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在实验模型中通过快速药物输注终止心房颤动

Rapid drug infusion for termination of atrial fibrillation in an experimental model.

作者信息

Arzbaecher R, Gemperline J, Haklin M, Buscemi P

机构信息

Illinois Institute of Technology, Chicago, USA.

出版信息

Pacing Clin Electrophysiol. 1998 Jan;21(1 Pt 2):288-91. doi: 10.1111/j.1540-8159.1998.tb01106.x.

Abstract

Episodes of paroxysmal atrial fibrillation (PAF) in the ambulatory patient might be terminated promptly by intravenous infusion from an implanted drug delivery system. We have explored this concept in a series of experiments using rapid intra-atrial infusions in dogs. In the acute studies, rapid intra-atrial infusions of procainamide were delivered during continual measurements of epicardial monophasic action potentials (MAP), atrial effective refractory periods (ERP), and right to left atrial conduction times (CT) in 9 dogs. In the chronic studies, 20 episodes of sustained PAF were induced in 4 dogs after six weeks of rapid or burst atrial pacing from a specially programmed implanted pacemaker. Rapid infusions of procainamide were then delivered to the right atrium through a previously implanted catheter connected to a subcutaneous access port. Procainamide significantly increased the duration of the atrial MAP, ERP and CT in the acute experiments. It also terminated induced PAF within five minutes of the end of infusion in all twenty of the chronic experiments. We conclude that rapid intra-atrial infusion of procainamide is very effective in this animal model of PAF, and that such infusion prolongs atrial MAP, ERP and CT.

摘要

门诊患者的阵发性心房颤动(PAF)发作可能通过植入式药物输送系统静脉输注迅速终止。我们在一系列实验中探讨了这一概念,这些实验采用在犬类中进行快速心房内输注的方法。在急性研究中,在持续测量9只犬的心外膜单相动作电位(MAP)、心房有效不应期(ERP)以及右至左心房传导时间(CT)的过程中,进行了普鲁卡因胺的快速心房内输注。在慢性研究中,经过六周由专门编程的植入式起搏器进行快速或猝发性心房起搏后,4只犬诱发了20次持续性PAF发作。然后通过连接到皮下接入端口的先前植入的导管将普鲁卡因胺快速输注到右心房。在急性实验中,普鲁卡因胺显著增加了心房MAP、ERP和CT的持续时间。在所有20次慢性实验中,它还在输注结束后五分钟内终止了诱发的PAF。我们得出结论,在这种PAF动物模型中,快速心房内输注普鲁卡因胺非常有效,并且这种输注可延长心房MAP、ERP和CT。

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