Why the study?
Does prothrombin complex concentrate improve effective haemostasis in patients with vitamin K antagonist-associated bleeding?
Does prothrombin complex concentrate improve effective haemostasis in patients with vitamin K antagonist-associated bleeding?
Prothrombin complex concentrate achieves effective haemostasis in the majority of patients with VKA-associated bleeding, though 30-day mortality remains high primarily due to intracranial hemorrhage.
May support PCC consideration in VKA bleeding; leaves open net clinical benefit and need for RCTs.
Unlabelled Box •Data on clinical outcome of vitamin K antagonist (VKA)‐associated bleeding is scarce. •Cohort study of patients with VKA bleeds treated with prothrombin complex concentrate (PCC). •Effective haemostasis was achieved in 68% of patients with a VKA‐associated bleeding. •Thromboembolism rates were low and mortality rates high at 30 days after PCC administration. Background Vitamin K antagonists (VKA) are used for the treatment of thromboembolism. Patients with severe VKA‐associated bleeding require immediate restoration of haemostasis. Clinical studies on the effect of prothrombin complex concentrate (PCC) are heterogeneous with respect to outcome of bleeding. Objective To evaluate the clinical outcome of patients treated with PCC for VKA‐associated bleeding. Methods We performed a cohort study of consecutive patients who received PCC for VKA‐related bleeding in five Dutch hospitals. Data were collected by chart review on the bleeding event, international normalized ratio (INR), haemostatic efficacy, thromboembolic (TE) complications, and mortality. The primary outcome was effective haemostasis, assessed by an adaptation of the Sarode criteria with a surrogate outcome for patients with ICH without repeat CT. Results One hundred patients were included. Mean age was 74 years, 54% were male and 79% received VKA for atrial fibrillation. Most patients presented with ICH (41%) or GI bleeding (36%). Effective haemostasis was achieved in 67/98 (68%) patients using the adapted classification. Surrogate outcomes were applied for 32 patients and data for two patients was missing. Median pre‐treatment INR was 3.9 (IQR 2.9‐5.8). One hour after PCC infusion, the INR was available for 50 patients and of these, 35 (70%) had an INR ≤1.4. TE complications occurred in five patients and 22 died (60% bleeding‐related) within 30 days. Conclusion PCC achieved effective haemostasis in 68% of evaluable patients with VKA‐associated bleeding. TE complication rates were low, but mortality rates were high, due to the large number of patients with ICH.
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Brekelmans et al. (2017) studied this question.
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