帕罗西汀联合小剂量非典型抗精神病药物治疗老年期和非老年期广泛性焦虑障碍的疗效对比分析
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  • 英文篇名:A comparative analysis of paroxetine combined with low-dose atypical antipsychotic drugs in the treatment of generalized anxiety disorder in the elderly and non-elderly
  • 作者:黄鹃 ; 张涛 ; 向波
  • 英文作者:HUANG Juan;ZHANG Tao;XIANG Bo;Southwest Medical University,Southwest Medical University Affiliated Hospital;
  • 关键词:广泛性焦虑障碍 ; 帕罗西汀 ; 非典型抗精神病药物
  • 英文关键词:general anxiety disorder;;paroxetine;;atypical antipsychotic drugs
  • 中文刊名:YWYB
  • 英文刊名:Chinese Journal of Drug Dependence
  • 机构:西南医科大学,西南医科大学附属医院;
  • 出版日期:2019-06-15
  • 出版单位:中国药物依赖性杂志
  • 年:2019
  • 期:v.28;No.137
  • 基金:四川省科技厅项目(2017JY0322);; 泸州市科技局项目[2015-S-45(5/5)];; 泸州市-西南医科大学创新团队联合项目(2016LZXNYD-T08)
  • 语种:中文;
  • 页:YWYB201903012
  • 页数:7
  • CN:03
  • ISSN:11-3920/R
  • 分类号:76-82
摘要
目的:比较帕罗西汀联合小剂量非典型抗精神病药物治疗老年期和非老年期广泛性焦虑障碍的疗效、安全性差异。方法:选取2017.1.1-2018.11.15日于西南医科大学附属医院精神科住院的满足ICD-10广泛性焦虑障碍诊断标准的患者188例,据年龄分成老年组(年龄大于等于60岁)和非老年组(年龄小于60岁),老年组和非老年组均随机分为实验组和对照组,实验组给予帕罗西汀联合非典型抗精神病药物(包括奥氮平片、富马酸喹硫平片)治疗,对照组仅给予帕罗西汀治疗,分别于治疗前和治疗后2周使用汉密尔顿焦虑量表(HAMA)评估临床疗效,个人与社会表现量表(PSP)评估社会功能,药物不良反应量表(UKU)、胃肠道症状评定量表(GSRS)评定不良反应。结果:(1)治疗前HAMA、PSP得分比较:老年和非老年的实验组、对照组治疗前HAMA、PSP评分均无统计学差异(P> 0.05),老年实验组和非老年实验组HAMA、PSP评分无统计学差异(P> 0.05),老年对照组和非老年对照组HAMA、PSP评分无统计学差异(P> 0.05);(2)治疗2周后与治疗前HAMA、PSP对比:老年、非老年实验组均较对照组HAMA减分率更高、PSP加分率更高(P <0.05),非老年实验组较老年实验组HAMA减分率高、PSP加分率更高(P <0.05);(3)治疗2周后药物副作用结果:老年、非老年实验组副作用发生率较对照组无差异(P> 0.05),老年实验组较非老年实验组副作用发生率无差异(P> 0.05),老年对照组较非老年对照组无差异(P> 0.05)。结论:老年组和非老年组帕罗西汀联用非典型抗精神病药物的疗效均较单用帕罗西汀更好,社会功能恢复更好,帕罗西汀联用非典型抗精神病药物治疗非老年期广泛性焦虑障碍较老年期广泛性焦虑障碍疗效更好,社会功能恢复更好,副反应发生率无显著差异。
        Objective: To compare the efficacy and safety of paroxetine tablets combined with low-dose atypical antipsychotic drugs in the treatment of generalized anxiety disorder in the elderly and non-elderly individuals.Methods: The 188 patients who met the diagnostic criteria of generalized anxiety disorder according to ICD-10 were selected from the psychiatric department of the Affiliated Hospital of Southwest Medical University from January 1,2017 to November 15,2018.The participants were divided into the elderly group( older than 60 years old) and the non-elderly group( younger than 60 years old).The elderly group and the non-elderly group were randomly divided into the experimental group and the control group.The experimental group was given paroxetine tablets combined with atypical antipsychotic drugs( including olanzapine and quetiapine fumarate).The control group was treated with paroxetine alone.The clinical efficacy was assessed by Hamilton Anxiety Scale( HAMA) before and 2 weeks after treatment.The social function was assessed by Personal and Social Performance Scale( PSP).The adverse reactions and gastrointestinal symptoms were assessed by UKU and GSRS scale,respectively.Results:( 1) There was no statistical difference in HAMA and PSP scores among these groups before treatment( P > 0.05);( 2) After 2 weeks of treatment,the HAMA reduction rate and PSP increase rate of the elderly and non-elderly experimental group were higher than those of control group( P < 0.05),and the HAMA reduction rate and PSP increase rate of the non-elderly experimental group were higher than those of elderly experimental group( P < 0.05);( 3) The side effects of drugs after 2 weeks of treatment: there was no difference in the incidence of side effects among all these groups( P >0.05).Conclusion: The effect of paroxetine combined with atypical antipsychotics in elderly and non-elderly groups was better than that of paroxetine alone,and the recovery of social function was also better in combination group.In addition,the effect of paroxetine combined with atypical antipsychotics in non-elderly patients with generalized anxiety disorder was better than that in elderly patients,and the recovery of social function was also better.There was no significant difference in the incidence of side effects between groups.
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