Cargando…

Out‐of‐hospital cardiac arrest and differential risk of cardiac and non‐cardiac QT‐prolonging drugs in 37 000 cases

AIMS: Drugs that prolong the QT interval, either by design (cardiac QT‐prolonging drugs: anti‐arrhythmics) or as off‐target effect (non‐cardiac QT‐prolonging drugs), may increase the risk of ventricular arrhythmias and out‐of‐hospital cardiac arrest (OHCA). Risk mitigation measures were instituted,...

Descripción completa

Detalles Bibliográficos
Autores principales: Eroglu, Talip E., Barcella, Carlo A., Blom, Marieke T., Mohr, Grimur H., Souverein, Patrick C., Torp‐Pedersen, Christian, Folke, Fredrik, Wissenberg, Mads, de Boer, Anthonius, Schwartz, Peter J., Gislason, Gunnar H., Tan, Hanno L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9291302/
https://www.ncbi.nlm.nih.gov/pubmed/34374122
http://dx.doi.org/10.1111/bcp.15030
_version_ 1784749113006358528
author Eroglu, Talip E.
Barcella, Carlo A.
Blom, Marieke T.
Mohr, Grimur H.
Souverein, Patrick C.
Torp‐Pedersen, Christian
Folke, Fredrik
Wissenberg, Mads
de Boer, Anthonius
Schwartz, Peter J.
Gislason, Gunnar H.
Tan, Hanno L.
author_facet Eroglu, Talip E.
Barcella, Carlo A.
Blom, Marieke T.
Mohr, Grimur H.
Souverein, Patrick C.
Torp‐Pedersen, Christian
Folke, Fredrik
Wissenberg, Mads
de Boer, Anthonius
Schwartz, Peter J.
Gislason, Gunnar H.
Tan, Hanno L.
author_sort Eroglu, Talip E.
collection PubMed
description AIMS: Drugs that prolong the QT interval, either by design (cardiac QT‐prolonging drugs: anti‐arrhythmics) or as off‐target effect (non‐cardiac QT‐prolonging drugs), may increase the risk of ventricular arrhythmias and out‐of‐hospital cardiac arrest (OHCA). Risk mitigation measures were instituted, in particular, surrounding prescription of cardiac QT‐prolonging drugs. We studied OHCA risk of both drug types in current clinical practice. METHODS: Using data from large population‐based OHCA registries in the Netherlands and Denmark, we conducted two independent case–control studies. OHCA cases with presumed cardiac causes were matched on age/sex/index date with up to five non‐OHCA controls. We calculated odds ratios (ORs) for the association of cardiac or non‐cardiac QT‐prolonging drugs with OHCA risk using conditional logistic regression analyses. RESULTS: We identified 2503 OHCA cases and 10 543 non‐OHCA controls in the Netherlands, and 35 017 OHCA cases and 175 085 non‐OHCA controls in Denmark. Compared to no use of QT‐prolonging drugs, use of non‐cardiac QT‐prolonging drugs (Netherlands: cases: 3.0%, controls: 1.9%; Denmark: cases: 14.9%, controls: 7.5%) was associated with increased OHCA risk (Netherlands: OR 1.37 [95% CI: 1.03–1.81]; Denmark: OR 1.63 [95% CI: 1.57–1.70]). The association between cardiac QT‐prolonging drugs (Netherlands: cases: 4.0%, controls: 2.5%; Denmark: cases: 2.1%, controls: 0.9%) and OHCA was weaker (Netherlands: OR 1.17 [95% CI: 0.92–1.50]; Denmark: OR 1.21 [95% CI: 1.09–1.33]), although users of cardiac QT‐prolonging drugs had more medication use and comorbidities associated with OHCA risk than users of non‐cardiac QT‐prolonging drugs. CONCLUSION: In clinical practice, cardiac QT‐prolonging drugs confer lower OHCA risk than non‐cardiac QT‐prolonging drugs, although users of the former have higher a priori risk. This is likely due to risk mitigation measures surrounding prescription of cardiac QT‐prolonging drugs.
format Online
Article
Text
id pubmed-9291302
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-92913022022-07-20 Out‐of‐hospital cardiac arrest and differential risk of cardiac and non‐cardiac QT‐prolonging drugs in 37 000 cases Eroglu, Talip E. Barcella, Carlo A. Blom, Marieke T. Mohr, Grimur H. Souverein, Patrick C. Torp‐Pedersen, Christian Folke, Fredrik Wissenberg, Mads de Boer, Anthonius Schwartz, Peter J. Gislason, Gunnar H. Tan, Hanno L. Br J Clin Pharmacol Original Articles AIMS: Drugs that prolong the QT interval, either by design (cardiac QT‐prolonging drugs: anti‐arrhythmics) or as off‐target effect (non‐cardiac QT‐prolonging drugs), may increase the risk of ventricular arrhythmias and out‐of‐hospital cardiac arrest (OHCA). Risk mitigation measures were instituted, in particular, surrounding prescription of cardiac QT‐prolonging drugs. We studied OHCA risk of both drug types in current clinical practice. METHODS: Using data from large population‐based OHCA registries in the Netherlands and Denmark, we conducted two independent case–control