Gundry S R, Black K, Izutani H
Loma Linda University Medical Center, Loma Linda, CA 92354, USA.
J Thorac Cardiovasc Surg. 2000 Sep;120(3):473-7. doi: 10.1067/mtc.2000.108596.
As heart surgery becomes increasingly focused on minimally invasive techniques, it has become apparent that conventional techniques of anastomosis will need to be severely altered or abandoned. Toward that end, we developed and tested in vitro and in vivo coronary artery bypass graft anastomoses using a biologic glue formulated from bovine albumin and glutaraldehyde. We used a double-balloon catheter as a temporary internal stent to create and seal the anastomosis during gluing.
Initially, anastomoses were made between cryopreserved human saphenous vein segments and coronary arteries in vitro on 12 intact bovine hearts. A total of 42 anastomoses were created with the catheter system introduced into the distal end of the graft, exiting the back wall, and entering the anterior wall of the coronary artery. Two balloons (one in the graft and one in the coronary artery) held the anastomosis stable while the biologic glue was applied externally and allowed to set for 2 minutes. The balloon catheter was then removed from the end of the graft simulating a side-to-side internal thoracic artery anastomosis. After the graft had been flushed to assure distal end patency, the open end of the graft was clipped, turning the anastomosis into an end-to-side graft. A pressure transducer was then attached to the graft and saline solution forcefully infused.
All grafts easily held a pressure of 300 mm Hg; 10 grafts were tested up to 560 mm Hg without leaks. Distal and proximal coronary artery patency was checked by examining flow out of the coronary ostia and by cutting arteries distal to the grafts. All anastomoses were patent on being opened and no glue was seen intraluminally. Subsequently, 3 anastomoses of the left internal thoracic artery to the left anterior descending artery have been constructed in goats, with autopsies at 24 hours, 10 months, and 1 year revealing patent anastomoses.
A biologic glue and catheter system has been developed that allows a coronary anastomosis with a high bursting strength to be performed. When the system has been further developed and tested, truly minimally invasive heart surgery may be possible.
随着心脏手术越来越注重微创技术,很明显传统的吻合技术将需要大幅改变或摒弃。为此,我们研发并在体外和体内测试了使用由牛白蛋白和戊二醛配制的生物胶水进行冠状动脉搭桥移植吻合术。我们使用双球囊导管作为临时内部支架,在胶合过程中创建并密封吻合口。
最初,在12颗完整的牛心脏上,于体外在冷冻保存的人隐静脉段与冠状动脉之间进行吻合。通过将导管系统引入移植物远端、穿出后壁并进入冠状动脉前壁,共创建了42个吻合口。在外部涂抹生物胶水并使其凝固2分钟时,两个球囊(一个在移植物中,一个在冠状动脉中)保持吻合口稳定。然后从移植物末端移除球囊导管,模拟胸内动脉侧侧吻合。在冲洗移植物以确保远端通畅后,夹住移植物的开放端,将吻合口变为端侧移植物。然后将压力传感器连接到移植物上,并强力注入盐溶液。
所有移植物都能轻松承受300毫米汞柱的压力;10个移植物在高达560毫米汞柱的压力下进行测试,无渗漏。通过检查冠状动脉开口处的血流以及切割移植物远端的动脉来检查冠状动脉远端和近端的通畅情况。所有吻合口在打开时均通畅,管腔内未见胶水。随后,在山羊身上构建了3个左胸内动脉与左前降支动脉的吻合口,在24小时、10个月和1年时进行尸检,显示吻合口通畅。
已研发出一种生物胶水和导管系统,可进行具有高破裂强度的冠状动脉吻合。当该系统得到进一步研发和测试后,真正的微创心脏手术或许可行。