Efficacy of Tranexamic Acid for Reducing Blood Loss and Blood Transfusion After Periacetabular Osteotomy
Status: | Enrolling by invitation |
---|---|
Conditions: | Orthopedic |
Therapuetic Areas: | Orthopedics / Podiatry |
Healthy: | No |
Age Range: | 12 - 45 |
Updated: | 2/23/2019 |
Start Date: | October 2014 |
End Date: | June 2019 |
The Effect of Intravenous Tranexamic Acid on Blood Loss and Transfusion After Periacetabular Osteotomy: a Prospective, Double-blinded, Randomized Controlled Trial
The goal of this randomized controlled, double-blinded trial is to assess the efficacy of
intravenous tranexamic acid, a drug, in reducing blood loss and transfusion in patients
undergoing periacetabular osteotomy, an elective reorientation procedure for the hip joint.
The investigators hypothesize that tranexamic acid will be more effective than placebo
(normal saline solution) in reducing blood loss and transfusion after periacetabular
osteotomy.
intravenous tranexamic acid, a drug, in reducing blood loss and transfusion in patients
undergoing periacetabular osteotomy, an elective reorientation procedure for the hip joint.
The investigators hypothesize that tranexamic acid will be more effective than placebo
(normal saline solution) in reducing blood loss and transfusion after periacetabular
osteotomy.
Periacetabular osteotomy (PAO) is an elective reorientation surgery for the hip joint,
typically for the treatment of hip dysplasia in young, otherwise healthy patients, which
requires multiple pelvic osteotomies around the acetabulum. A major source of its
perioperative morbidity is blood loss. The principal cause of postoperative blood loss after
PAO is surgical trauma, with secondary activation of both the coagulation cascade and local
fibrinolysis. In the PAO literature, allogeneic transfusion rates are as high as 58%, and
blood loss can range to nearly 4 L. The risk of excessive blood loss and blood transfusion in
young, healthy patients after elective surgery is an event that can be reduced with blood
conservation protocols, which can include pharmacological agents. Tranexamic acid is a
synthetic derivative of the amino acid lysine and a competitive inhibitor of plasminogen
activation that interferes with fibrinolysis. Multiple studies and meta-analyses have shown
that intravenous administration of the antifibrinolytic agent tranexamic acid reduces
postoperative bleeding and the need for transfusion during joint replacement surgery.
However, no published data exists to support its use during PAO. We hypothesize that
intravenous tranexamic acid will reduce perioperative blood loss and, thus, transfusion
requirement in patients undergoing PAO. A total of 80 patients will be enrolled. Patients
will be randomized to receive either intravenous tranexamic acid versus placebo (normal
saline) during PAO. Calculated total blood loss (primary outcome) will be determined, and
intraoperative cell saver utilization (secondary outcome), and (3) postoperative allogeneic
blood transfusion (secondary outcome) will be recorded. Patients will be followed for a total
of 6 weeks after surgical intervention. If the use of IV tranexamic acid in the PAO patient
population significantly reduces total perioperative blood loss, then it would provide an
efficacious and inexpensive method for reducing postoperative morbidity after PAO.
typically for the treatment of hip dysplasia in young, otherwise healthy patients, which
requires multiple pelvic osteotomies around the acetabulum. A major source of its
perioperative morbidity is blood loss. The principal cause of postoperative blood loss after
PAO is surgical trauma, with secondary activation of both the coagulation cascade and local
fibrinolysis. In the PAO literature, allogeneic transfusion rates are as high as 58%, and
blood loss can range to nearly 4 L. The risk of excessive blood loss and blood transfusion in
young, healthy patients after elective surgery is an event that can be reduced with blood
conservation protocols, which can include pharmacological agents. Tranexamic acid is a
synthetic derivative of the amino acid lysine and a competitive inhibitor of plasminogen
activation that interferes with fibrinolysis. Multiple studies and meta-analyses have shown
that intravenous administration of the antifibrinolytic agent tranexamic acid reduces
postoperative bleeding and the need for transfusion during joint replacement surgery.
However, no published data exists to support its use during PAO. We hypothesize that
intravenous tranexamic acid will reduce perioperative blood loss and, thus, transfusion
requirement in patients undergoing PAO. A total of 80 patients will be enrolled. Patients
will be randomized to receive either intravenous tranexamic acid versus placebo (normal
saline) during PAO. Calculated total blood loss (primary outcome) will be determined, and
intraoperative cell saver utilization (secondary outcome), and (3) postoperative allogeneic
blood transfusion (secondary outcome) will be recorded. Patients will be followed for a total
of 6 weeks after surgical intervention. If the use of IV tranexamic acid in the PAO patient
population significantly reduces total perioperative blood loss, then it would provide an
efficacious and inexpensive method for reducing postoperative morbidity after PAO.
Inclusion Criteria:
- Age greater than or equal to 12 years old
- Age less than or equal to 45 years old
- Indicated for elective periacetabular osteotomy
Exclusion Criteria:
- Preoperative use of an anticoagulant (Plavix, warfarin, lovenox, etc.)
- History of hypersensitivity to tranexamic acid
- History of thromboembolic event (e.g., Pulmonary embolism or Deep vein thrombosis)
- History of subarachnoid hemorrhage
- History or evidence of hepatic dysfunction (aspartate transaminase-alanine
transaminase ratio greater than 60) or renal dysfunction (Creatinine greater than 1.5
mg/dL, or glomerular filtration rate less than 30 mL/minute)
- History of seizure
- Coronary stents or prior diagnosis of coronary artery disease
- Color blindness
- Leukemia
- Congenital or acquired coagulopathy as evidence by international normalized ratio
(INR) greater than 1.4 or partial thromboplastin time (PTT) > 1.4 times normal, or
Platelets less than 150,000/mm^3 on preoperative laboratory testing
- Use of hormone replacement therapy or hormonal contraceptive agent within 7 days prior
to surgery
- Pregnant
- Breastfeeding
- Donated preoperative autologous blood
- Younger than 12-years-old and older than 45-years-old
- Preoperative hemoglobin less than 10 g/dL
- Concomitant open procedures (e.g., femoral osteotomy or osteochondral allograft)
- Patients with any contraindication to neuraxial anesthesia:
- Patient refusal
- History of lumbar spinal fusion
- Infection at the site of the epidural
- Coagulopathy, as defined above
- Ventriculoperitoneal shunt
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