Tranexamic acid, an anti-fibrinolytic agent, is commonly given after induction of general anesthesia in patients undergoing hip and knee arthroplasty. This medication has been associated with decreased blood loss during these procedures, decreased rate of blood transfusion, decreased hospital costs, and no increased risk of thrombotic complication. Given the safety and efficacy of this medication in one subspeciality of orthopedics, it is warranted to investigate the use of it in another subspeciality where blood loss is also of concern. It is also of the utmost importance to identify medications that can safely be given to our population to not only improve patient outcomes but also decrease patient costs in the setting of significant disparities. The application of these findings to orthopedic trauma is not something that has been largely studied or appears in the literature. We hope to fill this gap of knowledge to allow for the application of a safe and beneficial medication to a much larger subset of patients than that that is already receiving the medication routinely. The use of TXA in orthopedic patients who are on anticoagulation versus those who are not is also not something that has been previously studied and another knowledge gap that we hope to fill.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
200
orthopedic trauma patients who are on anticoagulation
Community Regional Medical Center
Fresno, California, United States
Estimated blood loss (EBL) comparison between those who received TXA vs no TXA
Less estimated blood loss after surgery for patients who were administered TXA
Time frame: EBL note is made post-procedure by surgical team, and research team will collect data at least one month post-procedure
Hospital Length of Stay for Patients who received TXA vs no TXA
Patient medical records will be reviewed post-operatively and data will be collected in our study specific data sheet.
Time frame: EBL note is made post-procedure by surgical team, and research team will collect data at least one month post-procedure
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