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Effect of tranexamic acid on children with traumatic bleeding: A systematic review and meta-analysis
Yu-Cheng Lin1, Tsu-Hsien Wang2, Yi-No Kang3
1Department of Medicine, Taipei Tzu Chi Hospital, Buddhist Tzu Chi Foundation, New Taipei City, Taiwan.
Insights
Tranexamic acid (TXA) effectively reduces mortality in pediatric trauma patients. While generally safe, further research is needed to optimize TXA dosing and timing for best outcomes in children.
Area of Science:
- Pediatric Emergency Medicine
- Trauma Surgery
- Pharmacology
Background:
- Traumatic bleeding in children poses significant mortality risks.
- Evaluating antifibrinolytic agents like tranexamic acid (TXA) is crucial for improving outcomes.
Purpose of the Study:
- To systematically review and meta-analyze the efficacy and safety of TXA for pediatric traumatic bleeding.
- To assess TXA's impact on mortality, morbidity, and adverse events in pediatric trauma.
Main Methods:
- Comprehensive literature search of major databases for relevant cohort and randomized controlled trials.
- Inclusion criteria excluded studies on other anti-bleeding agents or patients with pre-existing bleeding disorders.
- Statistical analysis utilized random-effects models to calculate odds ratios for key outcomes.
Main Results:
- Ten studies (34,144 children) were analyzed, including one RCT and nine retrospective cohorts.
- TXA significantly reduced mortality (OR 0.58), particularly with a 1g initial dose.
- No significant differences were observed in ICU admission, surgical intervention, or hospital stay; a slight increase in seizures was noted, but no increase in thromboembolic events.
Conclusions:
- TXA demonstrates potential benefits in reducing mortality for pediatric trauma patients.
- The overall safety profile of TXA in this population appears favorable.
- Further research is warranted to establish optimal dosing and timing for TXA administration in pediatric trauma.
Background:
This systematic review and meta-analysis aimed to evaluate the efficacy and safety of tranexamic acid (TXA) in the treatment of traumatic bleeding in children.
Methods:
We searched Cochrane Central Register of Controlled Trials, Cochrane Database of Systematic Reviews, Embase, MEDLINE, Web of Science for relevant cohort and randomized controlled trials, excluding studies with other anti-bleeding treatments or patients with underlying bleeding disorders. Outcomes included mortality, ICU admission, surgical intervention, transfusions, hospital stay, seizures, and thromboembolic events. Statistical analysis employed odds ratios (OR) in random-effects models.
Results:
Ten studies (1 randomized controlled trial, 9 retrospective cohorts; n = 34,144) were included. The pooled results revealed that TXA significantly reduced mortality (OR 0.58; 95 % CI, 0.38-0.89), especially with a 1 g initial dose. However, no significant differences were found in other outcomes. TXA use was associated with a slight increase in seizures but no rise in thromboembolic events. The overall safety profile was favorable.
Conclusion:
Our study highlights the potential benefits of TXA in reducing mortality in pediatric trauma cases and underscores the need for further research to determine optimal dosing and timing strategies.
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