Next Article in Journal
Sexually Transmitted Infections in 2000–2018 in a Specialised Centre: Comparison between Pre-Crisis, Crisis, and Post-Crisis Period
Previous Article in Journal
Dinutuximab Beta Maintenance Therapy in Patients with High-Risk Neuroblastoma in First-Line and Refractory/Relapsed Settings—Real-World Data
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
JCM
Volume 12
Issue 16
10.3390/jcm12165253
jcm-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Prophylactic Administration of Tranexamic Acid Reduces Blood Products’ Transfusion and Intensive Care Admission in Women Undergoing High-Risk Cesarean Sections

by
Yair Binyamin
1,*,
Amit Frenkel
2,
Igor Gruzman
1,
Sofia Lerman
1,
Yoav Bichovsky
2,
Alexander Zlotnik
1,
Michael Y. Stav
3,
Offer Erez
4 and
Sharon Orbach-Zinger
3
1
Department of Anesthesiology, Soroka University Medical Center, The Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva 84101, Israel
2
General Intensive Care Department, Soroka University Medical Center, The Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva 84101, Israel
3
Department of Anesthesia, Beilinson Hospital, Rabin Medical Center Associated with Sakler Medical School, Tel Aviv University, Tel Aviv 6423906, Israel
4
Division of Obstetrics and Gynecology, Soroka University Medical Center, The Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva 84101, Israel
*
Author to whom correspondence should be addressed.
J. Clin. Med. 2023, 12(16), 5253; https://doi.org/10.3390/jcm12165253
Submission received: 10 July 2023 / Revised: 7 August 2023 / Accepted: 9 August 2023 / Published: 12 August 2023
(This article belongs to the Section Intensive Care)
Review Reports Versions Notes

Abstract

:
Postpartum hemorrhage (PPH) remains a major cause of maternal mortality. Tranexamic acid (TxA) has shown effectiveness in reducing PPH-related maternal bleeding events and deaths. We conducted a cohort study including parturient women at high risk of bleeding after undergoing a cesarean section (CS). Participants were divided into two groups: the treatment group received prophylactic 1-g TxA before surgery (n = 500), while the comparison group underwent CS without TxA treatment (n = 500). The primary outcome measured increased maternal blood loss following CS, defined as more than a 10% drop in hemoglobin concentration within 24 h post-CS and/or a drop of ≥2 g/dL in maternal hemoglobin concentration. Secondary outcomes included PPH indicators, ICU admission, hospital stay, TxA complications, and neonatal data. TxA administration significantly reduced hemoglobin decrease by more than 10%: there was a 35.4% decrease in the TxA group vs. a 59.4% decrease in the non-TxA group, p < 0.0001 and hemoglobin decreased by ≥2 g/dL (11.4% in the TxA group vs. 25.2% in non-TxA group, p < 0.0001), reduced packed red blood cell transfusion (p = 0.0174), and resulted in lower ICU admission rates (p = 0.034) and shorter hospitalization (p < 0.0001). Complication rates and neonatal outcomes did not differ significantly. In conclusion, prophylactic TxA administration during high-risk CS may effectively reduce blood loss, providing a potential intervention to improve maternal outcomes.

1. Introduction

During delivery, there is an activation of the fibrinolytic system, seen in the increased plasma urokinase-plasminogen activator (u-PA) or tissue plasminogen activator (t-PA) levels and decreased plasminogen activator inhibitor 1 (PAI-1) [1]. Previous studies have shown that tranexamic acid (TxA) significantly reduced maternal death due to postpartum hemorrhage (PPH) and reduced bleeding in cesarean and other surgeries [2,3,4,5,6,7,8]. A randomized control trial provide evidence of TXA reducing estimated blood loss (but not blood loss based on gravimetric assessment) in patients undergoing cesarean delivery [9].
Because of this evidence, its low cost, and the fact that it does not require refrigeration, the World Health Organization (WHO) classified it as an essential medicine, especially in low-resource countries [10].
Because of its effectiveness in reducing the risk of death from PPH, there is growing interest in its use as prophylaxis for prevention of PPH during cesarean sections (CS) and delivery [9,11,12,13,14].
Although there is controversy regarding this latter point, most articles conclude that there is no role for prophylactic TXA given in all CS. However, most of these studies excluded women at high risk of bleeding [9,11].
We hypothesized that these parturients may be the ones that would most benefit from prophylactic TxA and, therefore, we decided to conduct an exploratory cohort impact study to determine the prophylactic effect of TxA administration during CS of women at high risk of obstetrical hemorrhage (multiple pregnancy, third cesarean section and above, macrosomia, placental abruption, placenta previa with bleeding, abnormal placentation disorders, PET with severe characteristics, HELLP syndrome, and eclampsia) on hemoglobin, other parameters of PPH, ICU admission and length of hospital stay, TXA complications, and neonatal outcome.

