Coagulation Disorders Overview
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Questions and Answers

What is the primary cause of coagulopathy?

  • Increased levels of vitamin K
  • Excessive hydration leading to dilutional coagulopathy
  • Genetic mutations affecting hemoglobin
  • Alterations in platelets, clotting factors, or both (correct)
  • Which condition is characterized by a normal platelet production but a decreased lifespan due to antiplatelet antibodies?

  • Heparin-induced thrombocytopenia (HIT)
  • Thrombotic thrombocytopenic purpura (TTP)
  • Idiopathic or immune thrombocytopenic purpura (ITP) (correct)
  • Disseminated intravascular coagulation (DIC)
  • What happens in thrombotic thrombocytopenic purpura (TTP)?

  • Platelets form microclots disrupting organ function (correct)
  • Platelet production is significantly increased
  • There is a complete absence of clotting factors
  • Platelets abnormally aggregate, leading to excessive bleeding
  • What is the mortality rate for untreated thrombotic thrombocytopenic purpura (TTP)?

    <p>10-20%</p> Signup and view all the answers

    Which coagulopathy is caused by heparin treatment resulting in an unexplained low platelet count?

    <p>Heparin-induced thrombocytopenia (HIT)</p> Signup and view all the answers

    What is the risk for a client diagnosed with disseminated intravascular coagulation (DIC)?

    <p>Risk for internal and external bleeding and organ damage</p> Signup and view all the answers

    In hemophilia, what factor deficiencies are primarily involved?

    <p>Factor VIII or Factor IX</p> Signup and view all the answers

    What characterizes an autoimmune disorder as a cause of coagulopathy?

    <p>Normal production of platelets and clotting factors but immune system attacks</p> Signup and view all the answers

    Which risk factor is specifically associated with Immune Thrombocytopenic Purpura (ITP)?

    <p>Recent viral infection in children</p> Signup and view all the answers

    What underlying condition is commonly associated with Heparin-Induced Thrombocytopenia (HIT)?

    <p>Receiving heparin for longer than 1 week</p> Signup and view all the answers

    Which of the following conditions is NOT a risk factor for Thrombotic Thrombocytopenic Purpura (TTP)?

    <p>Family history of clotting disorders</p> Signup and view all the answers

    Which of these conditions is one of the risk factors for developing disseminated intravascular coagulation (DIC)?

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

    Among the following, which factor significantly increases the risk of HIT in patients?

    <p>Administration of heparin for more than one week</p> Signup and view all the answers

    What is a common symptom of microvascular thrombosis?

    <p>Petechiae and ecchymoses</p> Signup and view all the answers

    What vital sign changes may indicate excessive bleeding?

    <p>Tachycardia and hypotension</p> Signup and view all the answers

    Which finding is associated with organ failure due to microemboli?

    <p>Cyanosis of nail beds</p> Signup and view all the answers

    Which of the following is least likely to be observed with spontaneous bleeding disorders?

    <p>Recurrent infections</p> Signup and view all the answers

    What physical symptom may indicate heparin-induced thrombocytopenia (HIT)?

    <p>Warmth and redness in lower extremities</p> Signup and view all the answers

    What is the expected reference range for hemoglobin in females?

    <p>12 to 16 g/dL</p> Signup and view all the answers

    Which laboratory test shows an increased level in patients with DIC?

    <p>D-dimer</p> Signup and view all the answers

    What is the expected reference range for platelet levels?

    <p>150,000 to 400,000 mm3</p> Signup and view all the answers

    Which of the following represents an increased laboratory finding in DIC?

    <p>Fibrin split product levels</p> Signup and view all the answers

    What is the expected reference range for prothrombin time?

    <p>11.0 to 12.5 seconds</p> Signup and view all the answers

    What is the primary focus of nursing interventions for a patient with disseminated intravascular coagulation (DIC)?

    <p>Assessing and correcting the underlying cause</p> Signup and view all the answers

    Which manifestation should a nurse monitor for as a sign of microemboli in a patient with DIC?

