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
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.
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
1461-1468Informations 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.