Patients with DM are more affected by coronary artery disease and when treated by PCI with stent implantation they remain at higher risk of in-stent restenosis and adverse cardiovascular events
The etiology of this failure is likely to be multifactorial such as diffuse disease progression, small vessel and endothelial dysfunction
The presence of DM (particularly insulin-treated DM) has been a consistent, independent predictor of in-stent restenosis
Facilitates mono directional drug release and less systemic exposure of drug leading to faster re-endothelialisation
Coating on the stent and exposed parts of the balloon facilitate homogeneous drug delivery which addresses diused proliferative disease and focal restenosis
Additional 0.5 mm coating beyond the proximal and distal edge of the Stent addresses the edge restenosis
The formation of circular film with biodegradable polymer facilitate maximum drug delivery in blood wet conditions