Literature DB >> 31709664

Fibrinogen concentrates in hereditary fibrinogen disorders: Past, present and future.

Alessandro Casini1, Philippe de Moerloose2.   

Abstract

Hereditary fibrinogen disorders (HFD) are rare coagulation disorders. Even if the spectrum of symptoms is broad depending on the sub-type, bleeding is the most common complication. Of the available sources of fibrinogen replacement, fibrinogen concentrate provides a safer and more effective option to treat and prevent bleeding. Recent clinical trials on established and new fibrinogen concentrates have increased our knowledge on the clinical pharmacology of these products, pointing out possible age and weight differences for dose adjustment. The efficacy of fibrinogen infusions has been demonstrated, especially for the management of acute bleeding with an excellent response based on investigator rating. The target fibrinogen levels in the setting of both minor and major surgeries have been better specified. The safety has been confirmed with a low number of adverse events but there still remains concern over possible thrombotic risks. Pharmacological, clinical aspects and future perspectives on the utilization of fibrinogen concentrates in the treatment and prevention of bleeding in patients with HFD are reviewed.
© 2019 John Wiley & Sons Ltd.

Entities:  

Keywords:  afibrinogenemia; bleeding; fibrinogen concentrate; hypofibrinogenemia; pharmacokinetics; thrombosis

Year:  2019        PMID: 31709664     DOI: 10.1111/hae.13876

Source DB:  PubMed          Journal:  Haemophilia        ISSN: 1351-8216            Impact factor:   4.287


  6 in total

1.  A Novel Nonsense Mutation in FGB (c.1421G>A; p.Trp474Ter) in the Beta Chain of Fibrinogen Causing Hypofibrinogenemia with Bleeding Phenotype.

Authors:  Tomas Simurda; Rui Vilar; Jana Zolkova; Eliska Ceznerova; Zuzana Kolkova; Dusan Loderer; Marguerite Neerman-Arbez; Alessandro Casini; Monika Brunclikova; Ingrid Skornova; Miroslava Dobrotova; Marian Grendar; Jan Stasko; Peter Kubisz
Journal:  Biomedicines       Date:  2020-12-13

2.  A novel fibrinogen γ-chain frameshift mutation, p. Cys365Phefs*41, causing hypofibrinogenemia with bleeding phenotype in a Chinese family.

Authors:  Weijie Zhou; Yan Huang; Jie Wei; Jun Li Wang; Boming Huang; Xiaoxuan Zhou; Jie Yan; Yangyang Wu; Faquan Lin; Wangrong Wen
Journal:  Ann Transl Med       Date:  2021-08

3.  [Analysis of gene mutation spectrum and pharmacokinetics of fibrinogen infusion in 146 cases of congenital fibrinogen disorders].

Authors:  L Y Huang; D L Zhang; R F Fu; W Liu; Y F Chen; F Xue; X F Liu; T T Bi; R C Yang; L Zhang
Journal:  Zhonghua Xue Ye Xue Za Zhi       Date:  2021-07-14

Review 4.  Heterogeneity of Genotype-Phenotype in Congenital Hypofibrinogenemia-A Review of Case Reports Associated with Bleeding and Thrombosis.

Authors:  Monika Brunclikova; Tomas Simurda; Jana Zolkova; Miroslava Sterankova; Ingrid Skornova; Miroslava Dobrotova; Zuzana Kolkova; Dusan Loderer; Marian Grendar; Jan Hudecek; Jan Stasko; Peter Kubisz
Journal:  J Clin Med       Date:  2022-02-18       Impact factor: 4.241

Review 5.  Women With Congenital Hypofibrinogenemia/Afibrinogenemia: From Birth to Death.

Authors:  Yan Zhang; Xiaohang Zuo; Yue Teng
Journal:  Clin Appl Thromb Hemost       Date:  2020 Jan-Dec       Impact factor: 2.389

6.  The Efficacy of Fibrinogen Concentrates in Relation to Cryoprecipitate in Restoring Clot Integrity and Stability against Lysis.

Authors:  Claire S Whyte; Akriti Rastogi; Ellis Ferguson; Michela Donnarumma; Nicola J Mutch
Journal:  Int J Mol Sci       Date:  2022-03-09       Impact factor: 6.208

  6 in total

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