论文部分内容阅读
目的探讨中药联合心理干预治疗产后抑郁的临床疗效。方法 112例产后抑郁患者,根据治疗方法不同分为研究组(采用中药联合心理干预治疗,60例)和对照组(采用心理干预治疗,52例)。比较两组患者治疗前后爱丁堡产后抑郁量表(EPDS)、焦虑自评量表(SAS)及抑郁自评量表(SDS)评分及治疗效果。结果研究组和对照组治疗前EPDS评分分别为(18.7±3.8)、(18.6±3.8)分,治疗后EPDS评分分别为(9.4±2.1)、(11.2±2.5)分,治疗后两组患者EPDS评分均较治疗前显著下降,且研究组低于对照组,差异具有统计学意义(P<0.05)。研究组患者治疗总有效率为95.0%,高于对照组的84.6%,差异具有统计学意义(P<0.05)。两组患者治疗后SDS评分及SAS评分均较治疗前显著下降,且研究组患者SDS评分及SAS评分均低于对照组,差异具有统计学意义(P<0.05)。结论在心理干预的基础上,给予中药治疗产后抑郁,能够显著改善焦虑、抑郁症状,提高临床疗效。
Objective To explore the clinical efficacy of traditional Chinese medicine combined with psychological intervention in the treatment of postpartum depression. Methods One hundred and twelve patients with postpartum depression were divided into study group (60 cases treated with traditional Chinese medicine combined with psychological intervention) and control group (52 cases treated with psychological intervention) according to different treatment methods. The Edinburgh Postnatal Depression Inventory (EPDS), Self-rating Anxiety Scale (SAS) and Self-rating Depression Scale (SDS) were compared between two groups before and after treatment. Results The scores of EPDS before and after treatment in the study group and the control group were (18.7 ± 3.8) and (18.6 ± 3.8), respectively. After treatment, the EPDS scores were (9.4 ± 2.1) and (11.2 ± 2.5) The score was significantly lower than before treatment, and the study group was lower than the control group, the difference was statistically significant (P <0.05). The total effective rate of the study group was 95.0%, which was higher than that of the control group (84.6%), the difference was statistically significant (P <0.05). After treatment, SDS score and SAS score decreased significantly in both groups, and the SDS score and SAS score of the study group were lower than those of the control group, the difference was statistically significant (P <0.05). Conclusion On the basis of psychological intervention, giving Chinese medicine treatment of postpartum depression can significantly improve anxiety and depression symptoms and improve clinical efficacy.