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艾司西酞普兰快速剂量滴定治疗广泛性焦虑障碍的对照研究
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摘要
目的:观察艾司西酞普兰快速滴定能否加快起效速度及提高8周疗效。方法:将78例符合ICD-10广泛性焦虑障碍的患者随机分成艾司西酞普兰快速滴定组(1周内艾司西酞普兰加量至20mg/日)(n=36)和艾司西酞普兰常规滴定组(2周内艾司西酞普兰加量至20mg/日)(n=42),治疗持续8周,用广泛性焦虑量表-7(GAD-7)评定患者焦虑症状及疗效,同时用TESS和实验室检查评估治疗安全性。结果:治疗1,2,4,8周末快速滴定组GAD-7减分率均大于常规滴定组。第1,2,4,8周末艾司西酞普兰快速滴定组的治愈率分别为11.1%,27.8%,50%,72.2%,常规滴定组治愈率分别为2.4%,11.9%,23.8%,50.0%,第1,2,4,8周末艾司西酞普兰快速滴定组的有效率分别为33.3%,50%,63.9%,88.9%,常规滴定组有效率分别为11.9%,26.2%,42.9%,66.7%,快速滴定组疗效优于常规滴定组(P<0.05)。两组不良反应差异无显著性。结论:艾司西酞普兰快速滴定治疗广泛性焦虑障碍可以加快起效速度,提高8周整体疗效,同时不会显著增加药物不良反应。
Objective:To explore weather fast up-titration of escitalopram can make GAD patients response quicker and elevate the efficacy by the end of the 8 week.Methods:78 patients who meet ICD-10 criteria for GAD were divided into escitalopram fast up-titration group(n=36) and normal up-titration group(n=42) randomly.The trial lasted 8 weeks.The anxiety status and efficacy was evaluated with GAD-7(Generalized Anxiety Disorder Scale-7)on the baseline,I~(st),2~(th),4~(th),8~(th) weekend respectively and the safety was evaluated by TESS and laboratory examination.Results:The GAD-7 scores in fast up-titration group declined quicker than that in normal up-titration group by the end of 1~(st),2~(th),4~(th),8~(th) week(P<0.05) respectively.The remission rate of fast up-titration group is 11.1%,27.8%,50%,72.2%,and response rate is 33.3%,50%,63.9%,88.9%,while the remission rate of normal up-titration group is 2.4%,11.9%,38.4%,50.0%,and response rate is 11.9%,28.6%,42.9%,66.7%at the end of 1~(st),2~(th),4~(th),8~(th) weekend.The whole efficacy of fast up-titration group is better than normal up-titration group(P<0.05).The side effects of both groups have no significant difference(P>0.05).Conclusion:Fast up-titration of Escitalopram demonstrated to be more effective in the treatment of GAD,and response faster,while the safety is similar.
引文
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