2. Materials and Methods

Study Design: The study was a pragmatic retrospective impact study, a secondary analysis of our previous study examining all CS [15].
Ethics: The hospital institutional review board approved the study and waived patient informed consent as this was a retrospective study (approval number 0054-20-SORof Soroka University Medical Center, Beer Sheva, Israel).
Eligibility: Starting in 2017, all women undergoing CS received prophylactic TXA. We collected data on 1000 high-risk women who underwent low segment CS, of which 500 received 1 g prophylactic TxA and 500 did not. CS at high risk of bleeding was defined as: multiple pregnancy, third cesarean section and above, macrosomia, placental abruption, placenta previa with bleeding, abnormal placentation disorders, PET with severe characteristics, HELLP syndrome, and eclampsia [16,17]. Exclusion criteria were intrauterine fetal demise.
Recruitment: Two time frames were analyzed: (1) the control group: women who had CS before the introduction of the routine administration of TxA (1 January 2014 until 30 September 2014), and (2) the study group: women who had prophylactic administration of TxA before CS (1 January 2019 until 14 September 2019). In order to ensure compliance; a five-year gap between the periods was chosen since the introduction of prophylactic TXA was carried out in a gradual manner.
Setting: Soroka University Medical Center (SUMC) is the largest maternal ward in the country, with over 17,000 deliveries yearly. It is a tertiary hospital located in the south of Israel.
Procedure: Study women received 1 g of TxA before skin incision, given over 30–60 s.
Organization: There was no change in anesthetic or surgical technique between the two time frames.
Follow up: Women were followed up for three months using the hospital’s computerized medical records.
Primary outcome: (1) incidence of women having a hemoglobin drop >10% 24 h after CS compared to pre-operative baseline and (2) incidence of women having a hemoglobin drop of ≥2 g/dL.
Secondary outcome: maternal outcome (hemoglobin change, estimated blood loss as assessed by surgeon, need for blood products (packed red blood cell, fresh frozen plasma, cryoprecipitate and platelets, cesarean hysterectomy) (blood products were given in case of a hemoglobin level below 7.0 or during active bleeding with clinical manifestations or when symptoms of anemia appeared), intensive care admission, length of hospital stay), TxA complications (acute renal failure, increase in creatinine, thromboembolism, seizures) and neonatal data (Apgar, pH). Follow up of complications was for a three-month period because of thromboembolic events being more common in the postpartum period until at least 12 weeks after delivery [18].
Statistical Analysis: Continuous parametric data are presented with their mean ± standard deviation and comparisons performed using the independent group’s Student’s t-test. Categorical data are presented as count (percentage) and comparisons are performed using the Chi-square test. The data were analyzed and processed using R software (version 4.0.0). Because there were two primary outcomes, a Bonferroni correction was made and p < 0.025 was considered significant for the primary outcome. As the secondary outcomes were exploratory, they were not corrected.
A multivariable logistic regression model was performed to assess the primary outcome hemoglobin decrease >10% while controlling for maternal age, BMI, parity, number of CS, pregnancy week and TxA administration.
Sample size calculation: The study by Lakshmi and Araham [19] reported that 40% of parturients that did not receive tranexamic acid had a drop of more than 10% in hemoglobin level 24 h after surgery compared to its level before surgery. We assumed that a risk reduction of 25% in the proportion of women with a hemoglobin drop of more than 10% to be a clinically significant difference. Based on these assumptions and a significance level (alpha) of 0.05 and a power of 90%, the number of parturients that needed to be included was 475 per group. Taking into account that data were lacking or insufficient, 5% of our samples, a minimum of 500 parturients per group was necessary.

