Evidence map›Paper›PMID 23187124›Full record

ArticleThe Journal of clinical investigation2012

Tranexamic acid concentrations associated with human seizures inhibit glycine receptors.

Irene Lecker, Dian-Shi Wang, Alexander D Romaschin, Mark Peterson, C David Mazer, Beverley A Orser

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 67 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
67citing papers in PubMed, 4 pooled it
7.7field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

67 citing papers in PubMed, 4 syntheses or guidelines pooled it, 196 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Pooled it
  5. Trial
  6. Trial
  7. Trial
  8. Trial
  9. A breath of fresh air: an updated review of nebulised tranexamic acid for post-tonsillectomy haemorrhage.European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery · 2026
    Review
  10. Tranexamic Acid in Pediatric Care: A Comprehensive Overview.The journal of pediatric pharmacology and therapeutics : JPPT : the official journal of PPAG · 2026
    Article
  11. Article
  12. Observational
  13. Article
  14. Efficacy of Tranexamic Acid on GABANeurochemical research · 2025
    Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. In vitro human ion channel assays predictive of drug-induced seizure.Toxicological sciences : an official journal of the Society of Toxicology · 2025
    Article
  20. Review

7 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 1 country.

Irene LeckerDepartment of Physiology, University of Toronto, Toronto, Ontario, Canada.
Dian-Shi Wang
Alexander D Romaschin
Mark Peterson
C David Mazer
Beverley A Orser
St. Michael's Hospital · CAUniversity of Toronto · CASunnybrook Health Science Centre · CA

Funding

Canadian Institutes of Health Research MOP-38028Canadian Institutes of Health Research MOP-79428
6 · The paper itself

Abstract

Antifibrinolytic drugs are widely used to reduce blood loss during surgery. One serious adverse effect of these drugs is convulsive seizures; however, the mechanisms underlying such seizures remain poorly understood. The antifibrinolytic drugs tranexamic acid (TXA) and ε-aminocaproic acid (EACA) are structurally similar to the inhibitory neurotransmitter glycine. Since reduced function of glycine receptors causes seizures, we hypothesized that TXA and EACA inhibit the activity of glycine receptors. Here we demonstrate that TXA and EACA are competitive antagonists of glycine receptors in mice. We also showed that the general anesthetic isoflurane, and to a lesser extent propofol, reverses TXA inhibition of glycine receptor-mediated current, suggesting that these drugs could potentially be used to treat TXA-induced seizures. Finally, we measured the concentration of TXA in the cerebrospinal fluid (CSF) of patients undergoing major cardiovascular surgery. Surprisingly, peak TXA concentration in the CSF occurred after termination of drug infusion and in one patient coincided with the onset of seizures. Collectively, these results show that concentrations of TXA equivalent to those measured in the CSF of patients inhibited glycine receptors. Furthermore, isoflurane or propofol may prevent or reverse TXA-induced seizures.

Indexed as

AdultAgedAged, 80 and overAminocaproic AcidAnimalsAnticonvulsantsAprotininBinding, CompetitiveCells, CulturedGABA-A Receptor Antagonistsgamma-Aminobutyric AcidGlycineHumansInhibitory Concentration 50Inhibitory Postsynaptic PotentialsIn Vitro TechniquesAminocaproic AcidAnticonvulsantsAprotininGABA-A Receptor Antagonistsgamma-Aminobutyric AcidGlycineIsofluranePropofolReceptors, GABA-AReceptors, GlycineTranexamic Acid

Identifiers

PMID23187124
PMCPMC3533541
OpenAlexW1999223726

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.