studies. OHCA cases with presumed cardiac causes were matched on age/sex/index date with up to five non‐OHCA controls. We calculated odds ratios (ORs) for the association of cardiac or non‐cardiac QT‐prolonging drugs with OHCA risk using conditional logistic regression analyses. RESULTS: We identified 2503 OHCA cases and 10 543 non‐OHCA controls in the Netherlands, and 35 017 OHCA cases and 175 085 non‐OHCA controls in Denmark. Compared to no use of QT‐prolonging drugs, use of non‐cardiac QT‐prolonging drugs (Netherlands: cases: 3.0%, controls: 1.9%; Denmark: cases: 14.9%, controls: 7.5%) was associated with increased OHCA risk (Netherlands: OR 1.37 [95% CI: 1.03–1.81]; Denmark: OR 1.63 [95% CI: 1.57–1.70]). The association between cardiac QT‐prolonging drugs (Netherlands: cases: 4.0%, controls: 2.5%; Denmark: cases: 2.1%, controls: 0.9%) and OHCA was weaker (Netherlands: OR 1.17 [95% CI: 0.92–1.50]; Denmark: OR 1.21 [95% CI: 1.09–1.33]), although users of cardiac QT‐prolonging drugs had more medication use and comorbidities associated with OHCA risk than users of non‐cardiac QT‐prolonging drugs. CONCLUSION: In clinical practice, cardiac QT‐prolonging drugs confer lower OHCA risk than non‐cardiac QT‐prolonging drugs, although users of the former have higher a priori risk. This is likely due to risk mitigation measures surrounding prescription of cardiac QT‐prolonging drugs. John Wiley and Sons Inc. 2021-08-28 2022-02 /pmc/articles/PMC9291302/ /pubmed/34374122 http://dx.doi.org/10.1111/bcp.15030 Text en © 2021 The Authors. British Journal of Clinical Pharmacology published by John Wiley & Sons Ltd on behalf of British Pharmacological Society. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Eroglu, Talip E.
Barcella, Carlo A.
Blom, Marieke T.
Mohr, Grimur H.
Souverein, Patrick C.
Torp‐Pedersen, Christian
Folke, Fredrik
Wissenberg, Mads
de Boer, Anthonius
Schwartz, Peter J.
Gislason, Gunnar H.
Tan, Hanno L.
Out‐of‐hospital cardiac arrest and differential risk of cardiac and non‐cardiac QT‐prolonging drugs in 37 000 cases
title Out‐of‐hospital cardiac arrest and differential risk of cardiac and non‐cardiac QT‐prolonging drugs in 37 000 cases
title_full Out‐of‐hospital cardiac arrest and differential risk of cardiac and non‐cardiac QT‐prolonging drugs in 37 000 cases
title_fullStr Out‐of‐hospital cardiac arrest and differential risk of cardiac and non‐cardiac QT‐prolonging drugs in 37 000 cases
title_full_unstemmed Out‐of‐hospital cardiac arrest and differential risk of cardiac and non‐cardiac QT‐prolonging drugs in 37 000 cases
title_short Out‐of‐hospital cardiac arrest and differential risk of cardiac and non‐cardiac QT‐prolonging drugs in 37 000 cases
title_sort out‐of‐hospital cardiac arrest and differential risk of cardiac and non‐cardiac qt‐prolonging drugs in 37 000 cases
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9291302/
https://www.ncbi.nlm.nih.gov/pubmed/34374122
http://dx.doi.org/10.1111/bcp.15030
work_keys_str_mv AT eroglutalipe outofhospitalcardiacarrestanddifferentialriskofcardiacandnoncardiacqtprolongingdrugsin37000cases
AT barcellacarloa outofhospitalcardiacarrestanddifferentialriskofcardiacandnoncardiacqtprolongingdrugsin37000cases
AT blommarieket outofhospitalcardiacarrestanddifferentialriskofcardiacandnoncardiacqtprolongingdrugsin37000cases
AT mohrgrimurh outofhospitalcardiacarrestanddifferentialriskofcardiacandnoncardiacqtprolongingdrugsin37000cases
AT souvereinpatrickc outofhospitalcardiacarrestanddifferentialriskofcardiacandnoncardiacqtprolongingdrugsin37000cases
AT torppedersenchristian outofhospitalcardiacarrestanddifferentialriskofcardiacandnoncardiacqtprolongingdrugsin37000cases
AT folkefredrik outofhospitalcardiacarrestanddifferentialriskofcardiacandnoncardiacqtprolongingdrugsin37000cases
AT wissenbergmads outofhospitalcardiacarrestanddifferentialriskofcardiacandnoncardiacqtprolongingdrugsin37000cases
AT deboeranthonius outofhospitalcardiacarrestanddifferentialriskofcardiacandnoncardiacqtprolongingdrugsin37000cases
AT schwartzpeterj outofhospitalcardiacarrestanddifferentialriskofcardiacandnoncardiacqtprolongingdrugsin37000cases
AT gislasongunnarh outofhospitalcardiacarrestanddifferentialriskofcardiacandnoncardiacqtprolongingdrugsin37000cases
AT tanhannol outofhospitalcardiacarrestanddifferentialriskofcardiacandnoncardiacqtprolongingdrugsin37000cases
AT outofhospitalcardiacarrestanddifferentialriskofcardiacandnoncardiacqtprolongingdrugsin37000cases