SLE and Rheumatoid Arthritis

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Questions and Answers

In a patient with Systemic Lupus Erythematosus (SLE), what clinical manifestation should prompt immediate notification to the healthcare provider due to potential cardiopulmonary complications?

  • Exacerbation of the malar rash after sun exposure.
  • Increased joint pain and stiffness in the extremities.
  • Reports of fatigue and generalized weakness.
  • Complaints of chest pain that worsens with breathing or movement. (correct)

A client with Rheumatoid Arthritis (RA) is prescribed corticosteroids to manage inflammation. Which focused assessment is most critical for the nurse to perform regularly?

  • Evaluating for signs of gastrointestinal bleeding.
  • Monitoring glucose levels for hyperglycemia. (correct)
  • Assessing for changes in range of motion and joint flexibility.
  • Monitoring for signs of skin breakdown and delayed wound healing.

Which diagnostic finding is most indicative of Hodgkin's Lymphoma when evaluating a patient with persistent lymphadenopathy?

  • Increased percentage of blast cells in bone marrow aspirate.
  • Presence of Reed-Sternberg cells on lymph node biopsy. (correct)
  • Detection of Bence-Jones protein in urine sample.
  • Elevated levels of Epstein-Barr virus antibodies in serum.

A patient with Multiple Myeloma is at risk for developing spinal cord compression. Which symptom should the nurse prioritize when assessing for this complication?

<p>Sudden onset of lower extremity weakness or paralysis. (C)</p> Signup and view all the answers

A patient diagnosed with Acute Myeloid Leukemia (AML) is undergoing induction chemotherapy. Which lab value would be most concerning during this phase of treatment?

<p>White blood cell count of 1,500/µL. (D)</p> Signup and view all the answers

What is the primary mechanism by which HIV compromises the immune system?

<p>Infection and destruction of CD4+ lymphocytes, leading to immunosuppression. (C)</p> Signup and view all the answers

A patient with advanced HIV is diagnosed with Pneumocystis jirovecii Pneumonia (PCP). What clinical finding is most indicative of this infection?

<p>Profound hypoxemia unresponsive to oxygen therapy. (B)</p> Signup and view all the answers

In a patient with Scleroderma, which of the following clinical manifestations is associated with increased pulmonary hypertension risk?

<p>Raynaud's phenomenon affecting the fingers and toes. (B)</p> Signup and view all the answers

Following a bone marrow transplant a patient with Acute Lymphoblastic Leukemia (ALL) has the following lab results: platelets 90,000 and WBC 3,000. What is the priority nursing intervention?

<p>Implement strict isolation protocols to prevent infection. (D)</p> Signup and view all the answers

For a patient receiving chemotherapy, what is the most critical aspect of central venous access device (CVAD) management to prevent complications?

<p>Monitoring for signs of infection at the insertion site and maintaining strict sterile technique. (A)</p> Signup and view all the answers

A client with a history of anaphylaxis after a bee sting is prescribed an epinephrine auto-injector. What education component of the medication teaching is most critical?

<p>Explaining that the medication can be injected through clothing if necessary. (D)</p> Signup and view all the answers

A patient is diagnosed with Chronic Myeloid Leukemia (CML) and prescribed a tyrosine kinase inhibitor (TKI). What is the most important instruction for the nurse to emphasize regarding medication adherence?

<p>Educating on the need for consistent, uninterrupted daily administration to maintain disease control. (B)</p> Signup and view all the answers

A patient with Non-Hodgkin’s Lymphoma is beginning treatment. Which preventative measure is most important to teach to maintain skin integrity during treatment?

<p>Wearing loose-fitting cotton clothing and avoid harsh soaps or lotions. (B)</p> Signup and view all the answers

A patient with Systemic Lupus Erythematosus (SLE) tests positive for the ANA and LE Cell Test. What is the significance of these findings related to the pathophysiology of SLE?

<p>Indicates a decreased tolerance to self due to an abnormal immune and phagocytic system. (D)</p> Signup and view all the answers

After completing chemotherapy for Acute Lymphoblastic Leukemia (ALL), a pediatric client is encouraged to slowly gain weight. Which rationale explains the importance of this recommendation?

<p>Slow weight gain prevents refeeding syndrome and supports metabolic balance. (D)</p> Signup and view all the answers

A client is undergoing a Mantoux skin test for tuberculosis (TB) screening. What type of hypersensitivity reaction is involved in a positive Mantoux test?

<p>Type IV hypersensitivity, a cell-mediated delayed reaction. (A)</p> Signup and view all the answers

Which of the following is an important teaching point the nurse must include when providing discharge instruction for a patient with scleroderma?

<p>All of the above (E)</p> Signup and view all the answers

A phlebotomist is stuck by a needle while collecting blood from a patient who is HIV positive. What is the most important initial action for the phlebotomist to take?

