无需开胸即可轻松获得左心室辅助系统。

ASAIO transactions Pub Date : 1991-07-01
E Sasaki, T Nakatani, Y Taenaka, H Noda, E Tatsumi, H Akagi, T Masuzawa, M Goto, M Sakaki, Y Matsuo
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引用次数: 0

摘要

在之前的一篇文章中,描述了一种左心室辅助系统(LVAS),该系统具有易于应用的经皮经间隔插管技术。该系统安全有效(最大输出大于3l /min),适合于主动脉内球囊泵送和开胸LVAS之间。但是放置的技术技巧有点复杂。插管系统得到了改进。在新系统中,入口插管最初用作鞘引入器,并在经间隔穿刺后迅速插入左心房。新型进口套管采用聚氯乙烯(TM100, Toyobo, Co., Ltd, Osaka, Japan)制成,采用聚酯增塑剂,具有优异的抗血栓性和低摩擦性。远端部分设计为灵活的螺旋钢丝,便于操作。在近端安装一个密封中心以防止出血。在慢性动物实验中检验了新系统的简单性和安全性。在经间隔穿刺后几秒钟内将入口插管置入左心房。在20天的激活期间,虽然没有使用抗凝剂,但没有发生全身性或肺栓塞发作。在x线透视下,拆除时插管周围未见血栓形成。术后第14天,中隔穿刺部位愈合。该系统已准备好临床应用,并显示出令人满意的安全性和可管理性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Easy access for a left ventricular assist system without thoracotomy.

In a previous article, a left ventricular assist system (LVAS) with a percutaneous transseptal cannulation technique for easy application was described. This system was safe and efficient (maximum output greater than 3 L/min) and fitted between the intraaortic balloon pumping and LVAS with thoracotomy. But technical skill for placement was slightly complicated. The cannulation system has been improved. In the new system, the inlet cannula is initially used as a sheath introducer and is quickly inserted into the left atrium after transseptal puncture. The new inlet cannula is made of polyvinyl chloride (TM100, Toyobo, Co., Ltd., Osaka, Japan), which has excellent antithrombogenicity and low friction using a polyester plasticizer. The distal part is designed to be flexible with a spiral wire for easy manipulation. A sealing hub was installed to prevent bleeding at the proximal The simplicity and safety of the new system were examined in chronic animal experiments. The inlet cannula was placed into the left atrium within a few seconds after transseptal puncture. During 20 days of activation, there were no episodes of systemic or pulmonary embolism, although no anticoagulant was used. Under fluoroscopy, there was no thrombus formation around the cannula at removal. On the 14th day after removal, the puncture site of the septum had healed. This system is ready for clinical use and shows promise of satisfactory safety and manageability.

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