

DOS Kongressen 2017 ·
153
Tranexamic acid does not increase the postopera-
tive risk of cardiovascular events or death after
total hip arthroplasty surgery. A population-based
study from the Danish Hip Arthroplasty Register
Alexander Dastrup, Anton Pottegård, Jesper Hallas, Søren Overgaard
Department of Orthopaedic Surgery, Odense University Hospital; Clinical Phar-
macology and Pharmacy, University of Southern Denmark; Clinical Pharmacolo-
gy and Pharmacy, University of Southern Denmark; Department of Orthopedic
Surgery and Traumatology, Odense University Hospital
Background:
There remain concerns that routine use of tranexamic acid (TXA)
during primary total hip arthroplasty (THA) might increase the postoperative
risk of cardiovascular events. We aimed to estimate the risks of primarily venous
thromboembolism (VTE) and secondarily; deep vein thrombosis (DVT), pulmo-
nary embolism (PE), myocardial infarction (MI), ischemic stroke and all-cause
mortality within 30 days after surgery.
Purpose / Aim of Study:
To determine the safety of perioperative tranexamic
acid during primary THA in Denmark.
Materials and Methods:
Using the Danish Hip Arthroplasty Register, the Dan-
ish National Patient Register and the Danish National Database of Prescriptions
we included a total of 45,290 patients with primary THA from 2006 to 2013.
38,586 patients received perioperative TXA while 6704 did not. 1:2 Propensity
score matching on age, gender, year of surgery, known risk factors for car-
diovascular disease, the Elixhauser Comorbidity Index and income resulted in a
final cohort of 6002 and 12,004 individuals, unexposed and exposed to TXA
respectively. Cox regression survival analysis was used to calculate hazard ratios
(HR) and 95% confidence intervals (CI) for the validated outcomes.
Findings / Results:
In the matched cohort we found no statistically significant
effect on VTE (HR = 1.18; 95% CI, 0.83- 1.68), DVT (HR = 1.15; 95% CI,
0.78-1.68), PE (HR = 1.50; 95% CI, 0.60-3.78), MI (HR = 0.83; 95% CI, 0.46-
1.50), ischemic stroke (HR = 0.89; 95% CI, 0.39-2.01) or all-cause mortality
(HR = 0.73; 95% CI, 0.41-1.28).
Conclusions:
Use of TXA is not associated with the risk of VTE, DVT, PE, MI,
ischemic stroke or all-cause mortality after primary THA. Perioperative use of
TXA for primary THA seems safe.
No conflicts of interest reported
105.