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Pre-operative tranexemic acid vs. etamsylate in reducing blood loss during elective cesarean section: randomized controlled trial

This article has been retracted. Retraction note.
  • Haitham Torky EMAIL logo , El-Sayed El-Desouky , Ibrahim Abo-Elmagd , Attia Mohamed , Ahmad Abdalhamid , Ashraf El-shahat , Sileem Ahmed Sileem , Mahmoud M. Tawfick , Ashraf Abo-Louz and Ahmed Hussein
Published/Copyright: October 19, 2020

Abstract

Objectives

To investigate whether etamsylate may be an alternative to tranexamic acid in reduction of blood loss during elective cesarean section.

Methods

Prospective double-blinded multi-center randomized controlled trial involving 180 qualified women equally divided into three groups each containing 60 women received either tranexamic acid, etamsylate or placebo 20 min before elective cesarean section and blood loss was estimated.

Results

Mean blood loss, cases needing blood transfusion and cases needing further interventions were significantly lower in tranexamic acid and etamsylate group than placebo group, while mean postoperative hemoglobin and hematocrite were significantly higher in both tranexamic acid and etamsylate as compared to placebo.

Conclusions

Etamsylate is an effective second-line therapy (after tranexamic acid) in reducing blood loss during elective cesarean section with low risk of side effects, therefore, it can be an effective alternative to tranexamic acid in cases with contraindications or anticipated to be at high-risk of developing side effects from tranexamic acid.


Corresponding author: Haitham Torky, Department of Obstetrics and Gynecology, October 6th University, Giza, Egypt, Phone: +201001230161, Fax: +20225240066, E-mail:

  1. Research funding: Pan-African Trial Registry Number PACTR201802002761404.

  2. Author contributions: All authors have accepted responsibility for the entire content of this manuscript and approved its submission.

  3. Competing interests: Authors state no conflict of interest.

  4. Informed consent: Informed consent was obtained from all individuals included in this study.

  5. Ethical approval: The Ethical Committee of blinded for peer review approved the study, which is in line with the Helsinki declaration and the study was registered in blinded for peer review.

References

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Received: 2020-06-15
Accepted: 2020-09-20
Published Online: 2020-10-19
Published in Print: 2021-03-26

© 2020 Walter de Gruyter GmbH, Berlin/Boston

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