Module 5: Hematological Emergency Overview
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Questions and Answers

What event initiates the physiological response of hemostasis?

  • Blood vessel dilation
  • Vascular injury (correct)
  • Platelet activation
  • Blood coagulation
  • What is the duration of the vasoconstriction response following an injury?

  • Up to 10 minutes (correct)
  • 1 to 2 minutes
  • 15 to 20 minutes
  • Indefinite duration
  • Which of the following describes the formation of a platelet plug?

  • Activated platelets stimulate the release of anticoagulants
  • Platelets adhere to injured vessels and secrete activating chemicals (correct)
  • Blood coagulation occurs prior to platelet adhesion
  • Platelets become less sticky upon contact with collagen
  • What is the primary function of red blood cells (RBCs)?

    <p>Facilitating tissue oxygenation</p> Signup and view all the answers

    What is the first step in the blood coagulation process upon vessel damage?

    <p>Formation of prothrombin activator</p> Signup and view all the answers

    What role do calcium ions play in the coagulation process?

    <p>They act as a co-factor for enzyme activity</p> Signup and view all the answers

    What happens to aging red blood cells in the body?

    <p>They lose elasticity and get trapped in small blood vessels</p> Signup and view all the answers

    What does a hematocrit value of 45% indicate?

    <p>45 mL of RBCs in 100 mL of blood</p> Signup and view all the answers

    How soon does blood coagulation begin after a vessel is severely ruptured?

    <p>Within seconds</p> Signup and view all the answers

    What happens to a clot after its formation within the first half hour?

    <p>It retracts and seals the vessel further</p> Signup and view all the answers

    What can a low reticulocyte count indicate?

    <p>Bone marrow disease or anemia</p> Signup and view all the answers

    Which of the following conditions could lead to a high hematocrit value?

    <p>Dehydration</p> Signup and view all the answers

    What is a critical function of the fibrous tissue that grows into the blood clot?

    <p>It seals the injured vessel permanently</p> Signup and view all the answers

    What is the normal lifespan of a red blood cell?

    <p>120 days</p> Signup and view all the answers

    How many oxygen molecules can each hemoglobin molecule carry?

    <p>Four oxygen molecules</p> Signup and view all the answers

    What prompts an increase in white blood cell (WBC) production?

    <p>Response to infections</p> Signup and view all the answers

    What percentage of total WBC count do neutrophils account for?

    <p>65%</p> Signup and view all the answers

    Which of the following conditions is NOT associated with an increased WBC count?

    <p>Healthy lifestyle</p> Signup and view all the answers

    What is the primary role of platelets in the circulatory system?

    <p>Facilitate blood clotting</p> Signup and view all the answers

    What is the primary treatment approach for primary polycythemia?

    <p>Phlebotomy and anticancer drug therapy</p> Signup and view all the answers

    Which of the following is NOT a common symptom of primary polycythemia?

    <p>Loss of smell</p> Signup and view all the answers

    Which factors are specifically evaluated during a Prothrombin time test?

    <p>V, VIIa, and X</p> Signup and view all the answers

    In which phase of disseminated intravascular coagulation (DIC) is bleeding most likely to occur?

    <p>Second phase characterized by depletion of clotting factors</p> Signup and view all the answers

    What happens to platelets when a blood vessel is damaged?

    <p>They swell and adhere to the vessel wall.</p> Signup and view all the answers

    What laboratory finding is indicative of disseminated intravascular coagulation?

    <p>Decreased fibrinogen concentration</p> Signup and view all the answers

    Which process is activated when the damage to a vessel is severe?

    <p>Clotting cascade</p> Signup and view all the answers

    What is the normal clotting time in healthy individuals?

    <p>7 to 10 minutes</p> Signup and view all the answers

    How does disseminated intravascular coagulation (DIC) typically affect the body?

    <p>It causes simultaneous clotting and bleeding due to misbalance.</p> Signup and view all the answers

    What is a major complication associated with primary polycythemia?

    <p>Development of other bone marrow diseases</p> Signup and view all the answers

    Which type of WBC makes up approximately 5% of the total WBC count?

    <p>Monocytes</p> Signup and view all the answers

    Which symptom is commonly linked to both primary polycythemia and disseminated intravascular coagulation?

    <p>Dizziness</p> Signup and view all the answers

    What is a critical clinical consequence of the processes in disseminated intravascular coagulation?

    <p>Multiple-system organ failure</p> Signup and view all the answers

    Which factor is NOT associated with the development of leukemia?

    <p>Nutritional deficiencies</p> Signup and view all the answers

    What primarily distinguishes acute leukemia from chronic leukemia?