3. Results

The clinical and demographic characteristics of the study groups are presented in Table 1. The two groups had no differences in demographic variable or baseline obstetric data.
Primary outcome: The rate of hemoglobin decrease by >10% was higher in the non-TxA vs. the TxA group (Non-TxA group 59.4% (297/500) vs. TxA group 35.4% (177/500), p < 0.0001). The rate of hemoglobin decrease by ≥2 gm/dL was higher in the non-TxA group versus the TxA group (non-TxA 25.2% (126/500) vs. TxA11.4% (57/500), p < 0.0001) (Table 2).
Secondary outcomes other indicators of PPH: The prophylactic administration of TxA was associated with a reduced delta hemoglobin (pre vs. post CS hemoglobin), estimated blood loss, packed red blood cell transfusion within 48 h of CS. There was no difference in need for hysterectomy or need for intraoperative blood transfusion (Table 2).
Secondary outcomes: ICU admission and hospital stay were shorter in the group that received TxA (Table 2).
Secondary outcomes: Complications. The groups had no difference in the rate of acute renal failure, delta creatinine concentrations, thromboembolic events, or seizures (Table 3). All patients who had seizures had a history of preeclampsia.
Secondary outcomes: Neonatal data. Neonatal outcomes are listed in Table 4. There were no significant between-group differences in the incidence of any neonatal outcome.
Multivariable regression: Using a multivariable logistic regression model where we controlled for maternal age, BMI, parity, number of CS, gestational age at surgery, anemia before surgery, and TxA administration, administration of prophylactic TxA and number of CS were independently associated with lower rates of hemoglobin drop >10% (TxA administration—β = 0.787, 95% CI 0.7410; 0.8359, p < 0.0001. number of CS—β = 0.9694, 95% CI 0.9462; 0.9933, p = 0.0126) (Table 5).
Using another multivariable logistic regression model controlling for maternal age, BMI, parity, number of CS, gestational age at surgery, anemia before surgery, and TxA administration, administration of prophylactic TxA was not significantly associated with rates of visual estimated blood loss >1000 mL (TxA administration-β = 0.778, 95% CI 0.5055; 1.1922, p = 0.2513) (Table 5).

4. Discussion

In this analysis of real-world data, we found that the use of TxA in high-risk CS decreased blood loss and the need for postoperative packed red blood cell transfusions, as well as decreasing ICU admissions and shortening hospitalization time. Using a multivariable logistic model controlling for other factors influencing PPH, we found that TxA administration was independently associated with decreased blood loss.
Although studies showing that the use of prophylactic TXA in all CS had questionable benefits [9,11,20,21,22], we believe that our study does provide evidence for its use prophylactically in high-risk women.
Different studies have used different outcome measures to assess bleeding. In the study by Senthilles, hemorrhage was defined as calculated estimated blood loss > 1000cc or administration of RBC infusions within two days of delivery [9]. Because we included women with preoperative anemia, we felt that it was more accurate to use an absolute measure, a decrease in hemoglobin of >2 gm or a percentage decrease greater than 10%.
In terms of secondary outcomes, we report here for the first time that the prophylactic administration of TxA reduces the rate of ICU admission in women at risk of obstetrical hemorrhage who undergo CS. This was observed in our study population, which was included in previous reports [2,9]. Moreover, an additional novel observation by our study is the shorter hospitalization among women who received prophylactic TxA treatment. This parameter was not measured in previous reports [9], but has a great impact on public health expenses and patients’ satisfaction.
In recent years, paradoxically, the overall rate of PPH in high-income countries has increased; however, it was not associated with a concomitant elevation in maternal mortality [23]. There are many possible factors that can result in maternal mortality, including increasing maternal age, the increased incidence of multiple gestation, higher rates of placenta previa and placenta accreta due to previous CS [23], and a higher rate of intrapartum CS. Most RCTs have been limited to low-risk pregnancies, and thus the specific dynamics of parturients expected to bleed have not been studied; thus, the importance of real-world data in examining PPH cannot be overemphasized.
Two studies are currently being conducted investigating the use of prophylactic TxA in other high-risk populations, including women with prepartum anemia and placenta previa [24,25]. A recent secondary analysis of a TRAAP2 study by Sentilhes suggests that TXA was not associated with a reduction in any hemorrhage-related outcome among women with multiple pregnancies [26].
We also investigated the effect of prophylactic TXA administration prior to skin incision rather than following the delivery of the neonate [9]. We are not able to discuss the neonatal outcome but rest assured that there is no difference in pH or Apgar score.
Our study did not show that TxA caused unexpected side effects. In a recent article examining World Health Organization database case safety reports, there were 29 cases of adverse renal vascular and ischemic complications, 42 reports of pulmonary embolisms, and 41 reports of peripheral embolism and thrombosis in women receiving TxA [27]. In this study, however, 52.9% of women received doses higher than 1gm. Likewise, in a French study describing 18 cases of renal cortical necrosis after postpartum hemorrhage, high dose TxA was used including a bolus of 1–4 gm followed by a maintenance infusion [28]. This finding is in contrast with the WOMAN’s trial [2], which included 20,000 women and did not find that the use of TXA was associated with the risks of renal failure, embolism, or seizures. The incidence of renal failure, seizures, or thromboembolic events in our study was 0.2%, 0.6%, and 0.2%, respectively; however, our study did not aim primarily to assess these outcomes. We used hemoglobin change rather than EBL as our primary measure of outcome. We decided to use hemoglobin change because EBL has been shown to underestimate blood loss, especially at high volumes. However, hemoglobin can also be influenced by other factors, including hemodilution.
The strengths of our study are our large numbers and the strict adherence to protocol. In Senthilles’ study, ¼ of women deviated from protocol [9]. In our study, as the use of TxA was part of a strictly protocolized regimen, we examined treatment as opposed to intention to treat.
Our study’s limitations include the retrospective data, which make some information from charts inaccessible. Second, the historical nature of the study may cause the difference in results to be secondary to the changes in practices, such as intrauterine tamponade balloon. Third, we have no information on whether the surgery was conducted during labor or before labor. Fourth, our cohort has a high gravida and parity and a very high prior CS history, which may make our generalizability limited. Fifth, numerators and incidence of complications were extremely low, especially ICU admission. Therefore, our study is unable to ascertain whether TxA is associated with a reduced risk of ICU admission or RBC transfusion. Unfortunately, we do not have data on patients who received a repeat dose of TxA; a recent article showed the utility of a repeat dose in cases of continued fibrinolytic activity [29].

