’ (73%). Family history of sudden death (36%) and hypokalaemia at presentation (27%) were common. 165 culpable drug exposures were reported, including antiarrhythmics (42%), of which amiodarone and flecainide were the most common. Sotalol, a beta-blocking agent with antiarrhythmic activity, was also common (15%). 26% reported multiple drugs, of which 84% reported at least one cytochrome (CYP) P450 inhibitor. Potential pharmacodynamics interactions identified were mainly QT prolongation (59%). CONCLUSIONS: Antiarrhythmics, non-cardiac drugs and drug combinations were found to be culpable in a large cohort of 124 clinically validated proarrhythmia cases. Potential clinical factors that may warn the prescriber of potential proarrhythmia include older women, underlying cardiovascular comorbidity, family history of sudden death and hypokalaemia.
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spelling pubmed-56524622017-10-27 Drugs and life-threatening ventricular arrhythmia risk: results from the DARE study cohort Coughtrie, Abigail L Behr, Elijah R Layton, Deborah Marshall, Vanessa Camm, A John Shakir, Saad A W BMJ Open Epidemiology OBJECTIVES: To establish a unique sample of proarrhythmia cases, determine the characteristics of cases and estimate the contribution of individual drugs to the incidence of proarrhythmia within these cases. SETTING: Suspected proarrhythmia cases were referred by cardiologists across England between 2003 and 2011. Information on demography, symptoms, prior medical and drug histories and data from hospital notes were collected. PARTICIPANTS: Two expert cardiologists reviewed data for 293 referred cases: 130 were included. Inclusion criteria were new onset or exacerbation of pre-existing ventricular arrhythmias, QTc >500 ms, QTc >450 ms (men) or >470 ms (women) with cardiac syncope, all secondary to drug administration. Exclusion criteria were acute ischaemia and ischaemic polymorphic ventricular tachycardia at presentation, structural heart disease, consent withdrawn or deceased prior to study. Descriptive analysis of Caucasian cases (95% of included cases, n=124) and culpable drug exposures was performed. RESULTS: Of the 124 Caucasian cases, 95 (77%) were QTc interval prolongation-related; mean age was 62 years (SD 15), and 63% were female. Cardiovascular comorbidities included hypertension (53%) and patient-reported ‘heart rhythm problems’ (73%). Family history of sudden death (36%) and hypokalaemia at presentation (27%) were common. 165 culpable drug exposures were reported, including antiarrhythmics (42%), of which amiodarone and flecainide were the most common. Sotalol, a beta-blocking agent with antiarrhythmic activity, was also common (15%). 26% reported multiple drugs, of which 84% reported at least one cytochrome (CYP) P450 inhibitor. Potential pharmacodynamics interactions identified were mainly QT prolongation (59%). CONCLUSIONS: Antiarrhythmics, non-cardiac drugs and drug combinations were found to be culpable in a large cohort of 124 clinically validated proarrhythmia cases. Potential clinical factors that may warn the prescriber of potential proarrhythmia include older women, underlying cardiovascular comorbidity, family history of sudden death and hypokalaemia. BMJ Publishing Group 2017-10-16 /pmc/articles/PMC5652462/ /pubmed/29042382 http://dx.doi.org/10.1136/bmjopen-2017-016627 Text en © Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2017. All rights reserved. No commercial use is permitted unless otherwise expressly granted. This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
spellingShingle Epidemiology
Coughtrie, Abigail L
Behr, Elijah R
Layton, Deborah
Marshall, Vanessa
Camm, A John
Shakir, Saad A W
Drugs and life-threatening ventricular arrhythmia risk: results from the DARE study cohort
title Drugs and life-threatening ventricular arrhythmia risk: results from the DARE study cohort
title_full Drugs and life-threatening ventricular arrhythmia risk: results from the DARE study cohort
title_fullStr Drugs and life-threatening ventricular arrhythmia risk: results from the DARE study cohort
title_full_unstemmed Drugs and life-threatening ventricular arrhythmia risk: results from the DARE study cohort
title_short Drugs and life-threatening ventricular arrhythmia risk: results from the DARE study cohort
title_sort drugs and life-threatening ventricular arrhythmia risk: results from the dare study cohort
topic Epidemiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5652462/
https://www.ncbi.nlm.nih.gov/pubmed/29042382
http://dx.doi.org/10.1136/bmjopen-2017-016627
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