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中国临床药理学与治疗学 ›› 2011, Vol. 16 ›› Issue (5): 574-578.

• 药物治疗学 • 上一篇    下一篇

艾司西酞普兰联合抗精神病药物治疗急性期精神分裂症伴发抑郁的疗效观察

江长旺, 施剑飞, 诸亚萍, 陶云海   

  1. 杭州市第七人民医院精神科, 杭州 310013,浙江
  • 收稿日期:2011-02-10 修回日期:2011-03-04 发布日期:2011-07-08
  • 通讯作者: 施剑飞,男,本科,主任医师,硕士生导师,研究方向:精神障碍的病理与临床治疗。Tel:0571-85126522 E-mail:shijf659293@163.com
  • 作者简介:江长旺,男,本科,副主任医师,主要从事精神科临床工作。Tel:0571-85126585 E-mail:jzwn8487@sina.com

Efficacy study of Escitalopram together with atypical antipsychotic in treating depression symptoms accompanied with acute schizophrenia

JIANG Chang-wang, SHI Jian-fei , ZHU Ya-ping, TAO Yun-hai   

  1. Psychiatry Department,Hangzhou Seventh Hospital, Hangzhou 310013,Zhejiang, China
  • Received:2011-02-10 Revised:2011-03-04 Published:2011-07-08

摘要: 目的: 了解艾司西酞普兰联合抗精神病药物治疗急性期精神分裂症伴发抑郁的疗效及安全性。方法: 收集急性期精神分裂症伴抑郁的患者,随机分为研究组及对照组,研究组使用抗精神病药物联合艾司西酞普兰治疗,对照组仅使用抗精神病药物治疗,研究时间为8周。运用简明精神病评定量表(BPRS)、汉密尔顿抑郁量表(HAMD) 17项及不良反应症状量表(TESS)对两组患者进行症状及不良反应的评定。根据临床常用抗精神病药物效价比的换算方法,将两组患者所用的抗精神病药物换算成氟哌啶醇剂量,然后进行比较。结果: 入组71例,完成研究68例。研究组HAMD评分在治疗第1周起便出现较入组时有显著性下降,治疗第2周起明显低于对照组,对照组HAMD评分在治疗第4周起才显示出较入组时有显著性下降。研究组BPRS评分在治疗第2、4、8周较入组时均有显著性的下降,也明显低于同期对照组BPRS评分。治疗第8周研究组患者痊愈率(42.8%)显著高于对照组(15.1%),P<0.05,研究组显效率(65.7%)略高于对照组(51.5%)。研究组抗精神病药物的平均最高剂量,1~8周的平均剂量及第8周的平均剂量均显著低于对照组的剂量。在治疗第2、4、8周,研究组TESS评分均显著低于对照组。结论: 艾司西酞普兰联合抗精神病药物能快速有效地治疗精神分裂症所伴发的抑郁症状,对精神病性症状的治疗有协同作用,并且安全性较好。

关键词: 精神分裂症, 抑郁, 艾司西酞普兰, 治疗, 随机对照临床试验

Abstract: AIM: To study the efficacy and safety of Escitalopram together with atypical antipsychotic in treating depression symptoms accompanied with acute schizophrenia.METHODS: 71 acute schizophrenia patients with depression were randomly assigned into two groups: the study group and the control group. Escitalopram, together with atypical antipsychotic, were given to patients in the study group; while only atypical antipsychotic were given to patients in the control group. The study period was 8 weeks. At the end of week 1, 2, 4, 8, BPRS, HAMD (as indicator of treatment effect) and TESS (as indicator of adverse effect) were assessed for all patients. The scores of BPRS and HAMD were analyzed using statistics package between the study group and the control group. The dosages of atypical antipsychotic, based on converted dosage of haloperidol, were compared between the two groups also.RESULTS: This study completed 68 observations. HAMD scores in the study group decreased starting from week 1, and were lower than those in the control group from week 2(the differences were significant), while HAMD scores in the control group did not decrease until week 4. At the end of week 2,4,8, BPRS scores in the study group decreased and were lower than those in the control group significantly . At the end of week 8, The recovery rate of study group (42.8%) was significantly higher than that of the control group(15.1%). 65.7% patients in the study group ameliorated while 51.5% patients did in the control group, the difference was not significantly. The average dosages (the peak dosage, the dosage during 8 weeks, and the dosage for week 8) in study group were significantly less than the control. The TESS scores in the study group were significantly less than the control at the week 2, 4, 8.CONCLUSION: Escitalopram together with atypical antipsychotic is able to cure the depression symptoms accompanied with schizophrenia rapidly and effectively. It is safe (with less adverse effect) also. Therefore, Escitalopram can be used as a cooperative medicine in the treatment of schizophrenia with depression symptoms.

Key words: Schizophrenia, Depression, Escitalopram, Treatment, Randomized controlled trial

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