Document Type : Original Article
Authors
Obstetrics and Gynecology Department, Faculty of Medicine, Al-Azhar University
Abstract
Keywords
Main Subjects
ROLE OF PROPHYLACTIC TRANEXAMIC ACID IN REDUCING BLOOD LOSS DURING ELECTIVE CESAREAN SECTION
By
Ahmed Mohamed El-Seadawy Ghanem, Mofeed Fawzy Mohamed, and Samir Khamis Galal
Obstetrics and Gynecology Department, Faculty of Medicine, Al-Azhar University
E-mail: elseadawy855@gmail.com.
ABSTRACT
Background: Post-partum hemorrhage (PPH) is a major cause of maternal mortality globally. Tranexamic acid, an anti-fibrinolytic agent is an attempt to prevent this complication.
Objective: To identify the efficacy of intravenous (IV) tranexamic acid in reducing blood loss during elective cesarean section (CS).
Patients and Methods: A Randomized Controlled Study was conducted on 200 women undergoing cesarean section. They were allocated to either Study or Control group by computer generated random number tables. Tranexamic acid (TXA) was given prior to surgery in study group in addition to the routine care (10 units of oxytocin added to the intravenous drip soon after baby delivery), whereas the control group had routine care alone. Blood loss was measured in both groups. Hemoglobin before and after surgery was estimated, and the percentage of difference was compared.
Results: There was a significant reduction in blood loss calculated from placental delivery till end of surgery: 391.95 ml in study group versus 633 ml in control group (p<0.000). Another parameter studied was the percentage of fall in hemoglobin before and after surgery. Postoperative hemoglobin was significantly higher in study group than control group (p<0.000); Reduction in hemoglobin was significantly less in study group than control group by (0.76 ± 0.29 gm/dl) (p<0.000). There were no immediate post-operative complications to the mother and neonate.
Conclusion: Tranexamic acid (TXA) significantly reduced the amount of blood loss during Elective Cesarean Section (CS). Use of TXA was not associated with adverse effects. Thus, TXA can be used safely and effectively in subjects undergoing CS.
Keywords: Fibrinolysis, Hemoglobin, Hemorrhage, Morbidity, Prevention, TXA.
INTRODUCTION
Cesarean section (CS) rate has increased in both developed and developing countries, which would result in an increased risk of PPH. Deaths due to PPH remain relatively common in some parts of the world. To lower this occurrence, it is very vital to reduce blood loss in CS (IKarnbo et al., 2012).
Management of hemorrhage after CS may range from administration of oxytocic and blood transfusion to more radical measures such as hysterectomy and use of anti-fibrinolytic agent such as tranexamic acid (TXA) (Ray et al., 2017).
A systematic review of randomized controlled trials of anti-fibrinolytic agents in elective surgical patients identified 211 randomized controlled trials. Prohaemostatic drugs such as Tranexamic acid provide a complementary biochemical haemostatic effect to the well proven uterotonics, especially oxytocin. Systemic anti-fibrinolytic agents are widely used in surgery (Henry et al., 2015).
Tranexamic acid has been shown to reduce uterine blood loss in non-surgical aspect. A study done on women with menorrhagia has showed significant reduction in mean menstrual blood loss in those treated with Tranexamic acid (Matteson et al., 2013).
The results showed that Tranexamic acid reduced the risk of blood transfusion by 39%. Tranexamic acid is an analogue of lysine that inhibits fibrinolysis by competitively binding to plasminogen. It prevents the lysis of formed clot by inhibiting activation of plasminogen and plasmin. It is ten times more potent than Amino- caproic acid (Viswanath et al., 2015).
Several Randomised controlled trials have analysed the prophylactic role of Tranexamic acid and have shown significant results in reducing blood loss, Tranexamic acid might reduce the need for hysterectomy, reduce the risk of severe anaemia and avoid the need for blood transfusion; hence, this could contribute significantly to the goal of reducing maternal mortality (Movafegh et al., 2011).
This work aimed to identify the efficacy of intravenous (IV) tranexamic acid in reducing blood loss during elective cesarean section (CS).
PATIENTS AND METHODS
A Randomized Controlled Study established in the branch of Obstetrics and Gynecology at Al-Hussein University Hospital and Mabrra Elmahalla Health Insurance from the first of May 2020 to the first of December 2020.
Inclusion Criteria:
• Parity not more than two.
• Singleton pregnancy.
• Delivery by elective LSCS.
• Subjects of age between 18 and 37 years.
• Gestational age of 37 to 42 weeks of pregnancy.
Exclusion Criteria:
• Parity more than two.
