Lower risk of stent thrombosis and restenosis with unrestricted use of (Abbott Laboratories) and Promus, Promus Element (Boston Scientific Corporation).
Dr. Antonio Colombos perspective on the Promus PREMIER Stent. 3:47. Dr. Antonio Colombo is Director of Interventional Cardiology at San Raffaele Hospital
Dual anti-platelet treatment is recommended for patients receiving coronary stents. everolimus-eluting coronary stent system [PROMUS Element] for the treatment of up to two de novo coronary artery lesions) trial. J. Am. Coll. Cardiol.
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75x20mm promus element plus stent was placed overlapping the 2 previous stents, inflated to 14-18 atm for 7-15 seconds. Multiple inflations, from 10-16atm for 17-24 seconds, were made with a 3. 5x15mm quantum maverick balloon. An unspecified promus stent was implanted in the left anterior descending artery and a 3. 0 x 15 mm promus stent was implanted in the right coronary artery.
The PROMUS Element Plus Everolimus-Eluting Platinum Chromium Coronary Stent System is indicated for improving luminal diameter in patients with symptomatic heart disease or documented silent ischemia due to de novo lesions in native coronary arteries ≥2.25 mm to ≤4.00 mm in diameter in lesions ≤34 mm in length.
everolimus-eluting coronary stent system [PROMUS Element] for the treatment of up to two de novo coronary artery lesions) trial. J. Am. Coll. Cardiol.
The C-Code used for the Promus PREMIER Everolimus-Eluting Platinum Chromium Coronary Stent System is C1874 Stent, coated/covered with delivery system. C-Codes are used for hospital outpatient device reporting for Medicare and some private payers.
4,0 χ 24 mm. Med stentballongen dilaterades ytterligare i området mellan de två sistnämnda stentarna. In- greppet skedde Stent occlusions/stent thrombosis. From other part of BS Promus Element. Medtronic HEART. SCAAR http://www.ucr.uu.se/scaar/index.php/stent-reports anlades en Promus Premier-stent.
The PROMUS Element stent has been shown to be MR Conditional (poses no known hazards under specified conditions) through non-clinical testing of single and overlapped configurations up to 74 mm. The conditions are as follows: Field strengths of 1.5 and 3 Tesla Static magnetic field gradient <900 gauss/cm (extrapolated)
Promus PREMIER Stent System Dr. Antonio Colombo gives an overview of the Promus PREMIER Stent’s flexibility, conformability, visibility, and Everolimus drug/PVDF-HFP polymer combination.
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Advanced Stent Technology to Launch Immediately in the United States. NATICK, Mass. --Continuing to advance leading drug-eluting stent (DES) technology, Boston Scientific Corporation has received U.S. Food and Drug Administration (FDA) approval for the Promus PREMIER™ Everolimus-Eluting Platinum Chromium Coronary Stent System, the company's next-generation durable polymer drug-eluting stent
The conditions are as follows: Field strengths of 1.5 and 3 Tesla Static magnetic field gradient <900 gauss/cm (extrapolated) Promus PREMIER Stent System Dr. Antonio Colombo gives an overview of the Promus PREMIER Stent’s flexibility, conformability, visibility, and Everolimus drug/PVDF-HFP polymer combination. Promus PtCr EES ranked #2 for the lowest relative risk of Def/Prob Stent Thrombosis SCAAR Registry 12 Promus PtCr EES reported numerically lowest Permanent Polymer ST rates in real-world SCAAR Registry More than 8 Million Promus PtCr DES implanted worldwide15 expandable stent, pre-mounted on a Monorail (MR) or Over-The-Wire (OTW) delivery catheter. The stent is made from a platinum chromium alloy (PtCr). The drug-polymer coating consists of a polymer, PVDF-HFP, and the active pharmaceutical ingredient, everolimus.
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Aug 14, 2017 - The Promus PREMIER drug-eluting stent from Boston Scientific features customized stent architecture for strength, pushability, and flexibility.
Acute stent occlusion or non-occlusive thrombus in a previously implanted stent (with acute clinical presentation) are now presented as Stent Thrombus for stents implanted since 2007. Presentation of reported restenosis are also added since 2007 for stents used i Sweden at least 1000 times. Methods: Patients with DM (1,855 of 5,054 patients, 36.7%) from 2 prospective registries (the EXCELLENT [Efficacy of Xience/Promus Versus Cypher in Reducing Late Loss After Stenting] registry and RESOLUTE-Korea [Registry to Evaluate the Efficacy of Zotarolimus-Eluting Stent]) who were treated with EES (n = 1,149) or ZES (n = 706) were compared.