5. Conclusions

Prophylactic TxA administration may reduce estimated blood loss and hemoglobin changes among women at high risk of obstetrical hemorrhage undergoing cesarean delivery in our cohort. Further high quality randomized controlled studies must be performed to confirm this finding.

Author Contributions

Y.B. (Yair Binyamin), Review & Editing; O.E., Methodology and Formal Analysis; S.L., Review & Editing; M.Y.S., Methodology and Formal Analysis; I.G. and A.Z., Conceptualization; A.F., Y.B. (Yoav Bichovsky) and Y.B. (Yair Binyamin), Validation; S.O.-Z., Writing—Original Draft Preparation & Supervision. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

The study was conducted according to the guidelines of the Declaration of Helsinki, and approved by the Institutional Review Board of Soroka university medical center, protocol code 0054-20-SOR.

Informed Consent Statement

Patient consent was waived due to the retrospective nature of the study.

Data Availability Statement

yairben1@gmail.com.

Acknowledgments

We would like to thank Hadar Sharvit for his assistance with the study.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Hellgren, M. Hemostasis during Normal Pregnancy and Puerperium. Semin. Thromb. Hemost. 2003, 29, 125–130. [Google Scholar] [CrossRef] [PubMed]
  2. Shakur, H.; Roberts, I.; Fawole, B.; Chaudhri, R.; El-Sheikh, M.; Akintan, A.; Qureshi, Z.; Kidanto, H.; Vwalika, B.; Abdulkadir, A.; et al. Effect of early tranexamic acid administration on mortality, hysterectomy, and other morbidities in women with post-partum haemorrhage (WOMAN): An international, randomised, double-blind, placebo-controlled trial. Lancet 2017, 389, 2105–2116, Erratum in: Lancet 2017, 389, 2104. [Google Scholar] [CrossRef] [PubMed]
  3. Electronic Medicines Compendium, Summary of Product Characteristics: Tranexamic Acid. Available online: http://www.medicines.org.uk/emc/medicine/1489 (accessed on 12 September 2021).
  4. CRASH-2 Trial Collaborators; Shakur, H.; Roberts, I.; Bautista, R.; Caballero, J.; Coats, T.; Dewan, Y.; El-Sayed, H.; Gogichaishvili, T.; Gupta, S.; et al. Effects of tranexamic acid on death, vascular occlusive events, and blood transfusion in trauma patients with significant haemorrhage (CRASH-2): A randomised, placebo-controlled trial. Lancet 2010, 376, 23–32. [Google Scholar] [CrossRef] [PubMed]
  5. Ker, K.; Edwards, P.; Perel, P.; Shakur, H.; Roberts, I. Effect of tranexamic acid on surgical bleeding: Systematic review and cumulative meta-analysis. BMJ 2012, 344, e3054. [Google Scholar] [CrossRef] [PubMed]
  6. Sentilhes, L.; Madar, H.; Mattuizzi, A.; Froeliger, A.; Merlot, B.; Elleboode, B.; Deneux-Tharaux, C. Tranexamic acid for childbirth: Why, when, and for whom. Expert Rev. Hematol. 2019, 12, 753–761. [Google Scholar] [CrossRef] [PubMed]
  7. Sentilhes, L.; Lasocki, S.; Ducloy-Bouthors, A.S.; Deruelle, P.; Dreyfus, M.; Perrotin, F.; Goffinet, F.; Deneux-Tharaux, C. Tranexamic acid for the prevention and treatment of postpartum haemorrhage. Br. J. Anaesth. 2015, 114, 576–587. [Google Scholar] [CrossRef]
  8. Jimenez-Rivera, J.J.; Iribarren-Sarrías, J.L.; Martínez-Sanz, R. Tranexamic Acid in Patients Undergoing Coronary-Artery Surgery. New Engl. J. Med. 2017, 376, 1893. [Google Scholar] [CrossRef]
  9. Sentilhes, L.; Sénat, M.V.; Le Lous, M.; Winer, N.; Rozenberg, P.; Kayem, G.; Verspyck, E.; Fuchs, F.; Azria, E.; Gallot, D.; et al. Tranexamic Acid for the Prevention of Blood Loss after Cesarean Delivery. N. Engl. J. Med. 2021, 384, 1623–1634. [Google Scholar] [CrossRef]
