Electrical Diseases of the Heart 2013
DOI: 10.1007/978-1-4471-4881-4_6
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Mechanisms of Cardiac Arrhythmia

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Cited by 3 publications
(1 citation statement)
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“…Previously, the only available pharmacological options for the rhythm control of AF were propafenone and flecainide (sodium channel blockers); sotalol and dofetilide (I Kr potassium channel blockers) and amiodarone and dronedarone (mixed ion channel blockers) [12]. The safety and efficacy of these drugs limits their use in clinical practice --for example, propafenone and flecainide are proarrhythmogenic, particularly in patients who have structural heart disease; sotalol can cause marked QT interval prolongation as well as being contraindicated in asthmatic patients and amiodarone-related toxicity is well described (although less important in the acute setting there have still been anecdotal reports of adverse effect after just a few days [13]).…”
Section: Rhythm Controlmentioning
confidence: 99%
“…Previously, the only available pharmacological options for the rhythm control of AF were propafenone and flecainide (sodium channel blockers); sotalol and dofetilide (I Kr potassium channel blockers) and amiodarone and dronedarone (mixed ion channel blockers) [12]. The safety and efficacy of these drugs limits their use in clinical practice --for example, propafenone and flecainide are proarrhythmogenic, particularly in patients who have structural heart disease; sotalol can cause marked QT interval prolongation as well as being contraindicated in asthmatic patients and amiodarone-related toxicity is well described (although less important in the acute setting there have still been anecdotal reports of adverse effect after just a few days [13]).…”
Section: Rhythm Controlmentioning
confidence: 99%