李日光 李国文 李惠香 王文军 李志英.螺环酮联合帕罗西汀治疗焦虑症的疗效及安全性分析[J].现代生物医学进展英文版,2014,14(22):4312-4314. |
螺环酮联合帕罗西汀治疗焦虑症的疗效及安全性分析 |
The Analysis of The Effect and Security of Buspirone Combined withParoxetine in Treating Anxiety |
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DOI: |
中文关键词: 焦虑症 螺环酮 帕罗西汀 疗效 安全性 |
英文关键词: Anxiety Buspirone Paroxetine Effect Security |
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中文摘要: |
目的:研究螺环酮联合帕罗西汀治疗焦虑症的疗效及其安全性。方法:选取2009 年1 月至2013 年8 月我院收治的符合诊
断标准的焦虑症患者244 例,按照知情同意原则随机分为治疗组(122 例)和对照组(122 例),治疗组给予丁螺环酮联合帕罗西汀
治疗,对照组仅给予螺环酮治疗。治疗10 周后,运用汉密尔顿焦虑量表(HAMA)及Montgomery -Asberg 抑郁量表(MADS)评价
疗效,运用治疗过程中不良反应症状量表(TESS)评价其安全性,比较两组患者的疗效及安全性。结果:治疗后两组的HAMA 及
MADS 评分均低于治疗前,且治疗组低于对照组,差异均有统计学意义(P<0.05);两组TEES 评分在治疗第2、4、6、8、10 周末均无
统计学差异(P>0.05)。结论:螺环酮联合帕罗西汀在治疗焦虑症时可提高疗效,且安全性高,可考虑在临床推广。 |
英文摘要: |
Objective:To study the effect and security of buspirone combined paroxetine in the treatment of anxiety.Methods:244 patients who were diagnosed with anxiety were chosen from 2009 January to 2013 Augst in our hospital, and were divided into
treatment group (122 cases) and control group (122cases) randomly according to the principle of informed and consent, treatment group
was treated with buspirone combined paroxetine, while the control group was treated with buspirone alone. after 10 weeks of treatment,
Hamilton anxiety scale (HAMA) and Montgomery -Asberg depression scale (MADS) were used to evaluate the effect and treatment
emergent symptom scale (TESS) was used to evaluate the security, the effect and security between two groups of patients was compared.Results:The score of HAMA and MADS of two groups after treatment were all lower than those before the treatment, and the scores of
the treatment group were lower than the control group, the differences were all statistically significant(P<0.05). There were no statistically
differences in the comparison of the scores of TEES between two groups in the 2, 4, 6, 8, 10 weeks of treatment (P>0.05).Conclusion:Buspirone combined paroxetine can improve the effect in treating anxiety and have high security, which could be considered to be widely
applied in clinic. |
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