Prourokinase in Acute Ischemic Stroke: A Review of Current Evidence
摘要
Stroke is one of the leading causes of long-term morbidity and mortality worldwide. The advent of intravenous thrombolysis in the management of acute ischaemic strokes has been rendered the first line for systemic reperfusion therapy. This paper aims to evaluate the efficacy and safety of prourokinase in the management of AIS, highlighting its prospective safety and concludes by emphasizing the need for further research.
A search was conducted across multiple electronic databases, including PubMed, Embase, Scopus, Web of Science, and the Cochrane Library, to identify relevant studies published from inception to 2025 that assessed the trends, efficacy, safety, and comparative effectiveness of prourokinase in the management of AIS.
Recent FindingsAIS is a condition with high prevalence and comorbidity. Pooled analyses of phase II randomized trials (PROACT) with inclusion criteria for the study of primarily MCA occlusion confirmed by angiography, absence of hemorrhage or major infarction on computed tomography (CT) scan, and presentation within 3–6 h showed 40% of r-ProUK subjects and 25% of controls had a modified Rankin score of 2 or less (P = 0.4). Although there were reported improvements in recanalization rates in acute ischemic strokes, the increased frequency of symptomatic early intracranial hemorrhage reported from the studies limits potential use.
SummaryRecombinant human prourokinase (rhPro-UK), a fibrin-specific plasminogen activator, has shown promising results from clinical trials. The full therapeutic potential in the global management of acute ischemic stroke will be realized with further research, regulatory evaluation, and integration into clinical guidelines.