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作 者:伍海姗[1] 常麦会[1] 李乐华[1] 赵靖平[1] 陈晋东[1] 潘腾苏[2] 谢世平[3] 陈斌[4] 陈艳卿[5] 赵振环[6] 高成阁[7] 杜波[8]
机构地区:[1]中南大学湘雅二医院精神卫生研究所,湖南长沙410011 [2]湖南省脑科医院,湖南长沙410007 [3]南京脑科医院,江苏南京210029 [4]北京安定医院,北京100088 [5]北京回龙观医院,北京100096 [6]广州市脑科医院,广东广州510370 [7]西安交通大学附属第一医院,陕西西安710061 [8]河北省精神卫生中心,河北保定071000
出 处:《中国新药与临床杂志》2011年第12期907-911,共5页Chinese Journal of New Drugs and Clinical Remedies
摘 要:目的评价国产艾司西酞普兰治疗抑郁症的疗效和安全性。方法本研究为多中心、开放性研究,共入组符合CCMD-3诊断标准的抑郁症患者238例,服用国产艾司西酞普兰片10~20 mg·d^(-1),疗程为6 wk。使用汉密尔顿抑郁量表17项(HAMD-17)、临床疗效总评量表(CGI,包括病情严重程度CGI-S、疗效总评CGI-I)分别在治疗wk 1、2、4、6末进行疗效评价,使用不良事件记录表并根据症状、体征、实验室和心电图检查结果评价药物安全性。结果共计232例完成研究,在各时点HAMD-17(P<0.01)、CGI-S(P<0.05)、CGI-I(P<0.01)的总分与治疗前比较,均有显著差异。总体有效率为82.8%,痊愈率为58.6%。不良反应发生率为11.2%,整体耐受性较好。结论国产艾司西酞普兰是一种安全、有效的抗抑郁药物。AIM To evaluate the clinical efficacy and safety of domestic escitalopram in the treatment of depression. METHODS Two hundred and thirty-eight patients met with CCMD-3 criteria of depressive disorder were included into the open, multicenter, six-week research with flexible dosages 10 - 20 mg. d-1 of escitalopram. The HAMD-17, CGI, adverse event rating scale and related laboratory examinations were used to assess the efficacy and safety of the treatment by the end of 1, 2, 4, 6 wk. RESULTS Two hundred and thirty-two patients completed the study. Results indicated a significant reduction in scores of HAMD-17 (P 〈 0.01 ), CGI- S (P 〈 0.05) and CGI-I (P 〈 0.01) in every treatment time points compared with those in baseline. The effective rate and cure rate was 82.8% and 58.6%, respectively. The adverse reaction rate was 11.2%, and all adverse reactions were well tolerated. CONCLUSION Generic escitalopram is an effective and safe antidepressant.
分 类 号:R749[医药卫生—神经病学与精神病学]
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