The STENT Thrombosis Study

Slides:



Advertisements
Similar presentations
SPIRIT IV A Prospective, Randomized Trial Comparing an Everolimus-Eluting Stent and a Paclitaxel-Eluting Stent in Patients with Coronary Artery Disease.
Advertisements

ARCTIC investigators COI D ISCLOSURE FOR D R. M ONTALESCOT : Research Grants to the Institution or Consulting/Lecture Fees from Abbott Vascular, Astra-Zeneca,
SCAAR: Lower late and very late stent thrombosis rates with new generation drug eluting stents compared to bare metal stents Christoph Varenhorst M.D Ph.D;
Www. Clinical trial results.org  Major Endpoints: Death, MI, stent thrombosis, TLR, TVR, MACE, and CKMB >3x nl  Major Endpoints: Death, MI, stent thrombosis,
Stenting and Angioplasty with Protection in Patients at High-Risk for Endarterectomy Presented by Jay Yadav, MD on behalf of the SAPPHIRE Investigators.
Basel Stent Cost-effectiveness Trial-Late Thrombotic Events (BASKET LATE) Trial Basel Stent Cost-effectiveness Trial-Late Thrombotic Events (BASKET LATE)
DR ALEX CHASE REGIONAL HEART CENTRE MORRISTON SWANSEA SLIDE MATERIAL:PERSONAL COMMUNICATION WITH AUTHORS ABBOTT, BOSTON SCIENTIFIC, CORDIS, MEDTRONIC TCT.
HORIZONS AMI Trial H armonizing O utcomes with R evascular IZ ati ON and S tents In A cute M ycoardial I nfarction H armonizing O utcomes with R evascular.
The REALITY Study Results. REALITY Study Design The REALITY Study : Prospective randomized clinical trial to evaluate the safety and efficacy of CYPHER®
Samsung Medical Center Sungkyunkwan University School of Medicine Hyeon-Cheol Gwon, Joo Yong Hahn, Young Bin Song, Kyung Woo Park, Yang Soo Jang, Hyo-Soo.
1 of Presented by Gregg W. Stone, MD, ACC PROMUS Stent is a private-labeled Xience V Everolimus Eluting Coronary Stent System manufactured.
TAXUS Landmark Analysis Impact of Long-Term Clopidogrel Usage on Death, Myocardial Infarction and Stent Thrombosis Gregg W. Stone, MD Stephen G. Ellis,
Endeavor Safety: Pooled Analysis of Early and Late Safety of a Zotarolimus-Eluting Stent Laura Mauri, MD, MSc Brigham and Women’s Hospital Harvard Clinical.
Paclitaxel Eluting Stent Versus Conventional Stent in ST-segment Elevation Myocardial Infarction (PASSION) Trial Presented at The American College of Cardiology.
When Should We Use a New DES ? Dr R H Stables Cardiothoracic Centre Liverpool UK.
Trial to Assess the Use of the Cypher Stent in Acute Myocardial Infarction Treated with Balloon Angioplasty (TYPHOON) Trial Presented at The American College.
For OMA distribution only. Trademarks may be registered and are the property of their respective owners. © 2012 Medtronic, Inc. All rights reserved DOC_1A.
Martin B. Leon, MD Key Messages Tryton Pivotal: Randomized Trial and
Jose M. de la Torre Hernández … in behalf of the 3D investigators
Clinical Trials and Outcomes with DES in CTO Revascularization
Stent Thrombosis and Optimal Duration of DAPT
XIENCE V vs TAXUS: Game Over! The Studies are Definitive
Are we ready to perform TAVI in Intermediate Risk Patients?
Randomisation before planned PCI with DES (n=2500)
For the HORIZONS-AMI Investigators
David J. Cohen, M.D., M.Sc. Director of Cardiovascular Research
Updates From SURTAVI in Intermediate Risk Patients
Harmonized Assessment by Randomized Multicenter Study of OrbusNEich’s COMBO StEnt Japan-USA HARMONEE: Primary Report of A Randomized Trial of a Bioabsorbable.
ABSORB Japan: 3-year Clinical and Angiographic Results of a Randomized trial Evaluating the Absorb Bioresorbable Vascular Scaffold vs. Metallic Drug-eluting.
The Tryton Bifurcation Trial:
Surrogate Endpoints Laura Mauri, MD, MSc Brigham and Women’s Hospital
Eric J Dippel, MD FACC Davenport, Iowa, USA February 19, 2017
LONG-DES II Trial Randomized Comparison of the Efficacy of Sirolimus-Eluting Stent Versus Paclitaxel-Eluting Stent in the Treatment of Long Native Coronary.
TAXUS IV Trial Slow-rate release polymer-based paclitaxel-eluting stent compared with bare stent in patients with single de novo coronary lesions Presented.
DES Should be Used as the Default Stent in ACS!
