Department of Orthopaedic Surgery, Hyogo Medical University, 1-1 Mukogawa-Cho, Nishinomiya City, Hyogo, 663-8501, Japan.
Department of Orthopaedic Surgery, Nishinomiya Kaisei Hospital, 1-4 Ohama-Cho, Nishinomiya City, Hyogo, 662-0957, Japan.
J Orthop Surg Res. 2023 Mar 8;18(1):178. doi: 10.1186/s13018-023-03666-z.
This randomized controlled study was undertaken to investigate the efficacy of intravenous tranexamic acid (TXA) administration in reducing perioperative blood loss in patients undergoing medial opening-wedge distal tibial tuberosity osteotomy (MOWDTO). It was hypothesized that TXA would reduce perioperative blood loss in MOWDTO.
A total of 61 knees in 59 patients who underwent MOWDTO during the study period were randomly assigned to either of the groups with intravenous TXA administration (TXA group) or without TXA administration (control group). In the TXA group, patients received 1000 mg of TXA intravenously before skin incision and 6 h after the first dose. The primary outcomes was the volume of perioperative total blood loss which calculated using the blood volume and hemoglobin (Hb) drop. The Hb drop was calculated as the difference between preoperative Hb and postoperative Hb at days 1, 3, and 7.
The perioperative total blood loss was significantly lower in the TXA group (543 ± 219 ml vs. 880 ± 268 ml, P < 0.001). The Hb drop was significantly lower at postoperative days 1, 3 and 7 in the TXA group than in the control group (day 1: 1.28 ± 0.68 g/dl vs. 1.91 ± 0.69 g/dl, P = 0.001; day 3: 1.54 ± 0.66 g/dl vs. 2.69 ± 1.00 g/dl, P < 0.001; day 7: 1.74 ± 0.66 g/dl vs. 2.83 ± 0.91 g/dl, P < 0.001).
Intravenous TXA administration in MOWDTO could reduce the perioperative blood loss. Trial registration The study was approved by the institutional review board. (Registered on 26/02/2019 Registration Number 3136). Level of Evidence Level I, randomized controlled trial.
本随机对照研究旨在探讨静脉注射氨甲环酸(TXA)在减少内侧开放楔形胫骨结节截骨术(MOWDTO)患者围手术期失血中的疗效。假设 TXA 将减少 MOWDTO 中的围手术期失血。
在研究期间接受 MOWDTO 的 59 名患者的 61 个膝关节被随机分配到接受静脉注射 TXA 组(TXA 组)或不接受 TXA 组(对照组)。在 TXA 组,患者在皮肤切口前静脉注射 1000mg TXA,第一次剂量后 6 小时再次注射。主要结局是使用血容量和血红蛋白(Hb)下降计算的围手术期总失血量。Hb 下降值为术前 Hb 与术后第 1、3 和 7 天 Hb 的差值。
TXA 组围手术期总失血量明显低于对照组(543±219ml 比 880±268ml,P<0.001)。TXA 组术后第 1、3 和 7 天的 Hb 下降值明显低于对照组(第 1 天:1.28±0.68g/dl 比 1.91±0.69g/dl,P=0.001;第 3 天:1.54±0.66g/dl 比 2.69±1.00g/dl,P<0.001;第 7 天:1.74±0.66g/dl 比 2.83±0.91g/dl,P<0.001)。
MOWDTO 中静脉注射 TXA 可减少围手术期失血。试验注册本研究经机构审查委员会批准。(于 2019 年 2 月 26 日注册,注册号 3136)。证据水平 I 级,随机对照试验。