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International Conference on Thrombosis, Bleeding Disorders & Hemostasis

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Bleeding Disorders and Therapeutic Approaches: Bleeding disorders are classified as disorders of primary hemostasis or disorders of secondary hemostasis. Bleeding disorders should always be considered life threatening. Even the stable patient with a bleeding disorder can decompensate rapidly from massive bleeding or bleeding into a vital organ. It also present for symptoms related to anemia from ongoing hemorrhage. Patients in an anemic crisis are depressed or moribund, with marked pallor, tachypnea, tachycardia, and bounding pulses. Once the patient has been stabilized, every effort should be directed toward the rapid establishment of a Diagnosis. Hemophilia is a rare bleeding disorder that results from reduced levels or lack of clotting factor VIII. The two most common types of hemophilia are FVIII deficiency- hemophilia A and FIX deficiency -hemophilia B. Idiopathic thrombocytopenic purpura (ITP) is a disorder that can lead to easy or excessive bruising and bleeding. The bleeding results from unusually low levels of platelets the cells that help your blood clot. Von Willebrand disease is a condition that can cause extended or excessive bleeding, normally it is a Coagulation Disorder. The condition is most often inherited but in rare cases may develop later in life. Polycythemia vera is a stem cell disorder characterized as a pan hyperplastic, malignant, and neoplastic marrow disorder. Its most prominent feature is an elevated absolute red blood cell mass because of uncontrolled red blood cell production. Current treatments for preventing thrombotic diseases are associated with a significant risk of bleeding. Improved anticoagulant agents are therefore still required.

Description

Bleeding Disorders and Therapeutic Approaches:

Bleeding disorders are classified as disorders of primary hemostasis or disorders of secondary hemostasis. Bleeding disorders should always be considered life threatening. Even the stable patient with a bleeding disorder can decompensate rapidly from massive bleeding or bleeding into a vital organ. It also present for symptoms related to anemia from ongoing hemorrhage. Patients in an anemic crisis are depressed or moribund, with marked pallor, tachypnea, tachycardia, and bounding pulses. Once the patient has been stabilized, every effort should be directed toward the rapid establishment of a Diagnosis. Hemophilia is a rare bleeding disorder that results from reduced levels or lack of clotting factor VIII. The two most common types of hemophilia are FVIII deficiency- hemophilia A and FIX deficiency -hemophilia B. Idiopathic thrombocytopenic purpura (ITP) is a disorder that can lead to easy or excessive bruising and bleeding. The bleeding results from unusually low levels of platelets the cells that help your blood clot. Von Willebrand disease is a condition that can cause extended or excessive bleeding, normally it is a Coagulation Disorder. The condition is most often inherited but in rare cases may develop later in life. Polycythemia vera is a stem cell disorder characterized as a pan hyperplastic, malignant, and neoplastic marrow disorder. Its most prominent feature is an elevated absolute red blood cell mass because of uncontrolled red blood cell production. Current treatments for preventing thrombotic diseases are associated with a significant risk of bleeding. Improved anticoagulant agents are therefore still required.

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