Why the study?
Do drug-eluting stents increase the risk of stent thrombosis compared to bare-metal stents?
Do drug-eluting stents increase the risk of stent thrombosis compared to bare-metal stents?
While drug-eluting stents reduce restenosis, they carry a risk of late stent thrombosis, making uninterrupted antiplatelet therapy crucial.
Emphasizes antiplatelet adherence to mitigate thrombosis with drug-eluting stents; leaves open confirmation of net benefit in randomized trials.
Drug-eluting stents reduce the occurrence of in-stent restenosis and the need for subsequent target vessel revascularization when compared with bare-metal stents. However, drug-eluting stents may be associated with delayed (or absent) endothelialization, localized hypersensitivity reactions and late stent thrombosis. Stent thrombosis is a catastrophic event, resulting in life-threatening complications. Although larger, adequately powered, randomized trials are needed to fully assess the net clinical effects of drug-eluting stents compared with bare-metal stents, the evidence, thus far, appears to suggest that the net clinical benefit of drug-eluting stents may outweigh their risks. Premature discontinuation of antiplatelet therapy is the most important predictor of stent thrombosis; therefore, patients who are candidates for implantation of drug-eluting stents should be screened for their ability to receive and tolerate uninterrupted antiplatelet therapy longer than is necessary with bare-metal stents.
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Ιoannis Iakovou (2008) studied this question.
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