Clopidogrel administration is commonly prescribed in patients undergoing percutaneous coronary intervention, in patients with previous stroke and in patients under chronic hemodialysis via fistulae. Patients with chronic renal failure present lower clopidogrel response compared to those with normal renal function. Ticagrelor is a new oral direct-acting antagonist, which provides greater platelet inhibition in both clopidogrel responders and non-responders. It has also been shown that in patients with chronic kidney disease (creatinine clearance \<60 mL/min)ticagrelor achieved an absolute risk reduction of cardiovascular death, myocardial infarction, and stroke greater than that of patients with normal renal function. Clopidogrel resistant patients as assessed by VerifyNow P2Y12(Accumetrics)will be administered after informed consent ticagrelor 90 mg twice daily for 15 days. Platelet reactivity will be determined at the end of the treatment period. Bleeding events, major adverse cardiac events and any side effects until Day 15 will be reported in a descriptive manner.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
SINGLE
Enrollment
20
Ticagrelor 90mg twice a day for 15 days
Agios Andreas General Hospital, Nephrology Department
Pátrai, Achaia, Greece
Cardiology Department Patras University Hospital
Rio, Achaia, Greece
Platelet reactivity assessed by VerifyNow P2Y12 assay
Time frame: Day 15
Bleeding events according to TIMI criteria
Major, minor or minimal bleeding events according to TIMI criteria
Time frame: Day 15
Major adverse cardiovascular events
Death, non-fatal myocardial infarction and stroke
Time frame: Day 15
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