The danger of hemophilia is mainly a lifelong tendency to bleed after minor trauma. Spontaneous bleeding can occur in severe cases without obvious trauma, and can cause complications such as chronic hemophilic arthropathy, which affects the patient’s work and life.
Hemophilia is a bleeding disorder with hereditary coagulation abnormality. Due to the defective gene of coagulation factor in the body, it leads to the lack of coagulation factor, abnormal coagulation function, and easy to bleed for life. Hemophilia can develop from birth and has a high rate of disability and death if not treated regularly. Those who receive standardized treatment can have relatively normal growth and development and avoid disability.
Specific treatments include supplementation of coagulation factors, cold precipitation, and plasma transfusion.
If a cerebral hemorrhage has occurred before, there is a higher chance of another cerebral hemorrhage with non-preventive treatment, which carries a risk of life-threatening injury. Hemophiliacs should also be careful to avoid trauma and tests and treatments that may cause injury, and avoid medications that affect platelet function such as aspirin.
Hemophiliacs are advised to actively standardize their treatment under the guidance of their doctors and undergo regular review.