    <p>Cyanotic nail beds</p> Signup and view all the answers

    What should be prioritized in the nursing care of a patient experiencing complications from blood transfusions?

    <p>Regularly assessing vital signs</p> Signup and view all the answers

    Which nursing intervention should be avoided to prevent the risk of cerebral hemorrhage in a patient with DIC?

    <p>Instructing to avoid Valsalva maneuver</p> Signup and view all the answers

    What laboratory values should be monitored closely in a patient diagnosed with disseminated intravascular coagulation (DIC)?

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

    Which medication is commonly used in the treatment of Thrombotic Thrombocytopenic Purpura (TTP)?

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

    What is the role of anticoagulants in Disseminated Intravascular Coagulation (DIC)?

    <p>To decrease the formation of microclots</p> Signup and view all the answers

    In the management of Heparin-Induced Thrombocytopenia (HIT), which type of medication is utilized?

    <p>Direct thrombin inhibitors</p> Signup and view all the answers

    Which class of medications is used in treating Immune Thrombocytopenic Purpura (ITP)?

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

    How do immunosuppressive therapies impact Thrombotic Thrombocytopenic Purpura (TTP)?

    <p>They decrease the intensity of complications</p> Signup and view all the answers

    What therapeutic procedure can be used for treating Thrombotic Thrombocytopenic Purpura (TTP)?

    <p>Plasma exchange</p> Signup and view all the answers

    In which situation is a splenectomy indicated for a patient with Immune Thrombocytopenic Purpura (ITP)?

    <p>After initial medical management failure</p> Signup and view all the answers

    What is a potential outcome if a patient with TTP does not receive timely treatment?

    <p>Progression to acute kidney failure</p> Signup and view all the answers

    Which of the following is a common medical management option for Immune Thrombocytopenic Purpura (ITP) before considering a splenectomy?

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

    What is the primary treatment goal in patients undergoing plasma exchange for TTP?

    <p>Remove antibodies and toxins from blood</p> Signup and view all the answers

    Study Notes

    Coagulation Disorders

    • Coagulation disorders arise from problems with platelets, clotting factors, or both.
    • Coagulopathy is any condition affecting blood clotting ability.
    • Suspected when standard bleeding-control methods fail.
    • Can develop secondary to autoimmune conditions or significant blood loss.
    • Microemboli paradoxically deplete clotting factors, leading to hemorrhages alongside intravascular clotting.

    Idiopathic (Immune) Thrombocytopenic Purpura (ITP)

    • An autoimmune disorder impacting platelet lifespan.
    • Antiplatelet antibodies shorten platelet life, despite normal production.
    • Can cause severe bleeding after procedures like C-sections or lacerations.
    • Mortality rate for adults with ITP is 5%.

    Thrombotic Thrombocytopenic Purpura (TTP)

    • Characterized by abnormal platelet clumping in capillaries due to autoimmune reaction.
    • Leads to low platelet count and inadequate clotting response to injury.
    • Can result in kidney failure, heart attack, stroke, and is deadly within three months if untreated.
    • Mortality rate is 10-20%.

    Heparin-Induced Thrombocytopenia (HIT)

    • An immunity-mediated clotting disorder triggered by heparin therapy.
    • Causes unexplained low platelet count.
    • Mortality rate is 30%.

    Disseminated Intravascular Coagulation (DIC)

    • A life-threatening condition with simultaneous clotting and anti-clotting mechanisms.
    • Patients risk both internal and external bleeding, organ damage due to micro-clots.

    Hemophilia

    • An inherited bleeding disorder due to deficiencies in factor VIII or factor IX.
    • Often triggered by minor trauma.
    • Relatively common, typically diagnosed in early childhood.
    • Affects over one million individuals.

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    Description

    This quiz covers the essential concepts related to coagulation disorders and specific conditions such as ITP and TTP. Explore the mechanisms behind coagulopathy, the implications of autoimmune reactions, and how these disorders affect bleeding and clotting. Test your knowledge on the key characteristics and impacts of these conditions.

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