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Will the New Antiplatelet Agents in the Pipeline Replace Clopidogrel?
Is There a Role for Long Term Use of Clopidogrel for Primary and Secondary Prevention After CHARISMA?
Lessons from the ISAR REACT Studies: How Should We Anticoagulate Our Patients for PCI
New Insights from ACUITY: When and How Should Bivalirudin be Used in ACS and NSTEMI?
Evolving Utility of Aspirin and Thienopyridines: New Insights Into Anti-Platelet Resistance






 

 

A Polypill Approach Improves Compliance

Adherence to optimal medical therapy remains poor following a MI. The FOCUS study has identified younger age, depression, complex medication regimen, poor insurance coverage and low social support as the major factors contributing to poor compliance. FOCUS also demonstrated that compliance can be significantly improved using a polypill strategy.

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Mortality Following Primary PCI

The association between time and cause of death in patients undergoing primary PCI for STEMI is poorly understood. A study of 13,447 patient-years identified cardiogenic shock and hypoxic brain injury as the main causes of death within the first 30 days. The vast majority of deaths beyond 30 days were noncardiac.

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Immature Platelets May Predict Adverse Events

Immature platelets (IPC) are less responsive to antiplatelet therapy and are easily measured as part of the complete blood count. A prospective cohort study of 89 patients with CAD has indicated that an IPC level ≥7,632 platelets/µl may predict MACE.

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Are Beta Blockers Going Out of Fashion

Beta-blockers are commonly used in patients with heart failure as well as those with AF. A meta-analysis of 10 randomized studies comparing beta-blockers versus placebo in heart failure with sinus rhythm or AF has indicated that all cause mortality was reduced in those with sinus rhythm but not AF.

For more, click here

 

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CRT2013
Untitled Document
 
Minimizing Femoral Artery Access Complications during PCI
- Michael S. Lee, MD
PROTECT Trial: 5 Year Outcomes
- Edoardo Camenzind, MD
Reduction in office blood pressure after renal denervation in a large real world patient population with uncontrolled hypertension: interim 12-month results from the Global SYMPLICITY Registry
- Felix Mahfoud, MD
SYMPLICITY HTN-3 Trial: 12-month outcomes following un-blinding of subjects at 6 months
- George L. Bakris, MD



Live Case Demonstration from Kusatsu Heart Center
Osamu Hatoh, MD
Treating CTO via Radial?
Richard R. Heuser, MD
Patient Selection for CTO Recanalization: What Are the Appropriate Criteria?
Tarek Helmy, MD
Treating CTOs: Is There Enough Evidence-Based Data or do We Need Further Randomized Clinical Trials?
Gerald S. Werner, MD, PhD
Indication for CTO PCI: Clinical Rationale and Appropriateness
J. Aaron Grantham, MD

Jeremiah Brown, MDBicuspid Aortic Valve and TAVI
- Eberhard Grube, MD


 Click here to visit the WEBEX archives


A Polypill Strategy to Improve Adherence: Results From the FOCUS Project.
J Castellano, et al.
JACC 2014; 64:2071-2082
Second-Generation Drug-Eluting Stent Implantation Followed by 6- Versus 12-Month Dual Antiplatelet Therapy: The SECURITY Randomized Clinical Trial.
A Colombo, et al.
JACC 2014; 64:2086-2097
Short- and Long-Term Cause of Death in Patients Treated With Primary PCI for STEMI.
F Pedersen, et al.
JACC 2014; 64:2101-2108
Age-Related Normative Changes in Phasic Orthostatic Blood Pressure in a Large Population Study: Findings From the Irish Longitudinal Study on Ageing (TILDA).
C Finucane, et al.
Circ 2014; 130:1780-1789
Clinical Trials in Peripheral Vascular Disease: Pipeline and Trial Designs: An Evaluation of the ClinicalTrials.gov Database.
S Subherwal, et al.
Circ 2014; 130:1812-1819
The Recognition and Significance of Pathological T-Wave Inversions in Athletes.
F Schnell, et al.
Circ 2014 Online.
Molecular Findings Among Patients Referred for Clinical Whole-Exome Sequencing.
Y Yang, et al.
JAMA 2014; 312:1870-1879
Efficacy of Beta Blockers in Patients With Heart Failure Plus Atrial Fibrillation: An Individual-Patient Data Meta-Analysis.
D Kotecha, et al.
The Lancet 2014 Online
Relation Between Coronary Arterial Dominance and Left Ventricular Ejection Fraction After ST-Segment Elevation Acute Myocardial Infarction in Patients Having Percutaneous Coronary Intervention.
C Veltman, et al.
AJC 2014; 114:1646-1650
Relation of Obstructive Sleep Apnea to Coronary Artery Calcium in Non-Obese Versus Obese Men and Women Aged 45–75 Years.
F Luyster, et al.
AJC 2014; 114:1690-1694
Antiplatelet and Anticoagulation Agents in Acute Coronary Syndromes: What Is the Current Status and What Does the Future Hold?
K Huber, et al.
AHJ 2014; 168:611-621
How Can We Optimize the Processes of Care for Acute Coronary Syndromes to Improve Outcomes?
L Wallentin, et al.
AHJ 2014; 168:622-631



