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Association of non-shockable initial rhythm and psychotropic medication in sudden cardiac arrest
BACKGROUND: Asystole (ASY) and pulseless electrical activity (PEA) have a poor outcome during sudden cardiac arrest (SCA). Psychotropic medication has been associated with a risk for sudden cardiac death (SCD). Our aim was to study the association of psychotropic medication with ASY/PEA during SCA....
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7182673/ https://www.ncbi.nlm.nih.gov/pubmed/32346603 http://dx.doi.org/10.1016/j.ijcha.2020.100518 |
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author | Kauppila, Janna P. Hantula, Antti Pakanen, Lasse Perkiömäki, Juha S. Martikainen, Matti Huikuri, Heikki V. Junttila, M. Juhani |
author_facet | Kauppila, Janna P. Hantula, Antti Pakanen, Lasse Perkiömäki, Juha S. Martikainen, Matti Huikuri, Heikki V. Junttila, M. Juhani |
author_sort | Kauppila, Janna P. |
collection | PubMed |
description | BACKGROUND: Asystole (ASY) and pulseless electrical activity (PEA) have a poor outcome during sudden cardiac arrest (SCA). Psychotropic medication has been associated with a risk for sudden cardiac death (SCD). Our aim was to study the association of psychotropic medication with ASY/PEA during SCA. METHODS AND RESULTS: A total of 659 SCA subjects were derived from the emergency data of Oulu University Hospital (2007–2012). Subjects with non-cardiac origin of SCA and over 30-minute delay to rhythm recording were excluded. Population included 222 subjects after exclusions (mean age 64 ± 14 years, 78% males). Initial rhythm was ventricular fibrillation (VF) or ventricular tachycardia (VT) in 123 (55%), ASY in 67 (30%) and PEA in 32 (14%) subjects. The delay (collapse to rhythm recording) was similar in VF/VT and ASY/PEA subjects (median 8 min [1st–3rd quartile 3–12 min] versus 10 [0–14] minutes, p = 0.780). Among VF/VT subjects underlying cardiac disease was more often ischemic compared to ASY/PEA subjects (85% versus 68%, p = 0.003). Psychotropic medication was associated with ASY/PEA rhythm (OR 3.18, 95%CI 1.40–7.23, p = 0.006) after adjustment for gender, age and underlying cardiac disease. Subsequently, antipsychotics (OR 4.27, 95%CI 1.28–14.25, p = 0.018) were more common in the ASY/PEA group. Benzodiazepines and antidepressants were not associated with ASY/PEA. CONCLUSION: Psychotropic medication and especially antipsychotics are associated with non-shockable rhythm during SCA and may lower the possibility of survival from the event. This might partly explain the risk of SCD related to psychotropic medication. |
format | Online Article Text |
id | pubmed-7182673 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-71826732020-04-28 Association of non-shockable initial rhythm and psychotropic medication in sudden cardiac arrest Kauppila, Janna P. Hantula, Antti Pakanen, Lasse Perkiömäki, Juha S. Martikainen, Matti Huikuri, Heikki V. Junttila, M. Juhani Int J Cardiol Heart Vasc Original Paper BACKGROUND: Asystole (ASY) and pulseless electrical activity (PEA) have a poor outcome during sudden cardiac arrest (SCA). Psychotropic medication has been associated with a risk for sudden cardiac death (SCD). Our aim was to study the association of psychotropic medication with ASY/PEA during SCA. METHODS AND RESULTS: A total of 659 SCA subjects were derived from the emergency data of Oulu University Hospital (2007–2012). Subjects with non-cardiac origin of SCA and over 30-minute delay to rhythm recording were excluded. Population included 222 subjects after exclusions (mean age 64 ± 14 years, 78% males). Initial rhythm was ventricular fibrillation (VF) or ventricular tachycardia (VT) in 123 (55%), ASY in 67 (30%) and PEA in 32 (14%) subjects. The delay (collapse to rhythm recording) was similar in VF/VT and ASY/PEA subjects (median 8 min [1st–3rd quartile 3–12 min] versus 10 [0–14] minutes, p = 0.780). Among VF/VT subjects underlying cardiac disease was more often ischemic compared to ASY/PEA subjects (85% versus 68%, p = 0.003). Psychotropic medication was associated with ASY/PEA rhythm (OR 3.18, 95%CI 1.40–7.23, p = 0.006) after adjustment for gender, age and underlying cardiac disease. Subsequently, antipsychotics (OR 4.27, 95%CI 1.28–14.25, p = 0.018) were more common in the ASY/PEA group. Benzodiazepines and antidepressants were not associated with ASY/PEA. CONCLUSION: Psychotropic medication and especially antipsychotics are associated with non-shockable rhythm during SCA and may lower the possibility of survival from the event. This might partly explain the risk of SCD related to psychotropic medication. Elsevier 2020-04-22 /pmc/articles/PMC7182673/ /pubmed/32346603 http://dx.doi.org/10.1016/j.ijcha.2020.100518 Text en © 2020 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Original Paper Kauppila, Janna P. Hantula, Antti Pakanen, Lasse Perkiömäki, Juha S. Martikainen, Matti Huikuri, Heikki V. Junttila, M. Juhani Association of non-shockable initial rhythm and psychotropic medication in sudden cardiac arrest |
title | Association of non-shockable initial rhythm and psychotropic medication in sudden cardiac arrest |
title_full | Association of non-shockable initial rhythm and psychotropic medication in sudden cardiac arrest |
title_fullStr | Association of non-shockable initial rhythm and psychotropic medication in sudden cardiac arrest |
title_full_unstemmed | Association of non-shockable initial rhythm and psychotropic medication in sudden cardiac arrest |
title_short | Association of non-shockable initial rhythm and psychotropic medication in sudden cardiac arrest |
title_sort | association of non-shockable initial rhythm and psychotropic medication in sudden cardiac arrest |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7182673/ https://www.ncbi.nlm.nih.gov/pubmed/32346603 http://dx.doi.org/10.1016/j.ijcha.2020.100518 |
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