  10. World Health Organization. Model List of Essential Medicines, 21st List; World Health Organization: Geneva, Switzerland, 2019.
  11. Pacheco, L.D.; Clifton, R.G.; Saade, G.R.; Weiner, S.J.; Parry, S.; Thorp, J.M.; Longo, M.; Salazar, A.; Dalton, W.; Tita, A.T.; et al. Tranexamic Acid to Prevent Obstetrical Hemorrhage after Cesarean Delivery. N. Engl. J. Med. 2023, 388, 1365–1375. [Google Scholar] [CrossRef]
  12. Heesen, M.; Böhmer, J.; Klöhr, S.; Rossaint, R.; VAN DE Velde, M.; Dudenhausen, J.W.; Straube, S. Prophylactic tranexamic acid in parturients at low risk for post-partum haemorrhage: Systematic review and meta-analysis. Acta Anaesthesiol. Scand. 2014, 58, 1075–1085. [Google Scholar] [CrossRef]
  13. Sentilhes, L.; Winer, N.; Azria, E.; Sénat, M.-V.; Le Ray, C.; Vardon, D.; Perrotin, F.; Desbrière, R.; Fuchs, F.; Kayem, G.; et al. Tranexamic Acid for the Prevention of Blood Loss after Vaginal Delivery. N. Engl. J. Med. 2018, 379, 731–742. [Google Scholar] [CrossRef] [PubMed]
  14. Simonazzi, G.; Saccone, G.; Berghella, V. Evidence on the use of tranexamic acid at cesarean delivery. Acta Obstet. Gynecol. Scand. 2016, 95, 837. [Google Scholar] [CrossRef] [PubMed]
  15. Binyamin, Y.; Orbach-Zinger, S.; Gruzman, I.; Frenkel, A.; Lerman, S.; Zlotnik, A.; Frank, D.; Ioscovich, A.; Erez, O.; Heesen, M. The effect of prophylactic use of tranexamic acid for cesarean section. J. Matern. Neonatal Med. 2022, 35, 9157–9162. [Google Scholar] [CrossRef] [PubMed]
  16. Sujata, N.; Tobin, R.; Kaur, R.; Aneja, A.; Khanna, M.; Hanjoora, V.M. Randomized controlled trial of tranexamic acid among parturients at increased risk for postpartum hemorrhage undergoing cesarean delivery. Int. J. Gynecol. Obstet. 2016, 133, 312–315. [Google Scholar] [CrossRef]
  17. Kawakita, T.; Mokhtari, N.; Huang, J.C.; Landy, H.J. Evaluation of Risk-Assessment Tools for Severe Postpartum Hemorrhage in Women Undergoing Cesarean Delivery. Obstet. Gynecol. 2019, 134, 1308–1316. [Google Scholar] [CrossRef]
  18. Kamel, H.; Navi, B.B.; Sriram, N.; Hovsepian, D.A.; Devereux, R.B.; Elkind, M.S. Risk of a Thrombotic Event after the 6-Week Postpartum Period. New Engl. J. Med. 2014, 370, 1307–1315. [Google Scholar] [CrossRef]
  19. Lakshmi, S.D. Role of Prophylactic Tranexamic Acid in Reducing Blood Loss during Elective Caesarean Section: A Randomized Controlled Study. J. Clin. Diagn. Res. 2016, 10, QC17–QC21. [Google Scholar] [CrossRef]
  20. Bellos, I.; Pergialiotis, V. Tranexamic acid for the prevention of postpartum hemorrhage in women undergoing cesarean delivery: An updated meta-analysis. Am. J. Obstet. Gynecol. 2021, 226, 510–523.e22. [Google Scholar] [CrossRef]
  21. Shander, A.; Javidroozi, M.; Sentilhes, L. Tranexamic acid and obstetric hemorrhage: Give empirically or selectively? Int. J. Obstet. Anesthesia 2021, 48, 103206. [Google Scholar] [CrossRef]
  22. Hofer, S.; Blaha, J.; Collins, P.W.; Ducloy-Bouthors, A.-S.; Guasch, E.; Labate, F.; Lança, F.; Nyfløt, L.T.; Steiner, K.; van de Velde, M. Haemostatic support in postpartum haemorrhage: A review of the literature and expert opinion. Eur. J. Anaesthesiol. 2022, 40, 29–38. [Google Scholar] [CrossRef]
  23. Owen, M.D.; Cassidy, A.; Weeks, A. Why are women still dying from obstetric hemorrhage? A narrative review of perspectives from high and low resource settings. Int. J. Obstet. Anesth. 2021, 46, 102982. [Google Scholar] [CrossRef] [PubMed]
