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首页> 外文期刊>Indian heart journal >A pilot study on the acute conversion and maintenance of sinus rhythm in rheumatic atrial fibrillation using oral flecainide
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A pilot study on the acute conversion and maintenance of sinus rhythm in rheumatic atrial fibrillation using oral flecainide

机译:使用口服絮状物急性转化和窦性心律急性转化维持的试验研究

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Background Achievement of sinus rhythm (SR) is an important goal in rheumatic atrial fibrillation (AF). Studies in rheumatic AF have often used amiodarone for rhythm control. Flecainide has not been studied in these patients due to concerns of underlying structural heart disease. Methods Pharmacological cardioversion by oral single loading dose (SLD) of Flecainide (4?mg/kg, ≤300?mg) was tested in 50 patients with rheumatic AF (MVA 1.51?±?0.19?mmsup2/sup, age 46.2?±?10.28?yrs, AF duration 3.10?±?1.7?yrs, LA size: 44.42?±?7.48?mm). Non-converters underwent DC cardioversion (DCC) at 24?h. All patients received oral flecainide and ββ/diltiazem at discharge. Results At 24?h, 38/50 (76%) achieved SR (2 with SLD; 36 after DCC). At 30 days (mean Flecainide dose 116.5?±?10.5?mg) successful maintenance of SR was noted in 31/38 (89%). At 1 year, 30/38 (79%) of the initial converters and 60% of the overall population maintained SR. Those in SR had significantly better NYHA Class (1.1?±?0.12 vs 1.3?±?0.10, p?=?0.03) and mean PCS8 score (50.11?±?5.337 vs 46.84?±?5.379, p?=?0.02). AF duration (OR 0.594 CI 0.375–0.940, p?=?0.02) and LA size (OR 0.840, CI 0.757–0.933, p?=?0.001) were found to be the only significant predictors of successful outcomes. Patients with AF duration 3.5 years and LA size 51?mm had 85% and 75% chance of maintaining SR at 1 year, respectively. Conclusion Flecainide is safe and effective for achieving and maintaining SR in patients of rheumatic AF who are unlikely to have underlying coronary artery disease or ventricular dysfunction.
机译:背景技术窦性心律(SR)是风神经心房颤动(AF)的重要目标。血压AF的研究经常使用胺碘酮进行节律控制。由于潜在的结构性心脏病的担忧,这些患者尚未在这些患者中研究过蜡烛。方法在50例风湿性AF(MVA1.51≤X±0.1​​9Ω患者中,通过口服单次装载剂量(SLD)(4×Mg / kg,≤300μmγ)进行药物心致(4×mg / kg,≤300μm)(mVa1.51Ω·±0.19Ω·mm 2 ,年龄46.2?±10.28?YRS,AF持续时间3.10?±1.7?YRS,LA尺寸:44.42?±7.48?mm)。非转换器在24℃下接受DC Cardioversion(DCC)。所有患者在放电时接受口服絮状虫和ββ/ Diltiazem。结果24?H,38/50(76%)达到SR(2带SLD; 36后DCC后)。在30天(平均絮状剂剂量116.5?±10.5?mg)在31/38(89%)中指出了SR的成功维护。在1年,30/38(79%)的初始转换器和60%的整体人口维持SR。 SR中的人具有明显更好的NYHA类(1.1?±0.12 Vs 1.3?±0.10,P?= 0.03)并平均PCS8得分(50.11?±5.337 Vs 46.84?±?5.379,p?=?0.02) 。 AF持续时间(或0.594 CI 0.375-0.940,P?= 0.02)和La尺寸(或0.840,CI 0.757-0.933,p?= 0.001)是成功结果的唯一重要预测因子。 AF持续时间<3.5岁的患者和LA尺寸<51?mm有85%和75%的机会分别保持1年的SR。结论Flecainide是安全可有效的,可实现和维持患者的患者,其不太可能具有潜在的冠状动脉疾病或心室功能障碍。

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