Sex-differences in short QT syndrome: a systematic literature review and pooled analysis

Short QT syndrome (SQTS) is an inherited arrhythmic disorder with a risk of sudden cardiac death (SCD).1,2 Patients may present with symptoms such as palpitations, which could suggest atrial arrhythmias. Several criteria to facilitate the diagnosis of SQTS have been proposed in 2011.3 The European S...

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Autores principales: El-Battrawy, Ibrahim (Autor) , Schlentrich, Kim (Autor) , Besler, Johanna (Autor) , Liebe, Volker (Autor) , Schimpf, Rainer (Autor) , Lang, Siegfried (Autor) , Odening, Katja Elisabeth (Autor) , Wolpert, Christian (Autor) , Zhou, Xiao-Bo (Autor) , Borggrefe, Martin (Autor) , Akın, Ibrahim (Autor)
Formato: Article (Journal)
Lenguaje:inglés
Publicado: 01 August 2020
In: European journal of preventive cardiology
Year: 2020, Volumen: 27, Número: 12, Pages: 1335-1338
ISSN:2047-4881
DOI:10.1177/2047487319850953
Acceso en línea:Verlag, kostenfrei, Volltext: https://doi.org/10.1177/2047487319850953
Verlag, kostenfrei, Volltext: https://academic.oup.com/eurjpc/article/27/12/1335/5950594
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Notas de Autor:Ibrahim El-Battrawy, Kim Schlentrich, Johanna Besler, Volker Liebe, Rainer Schimpf, Siegfried Lang, Katja E Odening, Christian Wolpert, Xiaobo Zhou, Martin Borggrefe, and Ibrahim Akin
Descripción
Sumario:Short QT syndrome (SQTS) is an inherited arrhythmic disorder with a risk of sudden cardiac death (SCD).1,2 Patients may present with symptoms such as palpitations, which could suggest atrial arrhythmias. Several criteria to facilitate the diagnosis of SQTS have been proposed in 2011.3 The European Society of Cardiology guidelines updated these criteria in 2015.4 It has been suggested that an implantable cardioverter defibrillator (ICD) is possibly a definitive option to prevent SCD in these patients.1,5 Some studies have recommended the use of hydroquinidine in high risk SQTS patients including those suffering from recurrent ventricular tachyarrhythmias.2,6
Notas:Gesehen am 10.08.2026
Descripción Física:Online Resource
ISSN:2047-4881
DOI:10.1177/2047487319850953