TY - JOUR
T1 - The effect of tranexamic acid in open reduction and internal fixation of pelvic and acetabular fracture
T2 - A systematic review and meta-analysis
AU - Kim, Chul Ho
AU - Hwang, Jaeho
AU - Lee, Soong Joon
AU - Yoon, Pil Whan
AU - Yoon, Kang Sup
N1 - Publisher Copyright:
© 2022 Lippincott Williams and Wilkins. All rights reserved.
PY - 2022/7/22
Y1 - 2022/7/22
N2 - Background: Pelvic bone fractures may cause extensive bleeding; however, the efficacy of tranexamic acid (TXA) usage in pelvic fracture surgery remains unclear. In this systematic review and meta-analysis, we aimed to evaluate the efficacy of TXA in open reduction and internal fixation surgery for pelvic and acetabular fracture. Methods: MEDLINE, Embase, and Cochrane Library databases were systematically searched for studies published before April 22, 2020, that investigated the effect of TXA in the treatment of pelvic and acetabular fracture with open reduction and internal fixation. A pooled analysis was used to identify the differences between a TXA usage group and a control group in terms of estimated blood loss (EBL), transfusion rates, and postoperative complications. Results: We included 6 studies involving 764 patients, comprising 293 patients who received TXA (TXA group) and 471 patients who did not (control group). The pooled analysis showed no differences in EBL between the groups (mean difference -64.67, 95% confidence interval [CI] -185.27 to -55.93, P =.29). The study period transfusion rate showed no significant difference between the groups (odds ratio [OR] 0.77, 95% CI 0.19-3.14, P =.71, I2= 82%), nor in venous thromboembolism incidence (OR 1.53, 95% CI 0.44-5.25, P =.50, I2= 0%) or postoperative infection rates (OR 1.15, 95% CI 0.13-9.98, P =.90, I2= 48%). Conclusions: Despite several studies having recommended TXA administration in orthopedic surgery, our study did not find TXA usage to be more effective than not using TXA in pelvic and acetabular fracture surgery, especially in terms of EBL reduction, transfusion rates, and the risk of postoperative complications.
AB - Background: Pelvic bone fractures may cause extensive bleeding; however, the efficacy of tranexamic acid (TXA) usage in pelvic fracture surgery remains unclear. In this systematic review and meta-analysis, we aimed to evaluate the efficacy of TXA in open reduction and internal fixation surgery for pelvic and acetabular fracture. Methods: MEDLINE, Embase, and Cochrane Library databases were systematically searched for studies published before April 22, 2020, that investigated the effect of TXA in the treatment of pelvic and acetabular fracture with open reduction and internal fixation. A pooled analysis was used to identify the differences between a TXA usage group and a control group in terms of estimated blood loss (EBL), transfusion rates, and postoperative complications. Results: We included 6 studies involving 764 patients, comprising 293 patients who received TXA (TXA group) and 471 patients who did not (control group). The pooled analysis showed no differences in EBL between the groups (mean difference -64.67, 95% confidence interval [CI] -185.27 to -55.93, P =.29). The study period transfusion rate showed no significant difference between the groups (odds ratio [OR] 0.77, 95% CI 0.19-3.14, P =.71, I2= 82%), nor in venous thromboembolism incidence (OR 1.53, 95% CI 0.44-5.25, P =.50, I2= 0%) or postoperative infection rates (OR 1.15, 95% CI 0.13-9.98, P =.90, I2= 48%). Conclusions: Despite several studies having recommended TXA administration in orthopedic surgery, our study did not find TXA usage to be more effective than not using TXA in pelvic and acetabular fracture surgery, especially in terms of EBL reduction, transfusion rates, and the risk of postoperative complications.
KW - TXA
KW - acetabular fracture
KW - blood loss
KW - complication
KW - pelvic bone fracture
KW - tranexamic acid
KW - transfusion
UR - http://www.scopus.com/inward/record.url?scp=85135092873&partnerID=8YFLogxK
U2 - 10.1097/MD.0000000000029574
DO - 10.1097/MD.0000000000029574
M3 - Article
C2 - 35866801
AN - SCOPUS:85135092873
SN - 0025-7974
VL - 101
SP - E29574
JO - Medicine (United States)
JF - Medicine (United States)
IS - 29
ER -