Effects of intracoronary low-dose prourokinase administration on ST-segment elevation in patients with myocardial infarction and a high thrombus burden: a randomized controlled trial

被引:5
作者
Cao, Mingkun [1 ]
Wang, Zhiyong [2 ]
Meng, Xiujie [3 ]
Xu, Zhiru [2 ]
Gao, Jiangfeng [2 ]
Zhu, Wangliang [2 ]
Yu, Suhua [4 ]
Zhang, Haijun [5 ]
机构
[1] Natl United Engn Lab Biomed Mat Modificat, Dezhou, Peoples R China
[2] Inner Mongolia Peoples Hosp, Internal Med Cardiovasc Dept, Hohhot, Inner Mongolia, Peoples R China
[3] Inner Mongolia Int Mongolian Med Hosp, Internal Med Cardiovasc Dept, Hohhot, Inner Mongolia, Peoples R China
[4] Blue Sail Pioneer Lab, JW Med Syst, Jiwei, Shandong, Peoples R China
[5] Tongji Univ, Shanghai Peoples Hosp 10, Sch Med, 301 Yanvhang Rd, Shanghai 200092, Peoples R China
关键词
Low-dose prourokinase; ST-elevation myocardial infarction; percutaneous coronary intervention; high thrombus burden; myocardial reperfusion; cardiac function; cardiac perfusion; PERCUTANEOUS CORONARY INTERVENTION; STREPTOKINASE; THROMBECTOMY; ASPIRATION; SARUPLASE; ALTEPLASE; FLOW;
D O I
10.1177/03000605221139723
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Objective: To evaluate the efficacy and safety of low-dose prourokinase (pro-UK) administration during primary percutaneous coronary intervention (PCI) for the treatment of acute ST-segment elevation myocardial infarction (STEMI) in patients with a high thrombus burden. Methods: A prospective, randomized controlled trial was conducted at the Inner Mongolia People's Hospital, China. Patients with STEMI and a high thrombus burden who underwent thrombus aspiration and primary PCI were randomly allocated to pro-UK administration or control groups. The primary endpoint was corrected thrombolysis in myocardial infarction (TIMI) frame count (CTFC). Results: There were no significant differences in the baseline demographics or clinical characteristics of the two groups. The CTFC, tissue myocardial perfusion grade, ST-segment resolution, and myocardial blush grade of the pro-UK group were significantly better than those of the control group. In addition, after 30 days of follow-up, the pro-UK group had better cardiac function and perfusion than the control group. There were no differences in the clinical outcomes or incidence of hemorrhage. Conclusions: Intracoronary low-dose pro-UK improves myocardial perfusion and cardiac function in patients with a high thrombus burden. Major hemorrhages still occur in patients administered pro-UK, but are no more frequent. Study registration: Chinese Clinical Trial Registry (ChiCTR1900022290).
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页数:12
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