BACKGROUND: The management of patients with acute ischemic stroke during treatment with non-vitamin K oral anticoagulants (NOAC) is challenging. Functional NOAC-plasma-levels could guide decisions on therapies.
METHODS: A standard operating procedure for patients on NOAC was established: Patients with a plasma level below 50 ng/mL were considered eligible for intravenous thrombolysis (IVT), while levels above 100 ng/mL constituted an exclusion criterion. Levels between 50 to 100 ng/mL allowed an individual decision (Figure 1). For patients on vitamin-K antagonists (VKA), a cutoff for IVT was set at INR 1.7. Mechanical recanalization (EVT) of a large vessel occlusion was indicated independently from coagulation testing. Consecutive patients were included in an observational registry starting in January 2014.
RESULTS: 523 patients (262 on NOAC and 261 on VKA) were included. Patients were on treatment with Apixaban (131), Rivaroxaban (85), Dabigatran (37), Edoxaban (9) or Phenprocoumon (261) within 48 hours prior to admission. The functional NOAC-plasma level was assessed in a total of 207 (79.0%) patients (Figure 2 and 3).
47 (18.0%) of the VKA patients and 42 (16.0%) of the NOAC patients underwent a recanalization therapy with IVT and/or EVT according to the standard operating procedure. Among the patients under VKA, 30 received IVT and 27 underwent EVT, including 10 who received both. 24 of the NOAC patients received IVT, 31 underwent EVT and 14 both. Successful mechanical recanalization (TICI 2b-3) was achieved in 23 (85.2%) VKA patients and 28 (90.3%) NOAC patients. There were no differences in rates of major intracranial hemorrhage, which occurred in 2 (4.3%) VKA and 2 (4.8%) NOAC patients; P=0.908. 11 (25.0%) patients on VKA and 17 (41.5%) patients on NOAC had a favorable outcome (mRS 0-2); P=0.107 (Figure 4).
CONCLUSION: The assessment of functional NOAC-plasma levels is feasible to support decisions on recanalization therapies. Under consideration of defined thresholds, no higher bleeding rates after treatment were observed when compared to established guidelines for patients under VKA.

Europe Stroke Organisation Conference