Please use this identifier to cite or link to this item: https://doi.org/10.1016/j.ijcard.2007.07.074
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dc.titleA novel drug-eluting stent using bioabsorbable polymer technology: Two-year follow-up of the CURAMI registry
dc.contributor.authorTin Hay, E.
dc.contributor.authorHou, X.-M.
dc.contributor.authorLim, J.
dc.contributor.authorLow, A.
dc.contributor.authorTeo, S.-G.
dc.contributor.authorTan, H.-C.
dc.contributor.authorLee, C.-H.
dc.date.accessioned2014-11-28T04:58:33Z
dc.date.available2014-11-28T04:58:33Z
dc.date.issued2009-01-09
dc.identifier.citationTin Hay, E., Hou, X.-M., Lim, J., Low, A., Teo, S.-G., Tan, H.-C., Lee, C.-H. (2009-01-09). A novel drug-eluting stent using bioabsorbable polymer technology: Two-year follow-up of the CURAMI registry. International Journal of Cardiology 131 (2) : 272-274. ScholarBank@NUS Repository. https://doi.org/10.1016/j.ijcard.2007.07.074
dc.identifier.issn01675273
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/112211
dc.description.abstractBackground: There are safety concerns on drug-eluting stents (DESs) using durable polymer. The long-term outcome of next generation DESs using bioabsorbable polymer technology remains unknown. Methods: From March to June, 2005, a novel sirolimus-eluting (170 μg/cm2), bioabsorbable polymer (PLA and PLGA, eroded over 45 days) coated stent was implanted for treatment of acute myocardial infarction (AMI) in 49 patients (male 86%, age 55 + 10 years, diabetes 31%). All culprits were de novo lesions in the native coronary artery. On discharge, aspirin and clopidogrel for 3 months followed by life-long aspirin were prescribed. Angiographic follow-up was performed at 8 months. Clinical follow-up was performed at 4, 9 and 24 months. Results: Angiographic success rate was 100%. In-hospital adverse events consisted of 1 death (2%). All except one patient (due to aspirin allergy) were compliant to the 3 months dual antiplatelet therapy, and there was no adverse event during this period. One patient developed re-infarction in another coronary territory at 6 months. Twenty-seven patients (56%) underwent 8-month angiographic follow-up (Table 3). At 24 months, 6 patients had 7 major adverse cardiac events (12.2%, 1 death, 2 re-infarctions and 4 target lesion revascularizations). There were no incidences of subacute or late stent thrombosis. Conclusions: The Cura stent, using bioabsorbable polymer technology, appears to be safe at 2 years follow-up. Although the angiographic follow-up parameters were unfavorable, this report paves the way for further studies on DES using bioabsorbable polymer technology. © 2007 Elsevier Ireland Ltd. All rights reserved.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1016/j.ijcard.2007.07.074
dc.sourceScopus
dc.subjectBioabsorbable
dc.subjectCoronary
dc.subjectDrug-eluting stent
dc.subjectPolymer
dc.subjectStent thrombosis
dc.typeArticle
dc.contributor.departmentCENTRE FOR WIRELESS COMMUNICATIONS
dc.description.doi10.1016/j.ijcard.2007.07.074
dc.description.sourcetitleInternational Journal of Cardiology
dc.description.volume131
dc.description.issue2
dc.description.page272-274
dc.description.codenIJCDD
dc.identifier.isiut000261834300022
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