Effect of Tranexamic Acid on Coagulation and Fibrin Clot Properties in Children Undergoing Craniofacial Surgery.


Journal

Thrombosis and haemostasis
ISSN: 2567-689X
Titre abrégé: Thromb Haemost
Pays: Germany
ID NLM: 7608063

Informations de publication

Date de publication:
Mar 2020
Historique:
pubmed: 6 2 2020
medline: 29 12 2020
entrez: 5 2 2020
Statut: ppublish

Résumé

 Craniosynostosis surgery in small children is very often associated with a high blood loss. Tranexamic acid (TXA) reduces blood loss during this procedure, although the potential underlying coagulopathy in these children is not known in detail. Objective was to determine the nature of any coagulopathy found during and after craniosynostosis surgery and to characterize the effect of TXA on fibrin clot formation, clot strength, and fibrinolysis.  Thirty children received either TXA (bolus dose of 10 mg/kg followed by 8 hours continuous infusion of 3 mg/kg/h) or placebo. Dynamic whole blood clot formation assessed by thromboelastometry, platelet count, dynamic thrombin generation/thrombin-antithrombin, clot lysis assay, and fibrinogen/factor XIII (FXIII) levels were measured. Additionally, clot structure was investigated by real-time live confocal microscopy and topical data analysis.  Increased ability of thrombin generation was observed together with a tendency toward shortened activated partial thromboplastin time and clotting time. Postoperative maximum clot firmness was higher among children receiving TXA. FXIII decreased significantly during surgery in both groups.Resistance toward tissue plasminogen activator-induced fibrinolysis was higher in children that received TXA, as evidenced by topical data analysis and by a significant longer lysis time. Fibrinogen levels were higher in the TXA group at 24 hours.  A significant coagulopathy mainly characterized by changes in clot stability and not parameters of thrombin generation was reported. Tranexamic acid improved clot strength and reduced fibrinolysis, thereby avoiding reduction in fibrinogen levels.

Identifiants

pubmed: 32016928
doi: 10.1055/s-0039-3402762
doi:

Substances chimiques

Hemoglobins 0
Tranexamic Acid 6T84R30KC1
Factor XIII 9013-56-3
Thrombin EC 3.4.21.5
Tissue Plasminogen Activator EC 3.4.21.68

Types de publication

Journal Article Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

392-399

Subventions

Organisme : NNF14OC0011787
ID : Novo Nordisk Fonden

Informations de copyright

Georg Thieme Verlag KG Stuttgart · New York.

Déclaration de conflit d'intérêts

The authors declare no conflicts of interest with regard to the present manuscript. Dr. Hvas reports other from CSL Behring, other from Astellas, and other from Bayer A/S, outside the submitted work. Dr. Rasmussen reports grants from Health Research Foundation of Central Denmark Region, during the conduct of the study.

Auteurs

Christian Fenger-Eriksen (C)

Department of Anaesthesiology, Aarhus University Hospital, Denmark.

Alexander D'Amore Lindholm (AD)

Department of Anaesthesiology, Aarhus University Hospital, Denmark.

Lisbeth Krogh (L)

Department of Anaesthesiology, Aarhus University Hospital, Denmark.

Tobias Hell (T)

Department of Mathematics, University of Innsbruck, Innsbruck, Austria.

Martin Berger (M)

Department of Mathematics, University of Innsbruck, Innsbruck, Austria.

Martin Hermann (M)

Department of General and Surgical Intensive Care Medicine, Medical University of Innsbruck, Innsbruck, Austria.

Dietmar Fries (D)

Department of General and Surgical Intensive Care Medicine, Medical University of Innsbruck, Innsbruck, Austria.

Niels Juul (N)

Department of Anaesthesiology, Aarhus University Hospital, Denmark.

Mads Rasmussen (M)

Department of Anaesthesiology, Aarhus University Hospital, Denmark.

Anne-Mette Hvas (AM)

Department of Clinical Biochemistry, Thrombosis and Hemostasis Research Unit, Aarhus University Hospital, Denmark.
Department of Clinical Medicine, Aarhus University, Denmark.

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Classifications MeSH