What is the recommended dosing of Tranexamic Acid (TXA) in patients undergoing organ transplantation?

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Last updated: August 26, 2025View editorial policy

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Tranexamic Acid Dosing in Organ Transplantation

For patients undergoing organ transplantation, tranexamic acid should be administered as a 10 mg/kg loading dose followed by a 1 mg/kg/hour infusion during the procedure, with dose reductions required in patients with renal dysfunction. 1

Rationale for TXA Use in Transplantation

Tranexamic acid (TXA) is particularly valuable during liver transplantation due to the hyperfibrinolytic state that occurs during the procedure:

  • Hyperfibrinolysis during liver transplantation is caused by high levels of tissue plasminogen activator release, especially during the anhepatic phase 1
  • Randomized controlled trials have demonstrated that antifibrinolytic treatment reduces blood loss and transfusion requirements in liver transplantation without increasing thrombotic events 1
  • TXA has replaced aprotinin (which was withdrawn due to mortality concerns in cardiac surgery) as the preferred antifibrinolytic agent for transplantation 1

Standard Dosing Protocol

The recommended dosing regimen for TXA in organ transplantation is:

  • Loading dose: 10 mg/kg IV administered over 10 minutes
  • Maintenance infusion: 1 mg/kg/hour during the procedure 2, 3

This dosing has been shown to significantly reduce:

  • Intraoperative blood loss (median 4.3L vs 8L with placebo) 3
  • Perioperative erythrocyte use (median 9 units vs 13 units) 3
  • Total perioperative donor exposure (20.5 units vs 43.5 units) 3

Renal Dose Adjustments

Since TXA is primarily eliminated through renal clearance (90% excreted in urine within 24 hours), dose adjustments are mandatory in patients with renal dysfunction 1:

Serum Creatinine TXA IV Dosage
1.36-2.83 mg/dL 10 mg/kg twice daily
2.83-5.66 mg/dL 10 mg/kg daily
>5.66 mg/dL 10 mg/kg every 48 hours or 5 mg/kg every 24 hours

Failure to adjust dosing in renal dysfunction can lead to serious complications including neurotoxicity and ocular toxicity 1.

Monitoring During TXA Administration

When administering TXA during organ transplantation, monitor:

  • Coagulation parameters (PT, APTT, fibrinogen) 1
  • Kidney function (serum creatinine) 1
  • Signs of thrombosis, especially in high-risk patients 4
  • Visual disturbances, seizures, or hypersensitivity reactions 4

Special Considerations for Different Transplants

Liver Transplantation

  • TXA has been extensively studied in liver transplantation and shown to be effective 3, 5
  • High-dose TXA (up to 20g total) has been used safely in liver transplantation studies 3
  • No increased risk of hepatic artery or portal venous thrombosis has been observed with proper dosing 3

Kidney Transplantation

  • More cautious dosing is required due to the recipient's compromised renal function
  • Follow renal dosing adjustments strictly 1
  • Monitor serum creatinine frequently as recommended by KDIGO guidelines 1

Contraindications and Cautions

TXA should be avoided or used with extreme caution in transplant patients with:

  • Active intravascular clotting
  • Subarachnoid hemorrhage
  • Hypersensitivity to TXA
  • History of seizures (TXA can lower seizure threshold)
  • Massive hematuria (risk of ureteric obstruction) 4

Efficacy Comparison

TXA has been shown to be superior to:

  • Epsilon-aminocaproic acid for reducing packed red blood cell usage during liver transplantation 5
  • Placebo in multiple studies 3, 5

The evidence strongly supports that proper TXA administration significantly reduces blood loss and transfusion requirements without increasing thrombotic complications in organ transplantation.

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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