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HYPERSENSITIVITY
REACTIONS
Result of excessive immune response to any type of
stimulus, usually does not occur with the first exposure
to an allergen. Rather, the reaction follows a
re-exposure after sensitization, or buildup of
antibodies, in a predisposed person.
re-exposure after sensitization,
buildup of antibodies
predisposed person.
HYPERSENSITIVITY REACTIONS
the reaction follows a (2) in a __
type 1 anaphylactic hypersensitivity
most severe
type 1 anaphylactic hypersensitivity
ONSET: immediate, unanticipated and often sever explosive allergic reaction
type 1 anaphylactic hypersensitivity
chracterized by:
edema in tissues (larynx), hypotension, bronchospasm and cardiovascular collapse (severe case)
type 1 anaphylactic hypersensitivity
examples:
anaphylaxis
allergic rhinitis
allergic asthma
urticaria
anaphylaxis
allergic rhinitis
allergic asthma
urticaria
type 1 anaphylactic hypersensitivity examples 4
edema in tissues (larynx), hypotension, bronchospasm and cardiovascular collapse (severe case)
type 1 anaphylactic hypersensitivity CHARACTERIZED BY (4)
TYPE II cytotoxic hypersensitivity
system mistakenly Identified a normal constituent of a body as foreign, may be the result of cross-reacting antibody, possibly leading to tissue and cell damage
TYPE II cytotoxic hypersensitivity
EXAMPLES
drug induced hemolytic anemia
good pasture syndrome
myasthenia gravis
drug induced hemolytic anemia
good pasture syndrome
myasthenia gravis
TYPE II cytotoxic hypersensitivity example 3
cross reacting antibody
TYPE II cytotoxic hypersensitivity may be a result of
cell damage
tissue damage
TYPE II cytotoxic hypersensitivity possibly leading to (2)
TYPE III immune complex hypersensitivity
increase in vascular permeability and tissue injury due to immune complexes that are formed when antigens bind to antibodies
TYPE III immune complex hypersensitivity
examples
Serum sickness
systemic Lupus erythematous
rheumatoid arthritis
acute glomerulonephritis
Serum sickness
systemic Lupus erythematous
rheumatoid arthritis
acute glomerulonephritis
TYPE III immune complex hypersensitivity examples 4
vascular permeability
tissue injury
antigens bind to antibodies
TYPE III immune complex hypersensitivity
increase in ___ and ___ due to immnue complexes that are formed when ___
TYPE VI delayed hypersensitivity
Onset: 24-72 hpurs after exposure to allergen
TYPE VI delayed hypersensitivity
Mediated by sensitized T cells and macrophages rather than antibodies
TYPE VI delayed hypersensitivity
EXAMPLES
contact dermatitis
poison IVY
transplant rejection
contact dermatitis
poison IVY
transplant rejection
TYPE VI delayed hypersensitivity examples 3
sensitized T cells
macrophages
antibodies
TYPE VI delayed hypersensitivity
mediated by ___ and __rather than __
IgE
Type 1 ANAPHYLACTIC (ig___
anaphylaxis (type 1)
An immediate immunologic reaction
between a specific antigen and an
antibody.
Anaphylactic reaction;
Anaphylactic shock
anaphylaxis (type 1) AKA 2
allergen
anaphylaxis (type 1) CAUSE: (substance that can cause an allergic reaction.)
anaphylaxis (type 1)
is a severe, whole-body allergic reaction to a chemical
that has become an allergen.
Skin allergy test
anaphylaxis DX
food (Peanuts, tree nuts, shellfish)
antibiotics
biologic agents
insect sting
latex
common cause 5
biologic agents
Animal serums (tetanus antitoxin,
snake venom antitoxin, rabies
antitoxin), antigens used in skin testing
penicillin
sulfa antibiotics
common antibiotic as cause of anaphylaxis (2)
Mild anaphylaxis
peripheral tingling, warmth, fullness of mouth and throat, nasal congestion. periorbital swelling, pruritus, sneezing, eye tearing
peripheral tingling, warmth, fullness of mouth and throat, nasal congestion. periorbital swelling, pruritus, sneezing, eye tearing
Mild anaphylaxis CLINICAL MANIFESTATION
Moderate anaphylaxis
mild symptom : ; flushing, warmth anxiety and itching
Moderate anaphylaxis
serious reaction:
bronchospasm and edema (airway and larynx) with dyspnea, cough and wheezing
FLUSHING, warmth, anxiety and itching
bronchospasm and edema (airway and larynx) with dyspnea, cough and wheezing
Moderate anaphylaxis CLINICAL MANIFESTATION
MILD 4
SERIOUS 5
Severe anaphylaxis
ONSET IS ABRUPT
Severe anaphylaxis
progressive rapidly to bronchospasm, laryngeal edema, sever dyspnea, cyanosis, hypotension, dysphagia, abd cramp, V/D, seizures. Cardia arrest and coma may follow
bronchospasm, laryngeal edema, sever dyspnea, cyanosis, hypotension, dysphagia, abd cramp, V/D, seizures
SEVERE anaphylaxis clinical manifestation 13
epinephrine
antihistamine and corticosteroid
aminophylline and corticosterois
IV fluids, volume expanders and vasopressor agents
CPR
educ on how to ad med and prevention of allergen
N MGT for anaphylaxis (6)
for urticaria and edema and to prevent
recurrence
Epinephrine:
1:1000 SQ/IM in the upper extremity or thigh, then followed by a
continuous IV infusion
Aminophylline and corticosteroids:
improve airway patency
IV fluids, volume expanders, and vasopressor agents:
to maintain blood pressure
and normal hemodynamic status
Strict avoidance of potential allergens
Avoid areas populated by insects, use appropriate clothing, and use insect repellants
Always carry an emergency kit containing epinephrine (EpiPen)
PREVENTION OF ANAPHYLAXIS 3
Airway compromise
Cardiovascular collapse
Neurological complications
Gastrointestinal and renal complications
Rebound (biphasic) reactions
COMPLICATIONS of anaphylaxis 5
Laryngeal edema
bronchospasm
severe respiratory distress
hypoxemia.
