Tranexamic Acid Dosing for Total Joint Arthroplasty

Arthropathy of Knee Clinical Trial

Official title:

Determining the Optimal Dose of Tranexamic Acid in Decreasing Blood Loss During Lower Extremity Total Joint Arthroplasty

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02584725
• Other study ID #: AAAM9601
• Status: Completed
• Phase: Phase 4
• Start date: December 2014
• Est. completion date: June 2015

Study information

• Verified date: October 2020
• Source: Columbia University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to determine the effect of increasing doses of tranexamic acid (TXA) on limiting blood loss during total knee and total hip arthroplasty as defined by a change in hemoglobin from pre-operative baseline to the first post-operative day.

Description:

The study is a prospective, randomized, double-blinded trial comparing three different doses of TXA (5mg/kg, 10mg/kg, 15mg/kg) in decreasing blood loss during and after total knee and total hip arthroplasty. Patients undergoing total knee arthroplasty and total hip arthroplasty will be analyzed separately, in sub-group analysis. The primary endpoint will be the change in hemoglobin from baseline to the first post-operative day (POD#1).

Patients will initially be identified by their orthopedic surgeon if they meet the inclusion and exclusion criteria. They will be informed about the study and provided with the consent form in the office, which they will be able to review further prior to the date of surgery. If the patient wishes to participate, formal written consent will be completed by one of the study investigators or a member of the regional anesthesia team. Patients will then be randomized to one of three groups. The anesthesia team responsible for the subject patient's care will receive two twenty milliliter syringes of medication. The syringe labeled "Study medication #1" will be administered intravenously over 20 minutes beginning at the start of surgical skin preparation, and the syringe labeled "Study medication #2" will be administered over 20 minutes beginning at the start of surgical wound closure. The syringes for group 1 (low-dose TXA) will each contain 5mg/kg TXA, diluted to 20 milliliters with saline. The syringes for group 2 (moderate-dose TXA) will each contain 10mg/kg TXA, diluted to 20 milliliters with saline. The syringes for group 3 (high-dose TXA) will each contain 15mg/kg TXA, diluted to 20 milliliters with saline. The anesthesia team will document the total intra-operative estimated blood loss as well as the amount of blood in the suction canister at the end of the surgery (as calculated by volume in the suction bucket minus volume of irrigation used).

The intraoperative course will be standardized for all patients included in the study. For total knee arthroplasty patients, the anesthesia will consist of a long-acting femoral or adductor canal peripheral nerve block, followed by a standardized spinal anesthetic using 15mg of plain isobaric bupivacaine. For total hip arthroplasty patients, the anesthesia will consist of a standardized spinal anesthetic using 15mg of plain isobaric bupivacaine. In those patients for whom spinal anesthesia is contraindicated or refused, general anesthesia will be performed and these patients will be excluded from the study. All patients initially enrolled, but excluded secondary to administration of a general anesthetic will be analyzed via an intention-to-treat method. Administration of intravenous crystalloid solutions will be per the discretion of the anesthesia team participating in the intra-operative portion of each patient's care, and will be documented for purposes of this study by the anesthesia team.

On PODs #0, #1 and #2, all patients will undergo standard post-operative blood work which includes a complete blood count. When working with physical therapy on POD#1 and POD#2, assessment of ability to sit, stand, and walk (yes/no) will be recorded. Assessment of pain scores via a VAS (0-10 scale, with 0 being no pain and 10 being the worst 05/26/2016 pain) will be recorded on POD#1 and POD#2. Assessment of subjective sense of overall wellbeing (a 0-10 scale, with 0 being the worst patients have ever felt, and 10 representing pre-operative baseline) will be recorded on POD #1 and #2. Patients will also be monitored via clinical exam for incidence of seizure, transient ischemic attack, stroke, myocardial infarction, deep venous thrombosis, and pulmonary embolus in the first 48 post-operatively.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 84
• Est. completion date: June 2015
• Est. primary completion date: June 2015
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Patients undergoing primary unilateral total knee arthroplasty or primary unilateral total hip arthroplasty under spinal anesthesia at Columbia University Medical Center/ New York Presbyterian Hospital.

Exclusion Criteria:

• Non-English speaking.

• Patient refusal to participate.

• Weight exceeding 100kg.

• Baseline hemoglobin of less than 10.

• Repeat, revision, or bilateral surgery.

• Known sensitivity or allergy to Tranexamic Acid.

• Active intra-vascular clotting.

• History of coagulopathy or congenital thrombophilia.

• Thromboembolic event in the 12 months prior to enrollment.

• Percutaneous coronary intervention requiring a drug eluting stent in the 12 months prior to enrollment.

• History of anticoagulant medication use unless stopped prior to surgery as recommended by and in accordance with the American Society of Regional Anesthesia Guidelines.

• Use of a general anesthetic in the current anesthetic.

• Blood transfusion for a hemoglobin value which deviates from the study's transfusion protocol.

Related Conditions & MeSH terms

• Arthropathy of Hip
• Arthropathy of Knee
• Joint Diseases

Intervention

Drug:
• Tranexamic Acid
Comparison of 3 different doses of the drug

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Columbia University

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change in Hemoglobin From Baseline to the First Post-operative Day (POD#1)		1 day
Secondary	Change in Hemoglobin From Baseline to POD#0		6 hours
Secondary	Change in Hemoglobin From Baseline to POD#2		2 days
Secondary	Number of Participants Requiring Blood Transfusion From the Intra-operative Period Into the End of POD#2	Number or count of participants requiring transfusion.	2 days
Secondary	Total Estimated Intra-operative Blood Loss		2 hours
Secondary	Volume of Blood in the Surgical Suction Canister at the End of Surgery		2 hours
Secondary	Count of Participants Able to Sit on Post-Operative Day 1 (POD1) and Post-Operative Day 2 (POD2)	Count of participants able to sit on POD1 and POD2 as assessed by a mobility assessment.	2 days
Secondary	Count of Participants Able to Stand on POD1 and POD2	Count of participants able to stand on POD1 and POD2 as assessed by a mobility assessment.	2 days
Secondary	Count of Participants Able to Walk on POD1 and POD2	Count of participants able to Walk on POD1 and POD2 as assessed by a mobility assessment.	2 days
Secondary	Visual Analog Scale (VAS) Pain Scores on POD#1 and POD#2	The VAS measures pain on a scale of 0-10, with 0=no pain and 10=worst possible pain.	2 days
Secondary	Wellbeing Questionnaire Score on POD#1 and POD#2	Patients' self-reported scores on a scale of overall feeling of wellbeing on POD#1 and POD#2. Scores range from 0-10, with 0= "worst I have ever felt" and 10= "feel just as well as before surgery."	2 days
Secondary	Count of Seizure, Transient Ischemic Attack, Stroke, Myocardial Infarction, Deep Venous Thrombosis, and Pulmonary Embolus		2 days