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Published Online
on June 15, 2009

Circulation. 2009
Published online before print June 15, 2009, doi: 10.1161/CIRCULATIONAHA.108.822791
A more recent version of this article appeared on June 30, 2009
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Submitted on September 18, 2008
Accepted on April 21, 2009

Triple Versus Dual Antiplatelet Therapy in Patients With Acute ST-Segment Elevation Myocardial Infarction Undergoing Primary Percutaneous Coronary Intervention

Kang-Yin Chen MD, Seung-Woon Rha MD*, Yong-Jian Li MD, Kanhaiya L. Poddar MBBS, Zhe Jin MD, Yoshiyasu Minami MD, Lin Wang MD, Eung Ju Kim MD, Chang Gyu Park MD, Hong Seog Seo MD, Dong Joo Oh MD, Myung Ho Jeong MD, Young Keun Ahn MD, Taek Jong Hong MD, Young Jo Kim MD, Seung Ho Hur MD, In Whan Seong MD, Jei Keon Chae MD, Myeong Chan Cho MD, Jang Ho Bae MD, Dong Hoon Choi MD, Yang Soo Jang MD, In Ho Chae MD, Chong Jin Kim MD, Jung Han Yoon MD, Wook Sung Chung MD, Ki Bae Seung MD, Seung Jung Park MD, for the Korea Acute Myocardial Infarction Registry Investigators

From the Korea University Guro Hospital, Seoul, Korea.

* To whom correspondence should be addressed. E-mail: swrha617{at}yahoo.co.kr.

Background—Whether triple antiplatelet therapy is superior or similar to dual antiplatelet therapy in patients with acute ST-segment elevation myocardial infarction undergoing primary percutaneous coronary intervention in the era of drug-eluting stents remains unclear.

Methods and Results—A total of 4203 ST-segment elevation myocardial infarction patients who underwent primary percutaneous coronary intervention with drug-eluting stents were analyzed retrospectively in the Korean Acute Myocardial Infarction Registry (KAMIR). They received either dual (aspirin plus clopidogrel; dual group; n=2569) or triple (aspirin plus clopidogrel plus cilostazol; triple group; n=1634) antiplatelet therapy. The triple group received additional cilostazol at least for 1 month. Various major adverse cardiac events at 8 months were compared between these 2 groups. Compared with the dual group, the triple group had a similar incidence of major bleeding events but a significantly lower incidence of in-hospital mortality. Clinical outcomes at 8 months showed that the triple group had significantly lower incidences of cardiac death (adjusted odds ratio, 0.52; 95% confidence interval, 0.32 to 0.84; P=0.007), total death (adjusted odds ratio, 0.60; 95% confidence interval, 0.41 to 0.89; P=0.010), and total major adverse cardiac events (adjusted odds ratio, 0.74; 95% confidence interval, 0.58 to 0.95; P=0.019) than the dual group. Subgroup analysis showed that older (>65 years old), female, and diabetic patients got more benefits from triple antiplatelet therapy than their counterparts who received dual antiplatelet therapy.

Conclusions—Triple antiplatelet therapy seems to be superior to dual antiplatelet therapy in patients with ST-segment elevation myocardial infarction undergoing primary percutaneous coronary intervention with drug-eluting stents. These results may provide the rationale for the use of triple antiplatelet therapy in these patients.


Key words: cilostazol • myocardial infarction • thrombosis • platelets


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Antiplatelet Polypharmacy in Primary Percutaneous Coronary Intervention: Trying to Understand When More Is Better
Ahmed Abdel-Latif and David J. Moliterno
Circulation 2009 119: 3168-3170. [Extract] [Full Text]



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A. Abdel-Latif and D. J. Moliterno
Antiplatelet Polypharmacy in Primary Percutaneous Coronary Intervention: Trying to Understand When More Is Better
Circulation, June 30, 2009; 119(25): 3168 - 3170.
[Full Text] [PDF]