Evidence map›Paper›PMID 42221451›Full record

Trial reportMedecine tropicale et sante internationale2026

[Evaluation of the Efficacy and Tolerance of Tranexamic Acid Combined with Inoserp

Sébastien Larréché, Noé Sodjinou, Naryanan Tourita, Seidou Alassane Ouorou, Éric Ganhouingnon, Édith Aloukoutou Layo, Achille Massougbodji, Jean-Philippe Chippaux

Abstract readRandomized Controlled TrialEnglish Abstract
In one paragraph

Trial report in Medecine tropicale et sante internationale, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Sébastien LarréchéService de biologie médicale, Hôpital national d'instruction des armées Bégin, 69 avenue de Paris, 94160 Saint-Mandé; École du Val-de-Grâce, 1 place Alphonse Laveran, 75005 Paris; UMR-S1144, Université Paris Cité, 4 avenue de l'observatoire, 75006, Paris, France.ORCID https://orcid.org/0000-0002-8961-7132
Noé SodjinouInstitut de recherche clinique du Bénin, Abomey-Calavi, Bénin.
Naryanan TouritaDépartement Santé, Université Senghor, 1, Place Ahmed Orabi, Al Mancheya, BP 415, 21111 Alexandrie, Égypte.
Seidou Alassane OuorouService des urgences, Hôpital Saint-Jean de Dieu, Tanguiéta, Bénin.ORCID https://orcid.org/0009-0005-6238-5852
Éric GanhouingnonLaboratoire de biologie, Hôpital Saint-Jean de Dieu, Tanguiéta, Bénin.ORCID https://orcid.org/0000-0003-4306-2079
Édith Aloukoutou LayoInstitut de recherche clinique du Bénin, Abomey-Calavi, Bénin.
Achille MassougbodjiInstitut de recherche clinique du Bénin, Abomey-Calavi, Bénin.ORCID https://orcid.org/0000-0001-7656-3553
Jean-Philippe ChippauxUniversité Paris Cité, IRD, Inserm, MERIT, F-75006 Paris, France.ORCID https://orcid.org/0000-0002-1976-8568

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Hemorrhagic syndrome accounts for a significant proportion of the mortality and morbidity associated with snakebites in sub-Saharan Africa. Hyperfibrinolysis, which has been reported in some cases, suggests the potential benefit of antifibrinolytics; however, these have been little studied in this context. This study aimed to evaluate the effectiveness of combining tranexamic acid and antivenom in treating hemorrhagic syndrome and coagulopathy associated with Materials and methods: Patients presenting with hemorrhagic syndrome due to envenomation were prospectively included at the Saint Jean de Dieu Hospital in Tanguiéta, Benin. Patients were randomized into two groups: one receiving antivenom and tranexamic acid (SAV + AT) and one receiving only antivenom (SAV). All patients received two vials of Inoserp Results: Twenty-five patients were included: Twelve patients were in the SAV + AT group, and thirteen patients were in the SAV group. Six patients in the SAV + AT group and five patients in the SAV group experienced persistent or recurrent bleeding (p = 0.695). There was no significant difference in WBCT at different time points between the two groups, nor in INR at 6 and 12 hours. There were no adverse effects suggesting intolerance to tranexamic acid (e.g., ocular abnormality, convulsions, or thrombosis), and plasma creatinine levels did not differ significantly between the two groups. Conclusion: Systematic use of tranexamic acid showed no benefit for hemorrhagic syndrome and coagulopathy associated with

Indexed as

Antifibrinolytic AgentsAntiveninsEchisHemorrhageSnake BitesTranexamic AcidViper VenomsAdultAnimalsBeninDrug Therapy, CombinationFemaleHumansMaleMiddle AgedProspective StudiesAntifibrinolytic AgentsAntiveninsTranexamic AcidViper VenomsAntifibrinolyticAntivenomBeninCoagulopathyFibrinolysisSnakebites, ViperidaeSub-Saharan Africa

Identifiers

PMID42221451
PMCPMC13216910

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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.