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Review of immunology from H&P in 6th ed chapt 19 are self study: Slides 1-17 Identify key material to review from Fundamentals and A&P
Self-tolerance Immunocompetent Antigens HLA Stem cell/figure19-3 Chart 19-1 Leukocytes/table 19-1 Absolute neutrophil count Left shift Vascular leak syndrome Sequence of inflammatory responses
Complement Agglutination Immunoglobulin Innate native immunity Natural active immunity Artificial active immunity Artificial passive immunity Natural passive immunity Hypersensitivity
THREE DIVISION OF IMMUNITY: FUNCTION INDEPENDENTLY AND INTERDEPENDENTLY TO PROVIDE COMPLETE IMMUNITY. 3
I.E.: tissue macrophages and granulocytes (neutrophils, basophils and eosinophils) Non Specific Response Initiated By Injury Or Invasion
Self study Question:
Cite two examples of an agent that can injure or invade.
Vasoconstriction followed by
increased capillary permeability to localize response phagocytosis assisted by complement activation to ingest debris release of chemical factors that enhance localization(vasoactive), attract factors that assist in inflammatory response (chemotaxis) and release of factors (cytokines) to stimulate production of granulocytes
Self study Question: How would you explain this event to a client in terms that they could understand?
Ignatavicius Figure 19-6 Steps of phagocytosis assisted by complement activation and fixation Complement coats the
antigen
Known as humoral immunity (B-lymphocytes action is predominant although assisted by Tlymphocytes) creates two types of cells : plasma cells and memory cells plasma cells secrete immunoglobulins in response to a specific antigen memory cells are dormant yet sensitized to the specific antigen in case of a repeated exposure
THE OLDER CLIENT HAS A REDUCED CAPACITY TO RESPOND, PRODUCE, AND SUSTAIN AN IMMUNE RESPONSE USING THIS MECHANISM
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AN ANTIGEN ENTERS THE BODY SENSITIZED B LYMPHOCYTES PRODUCE LARGE AMOUNTS OF ANTIBODIES IF REEXPOSED TO THE ANTIGEN MACROPHAGE AND T HELPER CELLS INTRODUCE ANTIGEN TO THE B LYMPHOCYTE
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Types of Immunity
Innate-native immunity
genetically predisposed; not an adaptive response
Active
natural: body responds to an antigen that is introduced naturally artificial: acquired immunity achieved through vaccines that have been attenuated to initiate exposure but not develop disease
Passive
natural:antibodies transferred to a fetus from mother artificial: injection of antibodies into a client
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Self Study Questions: What questions would you prepare to answer before administering a vaccine to identify what type of immunity the client will receive, and why? What additional questions would you ask if you had immune dysfunction, and why?
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Hypersensitivity reactions
allergy
Immunodeficiency
AIDS
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Beta agonists
Epinephrine 1:1000 aqueous solution
Epi-pen for SQ or IM injection
Histamine antagonists
Diphenhydramine (H1 antagonists) Ranitidine (H2 antagonists)
Alpha 1 agonists
Afrin (oxymetazoline)
IV corticosteroids
Solumedrol
Nursing Care of Clients Experiencing Hyperfunction of the Immune Response: Allergy and Autoimmunity
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Type 1: excess circulating IgE with mast ell release hay fever, atopic asthma and allergic rhinitis Type 2: IgG reacts with host cell as in Myasthenia gravis, autoimmune hemolytic anemia Type 3: immune complex formation causing damage as in SLE Type 4: delayed reaction from T lymphocytes as in poison ivy and PPD reaction Type 5: overreacting target cell caused by autoantibody stimulation (graves disease)
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Avoid offending antigen Apply OTC topical steroids Monitor for secondary infection No concern about progression to anaphylaxis since it is not a Type I reaction
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route can be inhaled, ingested, injected, contact (key point to remember every time a client has a new drug therapy initiated) life threatening form of Type I is called Anaphylaxis
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Incidence is increasing especially for individuals with frequent exposure may be mixed type I and Type IV
type IV are limited to cutaneous reactions
Health care workers Rubber industry workers Persons with spina bifida or urogenital abnormalities Persons who have undergone repeated or prolonged surgeries or mucous membrane exposure to latex devices, especially early in life Persons with an atopic history or history of food allergy (cross-reacting proteins, especially in banana, avocado, passion fruit, chestnut, kiwi fruit, melon, tomato, celery) Family history of allergy Source: Latex Allergy @ http://www.aafp.org/afp/980101ap/reddy.html
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Pathophysiology of TYPE I
First event can be local urticaria, pruritis, watery eyes, rhinitis Continuing events can lead to anaphylaxis with certain types of irritants, such as:
Latex, medications, peanut butter etc
More serious adverse event is call anaphylaxis
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Clinical Manifestations:
Sign and symptoms of allergic rhinitis, hay fever, allergic asthma, contact dermatitis, cutaneous rash (client-specific response)
Lab tests:
elevated eosinophils, IgE identification of specific allergens by RAST testing
Specialized tests:
skin testing food challenge
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antihistamines
inhibit vasodilation (Diphenhydramine)
leukotriene antagonists
block leukotriene receptor (Singulair)
desensitization therapy
allergy shots
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Nursing Care of Clients At risk for Experiencing Type I Latex allergy response
Nursing Care of Clients At risk for Experiencing Type I Latex allergy response (continued)
Assess for occupational exposure to latex Eliminate exposure to latex products Initiate health teaching
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Anaphylaxis
Life-threatening Type I hypersensitivity reaction Occurs rapidly, systemically Affects multiple organs
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Feelings of uneasiness, apprehension Weakness, impending doom Anxious and frightened Generalized pruritus/urticaria (hives) Angioedema
diffuse swelling of eyes, lips and tongue
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Bronchoconstriction Mucosal edema, excess mucus production Crackles, wheezing, diminished breath sounds Laryngeal edema, stridor, hypoxia, hypercapnia Hypotension, weak, rapid, irregular pulse Faintness, diaphoresis Loss of consciousness Dysrhythmias, shock
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Assess airway, breathing, circulation, and level of consciousness Administer Aqueous epinephrine 1:1000 dilution (1 mg/mL), 0.2 to 0.5 mL intramuscularly or subcutaneously every 5 minutes, as necessary,
should be used to control symptoms and increase blood pressure.
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Place in trendelenburg Establish airway with Endotracheal tube Administer oxygen Monitor HR and BP continually Start (2) IV NS 5-10ml/kg in first 5 minutes (may require 7 liters) and watch for fluid overload with heart disease
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Administer epinephrine IV
can be administered intravenously over several minutes and repeated as necessary in cases of anaphylaxis not responding to epinephrine injections and volume resuscitation.
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Summary
There are five types of hypersensitivity for which we are emphasizing understanding in Type 1 and Type 4. These types of hypersensivities both respond to irritant but follow a different course due to their individual pathophysiologies. Type I has the potential to be more life threatening, even if it is innocuous in its earliest presentation. Reduction of risk potential for anaphylaxis requires careful screening and analysis of high risk groups to minimize exposure. The life threatening reaction of anaphylaxis is managed using NIC: shock management and vasoactive agents that stop the capillary leaking that causes the shock condition. A review of the emergency medications emphasizing the mechanism of action, adverse effects, management side effects and contraindications are required when providing care.
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