School of Clinical medicine, Hospital of Chengdu University of Traditional Chinese Medicine, Chengdu, China.
Department of Gynecology and Obstetrics, East ward of Sichuan Provincial People's Hospital, Chengdu, China.
Explore (NY). 2020 Mar-Apr;16(2):110-115. doi: 10.1016/j.explore.2019.08.004. Epub 2019 Aug 13.
The aim of this study was to evaluate the efficacy and safety of motherwort injection (MI, Yi mu cao) in preventing post-abortion hemorrhage and promoting uterine retraction after induced abortion surgery.
In this multi-center randomized controlled trial undertaken between September 2014 and August 2016, 408 child-bearing age women who underwent induced abortion surgery and randomly assigned to two groups: MI group who received intramuscular MI treatment (n = 207) and no-treatment group (n = 201). The volume of vaginal bleeding and its duration were used as primary end points; and uterine size and dimension were measured as secondary end points. Blood coagulation indices, routine blood and adverse events were recorded to evaluate the safety.
The efficacy analysis was based on 366 patients. No significant difference were found in baseline characteristics between the two groups (P > 0.05). The amount of vaginal bleeding and duration of bleeding were significantly reduced in MI group compared with on-treatment group in Full Analysis Set (FAS) and Per Protocol Set (PPS) populations (P < 0.001). The volume and perimeter of the uterine dimensions in MI group were smaller than no-treatment group (P < 0.001). No significant abnormal vital signs were observed. Only 1 case of mild, transient erythema was found in MI group.
MI could reduce post-abortion hemorrhage and improve uterine retraction in women undergoing surgical induced abortion, without serious adverse events. It was a safe and effective treatment in preventing post-abortion hemorrhage after induced abortion.
本研究旨在评估益母草注射液(MI,益母草)在预防流产后出血和促进流产术后子宫收缩方面的疗效和安全性。
这是一项多中心随机对照试验,于 2014 年 9 月至 2016 年 8 月进行,将 408 名育龄期妇女随机分为 MI 组(n=207)和对照组(n=201)。以阴道出血量和持续时间为主要终点,子宫大小和形态为次要终点。记录凝血指标、血常规和不良反应,以评估安全性。
疗效分析基于 366 例患者。两组患者基线特征无显著差异(P>0.05)。MI 组在全分析集(FAS)和符合方案集(PPS)人群中,阴道出血量和出血持续时间均显著低于对照组(P<0.001)。MI 组子宫形态的体积和周长均小于对照组(P<0.001)。未观察到明显的生命体征异常。仅 MI 组 1 例出现轻度、短暂的红斑。
MI 可减少人工流产术后出血,促进子宫收缩,无严重不良事件。MI 是一种预防人工流产后出血的安全有效的治疗方法。