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Tranexamic acid may benefit patients with preexisting thromboembolic risk undergoing total joint arthroplasty: a systematic review and meta-analysis.
Dang, Xiangji; Liu, Mei; Yang, Qiang; Jiang, Jin; Liu, Yan; Sun, Hui; Tian, Jinhui.
Affiliation
  • Dang X; Evidence-based Medicine Center, School of Basic Medical Sciences, Lanzhou University, Lanzhou, P.R. China.
  • Liu M; Department of Pharmaceutical, Lanzhou University Second Hospital, Lanzhou, Gansu province, P.R. China.
  • Yang Q; The First Clinical Medical School, Gansu University of Chinese Medicine, Gansu, P.R. China.
  • Jiang J; Department of Neurosurgery, Lanzhou University Second Hospital, Lanzhou, Gansu province, P.R. China.
  • Liu Y; Department of Orthopedics, Lanzhou University Second Hospital, Lanzhou, Gansu province, P.R. China.
  • Sun H; Gansu High Throughput Screening and Creation Center for Health Products, School of Pharmacy, Lanzhou University, Lanzhou, P.R. China.
  • Tian J; Cuiying Biomedical Research Center, Lanzhou University Second Hospital, Lanzhou, Gansu province, P.R. China.
EFORT Open Rev ; 9(6): 467-478, 2024 Jun 03.
Article in En | MEDLINE | ID: mdl-38828967
ABSTRACT

Purpose:

This study sought to determine if the use of tranexamic acid (TXA) in preexisting thromboembolic risk patients undergoing total joint arthroplasty (TJA) was linked to an increased risk of death or postoperative complications.

Methods:

We conducted a comprehensive search for studies up to May 2023 in PubMed, Web of Science, EMBASE, and the Cochrane Library. We included randomized clinical trials, cohort studies, and case-control studies examining the use of TXA during TJA surgeries on high-risk patients. The Cochrane Risk of Bias instrument was used to gauge the excellence of RCTs, while the MINORS index was implemented to evaluate cohort studies. We used mean difference (MD) and relative risk (RR) as effect size indices for continuous and binary data, respectively, along with 95% CIs.

Results:

Our comprehensive study, incorporating data from 11 diverse studies involving 812 993 patients, conducted a meta-analysis demonstrating significant positive outcomes associated with TXA administration. The findings revealed substantial reductions in critical parameters, including overall blood loss (MD = -237.33; 95% CI (-425.44, -49.23)), transfusion rates (RR = 0.45; 95% CI (0.34, 0.60)), and 90-day unplanned readmission rates (RR = 0.86; 95% CI (0.76, 0.97)). Moreover, TXA administration exhibited a protective effect against adverse events, showing decreased risks of pulmonary embolism (RR = 0.73; 95% CI (0.61, 0.87)), myocardial infarction (RR = 0.47; 95% CI (0.40-0.56)), and stroke (RR = 0.73; 95% CI (0.59-0.90)). Importantly, no increased risk was observed for mortality (RR = 0.53; 95% CI (0.24, 1.13)), deep vein thrombosis (RR = 0.69; 95% CI (0.44, 1.09)), or any of the evaluated complications associated with TXA use.

Conclusion:

The results of this study indicate that the use of TXA in TJA patients with preexisting thromboembolic risk does not exacerbate complications, including reducing mortality, deep vein thrombosis, and pulmonary embolism. Existing evidence strongly supports the potential benefits of TXA in TJA patients with thromboembolic risk, including lowering blood loss, transfusion, and readmission rates.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: EFORT Open Rev Year: 2024 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: EFORT Open Rev Year: 2024 Document type: Article
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