WBC

WHITE BLOOD CELL DISORDERS

OBJECTIVES

  • The student will:
      - Understand and discuss the pathophysiology and causes of common white blood cell (WBC) disorders.
      - Understand and discuss diagnostics used to identify WBC disorders.
      - Understand treatment and nursing care of selected WBC disorders.

WHITE BLOOD CELLS (WBC) FUNCTIONS

  • Neutrophils:
      - Kill bacteria, fungi, and foreign debris.
  • Monocytes:
      - Clean up damaged cells.
  • Eosinophils:
      - Kill parasites, cancer cells, and are involved in allergic response.
  • Lymphocytes:
      - Help fight viruses and make antibodies.
  • Basophils:
      - Involved in allergic response.

CHEMOTHERAPY

  • Definition:
      - Use of chemicals to kill rapidly growing abnormal or cancerous cells in the body.
  • Types:
      - Many different types of chemotherapy exist.
  • Duration:
      - Each course typically takes 3-6 months.
      - Can be administered intravenously (IV) or orally (PO).
  • Outcomes:
      - Can be a cure for some cancers.

GOALS OF CHEMOTHERAPY

  • Primary Goal:
      - Destroy cancer cells.
  • Risk:
      - Greatest risk for infection occurs 7-10 days after starting (Nadir period).
  • Phases of Chemotherapy:
      - Induction:
        - Goal: Destroy remaining cancer cells.
        - Lasts several months.
      - Post-induction:
        - Goal: Maintain remission.
      - Maintenance:
        - Focus on avoiding disease resurgence.

EFFECTS OF CHEMOTHERAPY ON THE BODY

  • Side effects may include:
      - Pain
      - Trouble breathing
      - Hair loss
      - Mouth sores
      - Weakened immune system
      - Nausea
      - Vomiting
      - Constipation
      - Diarrhea
      - Bruising
      - Bleeding
      - Neuropathy
      - Rashes

NURSING CARE FOR PATIENTS UNDERGOING CHEMOTHERAPY

  • Nutritional support:
      - Dietary consult for appropriate nutrition.
  • Medications:
      - Megestrol and dronabinol for appetite stimulation.
      - Use of Ulcerease (mouth rinse) for mouth sores.
      - Ondansetron for nausea/vomiting.
  • Monitor for infection:
      - Infection is a leading cause of death in cancer patients.
      - Common sites of infection include lungs, gastrointestinal (GU) system, mouth, rectal area, peritoneal cavity, and blood (septicemia).
      - Advise patients at risk for neutropenia to contact healthcare provider (HCP) if temperature exceeds 100.4°F (38°C).
  • Use of Filgrastim:
      - A bone marrow stimulant to boost WBC production.

NEUTROPENIA

  • Definition:
      - Absolute Neutrophil Count (ANC) less than 1000 cells/mm³ (or 1 × 10⁹/L).
  • Clinical Manifestations:
      - Fever (may be low grade).
      - Sore throat and oral lesions.
      - Diarrhea.
      - Non-productive cough.
  • Diagnostics:
      - WBC with differential.
      - Leukopenia: normal count is 4,000.
      - ANC classifications:
        - Mild to moderate: 1000-500 cells/mm³.
        - Severe: less than 500 cells/mm³.

TREATMENT AND NURSING CARE FOR NEUTROPENIA

  • Infection risk monitoring:
      - Symptoms to watch for:
        - Fever >100.4°F.
        - Oral lesions, sore throat, etc.
  • Laboratory Tests:
      - Monitor ANC levels.
  • Treatment:
      - Blood cultures to detect infections if fever presents.
      - Start antibiotic therapy within 1 hour if infection is suspected.
      - Use of Filgrastim as a treatment option.

NEUTROPENIC PRECAUTIONS

  • Visitor Policy:
      - Visitors must announce themselves to the nurse before entering the room.
  • Handwashing Requirements:
      - Strict hand hygiene before patient care.
  • Room Maintenance:
      - Private room with a closed door.
      - No fresh fruits, vegetables, or flowers allowed.
      - No visitors or staff with infectious illnesses.
  • Articles Leaving Room:
      - No special precautions for items leaving the room.
      - No sick visitors or personnel allowed.

LEARNING CHECK EXAMPLE

  • The following situation requires nursing intervention:
      - C. The client’s grandson who is being treated for strep throat visits.

LEUKEMIA

  • Definition:
      - A group of malignant disorders characterized by abnormal leukocyte production.
  • Epidemiology:
      - 2019 estimates indicated 61,780 new cases with 22,840 deaths.
  • Risk Factors:
      - Genetics
      - Environmental exposures
      - Previous chemotherapy treatment
      - Viral infections

LEUKEMIA CLASSIFICATION

  • Acute Leukemia:
      - Abrupt onset and rapid progression.
      - Types:
        - Acute myeloid leukemia (AML):
          - Comprises 80% of acute leukemias in adults.
        - Acute lymphocytic leukemia (ALL):
          - Most common type of leukemia in children.
  • Chronic Leukemia:
      - Gradual onset and persistent progression.
      - Types:
        - Chronic myelogenous leukemia (CML).
        - Chronic lymphocytic leukemia (CLL):
          - Most common leukemia in adults.
      - Note: Memorization of details is not necessary.

