2016
DOI: 10.1016/j.jcin.2015.09.008
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Polymer-Free Biolimus A9-Coated Stents in the Treatment of De Novo Coronary Lesions

Abstract: The BFD, but not the BFD-LD, demonstrated noninferiority versus PES in terms of in-stent LLL, a surrogate of neointimal hyperplasia, at 12-month follow-up. At 5 years, clinical event rates were similar, without occurrence of stent thrombosis in all groups. (BioFreedom FIM Clinical Trial; NCT01172119).

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Cited by 71 publications
(29 citation statements)
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“…Higher rates of cardiac death and stent thrombosis often occur early in patients presenting with ST‐elevation myocardial infarction (STEMI) and late complications are more often seen in non‐ST‐elevation myocardial infarction (NSTEMI) . To improve clinical outcomes in patients presenting with ACS, novel stent technologies have been developed to target these complications after PCI, such as absorbable polymer stents (Mistent, Micell Technologies) , polymer‐free stents (biolimus stent, BioFreedom, Biosensor) , and the dual‐therapy stent (COMBO, OrbusNeich Medical) .…”
Section: Introductionmentioning
confidence: 99%
“…Higher rates of cardiac death and stent thrombosis often occur early in patients presenting with ST‐elevation myocardial infarction (STEMI) and late complications are more often seen in non‐ST‐elevation myocardial infarction (NSTEMI) . To improve clinical outcomes in patients presenting with ACS, novel stent technologies have been developed to target these complications after PCI, such as absorbable polymer stents (Mistent, Micell Technologies) , polymer‐free stents (biolimus stent, BioFreedom, Biosensor) , and the dual‐therapy stent (COMBO, OrbusNeich Medical) .…”
Section: Introductionmentioning
confidence: 99%
“…Notably, at 4 months, there was a significantly lower rate of lumen loss with the DCS than PES. The results demonstrated no inferiority to PES in the rate of lumen loss, a subclass of neointimal hyperplasia (Costa et al 2016). The use of nano-coatings on stents is being trialled currently in the United States: The COBRA PzF Stenting to Reduce the Duration of Triple Therapy in Patients Treated With Oral Anticoagulation Undergoing Percutaneous Coronary Intervention trial is ongoing and aims to investigate if the COBRA PzF stent with a polyzene-F nano-coating can successfully reduce bleeding compared to DES, through reducing the duration of oral anticoagulation therapy to 14 days, rather than the current 6 months, in patients undergoing PCI (US National Library of Medicine 2018).…”
Section: Nano-coated Stentsmentioning
confidence: 79%
“…After duplicate references were removed, we retrieved 1026 potentially relevant articles. In the present meta-analysis, we included 13 RCTs [ [16] , [17] , [18] , [19] , [20] , [21] , [22] , [23] , [24] , [25] , [26] , [27] , [28] ] consisting of 8021 patients with coronary artery disease who were randomized to receive PCI with either PF-DES (n = 4545) or DP-DES (n = 3476). Table 1 outlines the study characteristics of the included trials.…”
Section: Resultsmentioning
confidence: 99%