    <p>The maturity of the cancer cells</p> Signup and view all the answers

    Which of the following conditions is most closely associated with acute lymphocytic leukemia (ALL)?

    <p>Children younger than 15 years</p> Signup and view all the answers

    Which symptom is NOT commonly associated with leukemia?

    <p>Hair loss</p> Signup and view all the answers

    The diagnosis of leukemia is primarily confirmed by which procedure?

    <p>Bone marrow biopsy</p> Signup and view all the answers

    What is a common result of the proliferation of leukemic cells in the body?

    <p>Accumulation in vital organs</p> Signup and view all the answers

    Which type of leukemia primarily affects middle-aged adults?

    <p>Acute myelogenous leukemia (AML)</p> Signup and view all the answers

    Which symptom may indicate severe spleen enlargement in leukemia patients?

    <p>Abdominal fullness</p> Signup and view all the answers

    What is a common cause associated with Burkitt’s lymphoma in Africa?

    <p>Infection by Epstein-Barr virus</p> Signup and view all the answers

    Which factor is NOT linked to an increased risk of certain lymphomas?

    <p>Advanced age</p> Signup and view all the answers

    How does secondary polycythemia typically develop in individuals at high altitudes?

    <p>Reduced air pressure and low oxygen concentration</p> Signup and view all the answers

    What is the primary hormone responsible for stimulating red blood cell production in response to low oxygen levels?

    <p>Erythropoietin</p> Signup and view all the answers

    Which of the following describes primary polycythemia?

    <p>A bone marrow disorder leading to excessive RBC production</p> Signup and view all the answers

    Which symptom is NOT typically associated with lymphomas?

    <p>Increased appetite</p> Signup and view all the answers

    What type of polycythemia results from known physiological responses, such as living at high altitudes?

    <p>Secondary polycythemia</p> Signup and view all the answers

    Which characteristic is most closely associated with the condition known as polycythemia vera?

    <p>Increased red blood cell mass independent of erythropoietin</p> Signup and view all the answers

    Study Notes

    Module 5: Emergencies of Hematological Disorders

    • Module covers emergencies related to blood disorders
    • Objectives include describing blood physiology and components, discussing the pathophysiology and signs/symptoms of specific hematological disorders, outlining general assessment and management of patients with hematological disorders.

    Blood and Blood Components

    • Blood consists of cells and formed elements suspended in plasma
    • 95% of formed elements are red blood cells (RBCs/erythrocytes)
    • Remaining 5% consists of white blood cells (WBCs/leukocytes) and cell fragments (platelets)
    • Blood movement keeps formed elements dispersed throughout plasma, allowing various functions
    • Chief functions include: delivery of substances needed for cellular metabolism, defense against invading microorganisms and injury, and acid/base balance.
    • 55% of blood is plasma, 1% is buffy coat, 45% is red blood cells

    Cellular Components of Blood

    • Erythrocytes (RBCs)—non-nucleated, contain hemoglobin, responsible for oxygen transport, lifespan 80-120 days.
    • Leukocytes (WBCs)—nucleated, various types, crucial for immune defense, lifespan varies by type.
      • Lymphocytes
      • Monocytes
      • Macrophages
      • Eosinophils
      • Neutrophils
      • Basophils
    • Platelets (thrombocytes): Irregularly shaped cell fragments, involved in hemostasis, lifespan 8-11 days
    • Blood cells are formed within red bone marrow and other blood-forming organs.

    Laboratory Tests

    • Hematocrit: Percentage of red blood cells in total blood volume.
      • Normal values vary by sex.
    • Hemoglobin: Measures the amount of hemoglobin in the blood.
      • Normal values vary by sex.
    • Reticulocyte count: Measures the rate of RBC production.
      • Low count suggests decreased production, high count increased production

    White Blood Cells

    • WBCs arise from bone marrow and lymph glands, destroy foreign substances and debris
    • Healthy persons have 5,000-10,000 WBCs/mm³.

