Study protocol. TRAAP - TRAnexamic Acid for Preventing postpartum hemorrhage after vaginal delivery: a multicenter randomized, double-blind, placebo-controlled trial

被引:38
作者
Sentilhes, Loic [1 ]
Daniel, Valerie [2 ,3 ]
Darsonval, Astrid [2 ,3 ]
Deruelle, Philippe [4 ]
Vardon, Delphine [5 ]
Perrotin, Franck [6 ]
Le Ray, Camille [7 ,8 ]
Senat, Marie-Victoire [9 ]
Winer, Norbert [10 ]
Maillard, Francoise [8 ]
Deneux-Tharaux, Catherine [8 ]
机构
[1] Angers Univ Hosp, Dept Obstet & Gynecol, F-49933 Angers, France
[2] Angers Univ Hosp, Dept Pharm, F-49933 Angers, France
[3] Brest Univ Hosp, PPRIGO, Brest, France
[4] Jeanne Flandre Univ Hosp, Dept Obstet & Gynecol, Lille, France
[5] Caen Univ Hosp, Dept Obstet & Gynecol, Caen, France
[6] Tours Univ Hosp, Dept Obstet & Gynecol, Tours, France
[7] Cochin Univ Hosp, AP HP, Dept Obstet & Gynecol, Port Royal Matern Unit, Paris, France
[8] Paris Descartes Univ, Risks Pregnancy DHU, Ctr Epidemiol & Biostat,U1153, INSERM,Obstetr Perinatal & Pediat Epidemiol Res T, Paris, France
[9] Kremlin Bicetre Univ Hosp, AP HP, Dept Obstet & Gynecol, Paris, France
[10] Nantes Univ Hosp, Dept Obstet & Gynecol, Nantes, France
关键词
Postpartum hemorrhage; Treatment; Prevention; Tranexamic acid; Cesarean and vaginal deliveries; Thrombosis; ELECTIVE CESAREAN-SECTION; RENAL CORTICAL NECROSIS; REDUCING BLOOD-LOSS; 3RD STAGE; LABORATORY DETERMINATION; ACTIVE MANAGEMENT; VISUAL ESTIMATION; FIBRINOGEN; SEVERITY; EFFICACY;
D O I
10.1186/s12884-015-0573-5
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Background: Postpartum hemorrhage (PPH) is a major cause of maternal mortality, accounting for one quarter of all maternal deaths worldwide. Estimates of its incidence in the literature vary widely, from 3 % to 15 % of deliveries. Uterotonics after birth are the only intervention that has been shown to be effective in preventing PPH. Tranexamic acid (TXA), an antifibrinolytic agent, has been investigated as a potentially useful complement to uterotonics for prevention because it has been proved to reduce blood loss in elective surgery, bleeding in trauma patients, and menstrual blood loss. Randomized controlled trials for PPH prevention after cesarean (n = 10) and vaginal (n = 2) deliveries show that women who received TXA had significantly less postpartum blood loss without any increase in their rate of severe adverse effects. However, the quality of these trials was poor and they were not designed to test the effect of TXA on the reduction of PPH incidence. Large, adequately powered, multicenter randomized controlled trials are required before the widespread use of TXA to prevent PPH can be recommended. Methods and design: A multicenter, double-blind, randomized controlled trial will be performed. It will involve 4000 women in labor for a planned vaginal singleton delivery, at a term >= 35 weeks. Treatment (either TXA 1 g or placebo) will be administered intravenously just after birth. Prophylactic oxytocin will be administered to all women. The primary outcome will be the incidence of PPH, defined by blood loss >= 500 mL, measured with a graduated collector bag. This study will have 80 % power to show a 30 % reduction in the incidence of PPH, from 10.0 % to 7.0 %. Discussion: In addition to prophylactic uterotonic administration, a complementary component of the management of third stage of labor acting on the coagulation process may be useful in preventing PPH. TXA is a promising candidate drug, inexpensive, easy to administer, and simple to add to the routine management of deliveries in hospitals. This large, adequately powered, multicenter, randomized placebo-controlled trial seeks to determine if the risk-benefit ratio favors the routine use of TXA after delivery to prevent PPH.
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页数:13
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