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August 25, 2025International Journal of Childbirth0 citations

Two Different Doses of Tranexamic Acid for Reduction of Perioperative Blood Loss in Cesarean Section: A Randomized Controlled Study

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AEAhmed M. ElewaMEMomen ElkerkaryOTOmima T. Taha

Key Points

  • No significant difference in perioperative blood loss was observed between the two doses of tranexamic acid in the study.
  • The trial involved 100 women undergoing cesarean delivery, receiving either 10 mg/kg or 20 mg/kg of tranexamic acid.
  • Patients were matched based on inclusion and exclusion criteria to ensure comparable characteristics across groups.
  • The findings suggest that both dose regimens are equally effective in reducing blood loss during cesarean delivery.

Abstract

BACKGROUND: Cesarean delivery is a widely practiced obstetric surgery associated with blood loss. Different measures were described to decrease perioperative blood loss. Tranexamic acid proved effective in decreasing blood loss among women undergoing cesarean delivery. This study aimed to evaluate the difference between two dose regimens of tranexamic acid on blood loss among women undergoing cesarean delivery. METHODS: This randomized clinical trial was conducted at the operating theater of Suez Canal University Hospital from August 20, 2022, to February 23, 2023. We recruited women undergoing cesarean delivery after matching particular inclusion and exclusion criteria. These women received 10 mg/kg (group 1) or 20 mg/kg (group 2) of tranexamic acid before the skin incision. The primary objective was the amount of blood loss between both groups. RESULTS: The general characteristics of the patients in the two groups were comparable but for body mass index (BMI). There was no discernible difference in the perioperative blood loss between both groups ( p value .123). Five patients in group 1 (received 10 mg/kg tranexamic acid) and two patients in group 2 (received 20 mg/kg tranexamic acid) developed postpartum hemorrhage (blood loss >1,000 ml). Nausea was significantly higher in group 1, 22 (32.8%), compared with 13 (19.4%) in group 2 ( p value .077). None of the participants developed thromboembolic complications. Linear regression analysis revealed no significant factors associated with high bleeding risk except BMI. CONCLUSION: There was no difference between the two doses in perioperative blood loss among women undergoing cesarean delivery. CLINICAL TRIAL REGISTRATION NUMBER: PACTR202208859856197.

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Cite This Study

Elewa et al. (2025) studied this question.

synapsesocial.com/papers/68af5f13ad7bf08b1eae1eb3https://doi.org/10.1891/ijc-2024-0058
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