Rothman Orthopaedic Institute at Thomas Jefferson University, Philadelphia, PA; Department of Orthopaedic Surgery, Iran University of Medical Sciences, Tehran, Iran.
Rothman Orthopaedic Institute at Thomas Jefferson University, Philadelphia, PA.
J Arthroplasty. 2020 Mar;35(3):840-844. doi: 10.1016/j.arth.2019.10.029. Epub 2019 Oct 22.
Previous studies have demonstrated preoperative anemia to be a strong risk factor for periprosthetic joint infection (PJI) in total joint arthroplasty (TJA). Allogeneic blood transfusion can be associated with increased risk of PJI after primary and revision TJA. Tranexamic acid (TXA) is known to reduce blood loss and the need for allogeneic blood transfusion after TJA. The hypothesis of this study is that administration of intravenous TXA would result in a reduction in PJI after TJA.
An institutional database was utilized to identify 6340 patients undergoing primary TJA between January 1, 2013 and June 31, 2017 with a minimum of 1-year follow-up. Patients were divided into 2 groups based on whether they received intravenous TXA prior to TJA or not. Patients who developed PJI were identified. All PJI patients met the 2018 International Consensus Meeting definition for PJI. A multivariate regression analysis was performed to identify variables independently associated with PJI.
Of the patients included, 3683 (58.1%) received TXA and 2657 (41.9%) did not. The overall incidence of preoperative anemia was 16%, postoperative blood transfusion 1.8%, and PJI 2.4%. Bivariate analysis showed that patients who received TXA were significantly at lower odds of infection. After adjusting for all confounding variables, multivariate regression analysis showed that TXA is associated with reduced PJI after primary TJA.
TXA can help reduce the rate of PJI after primary TJA. This protective effect is likely interlinked to reduction in blood loss, lower need for allogeneic blood transfusion, and issues related to immunomodulation associated with blood transfusion.
先前的研究表明,术前贫血是全膝关节置换术(TJA)中假体周围关节感染(PJI)的一个强危险因素。同种异体输血可能与初次和翻修 TJA 后 PJI 的风险增加有关。氨甲环酸(TXA)已知可减少 TJA 后的出血量和异体输血的需求。本研究的假设是,静脉内给予 TXA 可降低 TJA 后的 PJI 发生率。
利用机构数据库,确定了 2013 年 1 月 1 日至 2017 年 6 月 31 日期间接受初次 TJA 的 6340 例患者,随访时间至少 1 年。根据患者是否在 TJA 前接受静脉内 TXA 将其分为两组。确定发生 PJI 的患者。所有 PJI 患者均符合 2018 年国际共识会议对 PJI 的定义。进行多变量回归分析以确定与 PJI 独立相关的变量。
纳入的患者中,3683 例(58.1%)接受了 TXA,2657 例(41.9%)未接受。术前贫血的总体发生率为 16%,术后输血率为 1.8%,PJI 发生率为 2.4%。双变量分析表明,接受 TXA 的患者感染的可能性明显较低。在调整所有混杂变量后,多变量回归分析显示,TXA 与初次 TJA 后 PJI 发生率降低相关。
TXA 有助于降低初次 TJA 后 PJI 的发生率。这种保护作用可能与减少出血量、降低异体输血需求以及与输血相关的免疫调节问题有关。