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Impact of Antiarrhythmic Drugs on the Outcome of Short QT Syndrome

Short QT syndrome (SQTS) is associated with sudden cardiac arrest. There are limited data on the impact of antiarrhythmic drugs on the outcome of SQTS. Materials and Methods: We studied data that describe the clinical outcome of 62 SQTS patients treated with antiarrhythmic drugs, who were recruited...

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Autores principales: El-Battrawy, Ibrahim, Besler, Johanna, Li, Xin, Lan, Huan, Zhao, Zhihan, Liebe, Volker, Schimpf, Rainer, Lang, Siegfried, Wolpert, Christian, Zhou, Xiaobo, Akin, Ibrahim, Borggrefe, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6688193/
https://www.ncbi.nlm.nih.gov/pubmed/31427960
http://dx.doi.org/10.3389/fphar.2019.00771
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author El-Battrawy, Ibrahim
Besler, Johanna
Li, Xin
Lan, Huan
Zhao, Zhihan
Liebe, Volker
Schimpf, Rainer
Lang, Siegfried
Wolpert, Christian
Zhou, Xiaobo
Akin, Ibrahim
Borggrefe, Martin
author_facet El-Battrawy, Ibrahim
Besler, Johanna
Li, Xin
Lan, Huan
Zhao, Zhihan
Liebe, Volker
Schimpf, Rainer
Lang, Siegfried
Wolpert, Christian
Zhou, Xiaobo
Akin, Ibrahim
Borggrefe, Martin
author_sort El-Battrawy, Ibrahim
collection PubMed
description Short QT syndrome (SQTS) is associated with sudden cardiac arrest. There are limited data on the impact of antiarrhythmic drugs on the outcome of SQTS. Materials and Methods: We studied data that describe the clinical outcome of 62 SQTS patients treated with antiarrhythmic drugs, who were recruited from a pool of patients diagnosed in our institution and also from known databases after a systematic search of the published literature. Results: Sixty-two SQTS patients treated with antiarrhythmic drugs were followed up over a median timeframe of 5.6 years (interquartile range 1.6–7.7 years). Six patients, in particular, received multiple drugs as a combination. Of the 55 patients treated with hydroquinidine (HQ), long-term prophylaxis was documented in 41 patients. Fourteen patients stopped treatment due to the following reasons: gastrointestinal intolerance (n = 4), poor compliance (n = 8), and no QTc prolongation (n = 2). Of the 41 patients treated with HQ, the QTc interval increased from 313.5 ± 17.2 to 380.1 ± 21.2 ms. Thirteen of the 41 patients suffered from at least one or more ventricular tachyarrhythmias (VAs) before HQ initiation. VAs are reduced in incidence after HQ treatment (13/41: 31% versus 3/41: 7.3%, p < 0.001). Conclusion: HQ increases the corrected QT interval and prevents VAs in the majority of the patients in this cohort. HQ is safe for use in SQTS patients, particularly due to its low rate of side effects. Other antiarrhythmic drugs might be useful, but the data justifying their use are sparse.
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spelling pubmed-66881932019-08-19 Impact of Antiarrhythmic Drugs on the Outcome of Short QT Syndrome El-Battrawy, Ibrahim Besler, Johanna Li, Xin Lan, Huan Zhao, Zhihan Liebe, Volker Schimpf, Rainer Lang, Siegfried Wolpert, Christian Zhou, Xiaobo Akin, Ibrahim Borggrefe, Martin Front Pharmacol Pharmacology Short QT syndrome (SQTS) is associated with sudden cardiac arrest. There are limited data on the impact of antiarrhythmic drugs on the outcome of SQTS. Materials and Methods: We studied data that describe the clinical outcome of 62 SQTS patients treated with antiarrhythmic drugs, who were recruited from a pool of patients diagnosed in our institution and also from known databases after a systematic search of the published literature. Results: Sixty-two SQTS patients treated with antiarrhythmic drugs were followed up over a median timeframe of 5.6 years (interquartile range 1.6–7.7 years). Six patients, in particular, received multiple drugs as a combination. Of the 55 patients treated with hydroquinidine (HQ), long-term prophylaxis was documented in 41 patients. Fourteen patients stopped treatment due to the following reasons: gastrointestinal intolerance (n = 4), poor compliance (n = 8), and no QTc prolongation (n = 2). Of the 41 patients treated with HQ, the QTc interval increased from 313.5 ± 17.2 to 380.1 ± 21.2 ms. Thirteen of the 41 patients suffered from at least one or more ventricular tachyarrhythmias (VAs) before HQ initiation. VAs are reduced in incidence after HQ treatment (13/41: 31% versus 3/41: 7.3%, p < 0.001). Conclusion: HQ increases the corrected QT interval and prevents VAs in the majority of the patients in this cohort. HQ is safe for use in SQTS patients, particularly due to its low rate of side effects. Other antiarrhythmic drugs might be useful, but the data justifying their use are sparse. Frontiers Media S.A. 2019-08-02 /pmc/articles/PMC6688193/ /pubmed/31427960 http://dx.doi.org/10.3389/fphar.2019.00771 Text en Copyright © 2019 El-Battrawy, Besler, Li, Lan, Zhao, Liebe, Schimpf, Lang, Wolpert, Zhou, Akin and Borggrefe http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
El-Battrawy, Ibrahim
Besler, Johanna
Li, Xin
Lan, Huan
Zhao, Zhihan
Liebe, Volker
Schimpf, Rainer
Lang, Siegfried
Wolpert, Christian
Zhou, Xiaobo
Akin, Ibrahim
Borggrefe, Martin
Impact of Antiarrhythmic Drugs on the Outcome of Short QT Syndrome
title Impact of Antiarrhythmic Drugs on the Outcome of Short QT Syndrome
title_full Impact of Antiarrhythmic Drugs on the Outcome of Short QT Syndrome
title_fullStr Impact of Antiarrhythmic Drugs on the Outcome of Short QT Syndrome
title_full_unstemmed Impact of Antiarrhythmic Drugs on the Outcome of Short QT Syndrome
title_short Impact of Antiarrhythmic Drugs on the Outcome of Short QT Syndrome
title_sort impact of antiarrhythmic drugs on the outcome of short qt syndrome
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6688193/
https://www.ncbi.nlm.nih.gov/pubmed/31427960
http://dx.doi.org/10.3389/fphar.2019.00771
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