Tranexamic Acid in Adult Spinal Deformity Surgery

Blood Loss, Surgical Clinical Trial

Official title:

Topical Tranexamic Acid as a Adjunct to Intravenous Tranexamic Acid in Adult Spinal Deformity Surgery

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT03553186
• Other study ID #: 2017-0920
• Status: Recruiting
• Phase: Phase 3
• Start date: July 11, 2018
• Est. completion date: March 2025

Study information

• Verified date: April 2024
• Source: Hospital for Special Surgery, New York
• Contact: Jordan A Gruskay, MD
• Phone: 2034647759
• Email: gruskayj[@]hss.edu
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Posterior spinal surgery for adult deformity is associated with high incidence of blood loss and need for blood transfusion and intraoperative blood salvage, with associated increased cost and risk for perioperative complications. Tranexamic acid (TXA) is relatively inexpensive anti-fibrinolytic agent that has been proven effective for decreasing intraoperative blood loss in various surgical specialties. Intravenous TXA (ivTXA) is routinely used at our institution for adult spinal deformity cases. Meanwhile, topical TXA (tTXA) is an attractive alternative/adjunct to ivTXA used with good results in orthopedic arthroplasty and cardiac surgery. To the investigators' knowledge, no data exists in the literature on the use of tTXA in either adult or pediatric spinal deformity surgery. The goal of this study is to determine the role tTXA has an adjunct to ivTXA in decreasing perioperative blood loss, drainage, transfusion requirements and length of stay following adult deformity spine surgery.

Description:

Blood loss is a significant issue in spinal deformity surgery, often requiring allogenic blood transfusion and/or intraoperative blood salvage and leading to increased risk of postoperative morbidity, increased length of stay, and higher total hospital costs. Tranexamic acid is an antifibrinolytic agent that is used in many surgical specialties to prevent perioperative blood loss. Intravenous (ivTXA) dosing has proven effective in reducing blood loss and perioperative transfusion in spinal surgery, while the topical (tTXA) form has been shown to be at least non-inferior to IV transfusion in the total arthroplasty literature. Intravenous TXA is routinely used at the investigators' institution in spinal deformity cases, but even with ivTXA infusion, perioperative blood loss remains a significant issue, with total estimated and calculated blood loss between ~1500-3000 mL. Usage of local tTXA in addition to ivTXA may provide additional benefits including an additive effect on decreasing blood loss, allowing for lowered dosages of ivTXA, decreasing risks associated with systemic exposure. Combination ivTXA and tTXA has shown excellent results in total joint arthroplasty. The objective of this study is to determine the additive benefit and risks of co-administration of the two in spinal deformity surgery. This population of spinal patients was chosen because the estimated blood loss is high and the potential clinical benefit of the intervention is large. Patients will be enrolled if they are undergoing surgery > 5 levels with extension to the pelvis. The investigators have previously utilized topical TXA for these cases by applying operative sponges soaked with solution into the wound during routine x-ray check following instrumentation, with anecdotally good effect. However, this practice has not been prospectively studied. In this prospective, randomized, blinded, placebo controlled study, a similar combined effect of ivTXA and tTXA on decreasing perioperative blood loss as seen in total joint arthroplasty, with a similar safety profile is expected.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 100
• Est. completion date: March 2025
• Est. primary completion date: March 2025
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 80 Years

Eligibility

Inclusion Criteria:

• Age 18-80

• Scheduled to undergo posterior long segment ( = 5 levels) posterior spinal fusion for adult scoliosis or degenerative joint diseae

• + fusion to pelvis

Exclusion Criteria:

• Surgical factors:

• Anterior Approach

• Presence or history of dural tear without repair as evidenced by pseudomeningocele on MRI imaging or by intraoperative exploration

• Patients donating autologous blood preoperatively

Patient factors:

• Diagnosis of renal (Cr>1.5 or CrCl <30ml/min) or hepatic insufficiency (AST, ALT 2x upper limit of normal)

• Diagnosis of seizure disorder or prior seizure

• History of thromboembolic events (CVA, TIA, DVT, PE) if within 1 year of surgery

• Hypercoagulability (e.g. antiphospholipid syndrome)

• History of coronary artery disease (stent, MI, +stress test) within 1 year of surgery

• Atrial fibrillation

• Concurrent anticoagulation therapy that cannot be discontinued within 3 days before surgery (Coumadin, plavix, LVX)

• Concurrent anticoagulation with ASA 325 that cannot be discontinued 10 days before surgery

• Bleeding disorder or abnormal preoperative coagulation profile (as identified by a preoperative platelet count of <100,000/mm3, an international normalized ratio of >1.4, or a prolonged partial thromboplastin time >1.4 times normal)

• Preexisting anemia <10 g/dL

• Color blindness or disturbance of color vision

• Leukemia or active cancer

• Religious restrictions on blood transfusion

• Pregnancy or women who are lactating/breastfeeding

Related Conditions & MeSH terms

• Blood Loss, Surgical
• Congenital Abnormalities
• Degenerative Lumbar Spinal Stenosis
• Spinal Deformity
• Spinal Stenosis

Intervention

Drug:
• Tranexamic Acid 100 MG/ML
TXA lavage solution (200 cc sterile normal saline + 5 g tranexamic acid 100mg/ml (50cc)) will be poured into the surgical field and left in contact for five minutes. This will occur after instrumentation. Excess solution will be suctioned away using a non-cell saver suction.
• Placebo
Placebo solution (200 cc sterile normal saline + placebo TXA ampule (50cc)) will be poured into the surgical field and left in contact for five minutes. This will occur after pedicle screw instrumentation. Excess solution will be suctioned away using a non-cell saver suction.

Locations

Country	Name	City	State
United States	Hospital for Special Surgery	New York	New York

Sponsors (1)

Lead Sponsor	Collaborator
Hospital for Special Surgery, New York

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Postoperative Drain output	Drain Output	48 hours
Secondary	Perioperative blood transfusion	Number of units of blood transfused perioperatively, including cell saver administration	Up to 30 days postoperatively
Secondary	Perioperative blood drop	CBC with hct/hg tracked postoperatively	Up to 72 hours postoperatively
Secondary	Perioperative adverse events	Minor and major adverse events occuring during hospitalization or after discharge	Up to 30 days postoperatively
Secondary	Length of stay	# of days from surgery to discharge	Up to 30 days postoperatively