THE PROBLEM OF PERMANENT VASCULAR ACCESS IN PATIENTS WITH CONGENITAL COMBINED COAGULATION DISORDER AND THROMBOHEMORRHAGIC SYNDROME (A CLINICAL CASE)

Abstract

Treatment of patients with congenital combined coagulation disorder and thrombohemorrhagic syndrome is associated with a number of difficulties, one of them is need of permanent vascular access in order to provide appropriate pathogenetic therapy. The article contains a clinical case, representing a subject matter of searching for means of providing a permanent vascular access in a child with congenital combined deficiency of vitamin K dependent clotting factors (II, VII, IX, X, S- and C-protieins) and severe course of thrombohemorrhagic syndrome.