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利培酮联合丙戊酸钠治疗急性躁狂症疗效及安全性

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目的:对利培酮联合丙戊酸钠治疗急性躁狂症的临床效果及安全性进行观察分析。方法:根据平行分组方法将我院近年来收治的90例急性躁狂症患者分为观察组(利培酮联合丙戊酸钠)与参考组(利培酮),各为45例,分别在治疗前、7d、14d、28d对两组患者BRMS评分进行观察,比较两组患者治疗效果及不良反应发生率。结果:治疗前两组患者BRMS评分比较无统计学意义(P>0.05),治疗后观察组7d、14d、28dBRMS评分明显优于参考组(P<0.05);观察组治疗总有效率明显大于参考组(P<0.05);两组患者不良反应发生率比较无统计学意义(P>0.05)。结论:利培酮联合丙戊酸钠治疗急性躁狂症效果确切,安全性高,可推广使用。
Risperidone combined valproate for the treatment of acute mania clinical efficacy and safety were observed and analyzed. Methods: According to the paral el-group approach in recent years, our hospital admitted 90 cases of acute mania patients were divided into observation group (risperidone combined VPA) with the reference group (risperidone), each of 45 cases, respectively, in before treatment, 7d, 14d, 28d BRMS scores of the two groups were observed, treatment groups were compared and incidence of adverse reactions. Results:Before treatment, the patients showed no statistical y significant BRMS score (P> 0.05), after treatment, the observation group 7d, 14d, 28dBRMS score significantly better than the reference group (P <0.05); observation group was significantly greater than the total efficiency reference group (P <0.05); groups incidence of adverse reactions in patients with no significant difference (P> 0.05). Conclusion: Risperidone treatment of acute mania combined effect of valproate precise, safe, can be widely used.

risperidonevalproateacute maniaefficacysafety

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新疆乌鲁木齐市第四人民医院精六科 830002

利培酮 丙戊酸钠 急性躁狂症 疗效 安全性

2014

中外健康文摘
中国中医药报社

中外健康文摘

影响因子:0.016
ISSN:1672-5085
年,卷(期):2014.(10)
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