Analysis of tranexamic acid usage in adult spinal deformity patients with relative contraindications: does it increase the risk of complications?

Author:

Mullin Jeffrey P.12,Soliman Mohamed A. R.13,Smith Justin S.4,Kelly Michael P.5,Buell Thomas J.6,Diebo Bassel7,Scheer Justin K.8,Line Breton9,Lafage Virginie10,Lafage Renaud10,Klineberg Eric11,Kim Han Jo12,Passias Peter G.13,Gum Jeffrey L.14,Kebaish Khaled15,Eastlack Robert K.16,Daniels Alan H.7,Soroceanu Alex17,Mundis Gregory16,Hostin Richard18,Protopsaltis Themistocles S.13,Hamilton D. Kojo6,Gupta Munish C.19,Lewis Stephen J.20,Schwab Frank J.10,Lenke Lawrence G.21,Shaffrey Christopher I.22,Bess Shay9,Ames Christopher P.8,Burton Douglas23

Affiliation:

1. Department of Neurosurgery, Jacobs School of Medicine and Biomedical Sciences at University at Buffalo, Buffalo, New York;

2. Department of Neurosurgery, Buffalo General Medical Center, Kaleida Health, Buffalo, New York;

3. Department of Neurosurgery, Faculty of Medicine, Cairo University, Cairo, Egypt;

4. Department of Neurosurgery, University of Virginia, Charlottesville, Virginia;

5. Department of Orthopedic Surgery, Rady Children’s Hospital, San Diego, California;

6. Department of Neurosurgery, University of Pittsburgh, Pittsburgh, Pennsylvania;

7. Department of Orthopedic Surgery, Brown University, Providence, Rhode Island;

8. Department of Neurological Surgery, University of California San Francisco, San Francisco, California;

9. Presbyterian St. Luke’s Medical Center, Denver, Colorado;

10. Department of Orthopedic Surgery, Lennox Hill Hospital, New York, New York;

11. Department of Orthopedic Surgery, University of Texas Health Houston, Houston, Texas;

12. Department of Orthopaedic Surgery, Hospital for Special Surgery, New York, New York;

13. Department of Orthopaedic Surgery, NYU Hospital for Joint Diseases, New York, New York;

14. Leatherman Spine Center, Louisville, Kentucky;

15. Department of Orthopaedic Surgery, Johns Hopkins University, Baltimore, Maryland;

16. Department of Orthopedic Surgery, Scripps Clinic, San Diego, California;

17. Department of Orthopedic Surgery, University of Calgary, Calgary, Alberta, Canada;

18. Department of Orthopaedic Surgery, Baylor Scoliosis Center, Plano, Texas;

19. Department of Orthopedic Surgery, Washington University, St. Louis, Missouri;

20. Department of Surgery, Division of Orthopedic Surgery, University of Toronto and Toronto Western Hospital, Toronto, Ontario, Canada;

21. Department of Orthopedic Surgery, Columbia University Medical Center, New York, New York;

22. Departments of Neurosurgery and Orthopedic Surgery, Spine Division, Duke University, Durham, North Carolina; and

23. Department of Orthopaedic Surgery, University of Kansas Medical Center, Kansas City, Kansas

Abstract

OBJECTIVE Complex spinal deformity surgeries may involve significant blood loss. The use of antifibrinolytic agents such as tranexamic acid (TXA) has been proven to reduce perioperative blood loss. However, for patients with a history of thromboembolic events, there is concern of increased risk when TXA is used during these surgeries. This study aimed to assess whether TXA use in patients undergoing complex spinal deformity correction surgeries increases the risk of thromboembolic complications based on preexisting thromboembolic risk factors. METHODS Data were analyzed for adult patients who received TXA during surgical correction for spinal deformity at 21 North American centers between August 2018 and October 2022. Patients with preexisting thromboembolic events and other risk factors (history of deep venous thrombosis [DVT], pulmonary embolism [PE], myocardial infarction [MI], stroke, peripheral vascular disease, or cancer) were identified. Thromboembolic complication rates were assessed during the postoperative 90 days. Univariate and multivariate analyses were performed to assess thromboembolic outcomes in high-risk and low-risk patients who received intravenous TXA. RESULTS Among 411 consecutive patients who underwent complex spinal deformity surgery and received TXA intraoperatively, 130 (31.6%) were considered high-risk patients. There was no significant difference in thromboembolic complications between patients with and those without preexisting thromboembolic risk factors in univariate analysis (high-risk group vs low-risk group: 8.5% vs 2.8%, p = 0.45). Specifically, there were no significant differences between groups regarding the 90-day postoperative rates of DVT (high-risk group vs low-risk group: 1.5% vs 1.4%, p = 0.98), PE (2.3% vs 1.8%, p = 0.71), acute MI (1.5% vs 0%, p = 0.19), or stroke (0.8% vs 1.1%, p > 0.99). On multivariate analysis, high-risk status was not a significant independent predictor for any of the thromboembolic complications. CONCLUSIONS Administration of intravenous TXA during the correction procedure did not change rates of thromboembolic events, acute MI, or stroke in this cohort of adult spinal deformity surgery patients.

Publisher

Journal of Neurosurgery Publishing Group (JNSPG)

Reference28 articles.

1. Increase in spinal deformity surgery in patients age 60 and older is not associated with increased complications;Sing DC,2017

2. Vertebral bone quality score independently predicts proximal junctional kyphosis and/or failure after adult spinal deformity surgery;Kuo CC,2023

3. Non-neurologic adverse events after complex adult spinal deformity surgery: results from the prospective, multicenter Scoli-RISK-1 study;Kwan KYH,2019

4. Outcomes of surgical treatment for 138 patients with severe sagittal deformity at a minimum 2-year follow-up: a case series;Scheer JK,2021

5. Incidence and predictors of all-cause mortality within one year after adult spinal deformity surgery;Zuckerman SL,2018

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