Gynuity Health Projects, New York, NY 10010, USA.
Lancet. 2010 Jan 16;375(9710):217-23. doi: 10.1016/S0140-6736(09)61923-1. Epub 2010 Jan 6.
Oxytocin, the gold-standard treatment for post-partum haemorrhage, needs refrigeration, intravenous infusion, and skilled providers for optimum use. Misoprostol, a potential alternative, is increasingly used ad hoc for treatment of post-partum haemorrhage; however, evidence is insufficient to lend support to recommendations for its use. This trial established whether sublingual misoprostol is non-inferior to intravenous oxytocin for treatment of post-partum haemorrhage in women receiving prophylactic oxytocin.
In this double-blind, non-inferiority trial, 31 055 women exposed to prophylactic oxytocin had blood loss measured after vaginal delivery at five hospitals in Burkina Faso, Egypt, Turkey, and Vietnam (two secondary-level and three tertiary-level facilities). 809 (3%) women were diagnosed with post-partum haemorrhage and were randomly assigned to receive 800 mug misoprostol (n=407) or 40 IU intravenous oxytocin (n=402). Providers and women were masked to treatment assignment. Primary endpoints were cessation of active bleeding within 20 min and additional blood loss of 300 mL or more after treatment. Clinical equivalence of misoprostol would be accepted if the upper bound of the 97.5% CI fell below the predefined non-inferiority margin of 6%. All outcomes were assessed from the time of initial treatment. This study is registered with ClinicalTrials.gov, number NCT00116350.
All randomly assigned participants were analysed. Active bleeding was controlled within 20 min after initial treatment for 363 (89%) women given misoprostol and 360 (90%) given oxytocin (relative risk [RR] 0.99, 95% CI 0.95-1.04; crude difference 0.4%, 95% CI -3.9 to 4.6). Additional blood loss of 300 mL or greater after treatment occurred for 139 (34%) women receiving misoprostol and 123 (31%) receiving oxytocin (RR 1.12, 95% CI 0.92-1.37). Shivering (152 [37%] vs 59 [15%]; RR 2.54, 95% CI 1.95-3.32) and fever (88 [22%] vs 59 [15%]; 1.47, 1.09-1.99) were significantly more common with misoprostol than with oxytocin. Six women had hysterectomies and two women died.
Misoprostol is clinically equivalent to oxytocin when used to stop excessive post-partum bleeding suspected to be due to uterine atony in women who have received oxytocin prophylactically during the third stage of labour.
缩宫素是产后出血的金标准治疗药物,但它需要冷藏、静脉输注,并且需要专业医护人员才能达到最佳效果。米索前列醇是一种潜在的替代品,越来越多地被临时用于治疗产后出血;然而,目前还没有足够的证据支持其使用。本试验旨在确定舌下含服米索前列醇是否不劣于静脉注射缩宫素,用于治疗接受预防性缩宫素治疗的产后出血女性。
在这项双盲、非劣效性试验中,来自布基纳法索、埃及、土耳其和越南的 5 家医院的 31055 名接受预防性缩宫素治疗的女性在阴道分娩后测量了失血量(有 2 家为二级医院,3 家为三级医院)。809 名(3%)女性被诊断为产后出血,并随机分配接受 800μg米索前列醇(n=407)或 40IU 静脉注射缩宫素(n=402)。医护人员和女性对治疗方案均不知情。主要终点是在 20 分钟内停止活动性出血,以及治疗后额外失血 300ml 或更多。如果 97.5%CI 的上限低于预先设定的非劣效性边界 6%,则接受米索前列醇的临床等效性。所有结果均从初始治疗时间开始评估。本研究在 ClinicalTrials.gov 注册,编号为 NCT00116350。
所有随机分配的参与者均被纳入分析。接受米索前列醇治疗的 363 名(89%)和接受缩宫素治疗的 360 名(90%)女性在初始治疗后 20 分钟内控制了活动性出血(相对风险 [RR]0.99,95%CI0.95-1.04;粗差值 0.4%,95%CI-3.9 至 4.6)。接受米索前列醇治疗的 139 名(34%)和接受缩宫素治疗的 123 名(31%)女性在治疗后额外失血 300ml 或更多(RR1.12,95%CI0.92-1.37)。接受米索前列醇治疗的 152 名(37%)和接受缩宫素治疗的 59 名(15%)女性出现了明显更多的寒战(RR2.54,95%CI1.95-3.32)和发热(RR1.47,95%CI1.09-1.99)。
在接受预防性缩宫素治疗的产妇中,当怀疑产后出血是由于子宫收缩乏力时,米索前列醇在停止过度产后出血方面与缩宫素具有临床等效性。