Application of human urokinase-type peptidase in preparing medicine for treating diabetes combined cerebral infraction
A technique for urokininogenase and diabetes, which is applied in the application field of preparing medicines for treating and/or preventing diabetes complicated with cerebral infarction, and can solve the problems of increased disability rate and mortality rate, poor prognosis, slow recovery from cerebral infarction and the like
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Embodiment 1
[0012] Example 1 Treatment of Human Urinary Kallikrein to Diabetic Patients with Cerebral Infarction
[0013] Experimental objects and grouping: 646 patients with cerebral infarction within 48 hours of onset were randomly selected clinically and divided into treatment group and control group. The treatment group was treated with human urokininogenase, and the control group was given routine treatment with Vibrasol. Among them, there were 532 cases of non-diabetic patients with cerebral infarction (149 cases in the control group and 383 cases in the treatment group), and 114 cases of diabetic patients with cerebral infarction (32 cases in the control group and 82 cases in the treatment group).
[0014] Analysis items: changes in neurological function of patients before and after treatment, using the European Stroke Scale (ESS). The course of treatment is 21 days.
[0015] Efficacy index: the curative effect is judged by the increase rate, and the calculation method is as foll...
Embodiment 2
[0026] Example 2 Effect of human urinary kallikrein on hemorheology in patients with diabetes mellitus complicated with cerebral infarction
[0027] Case selection: 95 cases of diabetic patients with cerebral infarction (44 cases were randomly divided into control group and 51 cases in treatment group), 92 cases of non-diabetic patients with cerebral infarction (42 cases were randomly divided into control group and 50 cases in treatment group). There was no significant difference in age, gender, lesion site and neurological deficit scores between the two groups (P>0.05), which were comparable.
[0028] Experimental method: The control group was given routine treatment with Vibrasol, and the treatment group was given urokininogenase treatment, and the course of treatment was 7 days.
[0029] Experimental indicators: Blood was drawn once before treatment and at the end of treatment in each group, and changes in hemorheology parameters such as whole blood viscosity, plasma viscos...
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