Efficacy and safety of quadruple therapy including tirofiban in the treatment of Chinese NSTE-ACS patients failing to receive timely percutaneous coronary intervention

Lan Li,1 Zhenrong Ge,1 Dengke Zhang,1 Jun Kuang,2 Xiang Ma,3 Shubin Jiang1 1Coronary Care Unit, The Traditional Chinese Medicine Hospital, Xinjiang Medical University, 2Department of Cardiology, General Hospital of Xinjiang Military Command, 3Department of Cardiology, First Affiliated Hospital of Xi...

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Main Authors: Li L (Author), Ge Z (Author), Zhang D (Author), Kuang J (Author), Ma X (Author), Jiang S (Author)
Format: Book
Published: Dove Medical Press, 2017-11-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Li L  |e author 
700 1 0 |a Ge Z  |e author 
700 1 0 |a Zhang D  |e author 
700 1 0 |a Kuang J  |e author 
700 1 0 |a Ma X  |e author 
700 1 0 |a Jiang S  |e author 
245 0 0 |a Efficacy and safety of quadruple therapy including tirofiban in the treatment of Chinese NSTE-ACS patients failing to receive timely percutaneous coronary intervention 
260 |b Dove Medical Press,   |c 2017-11-01T00:00:00Z. 
500 |a 1177-8881 
520 |a Lan Li,1 Zhenrong Ge,1 Dengke Zhang,1 Jun Kuang,2 Xiang Ma,3 Shubin Jiang1 1Coronary Care Unit, The Traditional Chinese Medicine Hospital, Xinjiang Medical University, 2Department of Cardiology, General Hospital of Xinjiang Military Command, 3Department of Cardiology, First Affiliated Hospital of Xinjiang Medical University, Urumqi, People’s Republic of China Background: Although it has been shown to be superior to simple antithrombotic drug therapy, most patients are unable to receive timely percutaneous coronary intervention (PCI) and are treated with conventional triple antithrombotic therapy (aspirin, clopidogrel, low-molecular-weight heparin). Here, we evaluate the efficacy and safety of adding low-dose tirofiban to this regimen. Methods: A total of 1,783 patient records (unable to receive PCI) indicating non-ST-segment elevation acute coronary syndrome (NSTE-ACS) were included. A total of 882 received conventional triple antithrombotic therapy; 901 received quadruple antithrombotic therapy. Efficacy was evaluated in terms of major adverse cardiovascular event (MACE) parameters. Safety was evaluated based on the occurrence of bleeding events. Data were collected over a 6-month period post treatment. Results: The rate of occurrence of MACE was significantly lower in the quadruple antithrombotic group (10.5% versus 14.1% at 6 months, P=0.02). The log-rank test showed improved survival in the quadruple antithrombotic group. Total bleeding events were higher in the quadruple antithrombotic group (9.7%) than in the triple antithrombotic group (7.1%) (P=0.04); however, this may be attributed to increased clinically insignificant minor bleeding events. Conclusion: Quadruple antithrombotic therapy demonstrated a superior alternative for the treatment of high-risk NSTE-ACS patients failing to receive PCI. Keywords: low-dose tirofiban, non-ST-segment elevation acute coronary syndrome, quadruple drug therapy  
546 |a EN 
690 |a low-dose tirofiban 
690 |a non-ST-segment elevation acute coronary syndrome 
690 |a quadruple drug therapy 
690 |a Therapeutics. Pharmacology 
690 |a RM1-950 
655 7 |a article  |2 local 
786 0 |n Drug Design, Development and Therapy, Vol Volume 11, Pp 3299-3307 (2017) 
787 0 |n https://www.dovepress.com/efficacy-and-safety-of-quadruple-therapy-including-tirofiban-in-the-tr-peer-reviewed-article-DDDT 
787 0 |n https://doaj.org/toc/1177-8881 
856 4 1 |u https://doaj.org/article/aaafb74b8a4b48d3bab330d60aa3d6ad  |z Connect to this object online.