Intracranial Hemorrhage Clinical Trial
Official title:
A Comparison of Recombinant Activated Factor VII, Prothrombin Complex Concentrate, and Fresh Frozen Plasma for Anticoagulation Reversal in Warfarin-Associated Acute Intracranial Hemorrhage: A Dose Ranging Pilot Study
The purpose of this dose-ranging pilot study is to compare Recombinant Activated Factor VII, Prothrombin Complex Concentrate and Fresh Frozen Plasma (each starting at low doses with escalation if necessary) for the reversal of warfarin in the setting of acute intracranial hemorrhage.
Both recombinant activated Factor VIIa (rFVIIa) as well as Prothrombin Complex Concentrate
(PCC) are labeled for the treatment of bleeding episodes in patients with hemophilia. Many
hospitals are also using each for the following unlabeled indications: bleeding rescue in
surgical patients, severe multiple trauma with ongoing bleeding, intracranial bleeding < 4
hours since symptom onset, traumatic head injury with evidence of expanding bleed,
retroperitoneal bleed, and life-threatening bleeding due to idiopathic coagulopathy. To our
knowledge, these two products have never been clinically compared head to head for the
reversal of warfarin in the setting of intracranial hemorrhage.
The rFVIIa (Novoseven) guidelines are based off of national data and utilize a dose range of
40-90 mcg/kg of ideal body weight (2.8-6.3 mg for a 70 kg. patient) with an additional dose
if needed. The dose cited in the literature for the management of intracerebral bleeds
ranges from 10 to 120 mcg/kg (0.7 - 8.4 mg for a 70 kg. patient,) with higher doses
associated with increased risk of thromboembolic events.
The recommended dosing of PCC is 30-50 i.u. per kilogram of ideal body weight with
additional dosing if needed. PCC (Profilnine®SD) is a mixture of the following vitamin
K-dependent clotting factors: II (prothrombin), VII (proconvertin), IX (plasma
thromboplastin component; PTC; Christmas factor), and X (Stuart-Prower factor). These
factors are required for the conversion of prothrombin to thrombin and thus adequate
hemostasis, and are synthesized in the liver.
Currently at the most hospitals around the country, fresh frozen plasma (FFP) is the
mainstay for reversal of warfarin-related coagulopathy in intracranial hemorrhage at the
discretion of the treating attending physician. We propose to study all the current reversal
practices in the intracranial hemorrhage population here at the University of Utah as part
of a quality improvement project for both patient safety and cost.
We will perform a safety and feasibility study comparing dosage regimens of rFVIIa, FIXa and
fresh frozen plasma (FFP) infusion in the normalization of coagulopathy in the context of
warfarin-related intracerebral hemorrhage. Our primary outcome is time to INR normalization
defined as INR≤ 1.3 on two consecutive readings separated by 2 hours.
;
Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
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