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3.
Int J Obstet Anesth ; 24(2): 174-9, 2015 May.
Article in English | MEDLINE | ID: mdl-25659517

ABSTRACT

Placental abruption may cause significant haemorrhage and coagulopathy that can progress rapidly due to simultaneous consumption and depletion of clotting factors. Plasma fibrinogen levels are predictive of further haemorrhage. Rapid detection and treatment of hypofibrinogenaemia is essential in the evolving clinical and haematological situation. The use of near-patient testing of coagulation using rotational thromboelastometry (ROTEM) allows dynamic monitoring of coagulopathy. Following the introduction of fibrinogen concentrate into our unit, a ROTEM-guided algorithm was developed for use in obstetric haemorrhage. We describe four cases of placental abruption, haemorrhage and severe coagulopathy that span the introduction of the algorithm. Three cases were associated with intrauterine death and the fourth with delivery of an extremely premature neonate. Rotational thromboelastometry was used in all cases but methods of fibrinogen replacement differ, illustrating evolving management of the condition in our unit.


Subject(s)
Abruptio Placentae/diagnostic imaging , Blood Coagulation Disorders/drug therapy , Fibrinogen/therapeutic use , Adolescent , Adult , Algorithms , Blood Coagulation/drug effects , Blood Coagulation Disorders/complications , Female , Humans , Pregnancy , Thrombelastography , Ultrasonography , Young Adult
4.
Anaesthesia ; 70(2): 166-75, 2015 Feb.
Article in English | MEDLINE | ID: mdl-25289791

ABSTRACT

We compared blood component requirements during major obstetric haemorrhage, following the introduction of fibrinogen concentrate. A prospective study of transfusion requirements and patient outcomes was performed for 12 months to evaluate the major obstetric haemorrhage pathway using shock packs (Shock Pack phase). The study was repeated after the pathway was amended to include fibrinogen concentrate (Fibrinogen phase). The median (IQR [range]) number of blood components given was 8.0 (3.0-14.5 [0-32]) during the Shock Pack phase, and 3.0 (2.0-5.0 [0-26]) during the Fibrinogen phase (p = 0.0004). The median (IQR [range]) quantity of fibrinogen administered was significantly greater in the Shock Pack phase, 3.2 (0-7.1 [0-20.4]) g, than in the Fibrinogen phase, 0 (0-3.0 [0-12.4]) g, p = 0.0005. Four (9.5%) of 42 patients in the Shock Pack phase developed transfusion associated circulatory overload compared with none of 51 patients in the Fibrinogen phase (p = 0.038). Fibrinogen concentrate allows prompt correction of coagulation deficits associated with major obstetric haemorrhage, reducing the requirement for blood component therapy and the attendant risks of complications.


Subject(s)
Algorithms , Fibrinogen/therapeutic use , Postpartum Hemorrhage/drug therapy , Thrombelastography/methods , Blood Coagulation/drug effects , Blood Transfusion/statistics & numerical data , Female , Hemostatics/therapeutic use , Humans , Pregnancy , Prospective Studies , Thrombelastography/statistics & numerical data , Treatment Outcome
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