How much do we need to provoke? Challenges and opportunities in refining the pharmacological tests to unmask Brugada syndrome.
作者信息
Menon Syamkumar Divakara
机构信息
McMaster University, Hamilton, ON, Canada.
出版信息
Indian Pacing Electrophysiol J. 2017 Jul-Aug;17(4):100-101. doi: 10.1016/j.ipej.2017.07.007. Epub 2017 Jul 11.
Abstract
摘要
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How much do we need to provoke? Challenges and opportunities in refining the pharmacological tests to unmask Brugada syndrome.我们需要多大程度的激发？完善药理学测试以揭示 Brugada 综合征中的挑战与机遇。
Indian Pacing Electrophysiol J. 2017 Jul-Aug;17(4):100-101. doi: 10.1016/j.ipej.2017.07.007. Epub 2017 Jul 11.
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本文引用的文献
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Evaluation of baseline ECG in patients undergoing Oral Flecainide Challenge test for suspected Brugada Syndrome: An analysis of lead II.对疑似布加综合征患者进行口服氟卡尼激发试验时基线心电图的评估：II导联分析
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Everybody has Brugada syndrome until proven otherwise?在未被证伪之前，每个人都患有布加综合征？
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Risk stratification in Brugada syndrome: results of the PRELUDE (PRogrammed ELectrical stimUlation preDictive valuE) registry.Brugada 综合征的风险分层：PRELUDE（程控电刺激预测价值）注册研究结果。
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Long-term prognosis of patients diagnosed with Brugada syndrome: Results from the FINGER Brugada Syndrome Registry.Brugada 综合征患者的长期预后：FINGER Brugada 综合征注册研究结果。
Circulation. 2010 Feb 9;121(5):635-43. doi: 10.1161/CIRCULATIONAHA.109.887026. Epub 2010 Jan 25.
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Mutations in sodium channel β1- and β2-subunits associated with atrial fibrillation.与心房颤动相关的钠通道β1和β2亚基突变。
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Mutation in glycerol-3-phosphate dehydrogenase 1 like gene (GPD1-L) decreases cardiac Na+ current and causes inherited arrhythmias.甘油-3-磷酸脱氢酶1样基因（GPD1-L）突变会降低心脏钠离子电流并导致遗传性心律失常。
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Sudden death in the young.年轻人猝死。
Heart Rhythm. 2005 Dec;2(12):1277-82. doi: 10.1016/j.hrthm.2005.09.008.
10
Brugada syndrome: report of the second consensus conference: endorsed by the Heart Rhythm Society and the European Heart Rhythm Association.布加综合征：第二届共识会议报告：得到心律学会和欧洲心律协会认可。
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