<p>Report the incident to occupational health and initiate post-exposure prophylaxis (PEP) as soon as possible. (A)</p> Signup and view all the answers

A patient with a diagnosis of Metastatic cancer has a potassium level of 2.9. Which assessment finding is most concerning?

<p>Cardiac dysrhythmias and ECG changes. (C)</p> Signup and view all the answers

A patient with a history of Rheumatoid Arthritis (RA) is at risk of developing symmetrical polyarthritis. What clinical manifestation in the patient's hands would warrant provider notification?

<p>Symmetric swelling, tenderness, and warmth in multiple joints of the hands. (B)</p> Signup and view all the answers

Flashcards

Systemic Lupus Erythematosus (SLE)

Auto-antibody production, more common in women, caused by an abnormal immune and phagocytic system that decreases tolerance to self.

Rheumatoid Arthritis

Autoimmune, inflammatory response causing immune cells to aggregate in small joints, leading to bone deformities.

Scleroderma

Collagenous tissue deposits in connective tissues, triggered by genetics and infection, affecting skin and internal organs.

Hypersensitivity 1: Anaphylaxis

IgE-mediated reaction causing vasodilation, bronchoconstriction, and potentially life-threatening symptoms.

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Hypersensitivity 2

Tissue-specific reactions mediated by IgG or IgM antibodies, such as mismatched blood transfusions or drug reactions.

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Hypersensitivity 3

Antigen-antibody immune complex deposition, leading to inflammation and tissue damage (e.g., post-strep glomerulonephritis).

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Hypersensitivity 4

T-cell mediated delayed reaction, such as contact dermatitis from poison ivy or a positive TB skin test.

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Pneumocystitis jirovecii Pneumonia

Fungal infection in the lungs often seen in immunocompromised individuals, leading to hypoxemia.

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Human Immunodeficiency Virus (HIV)

RNA retrovirus infecting CD4 lymphocytes and macrophages, requiring reverse transcriptase, integrase, and protease for replication.

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Chronic Myeloid Leukemia (CML)

Gradual onset, with fatigue, weight loss, bleeding, and a poor prognosis due to chemo resistance; characterized by high granulocyte count.

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Acute Myeloid Leukemia (AML)

Acute onset characterized by chromosomal abnormalities that cause blast cell proliferation; responds well to treatment.

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Multiple Myeloma

Plasma cell disorder where antibodies destroy healthy cells, leading to bone lesions and hypercalcemia.

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Acute Lymphoblastic Leukemia (ALL)

Childhood cancer with malignant transformation of B (lymphoblast) cells, leading to fever, infection, and anorexia; high remission rates.

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Hodgkin’s Lymphoma

Starts in lymph nodes and spreads; biopsy shows Reed-Sternberg cells; systemic symptoms include fever, sweating, and weight loss.

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Non-Hodgkin’s Lymphoma

Lymphoid neoplasm that starts in lymph nodes; manifestations include lymphadenopathy, fever, sweating, and weight loss/anorexia.

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Metastatic Cancer

Cancer spread related to circulatory flow, requiring cell survival; grading and staging are essential to determine the extent.

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Chemotherapy

Monitor WBC daily to detect complications from chemotherapy, administered via central venous access, to shrink and destroy cells.

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Normal WBC

The normal range for White blood cell count.

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Normal PLT

The normal range for Platelets.

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Prothrombin Time

Essential to check before surgery for coagulation.

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Study Notes

  • The notes below provide key information about various diseases and disorders, along with their clinical manifestations, diagnostic methods, and treatments.

Systemic Lupus Erythematosus (SLE)

  • Auto-antibody production occurs primarily in women with SLE.
  • An abnormal immune and phagocytic system leads to decreased tolerance to self.
  • Glomerulonephritis, indicating kidney involvement, signals systemic SLE.
  • Malar rash and cardiac/respiratory inflammation are clinical signs.
  • Diagnosis involves ANA and LE Cell Tests.
  • Advise patients to seek medical attention for chest pain with breathing/movement.
  • Education includes wearing sunscreen to prevent malar rash exacerbation.

Rheumatoid Arthritis

  • An autoimmune, inflammatory response causes immune cells to accumulate in small joints.
  • Bilateral-symmetrical polyarthritis, bone deformities, and fatigue are clinical manifestations.
  • Diagnosis is confirmed through labs and X-rays.
  • Educate patients about medications, encourage activity with rest, and adaptive equipment use.
  • Monitor glucose levels due to potential corticosteroid treatments.

Scleroderma

  • Collagenous tissue deposits occur in the body's connective tissues due to genetic factors and infection.
  • The condition can affect the skin or present systemically with internal organ involvement.
  • CREST (calcinosis, Raynaud's, esophageal dysfunction, sclerodactyly, telangiectasias) and vascular lesions on the lips are clinical signs.

Hypersensitivity Reactions

  • Type 1: Anaphylaxis
  • Type 2: Tissue-specific IgG/IgM (blood transfusions, medication transfusions)
  • Type 3: Antigen-antibody immune complex (strep leading to glomerulonephritis)
  • Type 4: Contact reaction
  • A positive Mantoux skin test for TB indicates a hypersensitivity reaction.

