Abstract

Abundant literature confirms that intravenous (IV) and intra-articular (IA) administration of tranexamic acid (TXA) reduces blood loss in total knee arthroplasty (TKA). Oral formulations of TXA exhibit profound cost-saving benefits. However, comparisons of the clinical efficacy among three different modalities of TXA administration have not been previously investigated in the setting of TKA with no closed suction drain and tourniquet. A total of 180 patients undergoing TKA were randomized to receive 2-g oral TXA 2 hours preoperatively, 20-mg/kg IV TXA 5 minutes prior to incision, or 2-g IA TXA. The primary outcome was 72-hour blood loss. Secondary outcomes were reductions in hemoglobin, the rate of transfusions, and adverse events. No significant differences were identified with regard to the mean 72-hour blood loss among the three groups (1003 mL in oral group, 1108 mL in IV group, and 1059 mL in IA group, respectively). Similarly, hemoglobin reduction was equivalent among the groups. Only one patient in IV group exhibited deep venous thrombosis. No difference was identified regarding transfusion rates. Oral TXA results in similar blood loss in TKA, with a profound cost-saving benefit, compared with the IA and IV formulations.

Highlights

  • Total knee arthroplasty (TKA) is associated with substantial intra- and postoperative blood loss that may carry a substantial risk of anemia and allogeneic transfusions[1,2]

  • Most studies focused on the investigation of IA and IV modalities of tranexamic acid (TXA) administration, but only two prospective studies investigated the efficacy of oral TXA administration compared to IV or IA TXA in total knee arthroplasty (TKA) when this trial was designed[11,12]

  • 180 enrolled study participants were included in the randomization in terms of interventions

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Summary

Introduction

Total knee arthroplasty (TKA) is associated with substantial intra- and postoperative blood loss that may carry a substantial risk of anemia and allogeneic transfusions[1,2]. Numerous randomized controlled trials confirmed that perioperative intravenous (IV), intra-articular (IA), and oral routes of TXA administration exhibited beneficial blood-saving effects and reduced transfusion requirements without www.nature.com/scientificreports/. The blood-sparing efficacy of oral TXA remains unclear in TKA without tourniquet and postoperative closed suction drain. Our randomized controlled trial was performed with an enhanced-recovery protocol to compare the efficacy of oral administration of TXA with that of IA and IV administration of TXA without the use of closed suction drain and tourniquet. We hypothesized that oral administration of TXA would produce an equivalent reduction in postoperative blood loss compared with IA and IV administration of TXA, with a better cost-effectiveness profile

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