Learning Objectives
Variable Response to Clopidogrel
Platelet Reactivity and Outcomes
Clopidogrel Metabolism
CYP450 Genetic Variants and PK/PD
CYP2C19 and Clinical Outcomes
Clopidogrel Boxed Warning
CYP2C19 and Treatment With Clopidogrel
CURRENT-OASIS 7: Study Design, Flow, and Compliance
CURRENT-OASIS 7: Clopidogrel Double (600 mg 150 mg/d x 7d 75 mg/d) vs Standard Dose (300 mg 75 mg/d)
CURRENT-OASIS 7: Clopidogrel Double- vs Standard-Dose Bleeding PCI Population
Tailoring Clopidogrel Dosing With Platelet Function Monitoring
GRAVITAS Study Design
GRAVITAS Primary End Point: CV Death, MI, Stent Thrombosis
GRAVITAS Pharmacodynamics: Effect of SD vs HD Clopidogrel
PRINCIPLE TIMI 44 PRIMARY EP: Acute Phase
PRINCIPLE TIMI 44 PRIMARY EP: Maintenance Phase
TRITON-TIMI 38 13,608 Patients With ACS and Planned PCI Randomized to Prasugrel (60/10) vs Clopidogrel (300/75)
TRITON-TIMI 38 Bleeding Events: Safety Cohort (N = 13,457)
TRILOGY-ACS Study Design
TRILOGY-ACS: Primary Efficacy End Point to 30 Months (Age < 75 years)
Ticagrelor Pharmacodynamics
Platelet Reactivity: Ticagrelor vs Prasugrel
PLATO Primary Efficacy End Point: CV Death, MI, or Stroke
PLATO: Bleeding
TRA-CER Primary End Point: CV Death, MI, Stroke, Hospitalization for Ischemia, Urgent Revascularization
TRA-CER: Bleeding Outcomes
CHAMPION PHOENIX Study Design
CHAMPION PHOENIX: Primary Efficacy Outcomes at 48 Hours, MITT
CHAMPION PHOENIX: Non-CABG Bleeding at 48 Hours
ESC NSTE-ACS Guidelines
Periprocedural Antithrombotic Medication in Primary PCI
Antiplatelet Therapy in UA/NSTEMI
Antiplatelet Therapy to Support Primary PCI for STEMI
Case 1
Case 2
Case 3
Conclusions
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References
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