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Antiarrhythmic Medication in Neonates and Infants with Supraventricular Tachycardia

Supraventricular tachycardia (SVT) is the most common arrhythmia in neonates and infants, and pharmacological therapy is recommended to prevent recurrent episodes. This retrospective study aims to describe and analyze the practice patterns, effectiveness, and outcome of drug therapy for SVT in patie...

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Autores principales: Bruder, Diana, Weber, Roland, Gass, Matthias, Balmer, Christian, Cavigelli-Brunner, Anna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9293794/
https://www.ncbi.nlm.nih.gov/pubmed/35258638
http://dx.doi.org/10.1007/s00246-022-02853-9
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author Bruder, Diana
Weber, Roland
Gass, Matthias
Balmer, Christian
Cavigelli-Brunner, Anna
author_facet Bruder, Diana
Weber, Roland
Gass, Matthias
Balmer, Christian
Cavigelli-Brunner, Anna
author_sort Bruder, Diana
collection PubMed
description Supraventricular tachycardia (SVT) is the most common arrhythmia in neonates and infants, and pharmacological therapy is recommended to prevent recurrent episodes. This retrospective study aims to describe and analyze the practice patterns, effectiveness, and outcome of drug therapy for SVT in patients within the first year of life. Among the 67 patients analyzed, 48 presented with atrioventricular re-entrant tachycardia, 18 with focal atrial, and one with atrioventricular nodal re-entrant. Fetal tachycardia was reported in 27%. Antiarrhythmic treatment consisted of beta-receptor blocking agents in 42 patients, propafenone in 20, amiodarone in 20, and digoxin in 5. Arrhythmia control was achieved with single drug therapy in 70% of the patients, 21% needed dual therapy, and 6% triple. Propafenone was discontinued in 7 infants due to widening of the QRS complex. After 12 months (6–60), 75% of surviving patients were tachycardia-free and discontinued prophylactic treatment. Patients with fetal tachycardia had a significantly higher risk of persistent tachycardia (p: 0.007). Prophylactic antiarrhythmic medication for SVT in infancy is safe and well tolerated. Arrhythmia control is often achieved with single medication, and after cessation, most patients are free of arrhythmias. Infants with SVT and a history of fetal tachycardia are more prone to suffer from persistent SVT and relapses after cessation of prophylactic antiarrhythmic medication than infants with the first episode of SVT after birth.
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spelling pubmed-92937942022-07-20 Antiarrhythmic Medication in Neonates and Infants with Supraventricular Tachycardia Bruder, Diana Weber, Roland Gass, Matthias Balmer, Christian Cavigelli-Brunner, Anna Pediatr Cardiol Original Article Supraventricular tachycardia (SVT) is the most common arrhythmia in neonates and infants, and pharmacological therapy is recommended to prevent recurrent episodes. This retrospective study aims to describe and analyze the practice patterns, effectiveness, and outcome of drug therapy for SVT in patients within the first year of life. Among the 67 patients analyzed, 48 presented with atrioventricular re-entrant tachycardia, 18 with focal atrial, and one with atrioventricular nodal re-entrant. Fetal tachycardia was reported in 27%. Antiarrhythmic treatment consisted of beta-receptor blocking agents in 42 patients, propafenone in 20, amiodarone in 20, and digoxin in 5. Arrhythmia control was achieved with single drug therapy in 70% of the patients, 21% needed dual therapy, and 6% triple. Propafenone was discontinued in 7 infants due to widening of the QRS complex. After 12 months (6–60), 75% of surviving patients were tachycardia-free and discontinued prophylactic treatment. Patients with fetal tachycardia had a significantly higher risk of persistent tachycardia (p: 0.007). Prophylactic antiarrhythmic medication for SVT in infancy is safe and well tolerated. Arrhythmia control is often achieved with single medication, and after cessation, most patients are free of arrhythmias. Infants with SVT and a history of fetal tachycardia are more prone to suffer from persistent SVT and relapses after cessation of prophylactic antiarrhythmic medication than infants with the first episode of SVT after birth. Springer US 2022-03-08 2022 /pmc/articles/PMC9293794/ /pubmed/35258638 http://dx.doi.org/10.1007/s00246-022-02853-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Article
Bruder, Diana
Weber, Roland
Gass, Matthias
Balmer, Christian
Cavigelli-Brunner, Anna
Antiarrhythmic Medication in Neonates and Infants with Supraventricular Tachycardia
title Antiarrhythmic Medication in Neonates and Infants with Supraventricular Tachycardia
title_full Antiarrhythmic Medication in Neonates and Infants with Supraventricular Tachycardia
title_fullStr Antiarrhythmic Medication in Neonates and Infants with Supraventricular Tachycardia
title_full_unstemmed Antiarrhythmic Medication in Neonates and Infants with Supraventricular Tachycardia
title_short Antiarrhythmic Medication in Neonates and Infants with Supraventricular Tachycardia
title_sort antiarrhythmic medication in neonates and infants with supraventricular tachycardia
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9293794/
https://www.ncbi.nlm.nih.gov/pubmed/35258638
http://dx.doi.org/10.1007/s00246-022-02853-9
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