Gynecological and obstetric outcome in the French cohort of women with factor XIII deficiency.


Journal

Thrombosis research
ISSN: 1879-2472
Titre abrégé: Thromb Res
Pays: United States
ID NLM: 0326377

Informations de publication

Date de publication:
07 2020
Historique:
received: 29 10 2019
revised: 17 03 2020
accepted: 08 04 2020
pubmed: 4 5 2020
medline: 22 5 2021
entrez: 4 5 2020
Statut: ppublish

Résumé

Congenital factor XIII deficiency is a very rare bleeding disorder affecting 33 patients in France. Besides its role in fibrin clot stabilization, factor XIII is involved in placental attachment. Fetal miscarriages represent a frequent and concerning issue for these patients. The aim of the present study was to describe clinical characteristics of women presenting severe congenital FXIII deficiency in France, to focus on gynecological and obstetrical events, and to report the management of these rare situations. We conducted a retrospective study in the French Hemophilia Comprehensive Care and Clinical Hemostasis Centers. Women between 15 and 65 years with factor XIII activity <10 IU dL Among 31 centers, eleven patients were included. The median age at diagnosis was 1.5 years (range: 0-35), and at inclusion it was 30 years (range: 15-63). Fetal miscarriage was the primary manifestations in 2 (18%) patients, the remaining were diagnosed during hemorrhage. Menorrhagias were reported by 2 women (27%), 13 pregnancies were reported by 9 women including one abortion. Every pregnancy was conducted under factor XIII substitution, no hemorrhagic episode was reported. Four patients (36%) experienced at least one fetal miscarriage with a total amount of 30 miscarriages with 6 occurring during substitution. Altogether, our data confirmed the high incidence of miscarriage in women with factor XIII deficiency. Good outcome of pregnancies required prophylaxis in accordance with international guidelines.

Identifiants

pubmed: 32360976
pii: S0049-3848(20)30117-1
doi: 10.1016/j.thromres.2020.04.010
pii:
doi:

Substances chimiques

Factor XIII 9013-56-3

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

22-25

Informations de copyright

Copyright © 2020 The Authors. Published by Elsevier Ltd.. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest All authors declare no conflicts of interest.

Auteurs

Lucia Rugeri (L)

Hospices Civils de Lyon, Unité Hémostase Clinique, Hôpital Louis Pradel, Hospices Civils de Lyon, Bron, France. Electronic address: lucia.rugeri@chu-lyon.fr.

Christophe Martinaud (C)

Department of Medical Biology, Military Medical Center Percy, Clamart, France.

Philippe Beurrier (P)

Centre de Traitement de l'Hémophilie, CHU Angers, Angers, France.

Yvonne Borg (Y)

Unité Hémostase et Centre Régional de Traitement des maladies Hémorragiques, Institut de Biologie Clinique, Hôpital Charles Nicolle, Rouen, France.

Hervé Chambost (H)

Centre for Bleeding Disorders, Pediatric Haematology Oncology Department, University Hospital La Timone, AP-HM, and Aix Marseille Univ, INSERM, INRA, C2VN, Marseille, France.

Mirela Chirila-Hetsch (M)

Service d'Hématologie, Hôpital de Valence, Valence, France.

Dominique Desprez (D)

Centre de Traitement de l'Hémophilie, CHU Strasbourg, Strasbourg, France.

Annie Harroche (A)

Hemophilia Care Centre, Hematology Unit, Hôpital Universitaire Necker Enfants Malades, Paris, France.

Vanessa Milien (V)

FranceCoag, University Hospital La Timone, AP-HM, Marseille, France.

Brigitte Pan-Petesch (B)

Unité Hémostase Service hématologie, CHU Brest, Brest, France.

Sandrine Meunier (S)

Hospices Civils de Lyon, Unité Hémostase Clinique, Hôpital Louis Pradel, Hospices Civils de Lyon, Bron, France.

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Classifications MeSH