Does tranexamic acid affect intraventricular hemorrhage growth in acute ICH? An analysis of the STOP-AUST trial

Author:

Yogendrakumar Vignan1ORCID,Wu Teddy Y2,Churilov Leonid13,Tatlisumak Turgut4,Strbian Daniel4,Jeng Jiann-Shing5,Kleinig Timothy J6,Sharma Gagan1,Campbell Bruce CV1,Zhao Henry1,Hsu Chung Y7,Meretoja Atte4,Donnan Geoffrey A1,Davis Stephen M1,Yassi Nawaf18

Affiliation:

1. Department of Neurology, Melbourne Brain Centre at the Royal Melbourne Hospital, University of Melbourne, Parkville, VIC, Australia

2. Department of Neurology, Christchurch Hospital, Christchurch, New Zealand

3. Melbourne Medical School, University of Melbourne, Heidelberg, VIC, Australia

4. Department of Neurology, Helsinki University Hospital, Helsinki, Finland

5. Department of Neurology, National Taiwan University Hospital, Taipei, Taiwan

6. Department of Neurology, Royal Adelaide Hospital, Adelaide, SA, Australia

7. Department of Neurology, China Medical University Hospital, Taichung, Taiwan

8. Population Health and Immunity Division, The Walter and Eliza Hall Institute of Medical Research, Parkville, VIC, Australia

Abstract

Background Trials of tranexamic acid (TXA) in acute intracerebral hemorrhage (ICH) have focused on the imaging outcomes of intraparenchymal hematoma growth. However, intraventricular hemorrhage (IVH) growth is also strongly associated with outcome after ICH. Revised definitions of hematoma expansion incorporating IVH growth have been proposed. Aims We sought to evaluate the effect of TXA on IVH growth. Methods We analyzed data from the STOP-AUST trial, a prospective randomized trial comparing TXA to placebo in ICH patients presenting ≤ 4.5 h from symptom onset with a CT-angiography spot sign. New IVH development at follow-up, any interval IVH growth, and IVH growth ≥ 1 mL were compared between the treatment groups using logistic regression. The treatment effect of TXA against placebo using conventional (> 6 mL or 33%), and revised definitions of hematoma expansion (> 6 mL or 33% or IVH expansion ≥ 1 mL, > 6 mL or 33%, or any IVH expansion, and > 6 mL or 33% or new IVH development) were also assessed. Treatment effects were adjusted for baseline ICH volume. Results The analysis population consisted of 99 patients (50 placebo, 49 TXA). New IVH development at follow-up was observed in 6/49 (12%) who received TXA and 13/50 (26%) who received placebo (aOR: 0.38 [95% CI: 0.13–1.13]). Any interval IVH growth was observed in 12/49 (25%) who received TXA versus 26/50 (32%) receiving placebo (aOR: 0.69 [95% CI: 0.28–1.66]). IVH growth ≥ 1 mL did not differ between the two groups. Using revised definitions of hematoma expansion, no significant difference in treatment effect was observed between TXA and placebo. Conclusions IVH may be attenuated by TXA following ICH; however, studies with larger cohorts are required to investigate this further. Registration http://www.clinicaltrials.gov ; Unique identifier: NCT01702636.

Funder

The Australian National Health and Medical Research Council

The Royal Melbourne Hospital Foundation

Publisher

SAGE Publications

Subject

Cardiology and Cardiovascular Medicine,Neurology (clinical)

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