• Twin pregnancy.
• Vaginal delivery or urgent C.S.
• Subjects of age less than 18 or more than 37.
• Subjects having medical problems like gestational hypertension, chronic hypertension and severe pre-eclampsia, renal disease, heart disease complicating pregnancy and having coagulation disorders.
• Subjects allergic to Tranexamic acid by previous history of allergy to it.
• Subjects with history of thromboembolic disorders.
• Subjects having tendency for increased bleeding like abnormal placentation, multiple pregnancy, polyhydramnios, previous two or more cesarean sections, and those who had blood transfusion due to anemia.
Blood loss was measured in both groups following placental delivery till the end of surgery. Blood collected in the suction container was noted, Soaked mops and operation table perineal sheet were weighed by electronic scale before and after the surgery. Blood collected in suction container, Amniotic fluid and the volume of blood lost before placental delivery were not included in the study. Hemoglobin and hematocrite value before and after surgery were estimated, and the percentage of difference was compared.
Participant:
The study was conducted among subjects at the Department of Obstetrics and Gynecology of Al-Hussein University Hospital and Mabrra Elmahalla Health Insurance who were to undergo elective cesarean section, after confirming the eligibility criteria for inclusion. All women had given a written consent after they were informed about the study aims and benefits. This research included 200 pregnant women who were divided into 2 equal groups:
Group I: Tranexamic acid was given prior to surgery in study group in addition to the routine care (10 units of oxytocin added to the intravenous drip soon after baby delivery).Tranexamic acid injection was prepared by diluting 1g (10ml) TXA in 100 ml of normal saline. TXA was administrated as intravenous infusion (over 15minutes) at least 20 minutes prior to skin incision.
Group II: Control group who had routine care alone.
Statistical analysis:
Information were gathered, amended, implicit and entered to the Factual Bundle for Sociology (IBM SPSS) variant 20 (statistical package for the social sciences) data were summarized as mean±Standed deviation, range and percentage. Both independent and paired t-test or Mann-Whitney U test were used for comparison of means. Chi square for comparison of qualitative data the P-value was considered significant when p ≤ 0.05.
RESULTS
This work included 200 pregnant women, divided into study (tranexamic) and control groups. No Significant difference between tranexamic and control groups regarding maternal age and gestational age, medical history, drug allergy, parity and gravidity (Table 1).
Table (1): Comparison between tranexamic and control groups regarding to maternal age, gestational age (GA), medical history, drug allergy, parity and gravidity
Groups Parameters |
Group 1 |
Group 2 |
P-value |
|
No. = 100 |
No. = 100 |
|||
Maternal age |
Mean ± SD |
28.51 ± 3.42 |
29.15 ± 3.64 |
0.202 |
Range |
23 – 37 |
23 – 37 |
||
Gravidity |
PG |
39 (39.0%) |
35 (35.0%) |
0.838 |
2 |
52 (52.0%) |
55 (55.0%) |
||
3 |
9 (9.0%) |
10 (10.0%) |
||
Parity |
0 |
39 (39.0%) |
35 (35.0%) |
0.769 |
1 |
55 (55.0%) |
60 (60.0%) |
||
2 |
6 (6.0%) |
5 (5.0%) |
||
Gestational age |
Mean ± SD |
38.34 ± 0.68 |
38.25 ± 0.54 |
0.301 |
Range |
37 – 40 |
37 – 39 |
||
Medical history |
Negative |
100 (100.0%) |
100 (100.0%) |
– |
Drug allergy |
Negative |
100 (100.0%) |
100 (100.0%) |
– |
There was a significant difference between tranexamic acid group and control group regarding blood loss from placental delivery to the end of the surgery (Table 2).
Table (2): Comparison between tranexamic and control groups regarding blood loss from placental delivery to the end of the surgery (mL)
Groups Blood loss |
Group 1 |
Group 2 |
P-value |
No. = 100 |
No. = 100 |
||
Mean ± SD |
391.95 ± 33.54 |
633 ± 16.55 |
<0.001 |
Range |
340 – 460 |
600 – 660 |
There was no significantly difference between two groups regarding preoperative hemoglobin, while there was a significant difference between tarnexamic group and control group regarding postoperative hemoglobin (Table 3).
