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中国临床药理学与治疗学 ›› 2017, Vol. 22 ›› Issue (10): 1152-1157.

• 药物治疗学 • 上一篇    下一篇

氨磺必利治疗精神分裂症疗效以及安全性研究

周 勇1,陈雪芳1,黄汉津2   

  1. 1 浙江省嘉兴市康慈医院精神科,桐乡 314500,浙江;2 浙江省温州市温州医科大学第二临床医院神经内科,温州 325001,浙江
  • 收稿日期:2017-01-16 修回日期:2017-04-03 出版日期:2017-10-26 发布日期:2017-11-13
  • 通讯作者: 黄汉津,男,主任医师,硕士研究生导师,研究方向:临床精神病学。 E-mail:hhj@wmu.edu.cn
  • 作者简介:周勇,男,硕士研究生,副主任医师,研究方向: 临床精神病学。 Tel:18657335738 E-mail:zhouyong19831124@sina.com
  • 基金资助:

    嘉兴市科技计划项目(2012AY1805)

Efficacy and safety of amisulpride for schizophrenia

ZHOU Yong 1, Chen Xuefang 1, HUANG Hanjin 2   

  1. 1 Department of Geriatrics, Kangci Hospital of Jiaxing, Tongxiang 314500, Zhejiang, China; 2 Department of Neurology, the Second Clinical Hospital of Wenzhou Medical University, Wenzhou 325001, Zhejiang, China
  • Received:2017-01-16 Revised:2017-04-03 Online:2017-10-26 Published:2017-11-13

摘要:

目的: 本研究主要探讨氨磺必利对照利培酮治疗精神分裂症的疗效以及安全性。方法: 共90例精神分裂症患者被随机分入氨磺必利组和利培酮组,各45例。在治疗前以及治疗后第2、4、8周末,使用阳性和阴性症状量表(positive and negative syndrome scale,PANSS)对病例精神症状进行评定,病情的严重程度采用临床大体疗效量表疾病严重程度(clinical global impressionsseverity of illness scale,CGI-S)评定,通过比较量表评分前后变化来评价疗效;副反应量表(TESS)评定不良反应的发生率以评价安全性。结果: 两组在各时点PANSS评分的总分和各因子分相比基线时均有显著性降低,且差异有统计学意义(P<0.05);与利培酮相比,氨磺必利组阴性症状评分明显下降,差异有统计学意义(P<0.05);两组间PANSS评分的总分、阳性症状和精神病理症状分在各时点比较差异无统计学意义(P>0.05)。与利培酮组相比,氨磺必利组CGI-S评分较基线时均有显著降低,差异有统计学意义(P<0.01),两组间CGI-S评分比较差异无统计学意义(P>0.05)。至研究结束,两组都没有发生严重的不良反应,经统计学检验,两组各种不良反应的发生率差异无统计学意义(P>0.05)。结论: 氨磺必利治疗精神分裂症疗效明显,能显著改善患者的阳性症状、阴性症状、一般病理症状,其疗效与利培酮相当,在改善阴性症状上优于利培酮。氨磺必利治疗精神分裂症耐受性好,未发生严重的不良反应。

关键词: 精神分裂症, 氨磺必利, 利培酮

Abstract:

AIM: To explore the efficacy and safety of amisulpride in treating patients with schizophrenia. METHODS: Ninety patients with schizophrenia were randomly divided into the experimental group (received amisulpride) and the control group (received risperidone) with forty-five cases in each group. The Positive and Negative Syndrome Scale (PANSS) was used to assess the patients' mental symptoms and the Clinical Global Impressions-Severity of Illness Scale (CGI-S) for the degree of severity; the efficacy was assessed through the changes of scores, the improvement rate and effective rate of symptoms. The Treatment Emergent Symptom Scale (TESS) was assessed to evaluate the adverse reactions. All scales were assessed before treatment and at the 2nd, 4th, 8th weekend after treatment. RESULTS:The scores of PANSS and all its factor scores at every time interval were significantly lower than those at baseline (P<0.05). The scores of negative symptoms in the experimental group were much lower than those in the control group at the 2nd, 4th, 8th weekend after treatment (P<0.05). There's no difference in total scores of PANSS, scores of positive symptoms and psychopathological symptoms between the two groups at every time interval (P>0.05). Scores of CGI-S in the experimental group was obviously lower than those at baseline in comparison with the control group (P<0.01). There's no difference in scores of CGI-S between the two groups (P>0.05). Both of two groups presents no severe adverse reactions after treatment, and no significant difference was observed between the two groups either (P>0.05). CONCLUSION: Both amisulpride and risperidone can obviously improve patiens' positive, negative and psychopathological symptoms. However, the efficacy on negative symptoms of amisulpride is better than that of risperidone. Amisulpride also exhibit better tolerance with no severe adverse reaction in treating schizophrenia.

Key words: schizophrenia, amisulpride, risperidone

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