Table 1.
Comparison of P2Y12 inhibitors.
Clopidogrel | Prasugrel | Ticagrelor | Cangrelor | |
---|---|---|---|---|
Chemical class | Thienopyridine | Thienopyridine | Cyclopentyl-triazolopyrimidine | Adenosine triphosphate analogue |
Route | Oral | Oral | Oral | Intravenous |
Prodrug | Yes (pro-drug, CYP dependent, 2 steps) | yes (pro-drug, CYP dependent, 1 step) | No | No |
Bioavailability | 15% | 79% | 36% | 100% |
Standard dosage | 600 mg LD, then 75 mg once a day | 60 mg LD, then 10 mg once a day | 180 mg LD, then 90 mg twice a day | 30 μg/kg bolus, then 4 μg/kg/min |
Reversibility of binding | Irreversible | Irreversible | Reversible | Reversible |
Onset of antiplatelet effect | 2–6 h | 0.5–4 h | 0.5–2 h | 2 min |
Level of platelet inhibition at steady state | 40–60% | 65–80% | 65–80% | 90–98% |
Offset of antiplatelet effect | 3–10 days | 5–10 days | 3–4 days | 30–60 min |
Recommended stop of treatment before surgery | 5 days | 7 days | 3–5 days | 1 h |
Excretion | 50% renal, 46% biliary | 68% renal, 27% feces | Biliary | Not dependent on hepatic or renal clearance mechanisms |
Kidney failure | No dose adjustment | No dose adjustment | No dose adjustment | No dose adjustment |
Dialysis or CrCl < 15 mL/min | Limited data | Limited data | Limited data | Limited data |
CrCl — creatinine clearance; LD — loading dose