Rekombinant faktor VIIa ved post partum-blødning

Anne Juul Wikkelsø, Jakob Stensballe

Abstrakt

Recombinant factor VIIa (rFVIIa) has of April 2022 been approved by the European Medicines Agency for treatment of severe postpartum haemorrhage. The extended approval is based on one small open-label, non-blinded randomized trial of 84 women from 2015 showing reduced "second line" treatment, but also increased risk of thromboembolism. Systematic use of tranexamic acid and timely coagulation assessment with thromboelastography/rotational thromboelastometry are not applied. Danish and international societies recommend that rFVIIa is reserved as a last option in severe life-threatening cases of postpartum haemorrhage.

Bidragets oversatte titelNot Available
OriginalsprogDansk
ArtikelnummerV07220423
TidsskriftUgeskrift for Laeger
Vol/bind184
Udgave nummer47
ISSN0041-5782
StatusUdgivet - 21 nov. 2022

Emneord

  • Female
  • Humans
  • Factor VIIa/therapeutic use
  • Postpartum Hemorrhage/drug therapy
  • Recombinant Proteins/therapeutic use
  • Randomized Controlled Trials as Topic

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