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作 者:张传海[1] 贺朝晖[1] 孙玉军[1] 王鹏举[1] 徐建龙[1] 吴鹏飞[1]
出 处:《中国健康心理学杂志》2013年第11期1629-1631,共3页China Journal of Health Psychology
基 金:2011年昆山市科技局指令性项目(编号:ks153)
摘 要:目的 观察喹硫平单药治疗躯体形式障碍的临床疗效、副反应.方法 选取我院门诊符合CCMD-3躯体形式障碍诊断标准患者按来院次序分为A(喹硫平单药)、B(文拉法辛单药)、C(喹硫平与文拉法辛合用)3组,每组各30例.分别给予喹硫平单药25~200mg/d、文拉法辛单药75~ 225 mg/d、喹硫平25~200mg/d与文拉法辛75~225mg/d合用治疗.治疗前与治疗第4、8周后评定症状自评量表(SCL-90),副反应量表(TESS).结果 3组SCL-90总分及各因子分评分在治疗4、8周后与治疗前比较差异有统计学意义(P<0.01).在4、8周后躯体化及总分方面,3组组间两两比较差异有统计学意义(P<0.01),合并用药组优于文拉法辛组,文拉法辛组优于喹硫平组.TESS无统计学意义.结论 喹硫平单药治疗躯体形式障碍疗效肯定,但疗效弱于文拉法辛单药,喹硫平与文拉法辛合用疗效最好,副反应相当.Objective To observe the clinical efficacy and side effects of quetiapine monotherapy in the treatment of somatoform disorders. Methods Patients in accordance with CCMD -3 with somatoform disorder diagnosis standard in our hospital outpatient service were divided into A (quetiapine), B (venlafaxine), C (quetiapine and venlafaxine)3 groups according to the visiting order, each group 30 cases, quetiapine 25 to 200 mg,venlafaxine 75 - 225 mg,25 ~ 200 mg of quetiapine and venlafaxine 75 - 225 mg of the treatment. Before and 4,8 weeks after treatment, SCL - 90 and TESS were used to assess . Results There were significant differences in SCL - 90 total score and factor scores of three groups between before treatment and in 4 weeks and 8 weeks after treatment(P 〈 0.01 ). In 4 weeks and 8 weeks after treatment, there were significant differences in SCL -90 total score and somatization among three groups (P 〈 O. 01 ) ,the drug combination group was better than the venlafaxine group, the venlafaxine group was better than the quetiapine group. There was no statistical significance in TESS (P 〉 0. 05). Conclusion Quetiapine monotherapy has certain curative effect in the treatment of somatoform disorders, but it is worse than venlafaxine, quetiapine with venlafaxine,their side effects are the same.
关 键 词:精神卫生 躯体形式障碍 随机对照试验 喹硫平 文拉法辛
分 类 号:R749[医药卫生—神经病学与精神病学]
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