Hemorrhage remains the leading cause of maternal death worldwide. Tranexamic acid has been shown to reduce rates of hemorrhage when given prophylactically prior to cesarean delivery. It has also been shown to be an effective treatment in response to hemorrhage after a vaginal delivery. The aim of this study is to assess the impact of TXA on hemorrhage rates when given prophylactically prior to all deliveries.
Hemorrhage remains the leading cause of maternal mortality worldwide. In a 2014 systematic analysis of the causes of maternal death, the World Health Organization (WHO) noted that even in the face of interventions developed to actively manage the third stage of labor, 27.1% of maternal deaths were directly attributable to excessive blood loss. Risk factors for postpartum hemorrhage (PPH) have been identified, but the majority of cases occur in low risk women. As such, the routine use of oxytocin in the third stage of labor is recommended in all women and has been well documented to reduce the risk of excessive blood loss. Uterotonics such as methylergonovine, 15-methyl PGF2α and misoprostol have shown to be particularly useful adjuncts as decreased uterine tone is the most common etiology of blood loss. More recently, tranexamic acid (TXA) has been shown to be efficacious in the prevention of postpartum hemorrhage in certain cohorts. Tranexamic acid exerts its effect through the binding of plasmin and subsequent inhibition of fibrin degradation. It is regarded as pregnancy category B by the Food and Drug Administration (FDA).
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
PREVENTION
Masking
NONE
Infusion of Tranexamic Acid (Cyklokapron) to all consented women with the delivery of the anterior shoulder of the infant
Navy Medical Center
San Diego, California, United States
Incidence of postpartum hemorrhage
Postpartum hemorrhage
Time frame: Up to six weeks from date of delivery
Postpartum blood loss
Estimated blood loss (EBL)
Time frame: Up to six weeks from date of delivery
Percent decrease in hematocrit
Hematocrit percentage
Time frame: 6 hours after hemorrhage event and as clinically indicated up to six weeks from date of delivery
Number of units of packed red blood cells transfused
Number of units of packed red blood cells transfused
Time frame: Up to six weeks from date of delivery
Number of units of platelets transfused
Number of units of platelets transfused
Time frame: Up to six weeks from date of delivery
Number of units of fresh frozen plasma transfused
Number of units of fresh frozen plasma transfused
Time frame: Up to six weeks from date of delivery
Number of units of cryoprecipitate transfused
Number of units of cryoprecipitate transfused
Time frame: Up to six weeks from date of delivery
Amount of methylergonovine administered
Amount of methylergonovine administered
Time frame: Up to six weeks from date of delivery
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Amount of 15-methyl prostaglandin F2(PGF2) administered
Amount of 15-methyl prostaglandin F2(PGF2) administered
Time frame: Up to six weeks from date of delivery
Amount of misoprostol administered
Amount of misoprostol administered
Time frame: Up to six weeks from date of delivery
Amount of oxytocin administered
Amount of oxytocin administered
Time frame: Up to six weeks from date of delivery
Exploratory laparotomy following vaginal delivery due to hemorrhage
Exploratory laparotomy, no hysterectomy
Time frame: Up to six weeks from date of delivery
Exploratory laparotomy following cesarean delivery due to hemorrhage
Exploratory laparotomy, no hysterectomy
Time frame: Up to six weeks from date of delivery
Hysterectomy
Number of hysterectomies performed as a result of postpartum hemorrhage
Time frame: Up to six weeks from date of delivery
Intensive Care Unit (ICU) admission
Number of subjects admitted to Intensive Care Unit diagnosed with postpartum hemorrhage
Time frame: Up to six weeks from date of delivery
Maternal thromboembolic events
Incidence of maternal thromboembolic events
Time frame: up to six weeks from date of delivery
Diagnosis of intraventricular hemorrhage in the neonate
Neonatal outcome intraventricular hemorrhage
Time frame: Up to six weeks from date of delivery
Diagnosis of anemia in the neonate
Neonatal outcome anemia
Time frame: Up to six weeks from date of delivery
Diagnosis of disseminated intravascular coagulation (DIC) in the neonate
Neonatal outcome DIC
Time frame: Up to six weeks from date of delivery
Diagnosis of neonatal sepsis
Neonatal outcome sepsis
Time frame: Up to six weeks from date of delivery
Diagnosis of hypoxic-ischemic encephalopathy (HIE) in the neonate
Neonatal outcome HIE
Time frame: Up to six weeks from date of delivery
Diagnosis of a seizure disorder in the neonate
Neonatal outcome seizure disorder
Time frame: Up to six weeks from date of delivery
Diagnosis of arrhythmia in the neonate
Neonatal outcome arrhythmia
Time frame: Up to six weeks from date of delivery
Diagnosis of heart failure in the neonate
Neonatal outcome heart failure
Time frame: Up to six weeks from date of delivery
Diagnosis of renal failure in the neonate
Neonatal outcome renal failure
Time frame: Up to six weeks from date of delivery
Diagnosis of hepatic failure in the neonate
Neonatal outcome hepatic failure
Time frame: Up to six weeks from date of delivery
Diagnosis of thromboembolic events in the neonate
Neonatal outcome thromboembolic event
Time frame: Up to six weeks from date of delivery
Maternal mortality
Incidence of maternal mortality
Time frame: Up to six weeks from date of delivery
Additional tranexamic acid administered
Additional tranexamic acid administered
Time frame: Up to six weeks from date of delivery
Rate of Bakri/balloon tamponade use
Bakri/balloon tamponade use
Time frame: Up to six weeks from date of delivery