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Purpose: To evaluate the effects of intravenous tranexamic acid (TA) and sublingual misoprostol on reducing bleeding after cesarean section.
Materials: One hundred and fifty-eight participants with term pregnancies scheduled for cesarean section were randomly divided into two groups. In M group, two sublingual misoprostol pills (400 mg) were administrated, immediately after the delivery. In TA group, ten minutes before skin incision, TA ampoule (1 g) was injected. In both groups, immediately after the delivery, 20 units of oxytocin in 1 L ringer lactate with speed of 1000 CC/h was injected. At the end of the operation, the amount of bleeding was measured based on the number of small and large gauzes, the blood in the suction container and the difference of patient's hemoglobin before and 24 h after surgery.
Results: Hemoglobin level reduction in the TA group was higher than the M group (- 2.45 ± 0.84 vs - 2.14 ± 1.38 g/dL) ( < 0.001). Furthermore, number of used gauze and blood suction in the TA group was significantly higher compared to sublingual misoprostol (4.67 ± 1.34 vs 3.25 ± 1.31 and 260.25 ± 79.06 vs 193.94 ± 104.79 cc, respectively) ( < 0.001). Mean blood pressure during the entire duration of surgery in the TA group decreased significantly as compared to the M group ( < 0.001).
Conclusion: Total bleeding was significantly lower in sublingual misoprostol as compared to the tranexamic acid group. Furthermore, in misoprostol group hemodynamic variables were stabilized greater than tranexamic acid group.
Registration Number: IRCT201708308611N6.
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http://dx.doi.org/10.1007/s13224-018-1181-x | DOI Listing |
J Surg Case Rep
April 2025
School of Medicine, College of Health Sciences, Addis Ababa University, Tikur Anbessa Specialized Hospital, Churchill Avenue, Lideta Sub-City, PO Box 5657, Addis Ababa, Ethiopia.
Misoprostol, a prostaglandin E1 analog, is widely used in obstetrics for abortion induction and labor management. Although generally safe, it can lead to rare complications such as uterine rupture, even in patients without prior uterine scarring. This case report describes a 27-year-old gravida 3, para 1 woman with no history of uterine surgery who presented with a second-trimester missed septic abortion.
View Article and Find Full Text PDFEur J Obstet Gynecol Reprod Biol X
March 2025
Tabriz University of Medical Sciences, Tabriz, Iran.
Background: The efficacy of different uterotonic agents is yet to be determined.
Methods: This was a randomized clinical trial on 240 pregnant mothers with a history of cesarean section in three groups: A: sublingual misoprostol and oxytocin, B: intrauterine misoprostol and oxytocin, and C: a higher dose of oxytocin alone. The intrapartum blood loss and the estimated blood loss within 24 h after surgery were compared between the groups.
Proc (Bayl Univ Med Cent)
January 2025
Department of Anesthesiology, Baylor Scott & White Medical Center - Temple, Temple, Texas, USA.
Objective: We hypothesized that patients who underwent cesarean delivery and received oxytocin boluses followed by an infusion would have a lower incidence of secondary uterotonic administration compared to patients who had an oxytocin infusion without boluses.
Methods: Patients who had cesarean deliveries at our hospital from September 1, 2021 through December 31, 2021 and from September 1, 2022 through December 31, 2022, corresponding to the oxytocin bolus and oxytocin infusion cohorts, respectively, were included. Patient demographic, physical, and clinical characteristic data were collected by a study investigator.
Eur J Contracept Reprod Health Care
April 2025
Department of Obstetrics & Gynecology, PGIMER, Chandigarh, India.
Primary Objective: A randomized study to compare the induction abortion interval (IAI) using two different routes of Low-dose misoprostol administration Sublingual (S/L) and vaginal, after priming with two sequential doses of mifepristone for second-trimester medical abortion.
Study Design: After randomization in two groups, participants received two doses of mifepristone (200 mg) 24 h apart. On day 3, 200mcg of misoprostol was given by S/L route to group 1 and by vaginal route to group 2, (400mcg among women with gestation ≤16 weeks) and every 6 hours for a maximum of 3 doses.