Chewed Versus Swallowed Ticagrelor in P2Y12 Inhibitor- Naive Patients Undergoing Percutaneous Coronary Intervention

被引:0
|
作者
Wilson, Thomas F. [1 ,2 ]
Ashraf, Muddasir [1 ]
Fuad, M. [1 ,2 ]
Nfor, Jan Tonga [1 ,2 ]
Kostopoulos, Louie [1 ,2 ]
Solis, Joaquin [1 ,2 ]
Khitha, Jayant [1 ,2 ]
Khraisat, Ahmad [1 ,2 ]
DeFranco, Anthony C. [1 ,2 ]
Bajwa, Tanvir [1 ,2 ]
Allaqaband, Suhail Q. [1 ,2 ,3 ]
机构
[1] Aurora Sinai Aurora St Lukes Med Ctr, Aurora Cardiovasc & Thorac Serv, Aurora Hlth Care, Milwaukee, WI USA
[2] Univ Wisconsin, Sch Med & Publ Hlth, Dept Cardiovasc Med, Madison, WI USA
[3] Aurora St Lukes Med Ctr, 2801 W Kinnickinn River Pkwy 880, Milwaukee, WI 53215 USA
关键词
acute coronary syndrome; antiplatelet medication; ticagrelor; loading dose; non-ST-segment; stable ischemic heart disease; ST-SEGMENT-ELEVATION; DUAL ANTIPLATELET THERAPY; ASSOCIATION TASK-FORCE; PLATELET INHIBITION; MYOCARDIAL-INFARCTION; P2Y(12) INHIBITORS; AMERICAN-COLLEGE; DOUBLE-BLIND; CLOPIDOGREL; PRETREATMENT;
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暂无
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Purpose Dual antiplatelet therapy is standard for patients undergoing percutaneous coronary intervention (PCI) with stents. Traditionally, patients swallow the loading dose of a P2Y12 inhibitor before or during PCI. Time to achieve adequate platelet inhibition after swallowing the loading dose varies significantly. Chewed tablets may allow more rapid inhibition of platelet aggregation. However, data for this strategy in patients with stable ischemic heart disease or non-ST-elevation acute coronary syndrome (NSTE-ACS) are less robust. Methods In this single-center prospective trial, 112 P2Y12-naive patients with stable ischemic heart disease or NSTE-ACS on aspirin therapy and who received ticagrelor after coronary angiography but before PCI were randomized to chewing (n=55) or swallowing (n=57) the ticagrelor loading dose (180 mg). Baseline variables were compared using 2-sample t-test and chi-squared/Fisher's exact tests as appropriate, with alpha set at 0.05. P2Y12 reaction units (PRU) were compared at baseline, 1 hour, and 4 hours using Wilcoxon rank-sum test. Patients then received standard ticagrelor dosing. Results After exclusions, P2Y12 PRU in the chewed and swallowed groups at baseline, 1 hour, and 4 hours after ticagrelor loading dose were 243 vs 256 (P=0.75), 143 vs 210 (P=0.09), and 28 vs 25 (P=0.89), respectively. No differences were found in major adverse cardiac events (MACE) or major bleeding at 30 days and 1 year. Conclusions In patients with stable ischemic heart disease or NSTE-ACS, chewing rather than swallowing ticagrelor may lead to slightly faster inhibition of platelet aggregation at 1 hour with no increase in MACE or major bleeding. (J Patient Cent Res Rev. 2023;10:50-57.)
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页码:50 / 57
页数:10
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