The antifibrinolytic and anti-inflammatory effects of multiple doses of oral tranexamic acid in total knee arthroplasty patients: a randomized controlled trial

被引:45
作者
Wang, D. [1 ]
Luo, Z. -Y. [1 ]
Yu, Z. -P. [1 ]
Liu, L. -X. [2 ]
Chen, C. [1 ]
Meng, W. -K. [1 ]
Yu, Q. -P. [3 ]
Pei, F. -X. [1 ]
Zhou, Z. -K. [1 ]
Zeng, W. -N. [3 ]
机构
[1] Sichuan Univ, West China Sch Med, West China Hosp, Dept Orthoped, Chengdu, Sichuan, Peoples R China
[2] Sichuan Univ, West China Sch Med, West China Hosp, Dept Neurosci, Chengdu, Sichuan, Peoples R China
[3] Third Mil Med Univ, Southwest Hosp, Ctr Joint Surg, Chengdu, Sichuan, Peoples R China
关键词
blood loss; inflammation; major surgery; thrombosis; tranexamic acid; TOTAL HIP-ARTHROPLASTY; PERIOPERATIVE BLOOD-LOSS; TOPICAL APPLICATION; RECOVERY; TOURNIQUET; MANAGEMENT; FIBRINOLYSIS; DRAINAGE; EFFICACY; BOLUSES;
D O I
10.1111/jth.14316
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Tranexamic acid (TXA) can reduce blood loss and the inflammatory response at multiple doses in total knee arthroplasty patients. However, the optimal regimen has not been determined. Objectives To identify the most effective regimen for achieving maximum reductions in blood loss and the inflammatory response. Patients/Methods Two hundred and seventy-five patients were randomized to receive a placebo (group A), a single 2-g oral dose of TXA 2 h preoperatively followed by 1 g of oral TXA 3 h postoperatively (group B), a single dose followed by 1 g of oral TXA 3 h and 7 h postoperatively (group C), a single dose followed by 1 g of oral TXA 3 h, 7 h and 11 h postoperatively (group D), or a single dose followed by 1 g of oral TXA 3 h, 7 h, 11 h and 15 h postoperatively (group E). The primary outcome was total blood loss on postoperative day (POD) 3. Secondary outcomes included a decrease in the hemoglobin level, coagulation parameters, inflammatory marker levels, and thromboembolic complications. Results Groups D and E had significantly lower blood loss and smaller decreases in hemoglobin level than groups A, B, and C, with no significant difference on POD 3 between groups D and E. Significantly enhanced coagulation was identified for the four multiple-dose regimens; however, all thromboelastographic parameters remained within normal ranges. Group E had the lowest inflammatory marker levels and pain, and the greatest range of motion. No thromboembolic complications were identified. Conclusion The four-dose regimen yielded the maximum reductions in blood loss and inflammatory response, improved analgesia, and promoted early rehabilitation. Further studies are required to ensure that these findings are reproducible.
引用
收藏
页码:2442 / 2453
页数:12
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