疏肝解郁胶囊联合西药治疗肝郁脾虚抑郁症的疗效观察
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摘要
目的:探讨肝郁脾虚型抑郁症患者应用疏肝解郁胶囊联合西药治疗临床疗效及其安全性进行评价,为临床诊断治疗提供一定的科学依据。方法:将本组纳入的132例肝郁脾虚型抑郁症患者根据随机数字表法随机分为对照组和观察组,每组各66例。对照组给予西药进行治疗,观察组在对照组治疗基础上结合疏肝解郁胶囊进行治疗;对比分析两组患者治疗后临床疗效、HAMD评分以及不良反应。结果:观察组治疗2个疗程后总有效率(89.39%)显著高于对照组(73.64%),且差异具有统计学意义(P<0.05);观察组治疗后HAMD评分(8.47±3.12)分显著低于对照组治疗后(13.18±2.39)分,且差异具有统计学意义(P<0.05);两组患者均未发生明显的不良反应。结论:肝郁脾虚型抑郁症患者应用疏肝解郁胶囊联合西药治疗临床疗效显著,不良反应少,临床上应用安全可靠,值得临床进一步推广应用。
Objective:To investigate the liver and spleen deficiency in patients with liver stagnation and depression application capsule combined with western medicine clinical efficacy and safety evaluation,to provide a scientific basis for clinical diagnosis and treatment.Methods:This group included 132 cases of liver and spleen deficiency in patients with depression were randomly divided into control group and observation group based on a random number table,66 cases in each group.Control group was given medicine for treatment,observation group combined liver qi stagnation capsules for treatment on the basis of the control group;comparative analysis of two groups of patients after clinical efficacy,HAMD score,and adverse reactions.Results:The total effective rate(89.39%) was significantly higher(73.64%) after 2 courses of treatment,and the difference was statistically significant(P<0.05);HAMD score after the observation group(8.47 ± 3.12) points significantly lower than in the control group(13.18 ± 2.39) points,and the difference was statistically significant(P<0.05);groups were no significant adverse reactions occur.Conclusion:Patients with depression liver qi stagnation liver spleen applications combined with western medicine capsule significant clinical efficacy,adverse reactions,the clinical application of safe,reliable,worthy of further clinical application.
引文
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