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Recent pharmacological management of oral bleeding in hemophilic patien
Background: Hemophilia is a hereditary bleeding disorder that can increase the risk of disease in oralcavity. Sometimes hemophilia is not always established already in a patient. The lack of awareness of hemophilia presence can cause serious problem. Purpose: The purpose of this review is to explain about dental bleeding manifestation and management in hemophilic patient. Reviews: Hemophilia can be
manifested as dental bleeding that cannot stop spontaneously. It should be treated with factor VIIII eitherby giving whole blood, fresh plasma, fresh frozen plasma, cryoprecipitate, and factor VIII concentrate.Factor VIII dose for hemophilia treatment can be calculated based on factor VIII present in hemophilia
patient’s body. Factor VIII can also be given as prophylaxis to prevent bleeding. Complications that can be caused by factor VIII replacement therapy are the presence of factor VIII inhibitor and transfusion related diseases. Treatment of dental bleeding due to hemophilia consists of factor replacement therapy and supportive therapy. Conclusion: Treatment of dental bleeding due to hemophilia consists of factor replacement therapy and supportive therapy. There are complications that can happen due to factor VIII replacement therapy that should be considered and anticipated.
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