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Welcome Ask The Experts March 24-27, 2007 New Orleans, LA.

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Presentation on theme: "Welcome Ask The Experts March 24-27, 2007 New Orleans, LA."— Presentation transcript:

1 Welcome Ask The Experts March 24-27, 2007 New Orleans, LA

2 Pretreatment with Thienopyridines
C. Michael Gibson, MS, MD Associate Professor of Medicine Harvard Medical School Chief of Clinical Research Cardiology Division Beth Israel Deaconess Medical Center Boston, MA

3 Emerging Data Regarding the Potential Benefits of Early Initiation of Clopidogrel Among ACS Patients
C. Michael Gibson, M.S., M.D.

4 Inhibition of Platelet Aggregation Following Clopidogrel Administration
Hochholzer W et al. Circulation. 2005;111

5 Clopidogrel Loading Dose Timing and Risk of MACE
Log Odds of Death, MI or UTVR at 28 Days Placebo - 2 Clopidogrel P = 0.020 for treatment / timing interaction - 3 - 4 - 5 - 6 5 10 15 20 25 30 Hours Prior to PCI of Study Drug Loading Dose J Am Coll Cardiol 2006;47:939–43.

6 Cumulative Holter Monitor Ischemia
5 10 15 Bival & post PCI Clop (n=101) Pre vs post PCI clop Among bival pts From 4-24 hrs HR = 7.28 p = 0.04 Cumulative minutes of ischemia (minutes per patient) Bival & pre PCI Clop (n=112) Epti & post PCI Clop (n=220) Epti & pre PCI Clop (n=217) 6 12 18 24 Hours after end of PCI CM Gibson ACC 2007

7 30 Day Primary Endpoint Adverse Events
Influence of Thienopyridine Exposure – PCI pts 30 Day Primary Endpoint Adverse Events RR [95%CI] 0.81 ( ) RR [95%CI] 0.96 ( ) RR [95%CI] 0.50 ( ) RR [95%CI] 1.07 ( ) RR [95%CI] 1.37 ( ) RR [95%CI] 0.61 ( ) Thienopyridine Exposed Not Thienopyridine Exposed

8 CURE: Major Bleeding in CABG Patients
Major or life-threatening bleeding w/in 7 days of CABG P=0.07 P=0.53 Clopidogrel stopped <5 days prior to CABG >5 days K.Fox et al, ESC 2002

9 ACUITY: Primary Outcomes in CABG Patients
Patients with and without a thienopyridine administered in-hospital prior to CABG P=0.066 P=0.013 P=0.362 *Heparin=unfractionated or enoxaparin

10 30 Day Outcomes – CABG Patients by Thienopyridine Status
Patients with and without a thienopyridine administered in-hospital prior to CABG Thieno (+) n=718 Thieno (-) n=820 P-value Resource Utilization Total LOS, median 12.1 9.0 <0.001 Pre-CABG LOS, median 4.6 2.5 Post-CABG LOS, median 6.9 5.8 Bleeding Endpoints Post CABG Major Bleeding 50.0% 50.5% 0.85 Post CABG Blood transfusions 38.2% 38.0% 0.96 24hr Chest Tube Output (median) 600.0 ml 550.0 ml 0.22

11 Question & Answer

12 Thank You! Please make sure to hand in your evaluation and pick up a ClinicalTrialResults.org flash drive


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