  24. Ker, K.; Roberts, I.; Chaudhri, R.; Fawole, B.; Beaumont, D.; Balogun, E.; Prowse, D.; Pepple, T.; Javaid, K.; Kayani, A.; et al. Tranexamic acid for the prevention of postpartum bleeding in women with anaemia: Study protocol for an international, randomised, double-blind, placebo-controlled trial. Trials 2018, 19, 712. [Google Scholar] [CrossRef] [PubMed]
  25. Sentilhes, L.; Deneux-Tharaux, C.; Roberts, I.; Ker, K. Tranexamic acid for the prevention of postpartum hemorrhage in women undergoing cesarean delivery. Am. J. Obstet. Gynecol. 2022, 226, 755–756. [Google Scholar] [CrossRef] [PubMed]
  26. Sentilhes, L.; Madar, H.; Le Lous, M.; Sénat, M.V.; Winer, N.; Rozenberg, P.; Kayem, G.; Verspyck, E.; Fuchs, F.; Azria, E.; et al. Tranexamic acid for the prevention of blood loss after cesarean among women with twins: A secondary analysis of the TRAnexamic Acid for Preventing Postpartum Hemorrhage Following a Cesarean Delivery randomized clinical trial. Am. J. Obstet. Gynecol. 2022, 227, 889.e1–889.e17. [Google Scholar] [CrossRef] [PubMed]
  27. Stämpfli, D.; Weiler, S.; Weiniger, C.F.; Burden, A.M.; Heesen, M. Renal ischemic adverse drug events related to tranexamic acid in women of child-bearing age: An analysis of pharmacovigilance data. Eur. J. Clin. Pharmacol. 2020, 77, 913–919. [Google Scholar] [CrossRef]
  28. Frimat, M.; Decambron, M.; Lebas, C.; Moktefi, A.; Lemaitre, L.; Gnemmi, V.; Sautenet, B.; Glowacki, F.; Subtil, D.; Jourdain, M.; et al. Renal Cortical Necrosis in Postpartum Hemorrhage: A Case Series. Am. J. Kidney Dis. 2016, 68, 50–57. [Google Scholar] [CrossRef]
  29. Ducloy-Bouthors, A.-S.; Gilliot, S.; Kyheng, M.; Faraoni, D.; Turbelin, A.; Keita-Meyer, H.; Rigouzzo, A.; Moyanotidou, G.; Constant, B.; Broisin, F.; et al. Tranexamic acid dose–response relationship for antifibrinolysis in postpartum haemorrhage during Caesarean delivery: TRACES, a double-blind, placebo-controlled, multicentre, dose-ranging biomarker study. Br. J. Anaesth. 2022, 129, 937–945. [Google Scholar] [CrossRef]
Table 1. Characteristics of the participants.
Table 1. Characteristics of the participants.
CharacteristicTranexamic Acid Group (N = 500)No Tranexamic Acid Group (N = 500)p Value
Age (years)32.30 ± 5.7332.88 ± 5.470.0987
Height (cm)161.3 ± 5.7161.7 ± 5.80.2157
Weight (Kg)81.05 ± 15.2880.65 ± 13.890.6587
Gravity—median (range)4 (1–25)4 (1–16)0.583
Parity—median (range)3 (0–12)3 (0–12)0.5865
Previous cesarean delivery—no. (%)339 (67.8%)338 (67.6%)0.9442
Number of cesarean delivery—median (range)3 (1–8)3 (1–8)0.8572
Gestational diabetes—no. (%)54 (10.8%)56 (11.2%)0.8414
HTN chronic—no. (%)13 (2.6%)13 (2.6%)1.000
Hypothyroidism—no. (%)21 (4.2%)18 (3.6%)0.6241
Kidney disease—no. (%)- (0.0%)- (0.0%)-
History of PPD—no. (%)8 (1.6%)9 (1.8%)0.8103
Anticoagulation Therapy32 (6.4%)23 (4.6%)0.2113
Pregnancy week36.75 ± 2.5536.56 ± 2.880.2697
Singletons406 (81.2%)415 (83%)0.4593
Twins88 (17.6%)81 (16.2%)0.5552
Triplets6 (1.2%)3 (0.6%)0.3173
Quadruplets0 (0%)1 (0.2%)0.3173
Placenta previa26 (5.2%)19 (3.8%)0.2846
Placenta accreta6 (1.2%)3 (0.6%)0.3173
PPD—Postpartum depression.
Table 2. Maternal outcomes.
Table 2. Maternal outcomes.
OutcomeTranexamic Acid Group
(N = 500)		No Tranexamic Acid Group
(N = 500)		p Value
Delta hemoglobin (gr/dL)0.85 ± 1.021.42 ± 1.01<0.0001
