Am J Perinatol
DOI: 10.1055/a-2353-0832
Original Article

When Are Pregnant Patients Receiving Tranexamic Acid during Delivery Hospitalization in the United States?

1   Division of Maternal-Fetal Medicine and Ultrasound, Department of Obstetrics and Gynecology, Washington University School of Medicine in St. Louis, St. Louis, Missouri
,
Seyedeh A. Miran
2   Department of Clinical Research and Leadership, George Washington University School of Medicine and Health Sciences, Washington, District of Columbia
,
Phillip Ma
2   Department of Clinical Research and Leadership, George Washington University School of Medicine and Health Sciences, Washington, District of Columbia
,
George Saade
3   Division of Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, Eastern Virginia Medical School, Norfolk, Virginia
,
Ian Roberts
4   Clinical Trials Unit, London School of Hygiene and Tropical Medicine, London, United Kingdom
,
5   Division of Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, George Washington University School of Medicine and Health Sciences, Washington, District of Columbia
6   Division of Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, Inova Health System, Falls Church, Virginia
› Author Affiliations
Funding This work was supported by the National Heart, Lung, and Blood Institute (grant no.: K23HL141640).

Abstract

Objective The World Health Organization recommends tranexamic acid (TXA) in the management of postpartum hemorrhage (PPH). However, the role of TXA in PPH prevention and the optimal timing of TXA administration remain unknown. Our objective was to describe the timing of TXA administration, differences in timing of TXA administration by mode of delivery, and current trends in TXA administration in the United States.

Study Design We conducted a descriptive study of trends in TXA administration using the Cerner Real-World Database. We identified 1,544,712 deliveries occurring at greater than 24 weeks' gestation from January 1, 2016, to February 21, 2023. Demographic data were collected including gestational age, mode of delivery, and comorbidities. The timing of TXA administration and differences in TXA timing by mode of delivery were also collected.

Results In our cohort, 21,433 patients (1.39%) received TXA. The majority of patients who received TXA were between ages 25 and 34 years old (55.3%), White (60.7%), and delivered between 37 and 416/7 weeks (81.4%). The TXA group had a higher prevalence of medical comorbidities including obesity (32.9 vs. 19.0%, p < 0.00001), preeclampsia (19.6 vs. 6.81%, p < 0.00001), and pregestational diabetes (3.27 vs. 1.36%, p < 0.00001). Among women who received TXA, 15.4% received it within 3 hours before delivery. Among patients who received TXA after delivery, 23.6% received TXA within 3 hours after delivery, whereas 35.7% received TXA between 10 and 24 hours after delivery. A total of 80.4% of patients who received TXA before delivery had a cesarean delivery.

Conclusion While TXA is most commonly administered after delivery, many patients are receiving TXA prior to delivery in the United States without clear evidence to guide the timing of administration. A randomized trial is urgently needed to determine the safety and efficacy of TXA when administered prior to delivery.

Key Points

  • TXA is used in the treatment of PPH.

  • The role of TXA in prevention of PPH is unclear.

  • Fewer than 2% of patients in the United States receive TXA at delivery.

  • TXA administration before delivery in the United States is rising.



Publication History

Received: 18 April 2024

Accepted: 20 June 2024

Accepted Manuscript online:
26 June 2024

Article published online:
18 July 2024

© 2024. Thieme. All rights reserved.

Thieme Medical Publishers, Inc.
333 Seventh Avenue, 18th Floor, New York, NY 10001, USA

 
  • References

  • 1 Joseph KS, Boutin A, Lisonkova S. et al. Maternal mortality in the United States: recent trends, current status, and future considerations. Obstet Gynecol 2021; 137 (05) 763-771
  • 2 Bonnar J, Davidson JF, Pidgeon CF, McNicol GP, Douglas AS. Fibrin degradation products in normal and abnormal pregnancy and parturition. BMJ 1969; 3 (5663) 137-140
  • 3 Ducloy-Bouthors AS, Duhamel A, Kipnis E. et al. Postpartum haemorrhage related early increase in D-dimers is inhibited by tranexamic acid: haemostasis parameters of a randomized controlled open labelled trial. Br J Anaesth 2016; 116 (05) 641-648
  • 4 Anaposala S, Kalluru PKR, Calderon Martinez E, Bhavanthi S, Gundoji CR. Postpartum hemorrhage and tranexamic acid: a literature review. Cureus 2023; 15 (05) e38736
  • 5 WOMAN Trial Collaborators. 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 (10084): 2105-2116
  • 6 World Health Organization (WHO). Updated WHO Recommendation on Tranexamic Acid for the Treatment of Postpartum Haemorrhage. Geneva, Switzerland: WHO; 2017
  • 7 Sentilhes L, Winer N, Azria E. et al; Groupe de Recherche en Obstétrique et Gynécologie. Tranexamic acid for the prevention of blood loss after vaginal delivery. N Engl J Med 2018; 379 (08) 731-742
  • 8 Sentilhes L, Sénat MV, Le Lous M. et al; Groupe de Recherche en Obstétrique et Gynécologie. Tranexamic acid for the prevention of blood loss after cesarean delivery. N Engl J Med 2021; 384 (17) 1623-1634
  • 9 Pacheco LD, Clifton RG, Saade GR. et al; Eunice Kennedy Shriver National Institute of Child Health and Human Development Maternal–Fetal Medicine Units Network. Tranexamic acid to prevent obstetrical hemorrhage after cesarean delivery. N Engl J Med 2023; 388 (15) 1365-1375
  • 10 Taeuber I, Weibel S, Herrmann E. et al. Association of intravenous tranexamic acid with thromboembolic events and mortality: a systematic review, meta-analysis, and meta-regression. JAMA Surg 2021; 156 (06) e210884
  • 11 Murao S, Nakata H, Roberts I, Yamakawa K. Effect of tranexamic acid on thrombotic events and seizures in bleeding patients: a systematic review and meta-analysis. Crit Care 2021; 25 (01) 380
  • 12 Shakur-Still H, Roberts I, Grassin-Delyle S. et al. Alternative routes for tranexamic acid treatment in obstetric bleeding (WOMAN-PharmacoTXA trial): a randomised trial and pharmacological study in caesarean section births. BJOG 2023; 130 (10) 1177-1186
  • 13 Hamilton BE, Martin JA, Osterman MJK. Births: provisional data for 2022. Vital Statistics Rapid Release; no. 28. Hyattsville, MD: National Center for Health Statistics; . June 2023
  • 14 Corbetta-Rastelli CM, Friedman AM, Sobhani NC, Arditi B, Goffman D, Wen T. Postpartum hemorrhage trends and outcomes in the United States, 2000–2019. Obstet Gynecol 2023; 141 (01) 152-161
  • 15 Litman EA, Ma P, Miran SA, Nelson SJ, Ahmadzia HK. Recent trends in tranexamic acid use during postpartum hemorrhage in the United States. J Thromb Thrombolysis 2023; 55 (04) 742-746
  • 16 Yang F, Wang H, Shen M. Effect of preoperative prophylactic intravenous tranexamic acid on perioperative blood loss control in patients undergoing cesarean delivery: a systematic review and meta-analysis. BMC Pregnancy Childbirth 2023; 23 (01) 420
  • 17 Sterling EK, Litman EA, Dazelle WDH, Ahmadzia HK. An update to tranexamic acid trends during the peripartum period in the United States, 2019 to 2021. Am J Obstet Gynecol MFM 2023; 5 (06) 100933
  • 18 Berghella V. Management of the third stage of labor: prophylactic pharmacotherapy to minimize hemorrhage. In: Post TW. ed. UpToDate, Waltham, MA;