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EDUC'AVK: reduction of oral anticoagulant-related adverse events after patient education: a prospective multicenter
Gilles Pernod1, José Labarère, Jacqueline Yver
1Department of Vascular Medicine, CHU Grenoble, Grenoble, France. GPernod@chu-grenoble.fr
Background:
Long-term oral anticoagulation treatment is associated with potential morbidity. Insufficient patient education is linked to poorly controlled anticoagulation. However the impact of a specific educational program on anticoagulation related morbidity remains unknown.
Objective:
To evaluate the effect of an oral anticoagulation patient education program in reducing both hemorrhagic and recurrent thrombotic complications.
Design/Participants:
We conducted a prospective, multicenter open randomized study, comparing an interventional group who received a specific oral anticoagulation treatment educational program with a control group. Eligible patients were older than 18 and diagnosed as having deep vein thrombosis or pulmonary embolism requiring therapy with a vitamin K antagonist for 3 months or more. Our primary outcome was the occurrence of hemorrhagic or thromboembolic events.
Results:
During the 3-month follow-up the main outcome criteria were observed 20 times (6.6% of patients), 5 (3.1%) in the experimental and 15 (10.6%) in the control group. Consequently, in multivariate analysis, the cumulative risk reduction in the experimental group was statistically significant (OR 0.25, 95% CI 0.1-0.7, p < 0.01).
Conclusions:
Patient education using an educational program reduced VKA-related adverse event rates.
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