Hemoglobin decrease ≥ 2 gr/dL—no (%)57 (11.4%)126 (25.2%)<0.0001
Hemoglobin drop >10%—no (%)177(35.4%)297 (59.4%)<0.0001
Estimated blood loss% (mL) 705.2 ± 178.06766.82 ± 172.48.26<0.0001
Estimated blood loss > 1000 mL—no (%)42 (8.4%)53 (10.6%)0.2808
Emergent hysterectomy—no (%)3 (0.6%)3 (0.6%)1
Packed red blood cell transfusion during surgery—no (%)7 (1.4%)15 (3%)0.1313
Packed red blood cell transfusion during surgery above 3 units1 (0.2%)3 (0.6%)0.3173
FFP transfusion during surgery—no (%)5 (1%)9 (1.8%)0.4194
Cryoprecipitate transfusion during surgery—no (%)5 (1%)6 (1.2%)1
Platelet transfusion during surgery—no (%)2 (0.4%)6 (1.2%)0.2869
Packed red blood cell transfusion 48 h—no (%)21 (4.2%)40 (8%)0.0174
FFP transfusion 48 h—no (%)5 (1%)6 (1.2%)1
Cryoprecipitate transfusion 48 h—no (%)4 (0.8%)4(0.8%)1
Platelet cell transfusion 48 h—no (%)3 (0.6%)4 (0.8%)1
ICU admission—no (%)2 (0.4%)9 (1.8%)0.034
Hospital stay (days)4.52 ± 1.485.12 ± 2.4<0.0001
Hospital stay > 5 days—no (%)59 (11.8%)109 (21.8%)<0.0001
Table 3. Complications.
Table 3. Complications.
ComplicationTranexamic Acid GroupNo Tranexamic Acid Groupp Value
Acute renal failure no (%)1 (0.2%)3 (0.6%)0.6164
Delta creatinine (mg/dL)−0.003 ± 0.11−0.006 ± 0.020.9276
Thromboembolic event no (%)1 (0.2%)
[DVT − 1]		2 (0.4%)
[DVT − 1, PE − 1]		1
Seizure no. (%)3 (0.6%)8 (1.6%)0.2252
Table 4. Neonate outcomes.
Table 4. Neonate outcomes.
OutcomeTranexamic Acid Group
N = 592		No Tranexamic Acid Group
N = 581		p Value
APGAR 1 min—median (range)9 (0–9)9 (0–9)0.1724
APGAR 1 min < 5—no (%)23 (3.89%)27 (4.64%)0.5157
APGAR 5 min—median (range)10 (0–10)10 (0–10)0.7422
APGAR 5 min < 5—no (%)11 (1.86%)15 (2.58%)0.4009
PH7.29 ± 0.0827.28 ± 0.0930.3314
PH < 7.2—no (%)35 (5.91%)50 (8.6%)0.07508
Table 5. Multivariable logistic regression model for the association between prophylactic tranexamic acid and hemoglobin drop > 10% and for the association between prophylactic tranexamic acid and visual EBL > 1000 mL.
Table 5. Multivariable logistic regression model for the association between prophylactic tranexamic acid and hemoglobin drop > 10% and for the association between prophylactic tranexamic acid and visual EBL > 1000 mL.
Multivariable Logistic Regression Model for the Association between Prophylactic Tranexamic Acid and Hemoglobin Drop >10%
Odds Ratio95% CIp  Value
Age0.994140.9681; 1.02070.6629
BMI1.004490.9784; 1.03120.7376
Parity1.062550.9936; 1.13700.0771
Number of CS0.880440.7917; 0.97810.0180
Pregnancy week1.00330.9558; 1.05310.8931
TxA administration0.38070.2931; 0.4932<0.0001
Anemia (Hb < 11.0)0.56260.4290; 0.7361<0.0001
Multivariable Logistic Regression Model for the Association between Prophylactic Tranexamic Acid and EBL > 1000 mL
Odds Ratio95% CIp  Value
Age0.98480.9414; 1.02960.5037
BMI0.99400.9498; 1.03790.7919
Parity1.11571.0063; 1.23230.0332
Number of CS1.0173930.8648; 1.19630.8345
Pregnancy week0.97480.9063; 1.05490.5091
TxA administration0.76900.4986; 1.17920.2303
Anemia (Hb < 11.0)1.19290.7698; 1.83650.4250
EBL—estimated blood loss.
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Binyamin, Y.; Frenkel, A.; Gruzman, I.; Lerman, S.; Bichovsky, Y.; Zlotnik, A.; Stav, M.Y.; Erez, O.; Orbach-Zinger, S. Prophylactic Administration of Tranexamic Acid Reduces Blood Products’ Transfusion and Intensive Care Admission in Women Undergoing High-Risk Cesarean Sections. J. Clin. Med. 2023, 12, 5253. https://doi.org/10.3390/jcm12165253