LEUKEMIA DIAGNOSTICS

  • Diagnostics:
      - Complete blood count (CBC) with differential.
      - Peripheral blood smear.
      - Bone marrow biopsy.
      - Lumbar puncture for staging classification.

LYMPHOMA

  • General Overview:
      - Incudes Hodgkin and Non-Hodgkin lymphoma.
      - Involves lymphatic system components including lymphatics, lymph nodes, thymus gland, bone marrow, and spleen.

HODGKIN LYMPHOMA

  • Characteristics:
      - Genetic, environmental, and Epstein-Barr virus contributions.
      - Lymph node malignancy characterized by the presence of Reed Sternberg Cells.
  • Demographics:
      - More common in age groups 15-30 years and after 55.
  • Clinical Manifestations:
      - Cervical lymph node enlargement.
      - Weight loss and fatigue.
      - Symptoms like fever, cough, and dysphagia.
      - B symptoms (drenching night sweats; weight loss >10% in 6 months; fever >100.4° F).
      - Pain at the disease site after consuming small amounts of alcohol (requires medical attention).

NON-HODGKIN LYMPHOMA

  • Characteristics:
      - Begins in lymphocytes without the presence of Reed Sternberg cells.
  • Incidence:
      - Most common blood cancer.
      - Linked to previous infections, notably H. pylori.

CLINICAL MANIFESTATIONS OF NON-HODGKIN LYMPHOMA

  • Painless lymph node enlargement.
  • Non-specific symptoms may include hepatomegaly, airway obstruction, and gastrointestinal symptoms.
  • Involvement in various areas of the body: tonsils, neck, thymus area, armpit, diaphragm, spleen, abdominal, pelvic, and groin areas.

NON-HODGKIN LYMPHOMA DIAGNOSTICS

  • Diagnostics:
      - Lymph node biopsy for confirmation.
      - Nursing considerations include infection and bleeding risks.
      - PET scan for staging purposes.

STAGING OF LYMPHOMA

  • Stages:
      - I: Above diaphragm
      - II: Below diaphragm
      - III: Involvement on both sides of the diaphragm
      - IV: Disseminated disease.

TREATMENT OF LYMPHOMA

  • Stage I and II:
      - External beam radiation.
  • Later stages:
      - Chemotherapy with additional treatments based on disease severity.

NURSING CARE FOR LYMPHOMA PATIENTS

  • Pain management:
      - Use NSAIDs, opioids, and corticosteroids as necessary.
  • Infection monitoring and management:
      - Careful assessment due to compromised immune systems.
  • Risk of bleeding:
      - Regular monitoring of blood counts and bleeding signs.
  • Psychosocial support needed:
      - Essential due to increased vulnerability during treatment.

MULTIPLE MYELOMA

  • Definition:
      - A malignancy of the plasma B cells.
  • Etiology:
      - Genetic predispositions, toxins, and viral exposure.
  • Demographics:
      - Men are affected more than women.
  • Survival Rate:
      - 5-year survival rate is approximately 45%.
      - Viral infections, such as HIV, may elevate the risk of developing multiple myeloma.

CLINICAL MANIFESTATIONS OF MULTIPLE MYELOMA

  • Disease often develops slowly with insidious onset; symptoms may not appear until advanced.
  • Notable symptoms include:
      - Bone pain and fractures.
      - Fatigue, weakness, and numbness.
      - Kidney dysfunction.
      - Hypercalcemia and hyperuricemia.
      - Increased risk of bleeding and infections due to poor bone marrow function.

DIAGNOSTICS AND TREATMENT OF MULTIPLE MYELOMA

  • Diagnostics:
      - CBC showing pancytopenia.
      - CMP with increased calcium and high serum creatinine.
      - Urinalysis demonstrating the presence of Bence Jones Protein.
      - Bone marrow biopsy confirms diagnosis.
  • Treatment options:
      - Chemotherapy and corticosteroids.
      - Multiple myeloma is seldom cured, but treatment can relieve symptoms and prolong survival.
      - Goals of management include pain control and preventing fractures.

NURSING CARE FOR MULTIPLE MYELOMA PATIENTS

  • Monitoring:
      - Infection risk and bleeding risk management.
      - Administration of IV fluids to maintain urine output at 1.5 to 2 L/day.
      - Use of IV furosemide for kidney protection.
      - Bisphosphonates (e.g., alendronate) may be useful.
  • Ambulation:
      - Encourage weight-bearing activities to help bones resorb calcium, preventing hypercalcemia.
  • Patient Safety:
      - High risk for falls due to potential pathologic fractures.