Treatment of post-partum haemorrhage with sublingual misoprostol versus oxytocin in women receiving prophylactic oxytocin: a double-blind, randomised, non-inferiority trial

被引:92
作者
Blum, Jennifer [1 ]
Winikoff, Beverly [1 ]
Raghavan, Sheila [1 ]
Dabash, Rasha [1 ]
Ramadan, Mohamed Cherine [2 ]
Dilbaz, Berna [3 ]
Dao, Blami [4 ]
Durocher, Jill [1 ]
Yalvac, Serdar [3 ]
Diop, Ayisha [1 ]
Dzuba, Ilana G. [1 ]
Ngoc, Nguyen Thi Nhu [5 ]
机构
[1] Gynu Hlth Projects, New York, NY 10010 USA
[2] El Gala Teaching Hosp, Dept Obstet & Gynecol, Cairo, Egypt
[3] MoH Etlik Zubeyde Hanim Womens Hlth Teaching & Re, Ankara, Turkey
[4] Ctr Hosp Souro Sanou, Dept Gynecol Obstet & Med Reprod, Bobo Dioulasso, Burkina Faso
[5] Ctr Res & Consultancy Reprod Hlth, Ho Chi Minh City, Vietnam
基金
比尔及梅琳达.盖茨基金会;
关键词
RECTALLY ADMINISTERED MISOPROSTOL; INTRAUTERINE MISOPROSTOL; MANAGEMENT;
D O I
10.1016/S0140-6736(09)61923-1
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background 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. Methods In this double-blind, non-inferiority trial, 31055 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 mu g 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. Findings 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. Interpretation 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.
引用
收藏
页码:217 / 223
页数:7
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