2006
DOI: 10.1002/ccd.20895
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First‐in‐human implantation of a fully bioabsorbable drug‐eluting stent: The BVS poly‐L‐lactic acid everolimus‐eluting coronary stent

Abstract: The first-in-human fully bioabsorbable drug-eluting stent (BVS poly-L-lactic acid everolimus-eluting coronary stent) implantation was performed at Auckland City Hospital, New Zealand as part of the ABSORB trial. There were no adverse events in-hospital or by 1 month. A stent that supports the vessel when needed, delivers an antiproliferative drug then disappears has theoretical advantages with regard to CT and MRI compatibility, restored vessel vasomotion, and facilitated future percutaneous intervention or su… Show more

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Cited by 118 publications
(59 citation statements)
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“…2 Currently, the everolimus-eluting BVS stent (Abbott Vascular, Santa Clara, USA), a coronary polymer stent based on PLLA, is being investigated in the ABSORB clinical trial. 19 Recent data on the in vivo performance of this stent, which has a strut thickness of 150 lm at a nominal diameter of 3.0 mm, is very promising and demonstrates an acute recoil comparable to a metallic stent. 25 A larger number of groups have already demonstrated the high potential of their technology in the experimental stage.…”
Section: Introductionmentioning
confidence: 94%
“…2 Currently, the everolimus-eluting BVS stent (Abbott Vascular, Santa Clara, USA), a coronary polymer stent based on PLLA, is being investigated in the ABSORB clinical trial. 19 Recent data on the in vivo performance of this stent, which has a strut thickness of 150 lm at a nominal diameter of 3.0 mm, is very promising and demonstrates an acute recoil comparable to a metallic stent. 25 A larger number of groups have already demonstrated the high potential of their technology in the experimental stage.…”
Section: Introductionmentioning
confidence: 94%
“…Bioresorbable scaffolds (BRS), developed to theoretically overcome most of such limitations, are the so-called 4th revolution in interventional cardiology and have the potential to significantly improve coronary artery disease treatment (6)(7)(8)(9)(10)(11).…”
Section: Introductionmentioning
confidence: 99%
“…In the ABSORB I Trial, 12 months after implantation restenosis rates were slightly higher in case of BVS (22.9 %) compared to BMS stents (19.3 %). The mean percent acute recoil was also higher for BVS stent (6.85 ± 6.96 % vs. 4.27 ± 7.08 %) [7][8][9][10]. On the basis of these results it was concluded that BVS stents were characterized by weaker scaffolding properties than the Xience V metallic implants.…”
Section: Introductionmentioning
confidence: 99%