Chapter 19-Immune disorders
Chapter 19: Nursing Care of Patients With Immune Disorders
Overview of Immune Disorders
Categories of Immune Disorders
Hypersensitivity Reactions
Autoimmune Disorders
Immune Deficiencies
Hypersensitivity Reactions
Definition: Injury to the body due to an exaggerated immune response.
Classification: By the method of tissue injury.
Type 1: Immediate hypersensitivity
Type 2: Cytotoxic hypersensitivity
Type 3: Immune complex-mediated hypersensitivity
Type 4: Delayed-type hypersensitivity
Type 1 Hypersensitivity Reaction
Mechanism: Involves immunoglobulin E (IgE) antibodies against soluble antigens, leading to mast cell degranulation.
Histamine Release: Occurs immediately; can range from mild to life-threatening.
Examples:
Food Intolerances
Common Conditions
Allergic Rhinitis
Symptoms: Sneezing, nasal itching, runny nose, itchy red eyes.
Atopic Dermatitis (Eczema)
Symptoms: Inflammation of skin leading to pruritus (itching), edema, dry skin, blisters.
Atopic Dermatitis Management
Care:
Ensure administration of prescribed antipruritics (medications to reduce itching).
Offer lukewarm soaks followed by emollient topical cream.
Rationale: Antipruritics help to reduce the itch-scratch cycle, while emollients alleviate dryness contributing to itching.
Anaphylaxis
Definition: Severe systemic type 1 reaction; widespread histamine release leading to:
Bronchial narrowing (stridor, wheezing, potential respiratory arrest)
Hypotension, tachycardia, risk of cardiac arrest
Anaphylaxis Treatment
Immediate Treatments:
Oxygen
Epinephrine
Antihistamines
Corticosteroids
Vasopressors
Mechanical Ventilation (if necessary)
Nursing Care:
Early recognition and maintenance of airway
Provide emotional support and education to patient
Urticaria (Hives)
Mechanism: Histamine release causes pruritic, raised, erythematous wheals on skin.
Therapeutic Interventions:
Epinephrine
Antihistamines
Corticosteroids
Histamine H2 Blockers
Angioedema
Definition: Swelling in submucosal/subcutaneous tissue due to increased vascular permeability.
Causes: Allergic reactions, ACE inhibitors, idiopathic causes, hereditary and acquired forms.
Symptoms: Painless, nonpruritic swelling that can be an emergency if it involves the airway.
Nursing Care for Type 1 Hypersensitivity Disorders
Monitoring:
Respiratory status and level of consciousness.
Stay with patient and provide information on their condition.
Document skin and lesions.
Education:
Importance of avoiding scratching; recommend applying pressure or rubbing rather than scratching.
Discuss need for medical alert identification and methods to avoid allergens.
Type 2 Hypersensitivity Reaction
Definition: Destruction of a substance containing an antigen.
Clinical Relevance: Beneficial in fighting pathogens but detrimental if incompatible red blood cells (RBCs) are detected as foreign.
Blood Typing:
Types: A, B, AB, O; Rh−, Rh+
O: Universal donor
AB: Universal recipient
Hemolytic Transfusion Reaction
Mechanism: When RBCs with foreign antigens are lysed rapidly, occluding blood vessels and causing ischemia and necrosis.
Risk: Life-threatening; prevention is critical.
Prevention Strategies:
Administer RhoGAM to Rh(D) negative patients exposed to Rh+ blood.
Careful administration of blood transfusions.
Nursing Care for Hemolytic Transfusion Reaction
Monitoring:
Monitor transfusion closely; if reaction symptoms occur, stop blood immediately.
Infuse normal saline with new tubing and follow agency reaction policy.
Return any unused blood and tubing to the blood bank.
Education:
Inform the patient about recognition of transfusion reactions.
Type 3 Hypersensitivity Reaction
Definition: Result from initial sensitization to an antigen, with reactions upon later exposures.
Manifestations:
Red edematous lesions, bleeding, and necrosis due to immune complexes formed by antigens and antibodies.
These complexes can lead to injuries within blood vessels when enzymes damage their walls.
Serum Sickness
Description: A rare type III hypersensitivity reaction where antigen-antibody complexes develop from exposure to nonhuman proteins (e.g., anti-venoms, rabies vaccines).
Onset Symptoms: Typically appear 7 to 21 days after exposure; brief and self-limiting if antigen exposure ceases.
Prognosis: Generally good.
Treatment: Based on symptoms and may include:
Antipyretics
Analgesics
Anti-inflammatories
Antihistamines
Corticosteroids
Group Activity
Objective: Compare and contrast the differential diagnosis of Serum Sickness vs Immediate Allergic Reaction considering
Type of Hypersensitivity
Causes
Symptoms
Pathophysiology
Treatments
Type 4 Hypersensitivity Reaction
Characteristics: Known as delayed-type hypersensitivity.
Example:
Contact Dermatitis: Occurs when chemicals contact the skin, leading T cells to secrete chemicals upon second exposure.
Common Triggers: Poison ivy, poison oak, and latex.
Symptoms: Reddened, pruritic areas with fragile vesicles.
Contact Dermatitis Management
Therapeutic Interventions:
Use antihistamines, topical drying agents, corticosteroids, topical immunomodulators for itching.
Consider tepid baths with baking soda or Aveeno, and wash skin with appropriate soap (Fels-Naptha).
Implement latex allergy protocols.
Autoimmune Disorders
Definition: Conditions in which the immune system fails to adequately recognize the body’s own cells, mistakenly targeting them as foreign and destroying them.
Pernicious Anemia
Mechanism: Antibodies against gastric parietal cells hinder the production of intrinsic factor, causing a vitamin B12 deficiency.
Consequences:
Red blood cells (RBCs) become deformed, leading to decreased production.
Symptoms: Weakness, anorexia, glossitis, pallor, and peripheral neuropathy.
Diagnostic Tests
Schilling Test: Used to evaluate vitamin B12 absorption.
Therapeutic Interventions:
Corticosteroids
Lifelong vitamin B12 supplementation
Nursing Care:
Education about vitamin B12 needs and care considerations due to fatigue.
Systemic Lupus Erythematosus (SLE)
Definition: An autoimmune disorder where the immune system attacks its own tissues and organs.
Subtypes:
Discoid Lupus Erythematosus (DLE): Primarily skin lesions.
Drug-Induced Systemic Lupus Erythematosus (DILE): Occurs after certain medications.
Presentation:
Chronic, inflammatory multisystem disorder characterized by various symptoms.
Population at Risk
Common Demographics: Young women, individuals with first-degree relatives with lupus, and higher prevalence in Black, Asian, Hispanic, and American Indian populations.
Signs and Symptoms of SLE
Vague Early Symptoms: Fatigue, fever.
Dermatological:
Butterfly rash, bruising, photosensitivity, alopecia, pain, pruritis.
Musculoskeletal:
Arthralgia (joint pain), arthritis.
Hematological:
Anemia, leukocytopenia, thrombocytopenia.
Cardiopulmonary:
Pericarditis, myocarditis, myocardial infarction, vasculitis, pleurisy, valvular disease.
Therapeutic Interventions for SLE
Management Strategies:
NSAIDs for pain and inflammation
Immunosuppressants
Corticosteroids for controlling flares
Antimalarial medications
Immunoglobulin therapy as needed.