Safety and efficacy of prourokinase injection in patients with ST-elevation myocardial infarction: Phase IV clinical trials of the prourokinase phase study
Heart and Vessels Dec 08, 2017
Zhao L, et al. - This research entailed the contemplation of the safety and efficacy with regard to infarct-related artery (IRA) patency of prourokinase (proUK) injection within 6 h after symptom onset, in patients with ST-elevation myocardial infarction (STEMI). Such a fibrinolysis therapy was discovered to be efficient and safe, displaying a very low rate of bleeding complications. It served as an alternative treatment option for STEMI patients, particularly in scenarios where primary PCI could not be offered in a timely manner.
Methods
- The recrutiment consisted of 1,851 patients with acute myocardial infarction who received thrombolytic therapy with proUK.
- They were injected with 20 mg proUK intravenously followed by intravenous infusion of 30 mg proUK within 30 min.
- IRA was determined via coronary angiography at 120 min after thrombolysis.
- A scrutiny was conducted of the efficacy and safety of proUK thrombolysis in the eligible candidates.
Results
- The findings illustrated successful clinical reperfusion in 1,580 patients (85.4%).
- Marked reduction was noted in the number of leads with ST segment elevation and the amplitude of ST segment elevation within 24 h after thrombolytic therapy with proUK.
- Death was reported in 83 patients (4.48%) by the end of follow-up (7 days after thrombolysis).
- The incidences of post-infarction angina, re-infarction or reocclusion, and emergency revascularization were 15.2, 4.21, and 8.27%, respectively.
- Subcutaneous or mucosal bleeding was determined to be the most common bleeding complication.
- The incidence of intracranial hemorrhage was found to be 0.32%.
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