![]() | Only 14 pages are availabe for public view |
Abstract Coronary artery bypass grafting using saphenous vein graft represents an important option in the treatment of intractable angina due to coronary artery occlusive disease. from its beginning in the late sixties[1], this procedure has been widely applied as a treatment for obstructive coronary artery disease.[2] Following coronary artery bypass surgery (CABG), 15% of vein grafts occlude in the first year, with increasing graft attrition rate of 1-4% per year, such that by 10 years after surgery, only 50-60% of grafts are patent. Up to 20% of patients experience recurrent angina in the first year after CABG, and up to 4% of patients per subsequent year. Furthermore, reoperation carries an increased risk of mortality (3-7%) and perioperative myocardial infarction (4-11%) [3, 4]. Percutaneous stenting of atherosclerotic vein graft lesions has been complicated by high rates of subsequent in-stent restenosis (ISR) and morbidity from distal embolisation of atherosclerotic debris [3, 4]. However, recent advances in drugeluting stents to reduce ISR for de novo lesions are likely to translate to reductions in ISR in vein graft treatment. The use of distal protection devices (DPDs), that trap material embolised at the time of intervention, reduce periprocedural myocardial infarction rates from 14-24% to 7-16% [4]. |