Serveur d'exploration Stress et Covid

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SARS-CoV-2, COVID-19 and inherited arrhythmia syndromes

Identifieur interne : 000191 ( 2020/Analysis ); précédent : 000190; suivant : 000192

SARS-CoV-2, COVID-19 and inherited arrhythmia syndromes

Auteurs : Cheng-I. Wu [Pays-Bas] ; Pieter G. Postema [Pays-Bas] ; Elena Arbelo ; Elijah R. Behr [Royaume-Uni] ; Connie R. Bezzina [Pays-Bas] ; Carlo Napolitano [Italie] ; Tomas Robyns [Belgique] ; Vincent Probst [France] ; Eric Schulze-Bahr [Allemagne] ; Carol Ann Remme [Pays-Bas] ; Arthur A. M. Wilde [Pays-Bas]

Source :

RBID : PMC:7156157

Abstract

Ever since the first case was reported at the end of 2019, the SARS-COV-2 virus and associated lung disease COVID-19 has spread throughout the world and has become a pandemic. In particular, the high transmission rate of the virus has made it a threat to public health globally. Currently, there is no proven effective therapy against the virus, and the impact on other diseases is also uncertain, especially inherited arrhythmia syndrome.

Arrhythmogenic effect of COVID-19 can be expected, potentially contributing to disease outcome. This may be of importance for patients with an increased risk for cardiac arrhythmias, either secondary to acquired conditions or co-morbidities or consequent to inherited syndromes. Management of patients with inherited arrhythmia syndromes such as Long QT syndrome, Brugada syndrome, Short QT syndrome and Catecholaminergic Polymorphic Ventricular Tachycardia in the setting of the COVID-19 pandemic may prove particularly challenging. Depending on the inherited defect involved, these patients may be susceptible to pro-arrhythmic effects of COVID-19-related issues such as fever, stress, electrolyte disturbances and use of antiviral drugs. We here describe the potential COVID-19 associated risks and therapeutic considerations for patients with distinct inherited arrhythmia syndromes and provide recommendations, pending local possibilities, for their monitoring and management during this pandemic.


Url:
DOI: 10.1016/j.hrthm.2020.03.024
PubMed: 32244059
PubMed Central: 7156157


Affiliations:


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PMC:7156157

Le document en format XML

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<name sortKey="Remme, Carol Ann" sort="Remme, Carol Ann" uniqKey="Remme C" first="Carol Ann" last="Remme">Carol Ann Remme</name>
<affiliation wicri:level="4">
<nlm:aff id="aff1">Amsterdam UMC, University of Amsterdam, Heart Center; Department of Clinical and Experimental Cardiology, Amsterdam Cardiovascular Sciences, Meibergdreef 9, 1105 AZ, Amsterdam, The Netherlands</nlm:aff>
<country xml:lang="fr">Pays-Bas</country>
<wicri:regionArea>Amsterdam UMC, University of Amsterdam, Heart Center; Department of Clinical and Experimental Cardiology, Amsterdam Cardiovascular Sciences, Meibergdreef 9, 1105 AZ, Amsterdam</wicri:regionArea>
<placeName>
<settlement type="city">Amsterdam</settlement>
<region nuts="2" type="province">Hollande-Septentrionale</region>
</placeName>
<orgName type="university">Université d'Amsterdam</orgName>
</affiliation>
<affiliation>
<nlm:aff id="aff2">European Reference Network for Rare and Low Prevalence Complex Diseases of the Heart (ERN GUARDHEART; http://guardheart.ern-net.eu)</nlm:aff>
</affiliation>
<affiliation>
<nlm:aff id="aff9">European Cardiac Arrhythmia genetics focus group of EHRA</nlm:aff>
</affiliation>
</author>
<author>
<name sortKey="Wilde, Arthur A M" sort="Wilde, Arthur A M" uniqKey="Wilde A" first="Arthur A. M." last="Wilde">Arthur A. M. Wilde</name>
<affiliation wicri:level="4">
<nlm:aff id="aff1">Amsterdam UMC, University of Amsterdam, Heart Center; Department of Clinical and Experimental Cardiology, Amsterdam Cardiovascular Sciences, Meibergdreef 9, 1105 AZ, Amsterdam, The Netherlands</nlm:aff>
<country xml:lang="fr">Pays-Bas</country>
<wicri:regionArea>Amsterdam UMC, University of Amsterdam, Heart Center; Department of Clinical and Experimental Cardiology, Amsterdam Cardiovascular Sciences, Meibergdreef 9, 1105 AZ, Amsterdam</wicri:regionArea>
<placeName>
<settlement type="city">Amsterdam</settlement>
<region nuts="2" type="province">Hollande-Septentrionale</region>
</placeName>
<orgName type="university">Université d'Amsterdam</orgName>
</affiliation>
<affiliation>
<nlm:aff id="aff2">European Reference Network for Rare and Low Prevalence Complex Diseases of the Heart (ERN GUARDHEART; http://guardheart.ern-net.eu)</nlm:aff>
</affiliation>
<affiliation>
<nlm:aff id="aff9">European Cardiac Arrhythmia genetics focus group of EHRA</nlm:aff>
</affiliation>
</author>
</analytic>
<series>
<title level="j">Heart Rhythm</title>
<idno type="ISSN">1547-5271</idno>
<idno type="eISSN">1556-3871</idno>
<imprint>
<date when="2020">2020</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc>
<textClass></textClass>
</profileDesc>
</teiHeader>
<front>
<div type="abstract" xml:lang="en">
<p>Ever since the first case was reported at the end of 2019, the SARS-COV-2 virus and associated lung disease COVID-19 has spread throughout the world and has become a pandemic. In particular, the high transmission rate of the virus has made it a threat to public health globally. Currently, there is no proven effective therapy against the virus, and the impact on other diseases is also uncertain, especially inherited arrhythmia syndrome.</p>
<p>Arrhythmogenic effect of COVID-19 can be expected, potentially contributing to disease outcome. This may be of importance for patients with an increased risk for cardiac arrhythmias, either secondary to acquired conditions or co-morbidities or consequent to inherited syndromes. Management of patients with inherited arrhythmia syndromes such as Long QT syndrome, Brugada syndrome, Short QT syndrome and Catecholaminergic Polymorphic Ventricular Tachycardia in the setting of the COVID-19 pandemic may prove particularly challenging. Depending on the inherited defect involved, these patients may be susceptible to pro-arrhythmic effects of COVID-19-related issues such as fever, stress, electrolyte disturbances and use of antiviral drugs. We here describe the potential COVID-19 associated risks and therapeutic considerations for patients with distinct inherited arrhythmia syndromes and provide recommendations, pending local possibilities, for their monitoring and management during this pandemic.</p>
</div>
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<name sortKey="Arrhenius, B" uniqKey="Arrhenius B">B. Arrhenius</name>
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<name sortKey="Kobayashi, S" uniqKey="Kobayashi S">S. Kobayashi</name>
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<name sortKey="Susa, T" uniqKey="Susa T">T. Susa</name>
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<name sortKey="Ishiguchi, H" uniqKey="Ishiguchi H">H. Ishiguchi</name>
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<name sortKey="Dalziel, S" uniqKey="Dalziel S">S. Dalziel</name>
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<name sortKey="Schulze Bahr, Eric" sort="Schulze Bahr, Eric" uniqKey="Schulze Bahr E" first="Eric" last="Schulze-Bahr">Eric Schulze-Bahr</name>
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