We have been using these devices in both open coronary bypass procedures (mainly in off pump procedures) and some robotically assisted closed chest coronary bypasses for over a year now with good results (they have already gained FDA approval). The purpose of the study is to document the results of using this technology in a closed chest setting. So, although the basic procedure will not change from our current practice the follow up will include a cardiac CT scan at 2 weeks, then again at 9 months to document the result of using this technology.
Tuesday, September 23, 2008
New device study
Starting a new study using an automated anastomotic device, the Cardica C Port Flex A (www.cardica.com), in robotically assisted coronary artery bypass operations. The C Port device produces a precise, consistent, compliant connection between two vessels. In previous studies it has been shown to have results (graft patency) superior to hand sewn anastomoses.
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