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Triple vs. Dual Antiplatelet Therapy in Patients With Acute Myocardial Infarction and Renal Dysfunction - Results From the Korea Acute Myocardial Infarction Registry

Authors
Choi, Young HwanSuh, Sang HeonChoi, Joon SeokKim, Chang SeongSim, Doo SunBae, Eun HuiLim, Sang YupMa, Seong KwonJeong, Myung HoKim, Soo Wan
Issue Date
10월-2012
Publisher
JAPANESE CIRCULATION SOC
Keywords
Acute myocardial infarction; Cilostazol; Glomerular filtration rate; Major adverse cardiac event; Thrombosis
Citation
CIRCULATION JOURNAL, v.76, no.10, pp.2405 - 2411
Indexed
SCIE
SCOPUS
Journal Title
CIRCULATION JOURNAL
Volume
76
Number
10
Start Page
2405
End Page
2411
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/107358
DOI
10.1253/circj.CJ-12-0236
ISSN
1346-9843
Abstract
Background: The question as to whether triple antiplatelet therapy is superior to dual antiplatelet therapy for patients with acute myocardial infarction (AMI) and renal dysfunction, who undergo percutaneous coronary intervention (PCI), is unresolved. Methods and Results: As part of the Korea Acute Myocardial Infarction Registry (KAMIR), 2,288 AMI patients with renal dysfunction (glomerular filtration rate <60 ml/min . 1.73m(2)) received either dual (aspirin plus clopidogrel; n=1,587) or triple (aspirin plus clopidogrel and cilostazol; n=701) antiplatelet therapy. Major adverse cardiac events (MACE) at 1 month and 1 year were compared between these 2 groups. On comparison with the dual therapy group, the triple therapy group had a similar incidence of major bleeding events but a significantly lower incidence of in-hospital mortality. The MACE rate at 1 month was significantly higher for the dual therapy group than for the triple therapy group (16.3% vs. 11.1%, P<0.05), and this difference was mainly attributed to death rather than repeat PCI (12.9% vs. 9.1%, P<0.05). The MACE rate at 1 year and the MACE-free survival time, however, did not differ between the groups. Conclusions: In AMI patients with renal dysfunction, triple antiplatelet therapy has a favorable in-hospital and short-term MACE impact, but it does not have an impact on the 1-year MACE-free survival. (Circ J 2012; 76: 2405-2411)
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