AMA Style

Binyamin Y, Frenkel A, Gruzman I, Lerman S, Bichovsky Y, Zlotnik A, Stav MY, Erez O, Orbach-Zinger S. Prophylactic Administration of Tranexamic Acid Reduces Blood Products’ Transfusion and Intensive Care Admission in Women Undergoing High-Risk Cesarean Sections. Journal of Clinical Medicine. 2023; 12(16):5253. https://doi.org/10.3390/jcm12165253

Chicago/Turabian Style

Binyamin, Yair, Amit Frenkel, Igor Gruzman, Sofia Lerman, Yoav Bichovsky, Alexander Zlotnik, Michael Y. Stav, Offer Erez, and Sharon Orbach-Zinger. 2023. "Prophylactic Administration of Tranexamic Acid Reduces Blood Products’ Transfusion and Intensive Care Admission in Women Undergoing High-Risk Cesarean Sections" Journal of Clinical Medicine 12, no. 16: 5253. https://doi.org/10.3390/jcm12165253

APA Style

Binyamin, Y., Frenkel, A., Gruzman, I., Lerman, S., Bichovsky, Y., Zlotnik, A., Stav, M. Y., Erez, O., & Orbach-Zinger, S. (2023). Prophylactic Administration of Tranexamic Acid Reduces Blood Products’ Transfusion and Intensive Care Admission in Women Undergoing High-Risk Cesarean Sections. Journal of Clinical Medicine, 12(16), 5253. https://doi.org/10.3390/jcm12165253

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop