摘要
目的:观察八珍益母胶囊辅助治疗初产妇产后恶露不尽的临床效果。方法:选取2020年6月到2023年12月期间我院60例产后恶露不尽的初产妇,以随机数表法分为对照组(30例,少腹逐瘀颗粒治疗)与观察组(30例,联合八珍益母胶囊治疗),治疗2w后,观察两组患者产后恶露排出情况、凝血指标以及临床疗效。结果:观察组恶露持续时间约27 d,短于对照组30 d,恶露量明显少于对照组(P<0.05);治疗后,观察组凝血酶时间、活化部分凝血活酶时间、凝血酶原时间、纤维蛋白原水平正向改善程度优于对照组(P<0.05);观察组总有效率93.33%,较对照组高且差异显著(P<0.05)。结论:八珍益母胶囊辅助治疗初产妇产后恶露不尽效果显著,可缩短患者恶露持续时间,减少患者恶露量,改善患者凝血状态。
Objective:Observation of the clinical effect of Bazhen Yimu capsule as an adjuvant treatment for prolonged lochia in primiparous women after delivery.Methods:Sixty primiparous women with postpartum lochia were selected from June 2020 to December 2023 in our hospital.They were randomLy divided into a control group(30 cases,treated with Shaofu Zhuyu Granules)and an observation group(30 cases,treated with Bazhen Yimu Capsules)using a random number table method.After 2 weeks of treatment,the lochia excretion,coagulation indicators,and clinical efficacy of the two groups of patients were observed.Results:The duration of lochia in the observation group was shorter than that in the control group,and the amount of lochia was significantly less than that in the control group(P<0.05);After treatment,the observation group showed a better positive improvement in thrombin time,activated partial thromboplastin time,prothrombin time,and fibrinogen levels than the control group(P<0.05);The total effective rate of the observation group was higher than that of the control group and the difference was significant(P<0.05).Conclusion:Bazhen Yimu Capsules have a significant effect in assisting the treatment of lochia in primiparous women after childbirth,which can shorten the duration of lochia,reduce the amount of lochia,and improve the coagulation status of patients.
作者
柯文敏
Ke Wen-min(Department of Obstetrics and Gynecology,Duchang Maternal and Child Health Hospital,Jiujiang 332000,Jiangxi,China)
出处
《四川生理科学杂志》
2024年第5期1059-1061,共3页
Sichuan Journal of Physiological Sciences
关键词
八珍益母胶囊
少腹逐瘀颗粒
初产妇
产后恶露不尽
临床疗效
Bazhen Yimu Capsules
Shaofu Zhuyu Granules
Primiparous women
Prolonged postpartum lochia
Clinical efficacy
