%0 Journal Article %T Effect of Intravenous Tranexamic Acid in Reducing Blood Loss during and after Elective Caesarean Section in a Third Level Health Institution: A Randomized Controlled Study %A Darlington Omawumi %A Emmanuel Oranu %A Rosemary Ogu %A Ngozi Orazulike %A Job Otokwala %J Open Journal of Obstetrics and Gynecology %P 265-279 %@ 2160-8806 %D 2023 %I Scientific Research Publishing %R 10.4236/ojog.2023.132028 %X Background: Blood loss during caesarean section (C/S) may lead to postpartum haemorrhage, and is one of the direct causes of maternal mortality and morbidity globally. Tranexamic acid is recommended in the treatment of postpartum haemorrhage (PPH) if oxytocin and other utertonics are ineffective in controlling PPH. In this centre it is not used prophylactically to reduce blood during caesarean section. Aim: To assess the effect of prophylactic intravenous tranexamic acid on blood loss during and after elective C/S at the University of Port Harcourt Teaching Hospital (UPTH). Methods: This was a prospective, single-blind, randomized, placebo-controlled interventional study conducted at the Obstetric theatre of UPTH from July 2020 to March 2021. Eligible women were randomized into two groups; seventy-two women received intravenous tranexamic acid while seventy-one women received a placebo. Socio-demographic data and the result of the study were collected through a proforma. Data collected was analyzed using Statistical Package for Social Sciences (SPSS) Version 22.0. The results were expressed in tables and charts as frequencies, percentages and mean. Chi-square test, Fisher¡¯s exact, and T-test were used to determine the relationship between variables. P-value ¡Ü 0.05 was considered statistically significant. Results: The findings showed that tranexamic acid significantly reduced mean blood loss during and after C/S (p-value < 0.01). The mean total blood loss from C/S to 2 hours post-surgery was significantly lower in the tranexamic acid group (624.88 ¡À 200.76 ml) in comparison to the placebo group (864.24 ¡À 229.09 ml), p-value = 0.001. The mean post-C/S packed cell volume (PCV) was significantly higher among the tranexamic acid group (30.68% ¡À 2.80%) in comparison to the placebo group (28.07% ¡À 3.27%), t = 5.131, p-value = 0.0001. The maternal side effects were nausea and vomiting, 9 (12.5%) and 1 (1.4%) participants respectively. Conclusion: