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A Point-of-Care Assay Could Identify High Platelet Reactivity After Clopidogrel Therapy and Impact of Triple Anti-Platelet Therapy on Platelet Reactivity in Type 2 Diabetic Patients
인제대학교 부산백병원¹ , 영남대학교 병원² , 계명대학교 동산병원³
김동기¹, 양태현¹ , 김두일¹ ,김동수¹ ,이상희² ,홍그루² ,박종선² , 김영조² , 박형섭³ ,조윤경³ ,허승호³ ,김권배³
Background: High platelet reactivity and impaired response to clopidogrel are common in type 2 diabetic patients. P2Y12 reaction unit (PRU) ≥240 after clopidogrel therapy, measured by a point-of-care assay, is associated with higher risk of adverse event after coronary stent implantation. Methods: We used a point-of-care assay (VerifyNow system) to evaluate the impact of diabetes mellitus on residual platelet reactivity in 544 patients undergoing dual or triple anti-platelet therapy who underwent DES implantation. All patients received a single 300 to 600 mg clopidogrel loading dose followed by 75 mg of clopidogrel daily and 100 mg of aspirin daily. Cilostazol daily dose of 200 mg was added in some patients by the discretion of the operators. Results: Platelet reactivity assessed by a point-of-care assay was higher in type 2 diabetic patients. Diabetic patients, compared with non-diabetic patients, manifested: 1) higher PRU value (Figure); 2) higher incidence of high platelet reactivity (HPR) which was defined as PRU ≥240 after clopidogrel therapy. We also found that higher PRU value and higher incidence of HPR noted in diabetic patients were consistent in patients undergoing triple anti-platelet therapy as well as dual anti-platelet therapy, however, higher PRU value and higher incidence of HPR in diabetic patients decreased with triple anti-platelet therapy. Conclusion: Type 2 diabetes mellitus is associated with high platelet reactivity and impaired response to clopidogrel, as assessed by a point-of-care assay. Addition of cilostazol to double anti-platelet therapy decrease PRU value and the incidence HPR in type 2 diabetic patients.
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