Decreased intermediate term patency of automated proximal anastomoses evaluated by sequential ultrafast CT

Objective: The Symmetry™ aortic connector creates proximal anastomoses of saphenous vein grafts using a nitinol implant. The device avoids partial clamping and thus possibly reduces neurologic complications. To evaluate graft patency, a single surgeon randomised study was performed in our institutio...

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Veröffentlicht in:European journal of cardio-thoracic surgery 2005-04, Vol.27 (4), p.579-583
Hauptverfasser: Dietrich, Markus, Martens, Sven, Kohlert, Melanie, Herzog, Christopher, Khan, Mohammad Fawad, Wimmer-Greinecker, Gerhard, Moritz, Anton
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Sprache:eng
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Zusammenfassung:Objective: The Symmetry™ aortic connector creates proximal anastomoses of saphenous vein grafts using a nitinol implant. The device avoids partial clamping and thus possibly reduces neurologic complications. To evaluate graft patency, a single surgeon randomised study was performed in our institution. Methods: Seventy-seven patients were randomised either to automated proximal anastomoses (group I, n=39, 61 vein grafts connected using the aortic connector, 47 as single, 15 as sequential bypasses) or controls (group II, n=38, 62 proximal anastomoses handsewn, 46 as single, 16 as sequential bypasses). Ultrafast CT-scans were performed on postoperative day 5 in 34 patients of group I and 16 patients of group II to evaluate early graft patency. Intermediate term patency was evaluated with ultrafast CT-scan in 30 patients of group I (46 grafts) and 25 patients of group II (39 grafts) 1 year after the operation. Results: Two early graft occlusions were detected in group I (3.8%). In group II all evaluated grafts were patent 5 days after surgery. 11.4 months after surgery, seven out of 46 grafts were found occluded (15.2%) in group I. In the control group, only one occlusion was detected (2.6%). Conclusions: We observed a trend towards an increased occlusion rate 1 year after surgery with automated connector devices. For evaluation of long-term patency larger patient groups have to be evaluated. Other benefits of these devices have to be proven to promote their clinical application.
ISSN:1010-7940
1873-734X
DOI:10.1016/j.ejcts.2004.12.050