NUR 344 Exam 2: Polycythemia and Platelets
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Questions and Answers

A patient with polycythemia vera is most likely to exhibit which combination of clinical manifestations?

  • Hypotension, cyanosis, and decreased RBC production.
  • Hypotension, pallor, and decreased erythropoietin levels.
  • Hypertension, pruritus after showering, and ruddy complexion. (correct)
  • Cyanosis, decreased erythropoietin levels, and hypertension.

A patient's platelet count returns as 100,000/μL. Which intervention is the priority, considering this result and the associated risks?

  • Instituting bleeding precautions and closely monitoring for signs of hemorrhage. (correct)
  • Immediately preparing the patient for elective surgery to mitigate risks.
  • Administering aspirin to prevent potential thrombotic events.
  • Starting cytoreductive therapy to lower the elevated platelet count.

What is the most critical dietary consideration for a patient undergoing warfarin therapy to maintain a stable INR?

  • Increasing the intake of alcohol and cranberry juice to potentiate the anticoagulant effects.
  • Maintaining a consistent daily intake of vitamin K to minimize fluctuations in coagulation. (correct)
  • Significantly increasing intake of dark leafy greens to improve overall health while on warfarin.
  • Avoiding vitamin K-rich foods entirely to enhance the drug's effect.

Which statement accurately describes the rationale behind avoiding NSAIDs in patients on warfarin therapy?

<p>NSAIDs increase the risk of bleeding when taken with warfarin due to their antiplatelet effects. (D)</p> Signup and view all the answers

A patient who has undergone a splenectomy is at increased risk for which of the following complications?

<p>Increased risk of thrombosis and DVT due to altered platelet storage and filtration. (B)</p> Signup and view all the answers

A nurse is providing post-operative education to a patient who underwent a bone marrow biopsy. Which instruction should the nurse emphasize to minimize complications?

<p>Avoid NSAIDs for pain management to prevent bleeding complications. (C)</p> Signup and view all the answers

A patient with anemia is likely to experience which cluster of clinical manifestations?

<p>Fatigue, dizziness, and shortness of breath. (A)</p> Signup and view all the answers

Which intervention is the highest priority for a patient experiencing a sickle cell crisis?

<p>Providing oxygen therapy and monitoring oxygen saturation. (D)</p> Signup and view all the answers

Which factor is most likely to precipitate a sickle cell crisis in a patient with sickle cell disease?

<p>High-altitude environments. (B)</p> Signup and view all the answers

Pernicious anemia is characterized by a deficiency in vitamin B12 caused by a lack of intrinsic factor. What is the primary consequence of this deficiency on red blood cells?

<p>Production of abnormally large, dysfunctional red blood cells. (A)</p> Signup and view all the answers

How would the health care provider typically address pernicious anemia, considering its underlying cause?

<p>Treating with regular vitamin B12 replacement via injections or nasal spray. (B)</p> Signup and view all the answers

What clinical manifestations are most indicative of autoimmune idiopathic thrombocytopenic purpura (ITP)?

<p>Easy bruising, petechiae, and prolonged bleeding. (C)</p> Signup and view all the answers

During the administration of a blood transfusion, what is the nurse’s most critical responsibility to ensure patient safety?

<p>Monitoring the patient closely for signs of a transfusion reaction, especially during the first 15 minutes. (A)</p> Signup and view all the answers

A patient receiving a blood transfusion develops a fever and chills. What immediate action should the nurse take?

<p>Immediately stop the transfusion, notify the provider, and follow agency protocol. (B)</p> Signup and view all the answers

What distinguishes a hemolytic transfusion reaction from a febrile non-hemolytic transfusion reaction (FNHTR)?

<p>A hemolytic reaction involves the immune system attacking the transfused blood cells, leading to their destruction, and this is a medical emergency, while FNHTR is a reaction to WBCs and is typically less severe. (C)</p> Signup and view all the answers

Which hematologic change is a typical age-related change in older adults?

<p>Decreased hemoglobin levels due to age-related bone marrow changes. (B)</p> Signup and view all the answers

How does the aging process typically affect the immune system's function in older adults?

