TCT-248 Absorb bioresorbable vascular scaffold in patients with or without diabetes mellitus: a sub-analysis of the Italian multicenter RAI Registry ( ClinicalTrials.gov Identifier: NCT02298413)

Patients treated with Absorb BVS because of in-stent restenosis or bypass graft disease were excluded from current analysis. At 1-year follow-up, no differences were found between groups in terms of a device-oriented composite end-point (DOCE) (4.3% vs. 6.6%; p=0.6) or its individual components (car...

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Veröffentlicht in:Journal of the American College of Cardiology 2017-10, Vol.70 (18), p.B103-B103
Hauptverfasser: Mojoli, Marco, Tarantini, Giuseppe, Masiero, Giulia, Loi, Bruno, Cortese, Bernardo, Ielasi, Alfonso, Varricchio, Attilio, Moretti, Luciano, Misuraca, Leonardo, Pasquetto, Giampaolo, Calabro', Paolo, Corrado, Donatella, Steffenino, Giuseppe
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Sprache:eng
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Zusammenfassung:Patients treated with Absorb BVS because of in-stent restenosis or bypass graft disease were excluded from current analysis. At 1-year follow-up, no differences were found between groups in terms of a device-oriented composite end-point (DOCE) (4.3% vs. 6.6%; p=0.6) or its individual components (cardiac death, target-vessel myocardial infarction and ischemia-driven TLR).
ISSN:0735-1097
1558-3597
DOI:10.1016/j.jacc.2017.09.321