Effect of Intravenous Tranexamic Acid Administration on Blood Loss during and after Caesarean Delivery: A Randomised Controlled Study
Introduction: India remains a major contributor to maternal deaths in the world. Haemorrhage after delivery (both vaginal & caesarean) is the leading cause. To reduce the haemorrhage, oxytocics are routinely used. In heavy bleeding, blood transfusion may be required and in few cases obstetri...
Main Authors: | , , |
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Format: | Article |
Language: | English |
Published: |
JCDR Research and Publications Pvt. Ltd.
2020-10-01
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Series: | International Journal of Anatomy Radiology and Surgery |
Subjects: | |
Online Access: | http://www.ijars.net/articles/PDF/2565/44228_CE[Ra1]_F(SHU)_PF1(Kri_SHU)_PFA(SHU)_GC(SHU)_PN(SHU).pdf |
Summary: | Introduction: India remains a major contributor to maternal
deaths in the world. Haemorrhage after delivery (both vaginal
& caesarean) is the leading cause. To reduce the haemorrhage,
oxytocics are routinely used. In heavy bleeding, blood transfusion
may be required and in few cases obstetric hysterectomy may
have to be done. Tranexamic Acid (TXA) injection has been
shown to be very effective in reducing blood loss in various
surgeries including Caesarean Section (CS).
Aim: To know the efficacy of intravenous TXA administration
in reducing blood loss during and 2 hours after caesarean
delivery.
Materials and Methods: This study was a randomised, placebo
controlled, clinical study in which patients scheduled for CS in
the District Hospital, Nadia were randomised into two groups,
using a random number table list to receive either 1 gm (in 10 mL)
of intravenous TXA dissolved in 20 mL of 5% dextrose solution
(study group; n=50) or placebo, i.e., 30 mL of 5% dextrose
solution (control group; n=50). Infusion was given 20 minutes
before spinal anaesthesia. Categorical (number & percentage of
patients) and continuous (Mean±Standard Deviation) variables
were compared across the groups using the Chi-Square test for
Independence of Attributes and unpaired t-test, respectively.
Results: The mean intraoperative, postoperative and total blood
loss were significantly lower in the study group (512.58, 65.06 &
577.64 mL, respectively) than the control group (731.68, 114.82
& 846.5 mL, respectively), p-value <0.001. There were five cases
(10%) with postpartum haemorrhage in control group, requiring
excess (>35 units) oxytocin infusion. There was significant
difference in pre and postoperative pallor (24 vs 37 patients in
study & control group respectively, p-value- 0.008), pulse rate
(mean difference 4.96/min in study group & 11.14/min in control
group, p-<0.001), haemoglobin (mean difference 0.13 gm% in
study & 1.28 gm% in control group, p-<0.001) level & packed cell
volume (mean difference 1% in study group & 3.34% in control
group, p-<0.001). Other vital parameters were not comparable.
None of the babies required admission in Neonatal Intensive
Care Unit (NICU). No sign of thrombosis was noted in any mother
of either group. Incidence of postoperative nausea (15 and 12
patients in study & control groups, p -0.499), vomiting (10 and 9
patients in study & control groups, p=0.799) were insignificant.
No cases of diarrhoea occurred in any group.
Conclusion: Preoperative treatment with intravenous TXA
significantly reduces blood loss related to caesarean delivery
without any significant adverse effects to both mother and
newborn. |
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ISSN: | 2277-8543 2455-6874 |