Tranexamic acid in spontaneous intracerebral hemorrhage: an updated systematic review and meta-analysis of randomized controlled trials.

Ann MedMar 3, 2026 (epub)
Clinical ResearchNeurologyHematologyOpen access

Cuilin Que, Luda Feng, Xinxing Lai et al.

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In 30 seconds

This systematic review and meta-analysis of randomized controlled trials assessed tranexamic acid (TXA) for spontaneous intracerebral hemorrhage. Nine trials initially enrolled 3,124 patients. Compared with control, TXA was not associated with significant differences in all-cause mortality (RR, 1.03; 95% CI [0.89-1.18]), hematoma expansion, functional independence, neurological impairment, or activities of daily living. Pooled results showed a reduction in hematoma volume from baseline (MD, -1.74; 95% CI [-2.47 to -1.02]), but adverse events did not differ significantly between groups.

Key findings

  • All-cause mortality did not differ significantly with TXA (RR, 1.03; 95% CI [0.89-1.18]).
  • TXA was not associated with significant differences in hematoma expansion (RR, 0.90; 95% CI [0.80-1.00]) or functional independence (RR, 1.02; 95% CI [0.92-1.12]).
  • Hematoma volume decreased from baseline in pooled data (MD, -1.74; 95% CI [-2.47 to -1.02]).
  • No significant difference in adverse events was observed between TXA and control groups.

Why it matters

The findings distinguish a reduction in hematoma volume from outcomes more directly relevant to patients, including survival and functional recovery. For spontaneous ICH, the pooled trial evidence did not show significant benefit in mortality, functional outcomes, or hematoma expansion, so the volume change alone should not be interpreted as evidence of improved clinical outcomes.

What to keep in mind

The abstract does not report further limitations; the findings are based on pooled randomized trials and should be interpreted in light of the reported confidence intervals.

Source

Published in Ann Med. This summary was written by xxcode from the publication's abstract and metadata. It is not peer reviewed and is not a substitute for the original article. For clinical decisions, review the original publication.

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