<p>Reduced cell function and increased inflammatory response. (B)</p> Signup and view all the answers

A patient with thrombocytosis is at risk for paradoxical bleeding. What statement accurately describes this phenomenon?

<p>The elevated platelet count interferes with platelet function, causing both clotting and bleeding issues. (B)</p> Signup and view all the answers

Following a splenectomy, a patient presents with signs of splenosis. What does this complication involve?

<p>The re-growth of the spleen from remaining splenic tissue scattered throughout the body. (A)</p> Signup and view all the answers

A patient with autoimmune idiopathic thrombocytopenic purpura (ITP) is prescribed corticosteroids. What is the primary goal of this treatment?

<p>To suppress the immune system's destruction of platelets. (B)</p> Signup and view all the answers

Which aspect of sickle cell disease directly alters the red blood cells’ ability to carry oxygen efficiently?

<p>The rigid, crescent shape of red blood cells impairs their flexibility and oxygen-carrying capacity. (A)</p> Signup and view all the answers

In managing a patient with sickle cell crisis, why is hydration a crucial intervention?

<p>Hydration improves blood flow and reduces sickling by decreasing blood viscosity. (A)</p> Signup and view all the answers

How does Warfarin affect the body's coagulation process to achieve its therapeutic effect.

<p>Inhibiting the synthesis of vitamin K-dependent clotting factors, thereby prolonging clotting time. (B)</p> Signup and view all the answers

A patient on warfarin therapy reports consuming large amounts of green tea daily. How does this affect their INR levels and overall anticoagulation therapy?

<p>Green tea will significantly lower the INR, increasing the risk of blood clots due to its high vitamin K content. (A)</p> Signup and view all the answers

Which statement accurately describes the implications for a patient with a change in CBC following a splenectomy?

<p>An elevated platelet count suggests an increased risk of thromboembolic events. (A)</p> Signup and view all the answers

What is the most accurate description of the purpose and process of a bone marrow biopsy?

<p>It involves extracting a sample of bone marrow fluid and cells via needle aspiration to diagnose blood disorders and assess cancer metastasis. (D)</p> Signup and view all the answers

A patient is diagnosed with polycythemia. What is the underlying mechanism contributing to the development of this condition?

<p>A genetic mutation or myeloproliferative disorder causing excessive red blood cell production. (B)</p> Signup and view all the answers

What is the function of the spleen regarding red blood cells?

<p>Filtering and maintaining red blood cells, and storing platelets. (B)</p> Signup and view all the answers

A patient receiving a blood transfusion reports back pain and has hematuria. Which transfusion reaction is most likely occurring, and what is the immediate nursing intervention?

<p>Hemolytic transfusion reaction; stop the transfusion immediately, notify the provider, and follow agency protocol. (A)</p> Signup and view all the answers

A patient with polycythemia vera would likely have which of the following?

<p>Genetic mutation in bone marrow (JAK2) (D)</p> Signup and view all the answers

Flashcards

Polycythemia

Condition with excess RBCs, thickening the blood, increasing risk of stroke and clotting.

Polycythemia Vera

Rare blood disorder from a genetic mutation (JAK2) causing excess RBC production.

Causes of Polycythemia

Genetic mutation, or myeloproliferative disorder (bone marrow produces too many RBCs).

Manifestations of Polycythemia Vera

Fatigue, headache, dizziness, tinnitus, HTN, thrombosis, pruritus after showers, ruddy complexion.

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Platelet Count

Normal range: 150,000-450,000. Below 150,000 indicates increased bleeding risk.

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Thrombocytopenia Risks & Treatment

Increased bleeding risk, spontaneous bleeding, risk during surgery/birth. Platelet transfusion, corticosteroids, splenectomy.

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Thrombocytosis Risks & Treatment

Increased clotting risk, DVT, stroke, PE, paradoxical bleeding. Treated with aspirin, cytoreductive therapy.

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Hematologic Changes in Older Adults

Decrease in blood volume, lower plasma protein, fewer RBCs, lower antibody levels and responses.

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Immune System Changes in Older Adults

Reduced cell function, increased inflammatory response, decreased adaptive immune response, increased autoimmune activity.

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Warfarin Therapy

Prevents DVT, atrial fibrillation, PE. Requires consistent Vitamin K intake to keep INR stable.

