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首页> 外文期刊>Journal of arrhythmia. >Comparison of the Effects of Na+ and K+ Channel Blockers on the Electrophysiological Properties of the Pulmonary Veins in Patients with Atrial Fibrillation
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Comparison of the Effects of Na+ and K+ Channel Blockers on the Electrophysiological Properties of the Pulmonary Veins in Patients with Atrial Fibrillation

机译:Na + 和K + 通道阻滞剂对心房颤动患者肺静脉电生理特性影响的比较

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Introduction: We assessed the effects of pilsicainide, a pure Na+ channel blocker, and nifekalant, a pure rapid delayed rectifier potassium current (IKr) blocker, on the electrophysiological characteristics within the pulmonary vein (PV) and at the PV-left atrial (LA) junction.Methods and Results: We used a basket catheter for PV mapping in 38 patients with paroxysmal atrial fibrillation (AF). Programmed stimulation was performed in the distal PV and PV-LA junction before and after the infusion of pilsicainide (1 mg/kg; n = 24) or nifekalant (0.3 mg/kg; n = 14). Both drugs significantly prolonged the effective refractory period (ERP) of the distal PV and PV-LA junction. Pilsicainide significantly decreased the ERP heterogeneity of the PV and PV-LA junction (36 ± 43 vs. 9 ± 60 ms, P 0:05). In contrast, nifekalant significantly increased the ERP heterogeneity of the PV and PV-LA junction (from 38 ± 34 to 60 ± 46 ms, P 0:01). Pilsicainide significantly prolonged the conduction time (S1-A1) from the distal PV to the PV-LA junction (from 42 ± 12 to 63 ± 26 ms, P 0:001), whereas this did not change with nifekalant.Conclusions: In AF patients, pilsicainide has antiarrhythmic effects mainly on the distal PV by modifying the ERP and conduction properties. In contrast, nifekalant has antiarrhythmic effects mainly on the PV-LA junction by modifying the ERP.
机译:简介:我们评估了纯净的Na + 通道阻滞剂pilsicainide和纯净的快速延迟整流钾电流(IKr)阻滞剂nifekalant对肺静脉(PV)和肺静脉内电生理特性的影响方法和结果:我们使用篮式导管对38例阵发性心房颤动(AF)患者进行PV定位。在输注比西卡尼(1 mg / kg; n = 24)或硝苯甲酸盐(0.3 mg / kg; n = 14)之前和之后,在远端PV和PV-LA交界处进行程序刺激。两种药物均显着延长了远端PV和PV-LA连接的有效不应期(ERP)。比西卡胺显着降低了PV和PV-LA连接的ERP异质性(36±43 vs. 9±60 ms,P <0:05)。相比之下,硝苯丙胺显着增加了PV和PV-LA连接的ERP异质性(从38±34到60±46 ms,P <0:01)。 Pilsicainide显着延长了从远端PV到PV-LA连接的传导时间(S1-A1)(从42±12到63±26 ms,P <0:001),而随硝苯丙胺没有改变。在房颤患者中,比西卡尼主要通过调节ERP和传导特性对远端PV产生抗心律不齐的作用。相比之下,硝苯卡那特主要通过修改ERP来对PV-LA连接产生抗心律失常作用。

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