Table (3): Comparison between tranexamic and control groups regarding hemoglobin (g/dL)
Groups Parameters |
Group 1 |
Group 2 |
P-value |
|
No. = 100 |
No. = 100 |
|||
Hb before |
Mean ± SD |
10.91 ± 1 |
11.14 ± 0.96 |
0.099 |
Range |
8.5 – 12.9 |
8.8 – 13 |
||
Hb after |
Mean ± SD |
10 ± 1.05 |
9.48 ± 0.91 |
<0.001 |
Range |
7.9 – 12.3 |
7.3 – 11.5 |
||
Paired t-test |
T |
14.890 |
52.579 |
|
P-value |
<0.001 |
<0.001 |
There was a significant difference between tranexamic group and control group regarding hemoglobin reduction (Table 4).
Table(4): Comparison between tranexamic and control groups regarding hemoglobin reduction g/dl
Groups HB difference |
Group 1 |
Group 2 |
P-value |
No. = 100 |
No. = 100 |
||
Mean ± SD |
-0.91 ± 0.61 |
-1.67 ± 0.32 |
0.001 |
Range |
-2.2 – 0.4 |
-2.7 – -1.3 |
There was no significantly difference between two groups regarding preoperative hematocrit value, while there was a significant difference between tranexamic group and control group regarding postoperative hematocrit value (Table 5).
Table (5): Comparison between tranexamic and control groups regarding hematocrit percent
Groups Parameters |
Group 1 |
Group 2 |
P-value |
|
No. = 100 |
No. = 100 |
|||
Haemtocrite before |
Mean ± SD |
34.68 ± 3.32 |
34.15 ± 2.8 |
0.220 |
Range |
26.5 – 42.1 |
26.1 – 42.1 |
||
Haemtocrite after |
Mean ± SD |
29.86 ± 3.09 |
28.62 ± 2.76 |
0.003 |
Range |
21.7 – 35 |
24 – 37 |
||
Paired t-test |
T |
52.402 |
25.804 |
|
P-value |
<0.001 |
<0.001 |
There was a significant difference between tranexamic group and control group regarding hematocrit reduction (Table 6).
Table (6): Comparison between tranexamic and control groups regarding hematocrit reduction (%)
Groups Haemtocrite difference |
Group 1 |
Group 2 |
P-value |
No. = 100 |
No. = 100 |
||
Mean ± SD |
-4.82 ± 0.92 |
-5.52 ± 2.14 |
0.003 |
Range |
-7.1 – -3 |
-12.2 – 2.4 |
DISCUSSION
Obstetric hemorrhage remains one of the major causes of maternal death in both developed and developing countries. Because of its importance as a leading cause of maternal mortality and morbidity, and because of evidence of substandard care in the majority of fatal cases, obstetric hemorrhage must be considered as a priority topic for national research development (Ducloy-Bouthors et al., 2016).
During placental delivery, fibrinogen and fibrin are rapidly degraded, whereas plasminogen activators and fibrin degradation products increase due to activation of the fibrinolytic system. This activation can last up to 6-10 h postpartum; causing more bleeding. Tranexamic acid competitively inhibits activation of plasminogen; thereby reducing conversion of plasminogen to plasmin (fibrinolysin).The antifibrinolytic potency of tranexamic acid was approximately 5 to 10 times that of aminocaproic acid. It was used in gynecological bleeding and major trauma (Viswanath et al., 2015).
Our study showed significant difference between tranexamic and controls as regards to blood loss and hemoglobin difference.
In our study, there was no significant difference as regard patient characteristics age, weight, parity and gestational age between study and control groups. This went with Movafegh et al. (2011), Goswami et al. (2013), Wang et al. (2015) and Lakshmi et al. (2016) who founded that patients’ characteristics in the study and control groups were similar, with no statistical difference between the two groups.
In our study, tranexamic acid significantly reduced bleeding during and after cesarean section. The study total blood loss was significantly less than control group these results agreed with the results of the three mentioned studies.
Goswami et al. (2013) showed significant difference in hemoglobin values in the pre- and post-operative periods. Wang et al. (2015) showed that declines in hemoglobin values after CS was significantly less in TXA group than in control group Lakshmi et al. (2016). Percentage of fall in hemoglobin before and after surgery, and the number of subjects who had more than 10% fall in hemoglobin. 9.3% of subjects in study group and 39% of subjects in control group had more than 10% fall in hemoglobin. Hb after CS was significantly greater in tranexamic group than control group.
In our study, there was a significant statistical difference in the vital data postoperatively between the two groups. Postoperative hemoglobin was significantly higher in study group than control group. Reduction in hemoglobin was significantly less in study group than control group. Also, post-operative hematocrit was significantly higher in study group than control group. Reduction in hematocrit was significantly less in study group than in control group. These results agreed with the results of the previous mentioned studies.