    Platelets

    • Platelets are small sticky cell fragments
    • Important in blood clotting following blood vessel injury
    • Form a platelet plug to stop bleeding

    Clotting Measurements

    • Clotting time is typically 7-10 minutes
    • Prothrombin time (PT) measures plasma clotting time.
    • Used to monitor patients on anticoagulants (eg, warfarin), screen for clotting disorders, liver failure.
    • Prolonged PT indicates problems with clotting factors

    Hemostasis

    • Initial physiologic response to wounding to stop bleeding
    • Involves vasoconstriction, platelet plug formation, coagulation, and the growth of fibrous tissue into the clot

    Specific Hematologic Disorders

    • Anemia, leukemia, leukopenia, lymphomas, polycythemia, disseminated intravascular coagulopathy (DIC), hemophilia, sickle cell disease, and multiple myeloma
    • These disorders are often grouped by the affected cell type(s)
      • RBC disorders
      • WBC disorders
      • Hemostasis disorders

    Anemia

    • Condition where hemoglobin or erythrocyte concentration is below normal.
    • Not a disease, but a symptom of underlying conditions.
    • Causes: blood loss, decreased production, and increased destruction of RBCs
    • Example types: iron-deficiency, pernicious, hemolytic

    Iron-Deficiency Anemia

    • Caused by inadequate iron intake or loss
    • RBCs produced are small and pale, have reduced oxygen-carrying capacity
    • Common cause is blood loss (menstruation, GI bleeding)

    Pernicious Anemia

    • Caused by deficiency of vitamin B12 (needed for RBC production)
    • Lack of intrinsic factor (stomach protein necessary for vitamin B12 absorption)
    • Results in large, immature RBCs
    • Causes neurological complications

    Hemolytic Anemia

    • Characterized by prematurely destroyed RBCs
    • Can be inherited (e.g., sickle cell anemia, thalassemia) or acquired (drug-induced)

    Acquired Disorders

    • Resulting from mechanical forces, autoimmune disorders, or infections.

    Signs and Symptoms of Anemia

    • Common symptoms: Fatigue, headaches, sore mouth/tongue, brittle nails, breathlessness, chest pain.
    • Additional symptoms related to low WBCs (leukopenia) or low platelets (thrombocytopenia) such as bleeding and other symptoms

    Diagnosis and Treatment

    • Patient history, blood tests, bone marrow biopsy determine diagnosis
    • Treatment varies dependent upon the underlying cause and severity of condition

    Leukemia

    • Cancer characterized by abnormal proliferation of WBCs (leukocytes)
    • Acute leukemia results from immature cells, chronic from more mature cells.
    • Causes: Genetic predisposition, exposure to radiation, certain viruses.
    • Symptoms: Abnormal blood cell counts, organ enlargement (spleen and liver), fatigue, frequent infections

    Leukopenia

    • Decrease in the number of WBCs
    • Risk of developing infections
    • Causes: Chemotherapy, radiation therapy, post-transplant medications, leukemia, certain anemias, and other diseases

    Lymphomas

    • General term for neoplastic disorders of lymphoid tissue.
    • Hodgkin lymphoma : Specific, curable form of lymphoma
    • Non-Hodgkin lymphoma: Unpredictable forms of lymphoma that have a high malignancy grade leading to more rapid progression compared to Hodgkin lymphoma.
    • Symptoms: Swelling of lymph nodes, fatigue, chills, night sweats, itching, cough, weight loss, shortness of breath and chest discomfort
    • Diagnosis and treatment vary dependent on the type of lymphoma

    Polycythemia

    • Increase in RBC mass.
    • Primary polycythemia: No clear cause.
    • Secondary polycythemia: natural response to chronic hypoxia (e.g., high altitude)
    • Often associated with dehydration.
    • Symptoms: Blurred vision, dizziness, generalized itching, headache

    Disseminated Intravascular Coagulation (DIC)

    • A complication of severe injury, trauma, or illness.
    • Characterized by abnormal clotting and bleeding simultaneously.
    • Often associated with hypotension, hypoperfusion, and organ ischemia.

    Hemophilia

    • Inherited bleeding disorder caused by deficiency in clotting factors.
    • Typically, factor VIII (hemophilia A) or factor IX (hemophilia B) are deficient.
    • Symptoms: Uncontrolled bleeding, easy bruising, prolonged bleeding time.
    • Treatment involves factor infusions

    Thrombocytopenia

    • Low platelet count
    • Causes: Reduced platelet production, increased platelet destruction, or splenic sequestration.
    • Symptoms: Small red or purple spots on skin, easy bruising, prolonged bleeding, nosebleeds, heavy menstrual bleeding.
    • Treatment: Careful monitoring, corticosteroids, platelet transfusions.

    General Assessment and Management of Patients With Hematologic Disorders

    • Thorough assessment and detailed history, vital signs, focused physical examination.
    • Patient should be evaluated for specific conditions like bruising, jaundice, and edema.
    • Determining the urgency of emergency transport.

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    Description

    This quiz covers the key concepts of emergencies related to hematological disorders. It includes essential information about blood physiology, components, and the assessment and management of patients suffering from these conditions. Test your knowledge on the pathophysiology and signs/symptoms of various blood disorders.

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