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Browsing by Author "Mumford, Andrew D. (7003755145)"

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    Publication
    Diagnosis and management of severe congenital protein C deficiency (SCPCD): Communication from the SSC of the ISTH
    (2022)
    Minford, Adrian (6602893631)
    ;
    Brandão, Leonardo R. (12788818600)
    ;
    Othman, Maha (7006122614)
    ;
    Male, Christoph (7003604062)
    ;
    Abdul-Kadir, Rezan (7004016849)
    ;
    Monagle, Paul (7004308240)
    ;
    Mumford, Andrew D. (7003755145)
    ;
    Adcock, Dorothy (7003902745)
    ;
    Dahlbäck, Björn (7103328699)
    ;
    Miljic, Predrag (6604038486)
    ;
    DeSancho, Maria T. (11138767900)
    ;
    Teruya, Jun (8679464900)
    Severe congenital protein C deficiency (SCPCD) is rare and there is currently substantial variation in the management of this condition. A joint project by three Scientific and Standardization Committees of the ISTH: Plasma Coagulation Inhibitors, Pediatric/Neonatal Thrombosis and Hemostasis, and Women’s Health Issues in Thrombosis and Hemostasis, was developed to review the current evidence and help guide on diagnosis and management of SCPCD. We provide a summary of the clinical presentations, differential diagnoses, appropriate investigations to confirm the diagnosis, approaches for management of the acute situation, and options for long-term management including subsequent pregnancies. We finally provide a set of recommendations to help in this regard. © 2022 The Authors. Journal of Thrombosis and Haemostasis published by Wiley Periodicals LLC on behalf of International Society on Thrombosis and Haemostasis.

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