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Dietary Considerations with Warfarin

Vitamin K consistency. Avoid drastic changes in intake of dark leafy greens, green tea, liver, asparagus.

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Substances Increasing Bleeding Risk with Warfarin

Alcohol, cranberry juice, ginger, garlic, turmeric, fish oil can increase bleeding risk.

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Function of the Spleen

Produces lymphocytes/macrophages, filters/maintains RBCs, stores platelets. Removal increases infection/clot risk.

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Implications of Splenectomy

Increased risk of infection and blood clots (thrombosis and DVT).

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Bone Marrow Biopsy

Needle inserted into iliac crest to take bone marrow sample. Used to diagnose hematologic disorders, evaluate low blood counts, assess metastatic cancer

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Nurse's Role During Bone Marrow Biopsy

Patient Education, Informed consent, preparation, assist provider/support patient

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Post-Bone Marrow Biopsy Teaching

Pain management (avoid NSAIDs), activity restrictions, site care, watch for bleeding/infection.

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Anemia - Clinical Manifestations

Reduction in RBCs, hemoglobin, or hematocrit, leading to fatigue, weakness, paleness, dizziness, SOB, chest pain, cold extremities.

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Sickle Cell Disease

Genetic disorder causing abnormally shaped, rigid, crescent-shaped RBCs, altering oxygen carrying ability.

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Interventions for Sickle Cell Crisis

Oxygen therapy, pain management, antibiotics, hydration, emotional support.

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Causes of Sickle Cell Crisis

Alcohol, dehydration, pregnancy, infection or hypoxia.

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Pernicious Anemia

Vitamin B-12 deficiency due to lack of intrinsic factor, leading to large, dysfunctional RBCs.

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Treatment for Pernicious Anemia

Vitamin B12 replacement (IM injections, oral supplements, nasal spray).

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Autoimmune Idiopathic Purpura (ITP)

Low platelet count due to an autoimmune response causing easy bruising, petechiae, prolonged bleeding.

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Manifestations of ITP

Easy bruising, petechiae, prolonged bleeding, heavy menstrual bleeding, nosebleeds, gum bleeds.

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Implications of Administering Blood

Restoration of blood levels, treatment of disorders, while considering risks, ethical and religious implications.

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Nurse's Responsibility Administering Blood

Verify order, assess patient, confirm blood product/type/identity, prepare equipment, monitor vitals/complications, document.

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How to Administer Blood

Verify order, patient, and blood compatibility. Start slow, vitals q15min for the first 15-30 and monitor for reaction.

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Complications of Blood Transfusion

Allergic reaction, FNHTR, hemolytic transfusion reaction, TRALI, circulatory overload, iron overload, infection.

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Thrombocytopenia

Low platelet count increasing the risk of bleeding.

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Study Notes

  • Study notes for NUR 344 Exam 2, Spring 2025

Polycythemia

  • Characterized by thickened blood due to excess RBCs.
  • Increases the risk of stroke and clotting.
  • Can result from genetic mutations or myeloproliferative disorders, where the bone marrow produces too many RBCs.

Polycythemia Vera

  • A blood disorder resulting from a genetic mutation (JAK2) in the bone marrow.
  • Leads to excess RBC production
  • Manifestations include fatigue, headaches, dizziness, tinnitus, hypertension, thrombosis, pruritus after showers, and a ruddy complexion

Platelet Count

  • Normal platelet count ranges from 150,000 to 450,000.
  • Thrombocytopenia: Platelet count below 150,000. -Increases bleeding risk, including spontaneous/internal bleeding and risks during surgery or birth.
    • Treatment may include platelet transfusions, corticosteroids, or splenectomy.
  • Thrombocytosis: Platelet count above 450,000.
    • Increases clotting risk, potentially leading to DVT, stroke, or PE.
    • Can paradoxically cause bleeding.
    • Treatment may involve aspirin or cytoreductive therapy.

