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氨磺必利联合艾司西酞普兰治疗阴性症状为主的精神分裂症42例 被引量:9

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摘要 目的探讨氨磺必利联合艾司西酞普兰对阴性症状为主的精神分裂症患者的临床疗效、安全性及对STROOP执行功能的影响。方法将83例以阴性症状为主的精神分裂症患者按随机数字表法分为两组:单用氨磺必利组(对照组)41例,氨磺必利联合艾司西酞普兰组(治疗组)42例,疗程8周。于治疗前及治疗后4,8周末分别采用阳性和阴性症状量表(PANSS)评定临床疗效,不良反应症状量表(TESS)评定药物不良反应,于治疗前及治疗8周后采用STROOP色词干扰试验评定患者执行功能。结果治疗8周后两组PANSS总分、阴性因子分及STROOP干扰命名项均较治疗前有显著降低。治疗后第8周末,治疗组的PANSS总分(50.3±10.9)分及阴性因子分(22.9±5.9)分显著低于对照组的PANSS总分(55.1±12.1)分及阴性因子分(26.5±4.1)分,差异有统计学意义;治疗组STROOP干扰命名成绩(38.9±14.3)个高于对照组(33.1±12.2)个,差异有统计学意义。两组不良反应均为轻度,差异无统计学意义(P>0.05)。结论在临床疗效及改善STROOP执行功能上,氨磺必利联合艾司西酞普兰治疗阴性症状为主的精神分裂症均较单用氨磺必利好。
出处 《医药导报》 CAS 北大核心 2014年第8期1056-1058,共3页 Herald of Medicine
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