Literature DB >> 33512441

Clinical phenotype, fibrinogen supplementation, and health-related quality of life in patients with afibrinogenemia.

Alessandro Casini1,2, Sylvia von Mackensen3, Cristina Santoro4, Claudia Djambas Khayat5, Meriem Belhani6, Cecil Ross7, Akbar Dorgalaleh8, Arshi Naz9, Ekrem Ünal10,11, Magy Abdelwahab12, Elise Dupuis Lozeron13, Nathalie Trillot14, Sophie Susen15, Flora Peyvandi16, Philippe de Moerloose2.   

Abstract

Due to the low prevalence of afibrinogenemia, epidemiologic data on afibrinogenemia are limited, and no data are available on health-related quality of life (HRQoL). We conducted a cross-sectional international study to characterize the clinical features, the fibrinogen supplementation modalities, and their impact on HRQoL in patients with afibrinogenemia. A total of 204 patients (119 adults and 85 children) from 25 countries were included. The bleeding phenotype was severe: 68 (33.3%) patients having at least one bleed per month and 48 (23%) a history of cerebral bleeding. About 35% (n = 72) of patients were treated with fibrinogen concentrates or cryoprecipitates as prophylaxis, 18.1% (n = 37) received ≥1 injection per week, and 16.6% (n = 34) were on home treatment. A thrombotic event was reported in venous and/or arterial territories by 37 (18.1%) patients. Thrombosis occurred even in young patients, and recurrence was frequent (7.4%). The total HRQoL was lower in children than in adults. Discomfort linked to treatment and limitations to sports and leisure were the main concerns. Women and children were particularly affected in family relationships. In multivariate analyses, younger age, residence in Asia or Africa, and a previous thrombotic event were statistically correlated with a worse HRQoL. In summary, our study underlines the severe bleeding and thrombotic phenotype and their impact on HRQoL in afibrinogenemia. The optimal strategy for fibrinogen supplementation needs to be determined. This trial was registered at www.clinicaltrials.gov as #NCT03484065.
© 2021 by The American Society of Hematology.

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Year:  2021        PMID: 33512441     DOI: 10.1182/blood.2020009472

Source DB:  PubMed          Journal:  Blood        ISSN: 0006-4971            Impact factor:   22.113


  3 in total

Review 1.  Extension of the Human Fibrinogen Database with Detailed Clinical Information-The αC-Connector Segment.

Authors:  Zofie Sovova; Klara Pecankova; Pavel Majek; Jiri Suttnar
Journal:  Int J Mol Sci       Date:  2021-12-23       Impact factor: 5.923

2.  Clinical, biological, and genetic features in an afibrinogenemia patient series in Algeria.

Authors:  Soraya Hadjali-Saichi; Philippe de Mazancourt; Jacqueline Tapon-Bretaudière; Tristan Mirault; Kahina Guenounou; Issam Frigaa; Anne-Marie Fischer; Ouerdia Chafa; Dominique Helley
Journal:  Haemophilia       Date:  2022-04-30       Impact factor: 4.263

3.  A homozygous duplication of the <I>FGG</i> exon 8-intron 8 junction causes congenital afibrinogenemia. Lessons learned from the study of a large consanguineous Turkish family.

Authors:  Michel Guipponi; Frédéric Masclaux; Frédérique Sloan-Béna; Corinne Di Sanza; Namik Özbek; Flora Peyvandi; Marzia Menegatti; Alessandro Casini; Baris Malbora; Marguerite Neerman-Arbez
Journal:  Haematologica       Date:  2022-05-01       Impact factor: 11.047

  3 in total

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