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使用伊布利特聚合物涂层起搏电极预防犬急性诱发性心房扑动。

Prevention of acute inducible atrial flutter in dogs by using an ibutilide-polymer-coated pacing electrode.

作者信息

Labhasetwar V, Strickberger S A, Underwood T, Davis J, Levy R J

机构信息

University of Michigan Medical School, Ann Arbor, USA.

出版信息

J Cardiovasc Pharmacol. 1998 Mar;31(3):449-55. doi: 10.1097/00005344-199803000-00017.

Abstract

Atrial arrhythmias (atrial fibrillation or atrial flutter) after coronary artery bypass graft surgery are difficult to prevent or treat and often result in significant morbidity. Prior experimental studies by our group showed improved therapeutic efficacy for antiarrhythmic drugs delivered via controlled-release polymeric matrices implanted on the epicardial surface. These experiments were conducted to test the hypothesis that direct atrial epicardial administration of ibutilide from a controlled-release system (compared with intravenous administration) can reduce the inducibility of atrial flutter in the acute postoperative atrial myocardium. Polymeric sustained-release preparations were formulated by solvent casting of an ibutilide and polyurethane (Pellathane) solution in tetrahydrofurane. Multilayer solvent-casted coatings on pacing electrode wires were carried out to fabricate a sustained-release electrode system. In animal model studies, each dog underwent a thoracotomy, followed by a right atriotomy that was repaired. Induction of atrial flutter was attempted by burst pacing with the bipolar pacing catheter. Sinus rhythm was restored with overdrive pacing. After determining the induction rate (percentage) of atrial flutter in the baseline state, a stainless-steel wire coated with the drug-delivery system, 10% ibutilide/90% polyurethane (n = 7), or without drug (polyurethane coating without ibutilide, n = 5; control) was sewn onto the right atrium. Systemic intravenous administration of ibutilide (1.2 microg/kg/h) also was carried out in a separate group of animals after atriotomy (n = 5). For ibutilide (at an estimated dose of 1.2 microg/kg/h), the atrial-flutter results were 41.85 +/- 2.21% induction for baseline compared with 12.42 +/- 5.26% (p = 0.02) after the ibutilide wire implant. In the control dogs, atrial flutter was induced 29.4 +/- 4.7% at baseline and 25.2 +/- 5.1% after implantation of the control wire (p = 0.4). Ibutilide coronary venous serum concentrations at the end of the ibutilide-polyurethane electrode experiments were 2.25 +/- 0.2 ng/ml (mean +/- SEM) versus systemic levels that were below the limits of detection. Systemic intravenous ibutilide infusions had no effect on the inducibility of atrial flutter. In conclusion, an epicardial implantable electrode coating with an ibutilide controlled drug-release system significantly reduced the inducibility of atrial flutter in an experimental atriotomy model. These results suggest that atrial arrhythmias occurring after coronary bypass surgery may be prevented by local atrial administration of ibutilide from a controlled-release pacing electrode.

摘要

冠状动脉搭桥手术后发生的房性心律失常(房颤或房扑)难以预防或治疗,且常导致严重的发病情况。我们团队之前的实验研究表明,通过植入心外膜表面的控释聚合物基质递送抗心律失常药物,治疗效果有所改善。进行这些实验是为了验证以下假设:与静脉给药相比,从控释系统直接在心外膜给予伊布利特可降低术后急性心房心肌中房扑的诱发性。通过将伊布利特和聚氨酯(佩拉坦)溶液在四氢呋喃中进行溶剂浇铸来制备聚合物缓释制剂。在起搏电极导线上进行多层溶剂浇铸涂层以制造缓释电极系统。在动物模型研究中,每只狗均接受开胸手术,随后进行右心房切开术并修复。尝试通过双极起搏导管进行猝发起搏来诱发房扑。通过超速起搏恢复窦性心律。在确定基线状态下房扑的诱发率(百分比)后,将涂有药物递送系统(10%伊布利特/90%聚氨酯,n = 7)或无药物(无伊布利特的聚氨酯涂层,n = 5;对照组)的不锈钢丝缝在右心房上。在另一组动物的心房切开术后,也进行了伊布利特的全身静脉给药(1.2微克/千克/小时,n = 5)。对于伊布利特(估计剂量为1.2微克/千克/小时),基线时房扑的诱发结果为41.85±2.21%,而在植入伊布利特钢丝后为12.42±5.26%(p = 0.02)。在对照犬中,基线时房扑的诱发率为29.4±4.7%,植入对照钢丝后为25.2±5.1%(p = 0.4)。在伊布利特 - 聚氨酯电极实验结束时,伊布利特冠状动脉静脉血清浓度为2.25±0.2纳克/毫升(平均值±标准误),而全身水平低于检测限。全身静脉输注伊布利特对房扑的诱发性没有影响。总之,带有伊布利特控释系统的心外膜可植入电极涂层在实验性心房切开术模型中显著降低了房扑的诱发性。这些结果表明,冠状动脉搭桥手术后发生的房性心律失常可能通过从控释起搏电极局部心房给予伊布利特来预防。

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