Published online May 6, 2023. doi: 10.12998/wjcc.v11.i13.2992
Peer-review started: January 9, 2023
First decision: February 20, 2023
Revised: March 8, 2023
Accepted: March 27, 2023
Article in press: March 27, 2023
Published online: May 6, 2023
Processing time: 105 Days and 21.8 Hours
Total shoulder arthroplasty (TSA) results in a large amount of perioperative blood loss due to severe trauma.
Therefore, through the inclusion of high-quality randomized controlled trials (RCTs), a meta-analysis was conducted to determine the efficacy and safety of intravenous tranexamic acid (TXA) in the perioperative period of TSA, thereby providing a high-quality evidence-based basis for clinical application.
The purpose of this meta-analysis was to investigate the safety and efficacy of intravenous TXA in TSA.
Meta-analysis.
A total of 5 RCTs with level 1 evidence were included. There were 369 cases, with 186 in the TXA group and 183 in the placebo group. The meta-analysis showed that TXA can significantly reduce total blood loss during the perioperative period [WMD = -249.56, 95% confidence interval (CI): -347.6 to -151.52, P < 0.0001], and the incidence of adverse reactions was low (OR = 0.36, 95%CI: 0.16-0.83, P = 0.02). Compared with the placebo group, the TXA group had significantly less total haemoglobin loss (WMD = -34.39, 95%CI: -50.56 to -18.22), less haemoglobin fluctuation before and after the operation (WMD = -0.6, 95%CI: -0.93 to -0.27) and less 24-h drain output (WMD = -136.87, 95%CI: -165.87 to -106.49). There were no significant differences in the operation time (P = 0.11) or hospital length of stay (P = 0.30) between the two groups.
The application of intravenous TXA in the perioperative period of TSA can significantly reduce the total volume of perioperative blood loss and reduce the incidence of adverse reactions, so TXA is worthy of widespread clinical use.
Multicentre, large-sample prospective RCTs are needed in the future to further verify the findings of this study. In TSA, the impact of intravenous TXA on medical costs and patient satisfaction in the postoperative period should also be evaluated, which will be conducive to comprehensive evaluation of the clinical value of intravenous TXA.