Abstract
Summary. This article presents a clinical case of an adolescent with severe hemophilia A and hemophilic arthropathy, who underwent indi- vidualized prophylactic treatment with extended half-life factor (F) VIII (efmoroctocog alfa). Transition to a pharmacokinetically tailored regimen, based on residual FVIII activity and the patient’s physical activity level, stabilized joint condition and regression of inflammatory changes as confirmed by magnetic resonance imaging. The findings support the effectiveness of a personalized approach combining early detection of subclinical joint damage and optimization of extended half-life FVIII therapy, resulting in improved joint health and quality of life.
For citation: Lemazina E.N., Shangareeva G.D., Gubaydullina D.G., Sadykov M.M. Personal experience of therapy individualization with prolonged FVIII in an adolescent with severe hemophilia A and hemophilic arthropathy. Tromboz, gemostaz i reologiya. 2025;(4):95–100. (In Russ.).
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