Pneumocystitis jirovecii Pneumonia

  • It is a fungal infection in the lungs, often seen in those with weakened immune systems (HIV/cancer).
  • Hypoxemia is a key clinical manifestation.

Human Immunodeficiency Virus (HIV)

  • Caused by a viral infection affecting CD4, lymphocytes, and macrophages.
  • As an RNA retrovirus, HIV converts to DNA to replicate and infect cells.
  • Transcriptase, integrase, and protease are essential for viral replication.
  • The primary replication site is the GI tract.
  • Risk factors include being a healthcare worker, unprotected sex, STIs, and being born to an infected mother (intrauterine, delivery, or breastfeeding).
  • Initially asymptomatic; females may experience vaginal itching with discharge.
  • Advanced HIV/AIDS symptoms include difficulty swallowing, SOB, productive cough, weight loss, chest pain, night sweats, and low CD4 count.
  • This can cause wasting syndrome, so monitor electrolytes.
  • Immunosuppressed patients: advise rest before meals, avoid cleaning litterboxes, thoroughly clean and cook raw foods, disinfect surfaces, and monitor temperatures.

Chronic Myeloid Leukemia (CML)

  • Gradual onset typically occurs between ages 40-50, with a poor prognosis due to chemo response.
  • Clinical signs: fatigue, weight loss, bleeding, discomfort, sweating, and high granulocyte count.
  • Diagnosis: bone marrow aspiration and CBC with differential.
  • Treatment: Tyrosine kinase inhibitor (PO), with emphasis on medication adherence.

Acute Myeloid Leukemia (AML)

  • Acute onset with a median age of 64.
  • Chromosomal problems lead to blast cell proliferation/mutation.
  • AML presents in myriad ways due to assorted chromosomal translocations or inversions.
  • Responds well to treatment.
  • Clinical signs: splenomegaly, bone pain, anemia, and thrombocytopenia.
  • Diagnosis: bone marrow aspiration, CBC, blood smear.
  • Treatment: Aggressive chemotherapy, starting with induction therapy.

Multiple Myeloma

  • Plasma cell disorder in antibody-secreting B lymphocytes.
  • Antibodies destroy healthy cells.
  • Clinical signs: bone lesions/issues and hypercalcemia.
  • Complications: spinal fracture and risk for spinal cord compression.
  • Diagnostic testing: Bone marrow biopsy and urinalysis for Bence-Jones protein.
  • Treatments: steroids, chemo, stem cell transplant, radiation.
  • Recommendations: increased daily water intake and maintain high UOP.

Acute Lymphoblastic Leukemia

  • Childhood cancer with malignant transformation of B (lymphoblast) cells.
  • Clinical presentation: Abrupt onset of symptoms (fever, infection, anorexia), severe headache, vomiting, and increased immature WBC count.
  • Diagnostic methods: bone marrow aspiration, CBC, and blood smear.
  • Treatment: Chemo and steroids.
  • High remission rates are typical.
  • Expected normal labs post-treatment: platelet 150,000-400,000 and WBC 5,000-10,000.
  • Encourage slow weight gain (1lb a week)

Hodgkin’s Lymphoma

  • It is a lymphoid neoplasm starting in lymph nodes, spreading to tissues/organs.
  • Clinical signs: Lymphadenopathy (cervical, supraclavicular, mediastinal, i.e., neck, shoulder, chest); B symptoms (fever, sweating, weight loss); pruritus; jaundice; herpes zoster.
  • Diagnostic identification: Biopsy showing Reed-Sternberg Cells with normal platelets.
  • Treatment: Chemo, stem cell transplant, and radiation.
  • Education: avoid drying soaps/lotions, wear cotton clothing, use electric razor.

Non-Hodgkin’s Lymphoma

  • Clinical signs: lymphadenopathy (abd, chest, neck) with fever, sweating, weight loss/anorexia; potential spinal cord compression.
  • Diagnosis often occurs at a late stage due to its less aggressive nature.
  • Treatment includes chemo, antibiotics, antifungals, antivirals, and pain management.
  • Education: exercise x 30 min 5x a week.

Metastatic Cancer

  • Pattern related to circulatory flow.
  • Cell survival is not guaranteed after entering circulation.
  • All tumors should undergo grading/staging.
  • Monitor WBC daily during chemotherapy; a critical drop is a complication.
  • Chemotherapy shrinks/destroys all cells.
  • Administration routes: Orally, IV, or directly into spinal fluid via central venous access device.

Laboratory Values

  • WBC: 5,000-10,000
  • PLT: 150,000-400,000
  • Prothrombin Time: 11-12.5 seconds
  • HCT: Male 42-52%, Female 37-47%
  • BUN: 10-20 mg/dL
  • Potassium: 3.5-5 mEq/L
  • Sodium: 135-145 mEq/L

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