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The creation of an arteriotomy during vascular intervention exposes the patient to a number of risks, and the reported probability of thromboembolic complications ranges from 0.3 to 1.6%. However, the use of a closure device seems to be an interesting alternative in selected cases. The aim of the study was to assess the safety and efficacy of the Viabahn in 45 consecutive cases. Forty-five patients undergoing femoral or popliteal artery revascularisation for arterial occlusive disease were included. The popliteal artery was crossed by a 8F or 10F sheath. At the beginning of the procedure, a 0.018-in. wire was inserted into the artery via the 10F sheath. When opening the artery, the guide wire was removed. After that, an endoprosthesis was inserted over a snare and pushed through the artery by a delivery system. There were 2 early failures, both due to unsatisfactory quality of the device. The mean follow-up was 8.8 months. All patients underwent follow-up angiography. The two devices were patent and the artery was satisfactorily sealed in all cases. The mean diameter of the vessels was 6.4 +/- 0.7 mm. The rate of minor complications was 12% and major complications were 3.3% (one major amputation of the lower limb). The patency rates were: 88% at 6 months, 81% at 12 months and 71% at 24 months. The presence of diabetes was significantly related to major complications and delayed patency rates. The three cases of major complications were due to two highly atherosclerotic and occluded vessels and one completely occluded vessel. The use of the Viabahn device is safe and enables satisfactory seal. The presence of diabetes and previous revascularisation surgery are high risk factors for major complications. The study was performed under angiographic control with
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