Patients with first venous thromboembolism (VTE) and high factor VIII (FVIII) are at increased risk of recurrence. It is unknown
whether these patients benefit from prolonged secondary thrombophrophylaxis. In a prospective trial patients with first spontaneous
VTE and FVIII levels >230 IU/dl were randomized to discontinue vitamin K Antagonist (VKA) after 6 months or to continue VKA
for additional 24 months. Patients were excluded if they had a natural inhibitor deficiency, lupus anticoagulant, cancer,
were pregnant, required long-term antithrombotic therapy or had acute-phase reaction. Primary study endpoints were symptomatic
recurrent VTE or major bleeding within 2 years. Follow-up was continued beyond 2 years. Of 3,219 screened patients 34 met
the inclusion criteria. Mean observation time was 37 months. Two of 17 patients allocated to discontinue VKA and two of 17
patients randomized to prolonged anticoagulation had recurrent VTE within 2 years. In the prolonged treatment group, one patient
had recurrence during VKA therapy and one patient 4 weeks after voluntary discontinuation of VKA. One major nonfatal bleeding
(severe epistaxis) after 10 months of VKA occurred in the prolonged treatment group. Five patients allocated to prolonged
anticoagulation had recurrent VTE after discontinuation of VKA. The probability of recurrence at 2 years after discontinuation
of VKA was 30% (95% CI 13–46%). Patients with high FVIII are at increased risk of recurrence. Our findings in a small number
of patients indicate that prolonged anticoagulation seems to be effective but that the benefit is not maintained after discontinuation
of anticoagulation.
Keywords Anticoagulation - High factor VIII - Recurrence of venous thromboembolism - Interventional trial