Am J Perinatol 2013; 30(05): 407-414
DOI: 10.1055/s-0032-1326986
Original Article
Thieme Medical Publishers 333 Seventh Avenue, New York, NY 10001, USA.

Can Intravenous Injection of Tranexamic Acid Be Used in Routine Practice with Active Management of the Third Stage of Labor in Vaginal Delivery? A Randomized Controlled Study

Kemal Gungorduk
1   Mardin Women and Children Hospital, Mardin, Turkey
,
Osman Asıcıoğlu
2   Department of Obstetrics and Gynecology, Kanuni Sultan Süleyman Teaching Hospital, Istanbul, Turkey
,
Gokhan Yıldırım
2   Department of Obstetrics and Gynecology, Kanuni Sultan Süleyman Teaching Hospital, Istanbul, Turkey
,
Cemal Ark
2   Department of Obstetrics and Gynecology, Kanuni Sultan Süleyman Teaching Hospital, Istanbul, Turkey
,
Ali İsmet Tekirdağ
2   Department of Obstetrics and Gynecology, Kanuni Sultan Süleyman Teaching Hospital, Istanbul, Turkey
,
Berhan Besımoglu
2   Department of Obstetrics and Gynecology, Kanuni Sultan Süleyman Teaching Hospital, Istanbul, Turkey
› Author Affiliations
Further Information

Publication History

02 February 2012

24 May 2012

Publication Date:
21 September 2012 (online)

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Abstract

Objective To estimate the effects of adding intravenous tranexamic acid (TA) to the standard active management of third-stage labor to reduce vaginal blood loss during the third and fourth stages of labor.

Study Design A prospective, double-blind, equivalence randomized, controlled study was performed. Women were randomly allocated to receive an intravenous infusion of TA (experimental group, n = 228) or 5% glucose (placebo group, n = 226) at delivery of the anterior shoulder. Active management of the third stage of labor, which includes prophylactic injection of 10 IU of oxytocin within 2 minutes of birth, early clamping of the umbilical cord, and controlled cord traction following delivery, was used in both groups. The primary outcome was mean blood loss during the third and fourth stages of labor.

Results Mean estimated blood loss at the third and fourth stages of labor was significantly lower in the experimental group than that in the placebo group (261.5 ± 146.8 mL versus 349.98 ± 188.85 mL, respectively; p < 0.001). The frequency of postpartum hemorrhage > 500 mL was also lower in the experimental group (4, 1.8%) compared with that in the placebo controls (15, [6.8%]; relative risk, 3.76; 95% confidence interval, 1.27 to 11.15; p = 0.01). No episode of thrombosis occurred in the women who received TA.

Conclusions The use of TA with standard active management of the third stage of labor reduced postpartum blood loss, and no increase in the incidence of thromboembolic events was observed.

Clinical Trial Registration

This trial is registered at clinicaltrials.gov (NCT01338454).