The clinical management of factor XI deficiency in pregnant women.


Journal

Expert review of hematology
ISSN: 1747-4094
Titre abrégé: Expert Rev Hematol
Pays: England
ID NLM: 101485942

Informations de publication

Date de publication:
07 2020
Historique:
pubmed: 22 5 2020
medline: 27 5 2021
entrez: 22 5 2020
Statut: ppublish

Résumé

Factor XI (FXI) deficiency is associated with highly variable bleeding, including excessive gynecologic and obstetrical bleeding. Since approximately 20% of FXI-deficient women will experience pregnancy-related bleeding, careful planning and knowledge of appropriate hemostatic management is pivotal for their care. In this manuscript, authors present our current understanding of the role of FXI in hemostasis, the nature of the bleeding phenotype caused by its deficiency, and the impact of deficiency on obstetrical care. The authors searched PubMed with the terms, 'factor XI', 'factor XI deficiency', 'women', 'pregnancy', and 'obstetrics' to identify literature on these topics. Expectations of pregnancy-related complications in women with FXI deficiency, including antepartum, abortion-related, and postpartum bleeding, as well as bleeding associated with regional anesthesia are discussed. Recommendations for the care of these women are considered, including guidance for management of prophylactic care and acute bleeding. FXI deficiency results in a bleeding diathesis in some, but not all, patients, making treatment decisions and clinical management challenging. Currently available laboratory assays are not particularly useful for distinguishing patients with FXI deficiency who are prone to bleeding from those who are not. There is a need for alternative testing strategies to address this limitation.

Identifiants

pubmed: 32437625
doi: 10.1080/17474086.2020.1772745
pmc: PMC7605282
mid: NIHMS1640557
doi:

Types de publication

Journal Article Meta-Analysis Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

719-729

Subventions

Organisme : NHLBI NIH HHS
ID : R35 HL140025
Pays : United States

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Auteurs

Allison P Wheeler (AP)

Department of Pathology, Microbiology and Immunology, Vanderbilt University , Nashville, TN, USA.
Department of Pediatrics, Vanderbilt University , Nashville, TN, USA.

Celeste Hemingway (C)

Department of Obstetrics and Gynecology, Vanderbilt University , Nashville, TN, USA.

David Gailani (D)

Department of Pathology, Microbiology and Immunology, Vanderbilt University , Nashville, TN, USA.

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Classifications MeSH