Key result
Factor Xa inhibitor-related intracranial hemorrhage treated with PCC showed similar effective hemostasis at 24 hours compared to VKA-related hemorrhage (73% vs 62%; adjusted OR 1.45; 95% CI 0.44-4.83).
Why the study?
Intracranial hemorrhage is a feared anticoagulation complication, and guidelines recommended prothrombin complex concentrate for factor Xa inhibitor-related bleeding before specific reversal agents were registered.
Does prothrombin complex concentrate (PCC) provide similar effective hemostasis in patients with factor Xa inhibitor-related intracranial hemorrhage compared to vitamin K antagonist-related intracranial hemorrhage?
Cohort (n=75)
Does prothrombin complex concentrate (PCC) provide similar effective hemostasis in patients with factor Xa inhibitor-related intracranial hemorrhage compared to vitamin K antagonist-related intracranial hemorrhage?
Odds Ratio: 1.45 (95% CI 0.44–4.83)
Absolute Event Rate: 73% vs 62%
Prothrombin complex concentrate provides similar rates of effective hemostasis for intracranial hemorrhage in patients on factor Xa inhibitors compared to those on vitamin K antagonists.
Suggests prothrombin complex concentrate may offer comparable hemostasis for factor Xa inhibitor-.
Intracranial hemorrhage (ICH) is the most feared complication of anticoagulation with a high mortality and morbidity. Before registration of a specific reversal agent for factor Xa inhibitors (FXa-I), international guidelines recommended prothrombin complex concentrate (PCC), which also is the specific reversal agent for vitamin K antagonists (VKA). In two contemporary cohorts, we compared clinical outcomes between patients with FXa-I and VKA related ICH treated with PCC between 2014 and 2018. Primary outcome was effective hemostasis after 24 h, according to the International Society of Thrombosis and Hemostasis definition. Safety outcomes were defined as venous and arterial thromboembolic complications and death within 30 days. Thirty-six patients with FXa-I-ICH and 39 patients with VKA-ICH were available for analysis. Baseline characteristics were comparable between both groups, except for time from start of symptoms to presentation at the hospital. In the FXa-I-ICH cohort, 24 (73%) patients achieved effective hemostasis compared to 23 (62%) patients in the VKA-ICH cohort (crude odds ratio [OR] 1.62 [95%CI 0.59-4.48], adjusted OR 1.45 [95%CI 0.44-4.83]). Eight (24%) patients with FXa-I-ICH deceased compared to 17 (45%) patients with VKA-ICH (crude OR 0.38 [95%CI 0.14-1.24], adjusted OR 0.41 [95%CI 0.12-1.24]). In this observational cohort study, the outcome of ICH managed with PCC was similar in patients with FXa-I-ICH and in patients with VKA-ICH.
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Bavalia et al. (2020) conducted a cohort in Intracranial hemorrhage (n=75). Factor Xa inhibitors vs. Vitamin K antagonists was evaluated on Effective hemostasis after 24 h (adjusted OR 1.45, 95% CI 0.44-4.83). Factor Xa inhibitor-related intracranial hemorrhage treated with PCC showed similar effective hemostasis at 24 hours compared to VKA-related hemorrhage (73% vs 62%; adjusted OR 1.45; 95% CI 0.44-4.83).
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