Sringamwong Wirawan, Saokaew Surasak, Mongkhon Pajaree
Obstetrics and Gynecology Unit, Phayao Hospital, Thailand.
Department of Pharmaceutical Care, School of Pharmaceutical Sciences, University of Phayao, Phayao, Thailand.
Ann Med Surg (Lond). 2022 Jun 4;78:103931. doi: 10.1016/j.amsu.2022.103931. eCollection 2022 Jun.
The study analyzed an optimal misoprostol dosage in prevention of postpartum hemorrhage (PPH). Also evaluated the side effects that might be related to dose of misoprostol.
A randomised study was performed in mothers who received cesarean section. Participants were divided into 3 groups of 400, 600 and 800 μg intrauterine misoprostol insertion combined with oxytocin. Clinical characteristics, laboratory testing and operative data were collected. The primary outcome was the amount of intra-operative blood loss and side effects were assigned as a secondary outcome.
There were 357 eligible cases, 119 cases in each group equally. Baseline characteristics were similar in between groups. Higher misoprostol dosage demonstrated lower blood loss. Mean blood loss was 509.1, 465.7 and 441.1 ml in the 400, 600 and 800 μg misoprostol groups respectively which were significant difference (p value 0.027). Post-hoc pairwise t-tests found that 800 μg group diminished blood loss than 400 μg group (p value 0.004). Intra-operative blood loss ≥500 ml occurred less frequently in patients receiving higher misoprostol dosage (p value 0.035). However, PPH was not identified difference between groups (p value 0.707). Nausea and vomiting were complained in less than 1% while none of the cases exhibited shivering. Pyrexia was identified in all groups, however, there was a trend towards lower dosage related to less percentage of pyrexia.
Either 400, 600 or 800 μg of misoprostol can prevent PPH similarly. However, the study prefers 400 μg misoprostol because of minimization the side effects.
本研究分析了预防产后出血(PPH)的米索前列醇最佳剂量。同时评估了可能与米索前列醇剂量相关的副作用。
对接受剖宫产的母亲进行了一项随机研究。参与者被分为三组,分别在子宫内插入400、600和800μg米索前列醇并联合使用缩宫素。收集临床特征、实验室检查和手术数据。主要结局是术中失血量,副作用作为次要结局。
共有357例符合条件的病例,每组119例。各组间基线特征相似。米索前列醇剂量越高,失血量越低。400、600和800μg米索前列醇组的平均失血量分别为509.1、465.7和441.1ml,差异有统计学意义(p值0.027)。事后两两t检验发现,800μg组的失血量低于400μg组(p值0.004)。接受较高米索前列醇剂量的患者术中失血量≥500ml的发生率较低(p值0.035)。然而,各组间产后出血无差异(p值0.707)。恶心和呕吐的发生率低于1%,且无一例出现寒战。所有组均出现发热,但有剂量越低发热百分比越低的趋势。
400、600或800μg米索前列醇预防产后出血的效果相似。然而,由于副作用最小化,本研究倾向于使用400μg米索前列醇。