ARCTIC-INTERRUPTION 2-year- Versus 1year Duration of Dual-Antiplatelet Therapy After DES implantation The randomized ARCTIC-Interruption Study JP Collet.
Instent Restenosis and Occlusion: Time for Surgical Revision?
MACE Trial Rationale, Study Design, and Current Status
Study Design AMI <12 hours, any age, cardiogenic shock excluded
on behalf of the ABSORB II Investigators
What Has Been Tried and What Is True?
BBK II Trial design: Patients undergoing a two-stent approach for a de novo bifurcation lesion were randomized in a 1:1 fashion to either culotte stenting.
Antiplatelet Therapy and Secondary Prevention
Primary endpoint at 1 year
The American College of Cardiology Presented by Dr. Maurits T. Dirksen
FAIR Trial design: Patients with SFA in-stent restenosis (ISR) were randomized to either a paclitaxel-coated balloon (DCB) (dose 3.5 μg/mm2) or routine.
REALITY: 8 month results
TUXEDO–India Trial design: Patients with type 2 diabetes mellitus (DM2) and coronary artery disease undergoing PCI were randomized to receive Taxus Element.
How and why this study may change my practice ?
Current update of cerebral embolic protection devices
EVERBIO II Trial design: Patients with CAD were randomized in a 1:1:1 fashion to either Absorb BVS, Biomatrix Flex stent [BES], or Promus Element EES.
ENDEAVOR IV: 5 Year Final Outcomes
For the HORIZONS-AMI Investigators
For the HORIZONS-AMI Investigators
ISAR-SAFE Trial design: Patients with DES PCI received 6 months of open-label DAPT with aspirin and clopidogrel. At 6 months, they were randomized in a.
The American College of Cardiology Presented by Dr. Raimund Erbel
ZEUS Trial design: Patients who were deemed uncertain DES candidates due to bleeding, thrombotic, or restenosis risk were randomized to receive either.
Large-Scale Registry Examining Safety and Effectiveness of Zotarolimus-Eluting and Sirolimus-Eluting Stents in Patients with Coronary Artery Disease Western.
Mortality Data From the BASKET LATE Trial and PREMIER Registry
SIRIUS: A U.S. Multicenter, Randomized, Double-Blind Study of the SIRolImUS-Eluting Stent in De Novo Native Coronary Lesions Presented at TCT 2002.
European Society of Cardiology Scientific Congress, September 2006
SORT-OUT III: A Prospective Randomized Comparison of Zotarolimus-Eluting and Sirolimus-Eluting Stents in Patients with Coronary Artery Disease Michael.
For the ACTION study group
ENDEAVOR III Multicenter Randomized Trial Clinical/MACE Angio/IVUS
ISAR-LEFT MAIN: A Randomized Clinical Trial on Drug-Eluting Stents for Unprotected Left Main Lesions J. Mehilli, MD Deutsches Herzzentrum Technische.
Comparison of Everolimus-Eluting and Paclitaxel-Eluting Stents: First Report of the Five-Year Clinical Outcomes from.
OPTIDUAL Trial design: Patients who received a drug-eluting stent and were event-free at 12 months were randomized to an additional 36 months of DAPT with.
The American College of Cardiology Presented by Dr. A. Abazid
NOBLE Trial design: Patients with unprotected left main disease were randomized to either PCI with a drug-eluting stent (DES) (88% biolimus) or CABG. They.
TYPHOON Trial Trial to Assess the Use of the Cypher Stent in Acute Myocardial Infarction Treated with Balloon Angioplasty (TYPHOON) Trial Presented at.
Presentation transcript:

The STENT Thrombosis Study 10,000 consecutive patients receiving DES at up to 12 sites Aspirin and clopidogrel responsiveness evaluated Using the Accumetrics VerifyNow system Clinical Follow-Up for 2-5 years Angiographic core lab assessment of all stent thromboses and 1:3 matching controls Supported by grants from Boston Scientific (lead contributor), Accumetrics, Abbott Vascular, Cordis, and Medtronic Presented at TCT 2006

The E-Select Registry and INSIGHT Randomized Trial 30,000 patient global registry + U.S. randomized trial of standard vs. long duration clopidogrel Sponsor: Cordis Corp. The PROTECT Randomized Trial 8,000 patient global randomized trial of the Endeavor vs. the Cypher stent. Primary Endpoint = stent thrombosis Sponsor: Medtronic Corp. Presented at TCT 2006