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Ann Thorac Surg 2004;78:1878-1879
© 2004 The Society of Thoracic Surgeons
Clinic for Cardiovascular Surgery, University Hospital Zürich, Rämistrasse 100, CH-8091 Zürich, Switzerland
oliver.reuthebuch{at}usz.ch
To the Editor:
We appreciate the interesting remarks of Matschke and associates regarding their findings of early graft occlusion using the Symmetry connector device. According to recently published reports [13] it appears that the occlusion or high-grade stenosis of saphenous vein grafts in coronary artery bypass grafting procedures done with the use of the Symmetry connector seems to occur at the level of the device, thus confirming our reported findings [4].
The rationale for these alarming observations is still unclear and is the subject of an ongoing debate. Currently, the following explanations are under discussion:
The anticoagulation protocol described by Matschke and co-workers addresses this potential mechanism of induced thrombogenicity by the Nitinol surface of the connector. In animal studies [6], implanted St. Jude medical connectors showed a complete neointimal covering after only 30 days, with no subsequent progression after 90 and 180 days. These findings suggest that after a period of 30 days, the implanted Nitinol surface might be covered, and thus thrombosis would not occur. However, in our series and in several reports, occlusions developed well beyond 30 days postoperatively, with 1 patient readmitted to the hospital because of angina 31 months after operation. Angiography revealed an occluded proximal connector, which was successfully dilated.
In summary, we believe that antiplatelet therapy is mandatory in patients with connector devices made of Nitinol. We are aware that this regimen addresses only one potential cause of stenosis or occlusion. Because of the convincing results of thrombosis prevention with clopidogrel or ticlopidine after stenting we do not think anticoagulation is necessary after implantation of a Nitinol connector. However, given our findings, we recommend strongly that antiplatelet therapy be continued more than 3 months postoperatively.
References
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