Clinically commonly used thrombolytic drugs are mainly urinary kinases and atipase (rt-PA). Atipase is an endogenetic enzyme with high specificity to fibrin. It can bind to fibrin in blood clots, activate the fibrinase in the blood, and degrade the fibrin, because it is mainly activated in the local thrombosis, and then play the effect of local thrombosis.<br><br>Khaled and other studies have concluded that intravenous rt-PA also has a positive effect on the recovery of nerve function in patients with acute isohemic cerebrovascular disease. Studies such as Maier's also suggest that rt-PA treatment can improve the functional prognosis of eligible patients, but further research is needed to confirm and determine the patient conditions most likely to benefit from it. Among them, blood glucose level is the main factor of thrombolytic effect, the higher the blood sugar level of patients before the application of thrombolytic drugs such as rt-PA, the worse the efficacy. The control of blood sugar within a certain range is beneficial to improve the therapeutic effect of thrombolytic drugs.<br>Due to the multi-mechanism disease of ischemic cerebrovascular disease, including local brain tissue ischemic, hypoxia, its brain cells appear electrochemical cascading waterfall-like reaction, and the signaling path in the damaged brain cells, which in turn leads to damage to the function of the central nervous system. Therefore, multi-target drugs are very important in their treatment. Butyl benzene has become an important auxiliary means of isomorphic cerebrovascular disease, and it is believed that it can also improve severe cognitive dysfunction syndrome caused by insufficient perfusion of brain tissue. Butylphenidate may have the following mechanisms for the treatment of isohemic cerebrovascular disease: by inhibiting the transition of M1 small glial cells/macrophages to M2 phenids, neurological damage and damage to the blood-brain barrier are mitigated. Butyl benzene sequentepsis treatment can also effectively improve the plasma level of 3-MST, reduce the plasma level of A beta 42, is conducive to improve the patient's life ability and nerve function, improve daily life activities, with high safety. 【22】。<br>Our study suggests that both groups of patients showed improved NHISS scores after treatment (p 0.05) than before treatment. However, the improvement was more pronounced in patients treated with atipase combined butyl benzene (p-0.00), about 67.5% of patients recovered well after treatment in the experimental group, and about 45% recovered well in nerve function after control group treatment (p-0.04), while there was no significant difference in the incidence of complications in both groups within 1 week of treatment (p-0.56).<br>To sum up: Atipase combined with butyl benzene to treat patients with acute pre-circulatory cerebral infarction symptoms improved significantly, high efficiency, nerve function recovery significantly, and the incidence of complications did not increase significantly.<br>The shortcoming of this study is that the number of cases included in the study is small and the follow-up time is short. Only patients within 6h of the disease were analyzed in general terms. There was no further refinement of the therapeutic effect and prognosticity of the application of atipase to butylphenidate in patients with different time windows. We are also actively accumulating cases, further refining the information on patient treatment within different time windows, and continuing to increase follow-up time with a view to elaborating in more detail on the shortcomings and long-term effects of the treatment.<br>References:
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