Grant Andrea L, Letson Hayley L, Morris Jodie L, McEwen Peter, Hazratwala Kaushik, Wilkinson Matthew, Dobson Geoffrey P
The Orthopaedic Research Institute of Queensland (ORIQL), 7 Turner St, Pimlico, Townsville, Queensland, 4812, Australia.
Heart, Trauma and Sepsis Research Laboratory, College of Medicine and Dentistry, James Cook University, 1 James Cook Drive, Townsville, Queensland, 4811, Australia.
J Orthop Surg Res. 2018 Jun 18;13(1):149. doi: 10.1186/s13018-018-0855-5.
Tranexamic acid (TXA) is commonly used in orthopedic surgery to reduce excessive bleeding and transfusion requirements. Our aim was to examine if TXA was required in all osteoarthritis patients undergoing TKA surgery, and its possible effects on systemic inflammation and coagulation properties.
Twenty-three patients (Oxford Score 22-29) were recruited consecutively; 12 patients received TXA before (IV, 1.2 g/90 kg) and immediately after surgery (intra-articular, 1.4 g/90 kg). Inflammatory mediators and ROTEM parameters were measured in blood at baseline, after the first bone-cut, immediately after surgery, and postoperative days 1 and 2.
After the bone cut and surgery, TXA significantly increased MCP-1, TNF-α, IL-1β and IL-6 levels compared to non-TXA patients, which was further amplified postoperatively. During surgery, TXA significantly prolonged EXTEM clot times, indicating a thrombin-slowing effect, despite little or no change in clot amplitude or fibrinogen. TXA was associated with three- to fivefold increases in FIBTEM maximum lysis (ML), a finding counter to TXA's antifibrinolytic effect. Maximum lysis for extrinsic and intrinsic pathways was < 8%, indicating little or no hyperfibrinolysis. No significant differences were found in postoperative hemoglobin between the two groups.
TXA was associated with increased systemic inflammation during surgery compared to non-TXA patients, with further amplification on postoperative days 1 and 2. On the basis of little or no change in viscoelastic clot strength, fibrinogen or clot lysis, there appeared to be no clinical justification for TXA in our group of patients. Larger prospective, randomized trials are required to investigate a possible proinflammatory effect in TKA patients.
氨甲环酸(TXA)常用于骨科手术,以减少术中出血过多和输血需求。我们的目的是研究是否所有接受全膝关节置换术(TKA)的骨关节炎患者都需要使用TXA,以及其对全身炎症和凝血特性的可能影响。
连续招募了23名患者(牛津评分22 - 29);12名患者在手术前(静脉注射,1.2 g/90 kg)和手术后立即(关节内注射,1.4 g/90 kg)接受TXA。在基线、首次截骨后、手术后立即以及术后第1天和第2天测量血液中的炎症介质和旋转血栓弹力图(ROTEM)参数。
与未使用TXA的患者相比,截骨和手术后,TXA显著增加了单核细胞趋化蛋白-1(MCP-1)、肿瘤坏死因子-α(TNF-α)、白细胞介素-1β(IL-1β)和白细胞介素-6(IL-6)水平,术后进一步升高。手术期间,TXA显著延长了EXTEM凝血时间,表明有凝血酶减慢作用,尽管凝块幅度或纤维蛋白原几乎没有变化。TXA与FIBTEM最大溶解率(ML)增加三到五倍有关,这一发现与TXA的抗纤维蛋白溶解作用相悖。外源性和内源性途径的最大溶解率<8%,表明几乎没有或没有纤维蛋白溶解亢进。两组患者术后血红蛋白无显著差异。
与未使用TXA的患者相比,TXA与手术期间全身炎症增加有关,术后第1天和第2天进一步加剧。基于粘弹性凝块强度、纤维蛋白原或凝块溶解几乎没有变化,在我们的患者组中,TXA似乎没有临床依据。需要更大规模的前瞻性随机试验来研究TKA患者中可能存在的促炎作用。