Postępowanie w stanach nagłych u pacjentów z hemofilią

Ewa Sikora, *Paweł Łaguna, Michał Matysiak

Summary
Haemophilia is congenital with haemorrhagic diathesis due to deficiency of VIII or IX o coagulation factor, which is manifested by an increased tendency to bleeds. The therapeutic procedure during bleeding is intravenous administration of missing IX or VIII coagulation factor. The article presents a diagram of emergency procedures during bleeding in different locations. When discussing these cases, we would like to emphasize that, regardless of the type of bleeding or injury, correct treatment is first and foremost substitution of the missing coagulation factor and then of imaging and laboratory diagnostics. Delayed administration of a factor concentrate may cause a risk to the patient's life.

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