活血息风化痰方治疗缺血性中风恢复期风痰瘀阻证的临床观察中医内科学专业论文.docxVIP

活血息风化痰方治疗缺血性中风恢复期风痰瘀阻证的临床观察中医内科学专业论文.docx

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PAGE PAGE 10 Clinical Observation on Treatment of Ischemic Stroke Recovery Period (Wind Phlegm Retention Syndrome) with Huoxue XifengHuatan Decoction Abstract Objective: Through this clinical trial, Huoxuexifeng huatan Decoction -n treatment of ischemic stroke recovery period (wind phlegm retention synd rome) a preliminary safety and efficacy evaluation. Methods: Select August 2009 - December 2010 between the First Aff- iliated Hospital of Guangxi Medical College Department of Neurology, Depar tment of Geriatrics, outpatient and inpatientmet the inclusion criteria of the 60 patients, using random number table, randomly assigned 1:1 to observe group and the control group. Control group received routine western medicine, the o bservation group routine western medicine on the basis of information given to Huoxuexifenghuatan Decoction (Chuan Xiong 15g, Tianqi 10g, earthworm 15g, leech 10g, centipede 1 article, Scorpio 6g, bile Southern Star 10g, Shicha ngpu 15g, amber 3g, ginseng 10g, etc), a/d, which amber Yan Mo, Affiliated medicine or drug room by a generation of fried, each dose of concentration for the two bags, each bag of 100ml, sooner or later the two sub-time blunt amber. 30 days for a course of treatment, 2 courses of treatment in both group . Before and after treatment of clinical neurological deficits and activities of daily living, quality of life and changes in TCM, and to evaluate drug safety. Results: 1、the treatment group were observed neurologic impairment and syndromes on the effect of improving significantly than the control group (P0.05). 2、the treatment group was observed neurological deficit score (NIH -SS score), activities of daily living (ADL), Barthel Index scores, QOL qualit- y of life index score, Hou points better than control group before treatment aft ter treatment (P0.05). 3、the general physical examination before and after tr -eatment in each group project, blood, urine, stool, ECG, liver function test re sults showed no significant

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