The Clinical Diagnosis and Management of Long QT Syndrome: Insights from the 2022 ESC Guidelines
نویسندگان
چکیده
Long QT syndrome (LQTS) is an uncommon disorder that characterized by prolongation and torsade de pointes leading to sudden cardiac death. It mainly triggered adrenergic activation. Since LQTS rare, it often underdiagnosed. The updated 2022 European Society of Cardiology (ESC) guidelines aim define the diagnosis spread its management. However, some unknowns uncertainties still exist regarding treatment LQTS. This commentary geared expansion clinical applications drug therapies for different subtypes based on ESC guidelines.
منابع مشابه
Guidelines for the diagnosis and management of familial long QT syndrome.
1.1 Definition and prevalence Long QT syndrome (LQTS) is a familial condition causing syncope and sudden death through rapid ventricular tachycardia (torsade de pointes), which can deteriorate to ventricular fibrillation, in otherwise fit and healthy young people. Prevalence is approximately 1 in 2,500. 1 Clinical diagnosis is made from a combination of suspicious history, family history and th...
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ژورنال
عنوان ژورنال: Reviews in Cardiovascular Medicine
سال: 2023
ISSN: ['2153-8174', '1530-6550']
DOI: https://doi.org/10.31083/j.rcm2406170