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Treatment of Human Urinary Kallidinogenase Combined with Maixuekang Capsule Promotes Good Functional Outcome in Ischemic Stroke

机译:人尿中激肽原酶联合麦血康胶囊的治疗促进缺血性卒中良好的功能预后

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摘要

>Aims: To evaluate the clinical efficacy of Human Urinary Kallidinogenase (HUK) and Maixuekang capsule in the treatment of acute ischemic stroke (AIS) patients.>Methods: In this study, from January 2016 to July 2016, 60 patients with acute ischemic stroke were enrolled and 56 patients with complete information of whom 21 patients received HUK+ basic treatment (HUK group), 16 patients received HUK+ Maixuekang capsule + basic treatment (HUK+ Maixuekang group), 19 patients received basic treatment (control group). 0.15 PNA unit of HUK injection plus 100 ml saline in intravenous infusion was performed in the HUK group and HUK+ Maixuekang group, with once a day for 14 consecutive days. 0.75 g Maixuekang capsules were taken in HUK+ Maixuekang group, with three times a day for 14 consecutive days. The National Institutes of Health Stroke Scale (NIHSS) scores in three groups were analyzed 7 days after treatment. The modified Rankin Scale (mRS) scores in three groups were analyzed 12 month after the treatment.>Results: No difference was found in the NIHSS scores, age, gender, and comorbidities between three groups before treatment (p > 0.05). Seven days after treatment, the NIHSS scores in the HUK group and HUK+ Maixuekang group were significantly decreased than before (p HUK = 0.001, p HUK+Maixuekang < 0.001), and lower than that in the control group (p HUK = 0.032; p HUK+Maixuekang < 0.001). Twelve months after treatment, good functional outcome rate (12 month mRS score ≤ 2) in the HUK group and HUK+ Maixuekang group was significantly higher than that in the control group (p HUK = 0.049, p HUK+Maixuekang = 0.032).>Conclusion: The treatment of HUK or HUK combined with Maixuekang capsule can effectively improve the neurological function and promote long-term recovery for AIS patients.
机译:>目的::评估人尿中的Kallidinogenase(HUK)和麦血康胶囊在急性缺血性中风(AIS)患者中的临床疗效。>方法: 2016年1月至2016年7月,共入选60例急性缺血性卒中患者,其中56例具有完整信息,其中21例接受了HUK +基本治疗(HUK组),16例接受了HUK +迈雪康胶囊+基本治疗(HUK +迈雪康组),19例接受基本治疗(对照组)。 HUK组和HUK +迈雪康组分别进行0.15 PNA HUK注射加100 ml生理盐水静脉滴注,连续14天,每天一次。 HUK +迈雪康组0.75克迈雪康胶囊,连续3天,每天3次。治疗7天后分析了三组美国国立卫生研究院卒中量表(NIHSS)评分。治疗后12个月对三组的改良兰金量表(mRS)得分进行了分析。>结果:治疗前三组之间的NIHSS得分,年龄,性别和合并症之间无差异(p > 0.05)。治疗7天后,HUK组和HUK +迈雪康组的NIHSS得分均较之前明显降低(p HUK = 0.001,p HUK + Maixuekang <0.001),低于对照组(p HUK = 0.032; p HUK +迈雪康<0.001)。治疗后12个月,HUK组和HUK +迈雪康组的良好功能转归率(12个月mRS评分≤2)显着高于对照组(p HUK = 0.049,p HUK + Maixuekang = 0.032)。 >结论: HUK或HUK联合麦雪康胶囊治疗可有效改善AIS患者的神经功能,促进其长期康复。

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