Movafegh et al. (2011) and Goswami et al. (2013) showed no statistically significant difference in the heart rates, respiratory rates and blood pressures in the two groups. Lakshmi et al. (2016) showed significant difference in the heart rates, respiratory rates and blood pressures in the two groups.
In our study, there was significant difference in vital data between the study group and control group post-oparative. The included patients were those who were term, singleton, going for elective cesarean section, and excluded patients with high risk of thrombo-embolism, ante-partum hemorrhage, abnormal site of the placenta, macrosomic baby, twin pregnancy and polyhydramnios. Movafegh et al. (2011), Goswami et al. (2013), Wang et al. (2015) and Lakshmi et al. (2016) showed the same inclusion and exclusion criteria.
We used placebo in the current study. Movafegh et al. (2011), Goswami et al. (2013), Wang et al. (2015) and Lakshmi et al. (2016) also used placebo.
CONCLUSION
The use of tranexamic acid prior to cesarean section was significantly effective in reducing blood loss during cesarean with no observed maternal or neonatal side effects.
REFERENCES
10. Wang HY, Hong SK, Duan Y and Yin HM. (2015): Tranexamic acid and blood loss during and after cesarean section: a meta-analysis. J Perinatol, 35(10):818-25.
دور حمض الترانيکساميک الوقائي في التقليل من فقدان الدم أثناء العملية القيصرية الاختياريه
أحمد محمد السعداوى غانم, مفيد فوزى محمد, سمير خميس جلال
قسم النساء والتوليد, کليه الطب, جامعة الازهر
E-mail: elseadawy855@gmail.com
خلفية البحث: يعد نزيف ما بعد الولادة من أهم الأسباب التى قد تؤدى إلى الوفاة عالميا .حمض الترانيکساميک الذى هو من الاحماض المضاده للفيبرين يعتبر محاولة لمنع هذه المشکلة.
وظائف البحث: هذا البحث يهدف إلى معرفة مدى کفاءه حقن حمض الترانيکساميک فى تقليل فقدان الدم أثناء الولادة القيصرية الاختيارية.
المرضى وطرق البحث : تم القيام بهذه الدراسة بطريقه عشوائية على مئتين من النساء اللواتى يخضعن لولادة قيصرية, تم وضعهم إما لمجموعه الدراسة أو مجموعة التحکم بنظام عشوائى عن طريق الکمبيوتر, وتم إعطاء حمض الترانيکساميک قبل العملية فى مجموعة الدراسة, بالإضافة إلى الرعاية الروتينية (إعطاء عشر وحدات من الأوکسيتوسين المضافة إلى التنقيط الوريدي بعد ولادة الطفل), بينما مجموعة التحکم لديها الرعاية الروتينية فقط .وقد تم حساب فقدان الدم, والهيموجلوبين قبل وبعد العملية والمقارنة للنسبة المئوية للفرق بينهما.
نتائج البحث : لوحظ وجود إنخفاض معتبر فى کمية الدم المفقود منذ ولادة المشيمة حتى الانتهاء من عملية الولادة بالکامل حيث وجد فى مجموعة الدراسة أن کمية الدم المفقود بما يعادل391.95 مل, بينما على الجه m الأخرى فى مجموعة التحکم وجد أن کمية الدم المفقود بما يعادل 633 مل, وقد وجد وحدة قياس أخرى لتحديد هذه النتائج وهى نسبة إنخفاض الهيموجلوبين فى الدم قبل وبعد العملية. وقد وجد أن نسبة الهيموجلوبين فى الدم ما بعد العملية کانت أعلى فى مجموعة الدراسة عن مجموعه التحکم. کما وجد أن النقص فى الهيموجلوبين فى الدم کان أقل بطريقة معتبرة فى مجموعة الدراسة عن مجموعة التحکم ولم توجد أى مشاکل بعد العملية سواء للأم أو للمولود.
الاستنتاج: حمض الترانيکساميک يقوم بتقليل فقدان الدم أثناء الولادة القيصرية الأختيارية بطريقة معتبرة, واستخدام حمض الترانيکساميک ليس له أى آثار أو أضرار جانبية . لذلک يتم إستخدام حمض الترانيکساميک بطريقه آمنه وفعالة للنساء اللواتى يخضعن لولادة قيصرية.
الکلمات الدالة: إنحلال الفيبرين; الهيموجلوبين; النزيف; الموت; المنع; حمض الترانيکساميک.
REFERENCES
10. Wang HY, Hong SK, Duan Y and Yin HM. (2015): Tranexamic acid and blood loss during and after cesarean section: a meta-analysis. J Perinatol, 35(10):818-25.