Skip to main content

Research Repository

Advanced Search

Tranexamic Acid Within 4.5 Hours of Intracerebral Hemorrhage With the CTA Spot Sign: Systematic Review and Individual Patient Meta-analysis

Yassi, Nawaf; Yogendrakumar, Vignan; Churilov, Leonid; Meretoja, Atte; Wu, Teddy; Campbell, Bruce C.V.; Strbian, Daniel; Jeng, Jiann-Shing; Woodhouse, Lisa J.; Ovesen, Christian; Law, Zhe Kang; Gu, Hong-Qiu; Nie, Ximing; Liu, Jingyi; Ma, Henry H.; Zhao, Henry; Bath, Philip M.; Liu, Liping; Sprigg, Nikola; Donnan, Geoffrey Alan; Davis, Stephen M.

Authors

Nawaf Yassi

Vignan Yogendrakumar

Leonid Churilov

Atte Meretoja

Teddy Wu

Bruce C.V. Campbell

Daniel Strbian

Jiann-Shing Jeng

Christian Ovesen

Zhe Kang Law

Hong-Qiu Gu

Ximing Nie

Jingyi Liu

Henry H. Ma

Henry Zhao

Liping Liu

Geoffrey Alan Donnan

Stephen M. Davis



Abstract

Background and Objectives The antifibrinolytic agent tranexamic acid has been tested in intracerebral hemorrhage trials with overall neutral results. Ongoing contrast extravasation on CT angiography (spot sign) can identify individuals with ongoing bleeding who may benefit from anti-fibrinolytic therapy. We aimed to investigate the effect of tranexamic acid on hematoma growth in patients with spot signs treated within 4.5 hours of onset. Methods We conducted a systematic review and individual patient meta-analysis, which we report according to the Preferred Reporting Items for Systematic Review and Meta-analyses of Individual Participant Data guidelines. PubMed and Embase were searched from inception to May 29, 2023, using the terms ((stroke) AND (randomised OR randomized) AND (tranexamic acid) AND (haemorrhage OR hemorrhage)). We included randomized trials comparing tranexamic acid with placebo in participants with primary intracerebral hemorrhage who had a spot sign and who had follow-up imaging within the required timeframe. Individual patient data were provided by each study and were integrated by the coordinating center. Data were pooled using a random-effects model. The primary endpoint was hematoma growth within 24 hours, defined as ≥33% relative or ≥6 mL absolute hematoma expansion compared with baseline, analyzed using mixed-effects–modified Poisson regression with robust standard errors, adjusted for baseline hematoma volume. Safety outcomes were mortality and major thromboembolic events within 90 days. Results Of 197 studies identified, 3 were eligible, contributing 162 participants for the primary analysis (60 female and 102 male). Hematoma growth occurred in 36 of 74 (49%) participants treated with tranexamic acid, compared with 48 of 88 (55%) participants treated with placebo (adjusted risk ratio 0.86, 95% CI 0.84–0.89, p < 0.001). Adjusted median absolute hematoma growth was 1.60 mL (95% CI 0.77–2.43) lower with tranexamic acid vs placebo. No differences in functional outcome or safety were observed. Discussion Tranexamic acid modestly reduced hematoma growth in patients with CT angiography spot signs treated within 4.5 hours of onset. Given the trials in the meta-analysis were individually neutral, these results require further validation before clinical application.

Citation

Yassi, N., Yogendrakumar, V., Churilov, L., Meretoja, A., Wu, T., Campbell, B. C., Strbian, D., Jeng, J.-S., Woodhouse, L. J., Ovesen, C., Law, Z. K., Gu, H.-Q., Nie, X., Liu, J., Ma, H. H., Zhao, H., Bath, P. M., Liu, L., Sprigg, N., Donnan, G. A., & Davis, S. M. (2024). Tranexamic Acid Within 4.5 Hours of Intracerebral Hemorrhage With the CTA Spot Sign: Systematic Review and Individual Patient Meta-analysis. Neurology, 103(12), https://doi.org/10.1212/wnl.0000000000210104

Journal Article Type Article
Acceptance Date Oct 10, 2024
Online Publication Date Nov 25, 2024
Publication Date Dec 24, 2024
Deposit Date Jan 10, 2025
Publicly Available Date Nov 26, 2025
Journal Neurology
Print ISSN 0028-3878
Electronic ISSN 1526-632X
Publisher American Academy of Neurology
Peer Reviewed Peer Reviewed
Volume 103
Issue 12
DOI https://doi.org/10.1212/wnl.0000000000210104
Public URL https://nottingham-repository.worktribe.com/output/42595080
Publisher URL https://www.neurology.org/doi/10.1212/WNL.0000000000210104
Additional Information Received: 2024-06-14; Accepted: 2024-10-10; Published: 2024-11-25