Poll Archives
Primary Outcomes of the EVOLVE II Trial
Dean J. Kereiakes, MD
AVOID Study
Dion Stub, MD
BASKET-PROVE II Trial
C.Kaiser, MD, et al.
Final Results of the Regional Systems of Care Demonstration Project: Mission: Lifeline STEMI Accelerator Study
Matthew W. Sherwood, MD, et al.
Dual Antiplatelet Therapy Beyond One Year After Drug-eluting Coronary Stent Procedures
Laura Mauri, MD, et al.
Randomized Trial of Atenolol Versus Losartan in Children and Young Adults with Marfan Syndrome
Ronald V. Lacro, MD, et al.
ITALIC Trial
Martine Gilard, MD, PhD, et al.
INHERIT Trial
Anna Axelsson, MD, et al.
Impact of a Multidisciplinary Management Program on Recurrent Hospitalization and Mortality in Older Individuals With Chronic Atrial Fibrillation: A Multi-Center Randomized Trial
Simon Stewart, MD, et al.
Low-dose aspirin for primary prevention of cardiovascular events in elderly Japanese patients with atherosclerotic risk factors: a randomized clinical trial
Yasuo Ikeda, MD, et al.
Update on PARADIGM-HF
John J.V. McMurray, MD, et al.
FACTOR-64 Randomized Clinical Trial
Joseph B. Muhlestein, MD, et al.
IMProved Reduction of Outcomes: Vytorin Efficacy International Trial
Eugene Braunwald, MD, et al.
Increased Risk of Ischemic Events Upon Discontinuation of Prasugrel After 12 or 30 Months of Therapy Following Placement of the TAXUS Liberte Paclitaxel- Eluting Coronary Stent
Kirk N. Garratt, MD, et al.
Six versus Twelve Months of Clopidogrel Therapy After Drug-Eluting Stenting - the Randomized, Double-Blind, Placebo-Controlled ISAR-SAFE Trial
Stefanie Schulz-Schupke, MD, et al.

Complex Patients Today and Tomorrow: Medtronic DES solutions from Resolute Integrity to bioresorbable stents
Prof. Sigmund Silber, MD
First Report on the Pivotal DESolve Nx trial: 6-month Clinical and Multimodality Imaging Results
Alexandre Abizaid, MD, PhD
One-Year Outcomes in 1010 Unselected Patients Treated with the PROMUS Element Everolimus-Eluting Stent: The Multicenter PROMUS Element European Post-Approval Surveillance Study
Raul Moreno, MD, et al.
Two-year clinical outcomes in the EVOLVE FHU trial
Ian Meredith, MD, PhD
BIOFLOW-II Trial
Stephan Windecker, MD, et al.

Outcomes in More Than 7000 Patients With Diabetes After Implantation of the Resolute Zotarolimus-eluting Stent
Rosli Mohd Ali, MD
Safety update and long-term clinical outcomes from all studies in the RESOLUTE Global Clinical Program
Carlo Di Mario, MD
Final Five-year Outcomes from the Randomized Comparison of Zotarolimus-eluting Stents With Everolimus-eluting Stents in the RESOLUTE All Comers Trial
Stephan Windecker, MD
Angina Status & TLF Creep: Bioabsorbable Stents (BAS) & Drug-Eluting Stents (DES)
Medtronic, Inc.
Clinical outcomes associated with dual antiplatelet therapy interruption following implantation of the ResoluteTM zotarolimus-eluting stent
Stephan Windecker, MD
Four-year Outcomes from the Randomized Comparison of a Zotarolimus-eluting and an Everolimus-eluting Stent in the RESOLUTE All Comers Trial
Patrick W Serruys MD, PhD
Resolute in Bifurcation Lesions: Data from the RESOLUTE Clinical Program
Prof. Ran Kornowski, MD



11/20/2014
New Data From EVOLVE Clinical Program Demonstrate SYNERGY™ Bioabsorbable Polymer Stent Meets Key Performance Endpoints

11/19/2014
Toshiba Enhances Radiation Dose Tracking System on Infinix

11/19/2014
Medtronic Bifurcated Endurant IIs AAA Stent Graft Launched in Europe and United States

11/19/2014
SVS and SIR to Initiate Large-Scale PRESERVE Study of IVC Filters in 2015

11/19/2014
Zoll to Acquire Philips’ InnerCool Business

11/19/2014
Enrollment Underway in BEST-CLI Randomized Trial

11/19/2014
Aptus Heli-FX EndoAnchor System to Be Distributed by Maquet in United Kingdom

11/19/2014
Endologix Completes Enrollment in the Nellix EVAS FORWARD-IDE Clinical Trial

11/11/2014
CSI’s COAST Study Begins Enrollment in Japan

11/11/2014
Abbott Enters Electrophysiology Market With Acquisition of Topera

11/11/2014
Hansen Medical Launches the Sensei X2 Robotic System

11/11/2014
Medtronic Launches Resolute Onyx DES After CE Mark Approval

11/11/2014
Venous Indication Approved for Cardinal Health’s MynxGrip Vascular Closure Device

10/15/2014
Occlutech Paravalvular Leak Closure Device Approved in Europe

10/15/2014
IDE Approved for Trial of Neovasc’s Tiara Transcatheter Mitral Valve

10/15/2014
FDA Approves Bracco Diagnostics’ Lumason Ultrasound Contrast Agent

10/15/2014
Merit Medical Unveils ThinkRadial Website and Educational Initiative

10/14/2014
InspireMD Resumes MGuard Prime Sales and Prioritizes DES and Carotid - New Product Programs

10/10/2014
C.R. Bard announces FDA approval of Lutonix 035 drug coated balloon catheter

10/9/2014
Covidien Begins Two Neurovascular Clinical Trials

10/9/2014
Endologix Completes Enrollment in EVAS FORWARD—GLOBAL Registry of Nellix System

10/9/2014
LEOPARD to Compare Endologix AFX System to Other Commercially Available EVAR Devices

10/9/2014
CFI Medical’s Zero-Gravity Suspended Radiation Protection System Approved in Europe
ACS & AMI
Angiomyogenesis & Cell Therapy
Carotid Interventions

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