Older Adult Immune System Changes

Hematologic changes:

  • Decrease in blood volume and lower plasma protein levels.
  • Bone marrow ages, resulting in fewer RBCs and lower hemoglobin levels
  • Antibody levels and immune responses are lower and slower

Immune System:

  • Reduced cell function and increased inflammatory response
  • Decreased adaptive immune response and increased autoimmune activity

Warfarin Therapy

  • Warfarin is an anticoagulant used to prevent DVT, atrial fibrillation, and PE.
  • Main risk is bleeding.
  • Avoid NSAIDs while on Warfarin.
    • Dietary considerations include maintaining consistent Vitamin K intake to stabilize INR levels.
    • Foods high in Vitamin K: dark leafy greens, green tea, liver, and asparagus.
    • Alcohol, cranberry juice, ginger, garlic, turmeric and fish oil can increase bleeding risk.

Spleen Function

  • Produces lymphocytes and macrophages.
  • Filters and maintains RBCs.
  • Stores platelets and blood.
  • Splenectomy implications:
    • Increased risk of infection and blood clots (thrombosis and DVT).
    • Potential changes in CBC.
    • Risk of splenosis (rupture of the spleen before removal).

Bone Marrow Biopsy

  • Involves inserting a needle into the iliac crest to collect a bone marrow sample used to diagnose hematologic disorders, evaluate low blood counts, and assess metastatic cancer.
  • Nurse's role:
    • Patient education and preparation.
    • Obtaining informed consent.
    • Assisting the provider and supporting the patient.
  • Post-biopsy teaching:
    • Pain management (avoid NSAIDs).
    • Activity restrictions and site care.
    • Monitoring for complications (bleeding, infection, pain) and arranging follow-up.

Anemia

  • Defined as a reduction in the number of RBCs, hemoglobin, or hematocrit
  • Clinical manifestations include fatigue, weakness, paleness, dizziness, SOB, chest pain, cold extremities, tachycardia, hypotension, heart murmurs, angina, dyspnea, increased RR, confusion, vertigo, tinnitus, and restless leg syndrome.

Sickle Cell Disease

  • Genetic blood disorder causing abnormally shaped, rigid RBCs.
  • Alters oxygen-carrying capacity.
  • Interventions for sickle cell crisis include oxygen therapy and monitoring, pain management (opioids, NSAIDs, PCAs), antibiotics (for infection), hydration (IV fluids), and emotional support.
  • Sickle cell crisis can be precipitated by alcohol, dehydration, pregnancy, infection, and hypoxia.

Pernicious Anemia

  • Vitamin B-12 deficiency due to lack of intrinsic factor.
  • Leads to larger, dysfunctional RBCs.
  • Treatment includes Vitamin B12 replacement via IM injections, oral supplements, or nasal spray, along with addressing the underlying autoimmune conditions.

Autoimmune idiopathic purpura (ITP)

  • Characterized by a low platelet count due to an autoimmune response.
  • Manifestations include easy bruising (purpura and ecchymosis), petechiae, prolonged bleeding, heavy menstrual bleeding (menorrhagia), nosebleeds (epistaxis), gum bleeds, and internal bleeding.

Administering Blood

  • Implications include restoration of blood levels and treatment of disorders, with considerations for risks/complications, ethical issues, religion, and informed consent.
    • Nurse responsibilities include verifying the order, assessing the patient, confirming blood product, type, and patient identity, preparing equipment and infusion rate, monitoring vitals, watching for complications, and documenting the procedure
  • Administration process includes verifying the order, patient, and blood compatibility, equipment preparation, connecting the blood and starting the transfusion slowly for the first 15 minutes with frequent vital sign checks.
    • Monitor for reactions and adjust transfusion rate.
  • Complications include:
    • Allergic reaction and Febrile Non-Hemolytic Transfusion Reaction (FNHTR).
      • FNHTR is caused by the body's reaction to WBCs in transfused blood.
      • Can be managed with acetaminophen.
    • Hemolytic Transfusion Reaction:
      • Immune system attacks the transfused blood.
      • Medical emergency.
    • Transfusion-related acute lung injury, circulatory overload, iron overload, infection, and thrombocytopenia.

Thrombocytopenia

  • Low platelet count

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Description

Study notes covering polycythemia, a condition with thickened blood due to excess RBCs and its risk factors. Also covers platelet counts, thrombocytopenia (low platelet count) and thrombocytosis (high platelet count) and their associated risks.

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