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

Blum Ms Gynuity Health Projects, New York, NY, United States|
Ngoc N.T.N. | Dzuba I.G. | Diop A. | Yalvac S. | Durocher J. | Dao B. | Dilbaz B. | Ramadan M.C. Center for Research and Consultancy in Reproductive Health, Ho Chi Minh City, Viet Nam| Raghavan S. MoH Etlik Zubeyde Hanim Women's Health Teaching and Research Hospital, Ankara, Turkey| Winikoff B. Department of Obstetrics and Gynecology, El-Gala Teaching Hospital, Cairo, Egypt|

The Lancet Số 9710, năm 2010 (Tập 375, trang 217-223)

ISSN: 1406736

ISSN: 1406736

DOI: 10.1016/S0140-6736(09)61923-1

Tài liệu thuộc danh mục: Scopus

Article

English

Từ khóa: misoprostol; oxytocin; adult; allergic reaction; article; Burkina Faso; clinical trial; controlled clinical trial; controlled study; diarrhea; double blind procedure; Egypt; female; fever; human; hysterectomy; major clinical study; maternal mortality; multicenter study; nausea; postpartum hemorrhage; priority journal; prophylaxis; randomized controlled trial; shivering; syncope; Turkey (republic); vaginal delivery; Viet Nam; vomiting; Administration, Sublingual; Adolescent; Adult; Developing Countries; Double-Blind Method; Female; Humans; Injections, Intravenous; Middle Aged; Misoprostol; Oxytocics; Oxytocin; Postpartum Hemorrhage; Pregnancy; Young Adult
Tóm tắt tiếng anh
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, 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 μg 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. Funding: The Bill & Melinda Gates Foundation. © 2010 Elsevier Ltd. All rights reserved.

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