Navigating Rare Coagulation Disorders In Pregnancy: A Case Series Emphasizing Multidisciplinary Care
DOI:
https://doi.org/10.64252/4j6sth24Abstract
Background: Inherited and acquired coagulation factor deficiencies in pregnancy are rare but pose significant risks to both mother and baby. Conditions like Factor XI, Factor VII, Factor XII deficiencies, and acquired hemophilia A present complex clinical and laboratory challenges that necessitate coordinated multidisciplinary care.
Objective: To present the clinical features, management, and outcomes of four pregnant women with rare coagulation disorders, emphasizing tailored, team-based strategies for safe delivery and postpartum care.
Methods and Cases:Four patients managed at our tertiary center with congenital Factor XI deficiency, Factor VII deficiency, Factor XII deficiency with renal anomaly, and postpartum acquired hemophilia A are described. Multidisciplinary collaboration guided individualized antenatal assessment, hemostatic support, anesthesia choice, and postpartum follow-up.
Conclusion: Early identification and personalized multidisciplinary management of coagulation disorders in pregnancy enable favorable maternal and neonatal outcomes. This case series offers practical insights for handling similarly rare, high-risk presentations.
