Percutaneous transluminal angioplasty PTA is an established method for treatment of peripheral artery disease PAD of the femoropopliteal artery. However, in up to % of patients restenosis and/or reocclusion remain a frequent complication occurring in the first year after the procedure. In this study, we focused on the influence of compromised postprocedural infrapopliteal runoff of the affected limb, on the hypercoagulability as detected by a global hemostasis assay and on genetic predisposition to hypercoagulability and on the regulation of the inflammation through the nuclear receptor related protein NuRR . Consecutive PAD patients treated by femoropopliteal PTA because of disabling claudication or critical limb ischemia were followed up by vascular ultrasound imaging at , , and months after the procedure. Venous blood samples for hemostasis, inflammation, and gene analysis were obtained before and h after PTA. One month after femoropopliteal PTA, % of patients with compromised runoff developed the combined end point restenosis/reocclusion in comparison to % with good runoff p = . . After months, the differences were no longer significant. It was concluded that compromised postprocedural infrapopliteal runoff predisposes to early restenosis/reocclusion after femoropopliteal PTA and that the deterioration of infrapopliteal runoff in the year after femoropopliteal PTA is accompanied by worsening of long-term femoropopliteal patency. Patients were genotyped for the prothrombotic gene polymorphisms platelet receptor glycoprotein IIIa T C, coagulation factor V G A, coagulation factor II G A, coagulation factor XII C -T, and plasminogen activator inhibitor-G G. We were not able to show any association between these polymorphisms and the restenosis/reocclusion rate in patients treated with femoropopliteal PTA. Furthermore, no association between thrombin generation and reste-