Tranexamic Acid in Patients Undergoing Liver Resection: The HeLiX Randomized Clinical Trial

JAMA. 2024 Oct 1;332(13):1080-1089. doi: 10.1001/jama.2024.11783.

Abstract

Importance: Tranexamic acid reduces bleeding and blood transfusion in many types of surgery, but its effect in patients undergoing liver resection for a cancer-related indication remains unclear.

Objective: To determine whether tranexamic acid reduces red blood cell transfusion within 7 days of liver resection.

Design, setting, and participants: Multicenter randomized clinical trial of tranexamic acid vs placebo conducted from December 1, 2014, to November 8, 2022, at 10 hepatopancreaticobiliary sites in Canada and 1 site in the United States, with 90-day follow-up. Participants, clinicians, and data collectors were blinded to allocation. A volunteer sample of 1384 patients undergoing liver resection for a cancer-related indication met eligibility criteria and consented to randomization.

Interventions: Tranexamic acid (1-g bolus followed by 1-g infusion over 8 hours; n = 619) or matching placebo (n = 626) beginning at induction of anesthesia.

Main outcomes and measures: The primary outcome was receipt of red blood cell transfusion within 7 days of surgery.

Results: The primary analysis included 1245 participants (mean age, 63.2 years; 39.8% female; 56.1% with a diagnosis of colorectal liver metastases). Perioperative characteristics were similar between groups. Red blood cell transfusion occurred in 16.3% of participants (n = 101) in the tranexamic acid group and 14.5% (n = 91) in the placebo group (odds ratio, 1.15 [95% CI, 0.84-1.56]; P = .38; absolute difference, 2% [95% CI, -2% to 6%]). Measured intraoperative blood loss (tranexamic acid, 817.3 mL; placebo, 836.7 mL; P = .75) and total estimated blood loss over 7 days (tranexamic acid, 1504.0 mL; placebo, 1551.2 mL; P = .38) were similar between groups. Participants receiving tranexamic acid experienced significantly more complications compared with placebo (odds ratio, 1.28 [95% CI, 1.02-1.60]; P = .03), with no significant difference in venous thromboembolism (odds ratio, 1.68 [95% CI, 0.95-3.07]; P = .08).

Conclusions and relevance: Among patients undergoing liver resection for a cancer-related indication, tranexamic acid did not reduce bleeding or blood transfusion but increased perioperative complications.

Trial registration: ClinicalTrials.gov Identifier: NCT02261415.

Publication types

  • Clinical Trial, Phase III
  • Multicenter Study
  • Pragmatic Clinical Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Antifibrinolytic Agents* / administration & dosage
  • Antifibrinolytic Agents* / adverse effects
  • Blood Loss, Surgical / prevention & control
  • Blood Loss, Surgical / statistics & numerical data
  • Double-Blind Method
  • Erythrocyte Transfusion / statistics & numerical data
  • Female
  • Hepatectomy* / adverse effects
  • Hepatectomy* / statistics & numerical data
  • Humans
  • Liver Neoplasms* / surgery
  • Male
  • Middle Aged
  • Perioperative Period / statistics & numerical data
  • Postoperative Complications* / epidemiology
  • Postoperative Complications* / etiology
  • Tranexamic Acid* / administration & dosage
  • Tranexamic Acid* / adverse effects

Substances

  • Antifibrinolytic Agents
  • Tranexamic Acid

Associated data

  • ClinicalTrials.gov/NCT02261415