Department of Orthopedic Surgery, Mayo Clinic, Jacksonville, Florida, USA.
Department of Radiology, Mayo Clinic, Jacksonville, Florida, USA.
J Surg Oncol. 2023 Oct;128(5):869-876. doi: 10.1002/jso.27391. Epub 2023 Jul 10.
Tranexamic acid (TXA) is an antifibrinolytic drug that has been shown to reduce blood loss following surgery. The use of TXA during orthopedic procedures has gained widespread acceptance, with multiple clinical studies demonstrating no increase in thrombotic complications. While TXA has been shown to be safe and effective for several orthopedic procedures, its use in orthopedic sarcoma surgery is not well established. Cancer-associated thrombosis remains a significant cause of morbidity and mortality in patients with sarcoma. It is unknown if intraoperative TXA use will increase the risk of developing a postoperative thrombotic complication in this population. This study aimed to compare the risk of postoperative thrombotic complications in patients who received TXA during sarcoma resection to patients who did not receive TXA.
A retrospective review was performed of 1099 patients who underwent resection of a soft tissue or bone sarcoma at our institution between 2010 and 2021. Baseline demographics and postoperative outcomes were compared between patients who did and did not receive intraoperative TXA. We evaluated 90-day complication rates, including: deep venous thrombosis (DVT), pulmonary embolism (PE), myocardial infarction (MI), cerebrovascular accident (CVA), and mortality.
TXA was used more commonly for bone tumors (p < 0.001), tumors located in the pelvis (p = 0.004), and larger tumors (p < 0.001). Patients who received intraoperative TXA were associated with a significant increase in developing a postoperative DVT (odds ratio [OR]: 2.22, p = 0.036) and PE (OR: 4.62, p < 0.001), but had no increase in CVA, MI, or mortality (all p > 0.05) within 90 days of surgery, following univariate analysis. Multivariable analysis confirmed that TXA was independently associated with developing a postoperative PE (OR: 10.64, 95% confidence interval: 2.23-50.86, p = 0.003). We found no association with DVT, MI, CVA, or mortality within 90 days postoperatively, following intraoperative TXA use.
Our results demonstrate a higher associated risk of PE following TXA use in sarcoma surgery and caution is warranted with TXA use in this patient population.
氨甲环酸(TXA)是一种抗纤维蛋白溶解药物,已被证明可减少手术后的失血。TXA 在骨科手术中的应用已得到广泛认可,多项临床研究表明不会增加血栓并发症的风险。虽然 TXA 已被证明在几种骨科手术中是安全有效的,但它在骨科肉瘤手术中的应用尚未得到充分确立。癌症相关的血栓仍然是肉瘤患者发病率和死亡率的一个重要原因。尚不清楚在这群患者中,术中使用 TXA 是否会增加术后发生血栓并发症的风险。本研究旨在比较在我院接受肉瘤切除术的患者中使用 TXA 和未使用 TXA 的患者术后血栓并发症的风险。
我们对 2010 年至 2021 年间在我院接受软组织或骨肉瘤切除术的 1099 例患者进行了回顾性分析。比较了术中使用 TXA 和未使用 TXA 的患者的基线人口统计学和术后结局。我们评估了 90 天的并发症发生率,包括:深静脉血栓形成(DVT)、肺栓塞(PE)、心肌梗死(MI)、脑血管意外(CVA)和死亡率。
TXA 更常用于骨肿瘤(p<0.001)、骨盆肿瘤(p=0.004)和更大的肿瘤(p<0.001)。接受术中 TXA 的患者发生术后 DVT(优势比 [OR]:2.22,p=0.036)和 PE(OR:4.62,p<0.001)的风险显著增加,但在术后 90 天内未增加 CVA、MI 或死亡率(所有 p>0.05),在单变量分析后。多变量分析证实,TXA 与术后发生 PE 独立相关(OR:10.64,95%置信区间:2.23-50.86,p=0.003)。我们发现,在术后 90 天内,术中使用 TXA 与 DVT、MI、CVA 或死亡率无关。
我们的结果表明,TXA 在肉瘤手术中的应用与 PE 发生风险增加相关,因此在该患者人群中使用 TXA 时需要谨慎。