Four-year clinical follow-up of the ABSORB everolimus-eluting bioresorbable vascular scaffold in patients with de novo coronary artery disease: the ABSORB trial

2012 ◽  
Vol 7 (9) ◽  
pp. 1060-1061 ◽  
Author(s):  
Dariusz Dudek ◽  
Yoshinobu Onuma ◽  
John Ormiston ◽  
Leif Thuesen ◽  
Karine Miquel-Hebert ◽  
...  
2013 ◽  
Vol 111 (7) ◽  
pp. 23B
Author(s):  
Michael Liang ◽  
Takashi Kajiya ◽  
Chi-Hang Lee ◽  
Mark Chan ◽  
Swee-Guan Teo ◽  
...  

2015 ◽  
Vol 170 (4) ◽  
pp. 641-651.e3 ◽  
Author(s):  
Dean J. Kereiakes ◽  
Stephen G. Ellis ◽  
Jeffrey J. Popma ◽  
Peter J. Fitzgerald ◽  
Habib Samady ◽  
...  

Kardiologiia ◽  
2018 ◽  
Vol 58 (12) ◽  
pp. 30-35 ◽  
Author(s):  
K. M. Vakkosov ◽  
N. A. Kochergin ◽  
K. A. Kozyrin ◽  
V. I. Ganjukov

The aim. Evaluates long­term clinical outcomes of percutaneous coronary intervention (PCI) with bioresorbable vascular scaffold (BVS) versus minimally invasive direct coronary artery bypass (MIDCAB) surgery for the treatment of left anterior descending (LAD) lesions.Methods and Results. In this single­center study were included 130 patients with stable angina and significant (≥ 70 %) LAD disease. Patients were randomly assigned in a 1:1 ratio to PCI with everolimus­eluting BVS (n=65) or MIDCAB (n=65). The primary end­point was major adverse cerebro­cardiovascular events (MACCE) and secondary was scaffold (graft) thrombosis at 1 year. The groups of patients were comparable for all baseline demographic, clinical and angiographic parameters. MACCE at 12 month occurred in 9.2 % of patients in the BVS group and in 4.6 % of patients in the MIDCAB group (p=0.3). There was no significant difference between the groups in rates of all cause death (1.5 % vs 1.5 %, p=1.0), myocardial infarction (3.1 % vs. 6.1 %, p=0.4), any revascularization (1.5 % vs. 6.1 %, p=0.1) and scaffold (graft) thrombosis (1.5 % vs. 1.5 %, p=1.00).Conclusion. At 12­month follow up, there was no significant difference in the rate of MACCE between PCI by BVS and MIDCAB in patients with isolated LAD lesions.


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