Impact of Fibrinogen Infusion on Thrombin Generation and Fibrin Clot Structure in Patients with Inherited Afibrinogenemia.


Journal

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

Informations de publication

Date de publication:
Sep 2022
Historique:
pubmed: 20 1 2022
medline: 31 8 2022
entrez: 19 1 2022
Statut: ppublish

Résumé

 Inherited afibrinogenemia is a very rare disease characterized by complete absence of fibrinogen in the circulation and an increased risk in both thrombosis and bleeding. Infusion of fibrinogen concentrate (FC) is the main approach for prevention and management of bleeding; however, it has been reported to carry a thrombotic risk.  We investigated the impact of a standard dose (40-100 mg/kg) of FC infusion on the thrombin generation (TG) parameters and the fibrin clot structure formed in plasma samples of patients with afibrinogenemia. Blood samples were collected from 20 patients before (T0) and 1 hour after infusion of FC (T1). TG was studied with calibrated automated thrombography. Fibrin clot structure was assessed with turbidimetry and scanning electron microscopy.  FC infusions (mean Clauss fibrinogen plasma level: 1.21 g/L at T1) led to a statistically significant increase in endogenous thrombin potential (ETP) (  In summary, fibrinogen infusion with a standard dose of FC increased but did not correct TG and led to formation of fibrin clots similar to those of patients with hypofibrinogenemia. All in all, our results do not support the biological evidence of hypercoagulability induced by FC in patients with afibrinogenemia.

Identifiants

pubmed: 35045578
doi: 10.1055/a-1745-0420
doi:

Substances chimiques

Hemostatics 0
Fibrin 9001-31-4
Fibrinogen 9001-32-5
Thrombin EC 3.4.21.5

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1461-1468

Informations de copyright

Thieme. All rights reserved.

Déclaration de conflit d'intérêts

A.C. reports grants, and fees paid to his institution from CSL Behring, Octapharma, Sobi, Shire, Takeda, Pentapharma, Biotest, and Novo Nordisk. T.L. reports grants, and fees paid to his institution from Stago and IRIS, outside the submitted work. The other authors do not report conflict of interest related to this study.

Auteurs

Claudia Khayat (C)

Department of Pediatrics, Hôtel-Dieu de France Hospital, Beirut, Lebanon.

Rita Marchi (R)

Department of Genetic Medicine and Development, Faculty of Medicine, University of Geneva, Geneva, Switzerland.

Stéphane Durual (S)

Biomaterials Laboratory, University Clinics of Dental Medicine, University of Geneva, Geneva, Switzerland.

Thomas Lecompte (T)

Faculty of Medicine, University of Geneva, Geneva, Switzerland.
Division of Angiology and Hemostasis, University Hospitals of Geneva, Geneva, Switzerland.

Marguerite Neerman-Arbez (M)

Department of Genetic Medicine and Development, Faculty of Medicine, University of Geneva, Geneva, Switzerland.

Alessandro Casini (A)

Faculty of Medicine, University of Geneva, Geneva, Switzerland.
Division of Angiology and Hemostasis, University Hospitals of Geneva, Geneva, Switzerland.

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Classifications MeSH