逍遥丸与艾司西酞普兰治疗血管性痴呆伴发抑郁的疗效对比分析
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  • 英文篇名:Comparative Analysis of Clinical Efficacy of Xiaoyao Pills and Escitalopram in Treatment of Vascular Dementia Patients with Depression
  • 作者:沈莹 ; 陈松 ; 余鸽 ; 杨华
  • 英文作者:SHEN Ying;CHEN Song;YU Ge;YANG Hua;Department of Geriatrics,Tongde Hospital of Zhejiang Province;Department of Psychiatry of The Seventh People's Hospital of Hangzhou;Department of Psychological Counseling,Tongde Hospital of Zhejiang;
  • 关键词:逍遥丸 ; 艾司西酞普兰 ; 血管性痴呆 ; 抑郁
  • 英文关键词:Xiaoyao Pill;;escitalopram;;vascular dementia;;depression
  • 中文刊名:ZYHS
  • 英文刊名:Chinese Archives of Traditional Chinese Medicine
  • 机构:浙江省立同德医院老年科;杭州市第七人民医院精神科;浙江省立同德医院心理咨询科;
  • 出版日期:2019-02-10
  • 出版单位:中华中医药学刊
  • 年:2019
  • 期:v.37
  • 基金:浙江省中医药科技计划项目(2016zb011)
  • 语种:中文;
  • 页:ZYHS201902034
  • 页数:4
  • CN:02
  • ISSN:21-1546/R
  • 分类号:142-145
摘要
目的:分析比较逍遥丸与艾司西酞普兰治疗血管性痴(vascular dementia,VD)呆伴发抑郁的临床疗效。方法:选取VD伴发抑郁患者100例,随机分为对照组和观察组,每组各50例。两组均给予奥拉西坦注射液+多奈哌齐片的血管性痴呆治疗,对照组患者在此基础上给予口服草酸艾司西酞普兰片,10 mg/次,1次/d,根据个人反应可逐渐增加至20 mg/d观察组患者给予逍遥丸治疗,8丸/次,3次/d;两组均以2周为1个疗程,治疗4疗程。测定治疗前后两组患者血清中BNDF、S100B蛋白、NE、DA、5-HT及Hcy的水平;观察两组治疗前后CSDD、MMSE、CDR及ADL评分,对比治疗后的临床疗效及不良反应。结果:治疗4周及治疗8周后CSDD各项评分及总分均较治疗前明显降低(P<0.05),但两组间比较没有统计学意义(P>0.05)。治疗后两组患者的MMES评分明显升高,与治疗前比较差异有统计学意义(P<0.05),但治疗后两组各评分比较没有统计学意义(P>0.05);两组治疗前后CDR评分均没有显著变化,比较没有统计学意义(P>0.05)。治疗4周及8周后两组患者ADL评分均显著降低,虽然观察组的ADL评分较对照组略高,但比较并没有明显差异(P>0.05)。治疗后两组患者的BNDF、NE、DA及5-HT水平均较治疗前显著升高(P<0.05),S100B及Hcy水平显著降低(P<0.05),对照组的5-HT升高幅度较观察组更为明显(P<0.05),而治疗后两组的BNDF、NE、DA、S100B及Hcy比较没有显著差异(P>0.05)。观察组的治疗临床总有效率为90.0%;对照组的临床总有效率为88.0%,两组比较没有统计学意义(P>0.05);治疗过程中观察组患者不良反应总发生率为8.0%;对照组患者不良反应总发生率为32.0%,两组比较有统计学意义(P<0.05)。结论:逍遥丸治疗血管性痴呆伴发抑郁的临床疗效与艾司西酞普兰基本一致,不良反应少于艾司西酞普兰,值得临床推广应用。
        Objective:To comparatively analyze the clinical efficacy of Xiaoyao Pill and escitalopram in the treatment of vascular dementia(VD) patients with depression.Methods:Totally 100 VD patients with depression were randomly divided into control group(n=50) and observation group(n=50).Both groups were treated with Donepezil Tablets and olaxetam injection, while patients in the control group were treated with oral oxalcitalopram oxalate 10 mg/time once a day.According to the individual reaction, the patients in the observation group could be treated with Xiaoyao Pills 3 times a day,20 mg/day, and the two groups were treated for 2 weeks as a course of treatment and 4 courses totally. We determined serum BNDFN S100 B protein, Neda-5-HT and Hcy in two groups before and after treatment. The levels of CDR and ADL were observed before and after treatment, and the clinical efficacy and adverse reactions were compared.Results: After 4 and 8 weeks treatment, the scores and total scores of CSDD were significantly lower than those before treatment(P<0.05), but there was no significant difference between the two groups(P>0.05).After treatment, the MMES score of the two groups was significantly higher than that before treatment(P<0.05), but there was no significant difference between the two groups after treatment(P>0.05), and there was no significant difference between the two groups' CDR score(P<0.05). There was no statistical significance(P>0.05).After 4 and 8 weeks of treatment, the ADL scores of the two groups were significantly decreased. Although the ADL score of the observation group was slightly higher than that of the control group, there was no significant difference between the two groups(P>0.05). There was no significant difference between the two groups(P>0.05). The total effective rate was 90.0% in the observation group.The total effective rate of the control group was 88.0 % and there was no significant difference between the two groups(P>0.05).The overall incidence of adverse reactions was 8.0% in the observation group.Conclusion:The clinical curative effect of Xiaoyao Pill on vascular dementia complicated with depression is consistent with that of escitalopram. The adverse reaction is less than that of escitalopram. It is worthy of clinical application.
引文
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