天麻钩藤颗粒联合美多芭治疗帕金森病的临床研究
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  • 英文篇名:Clinical study of Tianma Gouteng Granules combined with Madopar in the treatment of Parkinson disease
  • 作者:王郑 ; 赖天宝 ; 王小西 ; 李晓峰
  • 英文作者:WANG Zheng;LAI Tianbao;WANG Xiaoxi;LI Xiaofeng;Department of Neurology, Hangzhou Seventh People′ s Hospital;Department of Neurology, Zhongshan Hospital Affiliated to Xiamen University;Department of Pathology, the First Affiliated Hospital of Zhejiang University Medical School;Department of Neurology, Guangxi Zhuang Autonomous Region People′s Hospital;
  • 关键词:天麻钩藤颗粒 ; 美多芭 ; 帕金森病
  • 英文关键词:Tianma Gouteng Granules;;Medopar;;Parkinson disease
  • 中文刊名:YYCY
  • 英文刊名:China Medical Herald
  • 机构:杭州市第七人民医院神经内科;厦门大学附属中山医院神经内科;浙江大学医学院附属第一医院病理科;广西壮族自治区人民医院神经内科;
  • 出版日期:2019-01-15
  • 出版单位:中国医药导报
  • 年:2019
  • 期:v.16;No.496
  • 基金:国家自然科学基金资助项目(81502158)
  • 语种:中文;
  • 页:YYCY201902016
  • 页数:5
  • CN:02
  • ISSN:11-5539/R
  • 分类号:69-72+77
摘要
目的研究天麻钩藤颗粒联合美多芭治疗帕金森病(PD)的临床效果。方法选择2016年4月~2018年2月在杭州市第七人民医院接受治疗的PD患者174例,按照随机数表法将患者分为观察组和对照组,每组各87例。对照组予以美多芭治疗,观察组在对照组的基础上再增服天麻钩藤颗粒治疗,两组均治疗3个月,3个月为1个疗程。对比两组疗效、炎性指标及氧化应激指标,帕金森评分量表(UPDRS)评分和简易智能精神状态检查量表(MMSE)评分,以及用药安全性。结果观察组总有效率为96.55%,明显高于对照组(88.51%),差异有统计学意义(P <0.05)。治疗3个月后两组白细胞介素-4和超氧化物歧化酶水平高于治疗前,且观察组高于对照组;两组肿瘤坏死因子-α和丙二醛水平低于治疗前,且观察组低于对照组,差异有统计学意义(均P <0.05)。治疗3个月后两组MMSE评分明显高于治疗前,且观察组高于对照组;两组UPDRS评分明显低于治疗前,且观察组低于对照组,差异有统计学意义(均P <0.05)。观察组的不良反应总发生率为6.90%,与对照组(9.20%)比较,差异无统计学意义(P> 0.05)。结论天麻钩藤颗粒联合美多芭治疗PD效果显著,可有效改善患者的炎性状态及氧化应激水平,同时改善其认知功能,药物的安全性较好,值得给予推广。
        Objective To study the clinical efficacy of Tianma Gouteng Granules combined with Madopar in the treatment of Parkinson disease(PD). Methods From April 2016 to February 2018, 174 patients with PD admitted in Hangzhou Seventh People′ s Hospital were selected. According to the random number table method, the patients were divided into observation group and control group, 87 cases in each group. The control group was treated with Madopar and the observation group was treated with Tianma Gouteng Granules on the basis of the control group. The two groups were treated for 3 months, 3 months was 1 course of treatment. The efficacy, inflammatory index, oxidative stress index,unified parkinson disease rating scale(UPDRS), mini mental state examination(MMSE) and medication safety were compared. Results The total effective rate of the observation group was 96.55%, which was significantly higher than88.51% of the control group, the difference was statistically significant(P < 0.05). After 3 months of treatment, the level of nterleukin-4 and superoxide dismutase in both groups was higher than that before treatment, and the level in the observation group was higher than that in the control group, tumor necrosis factor-α and malonaldehyde level in the two groups was lower than before treatment, and the observation group was lower than the control group, the differences were statistically significant(all P < 0.05). After 3 months of treatment, the MMSE score of the two groups was significantly higher than that before treatment, and the observation group was higher than that of the control group, the UPDRS scores of the two groups were significantly lower than those before treatment, and the observation group was lowerthan that of the control group, the differences were statistically significant(all P < 0.05). The total incidence of adverse reactions in the observation group was 6.90%,compared with 9.20% of the control group, the differ-ence was not statistically significant(P > 0.05). Conclusion Tianma Gouteng Granules combined with Madopar is effective in the treatment of PD. It can effectively improve the inflammatory state and oxidative stress level of patients, and improve their cognitive function. The drug is safe and worthy of promotion.
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