anaphylaxis
Airway compromise (4)
Hypotension
shock
arrhythmias
cardiac arrest.
anaphylaxis
Cardiovascular collapse (4)
Hypoxic brain injury due to prolonged hypoxemia.
anaphylaxis
Neurological complications
acute kidney injury, bowel ischemia.
anaphylaxis
Gastrointestinal and renal complications 2
1–72 hours.
anaphylaxis
Rebound (biphasic) reactions (time of reoccurance)
TYPE II cytotoxic
MYASTHENIA
GRAVIS (MG)
MYASTHENIA
GRAVIS (MG)
A neuromuscular disorder characterized by failure
of transmission of nerve impulses at the myoneural
junction
nerve impulses
myoneural junction
A neuromuscular disorder characterized by failure
of transmission of __ at the __
MYASTHENIA
GRAVIS (MG)
caused by decreased functioning of
acetylcholine receptor sites. It is also associated
with autoimmune disorders
decrease function of acetycholine receptor sites
MYASTHENIA
GRAVIS (MG) MAY BE CAUSED BY
Autoimmune reaction: antibodies block or destroy acetylcholine (ACh)
receptors.
Thymus gland abnormalities (hyperplasia, thymoma).
More common in women <40 and men >60.
May be triggered or worsened by infection, surgery, stress, pregnancy,
certain medications (e.g., aminoglycosides).
factors influencing myasthenia gravis (1)
(hyperplasia, thymoma).
Thymus gland abnormalities (2)
aminoglycosides).
medication that may trigger MG
Autoimmune problem:
Blocked communication:
Less muscle stimulation:
Muscle weakness:
PATHOPHYSIOLOGY FOR MG
Muscle weakness associated with activity
relieved by rest,
Eyelid droopiness
double vision
impaired speech
difficulty swallowing
changes in facial expression
trouble breathing
MG CLINICAL MANIFESTATION 7
•Tensilon Test (Edrophonium Test)
MG DX
Tensilon
short – acting cholinergic – treatment for MG
IB
2MG
8MG
•Tensilon Test (Edrophonium Test)
administered __ (__ first, then __mg).
muscular strength
3 -5
Positive Tensilon test is observed as improvement in ___. Muscle weakness returns
in _ to _ minutes
Atropine sulfate (anticholinergic)
antidote for cholinergic is
Assess swallowing and gag reflex before feeding the client to prevent aspiration
Administer medications 20 to 30 minutes before meals to improve ability to swallow and prevent choking
Administer medications at an exact time to prevent myasthenic crisis that results to respiratory distress
Protect the client from falls due to muscle weakness
Implement aspiration precaution
Start meal with cold beverage. To contract muscles of the throat and
improve ability to swallow
Promote adequate ventilation to relieve respiratory difficulty
Avoid infections. Infections may trigger exacerbations of MG
Provide adequate rest with alternating activity
MG management (9)
•Plasmapheresis
separation of
antibodies from the
plasma to inhibit
autoimmune
response
Acetylcholinesterase Inhibitors/Cholinesterase Inhibitors
MANAGEMENT
•
Pharmacotherapy
Prostigmin (Neostigmine)
Mestinon (Pyridostigmine)
Mytelase (Ambenomium)
Acetylcholinesterase Inhibitors/Cholinesterase Inhibitors (3)
neuromuscular impulses
acetylcholine.
These medications transmit ___ by preventing the
destruction of ___
Monitor improvement of muscle strength and respirations
Observe the client for signs and symptoms of cholinergic crisis caused by
overdosing of the drug – muscle weakness, increased salivation, sweating,
tearing, and miosis
Have readily available on antidote for cholinergic crisis (Atropine Sulfate)
Encourage the client to wear Medic-Alert bracelet that indicates the health
problem and the drug taken
5. Instruct the client to take the medication before meals for best drug
absorption
6. Observe and report possible side effects and adverse reactions:
Nursing Interventions for Acetylcholinesterase Inhibitors 6
Nausea, vomiting, diarrhea, abdominal cramps
Increased salivation
Tearing
Miosis (constriction of pupils)
Possible hypertension
Acetylcholinesterase Inhibitors
side effects and adverse reactions:
Glucocorticoids
MEDICATION
for anti-inflammatory effects
Antacids
medication
(As protection)
To prevent gastrointestinal upset due to glucocorticoids
Thymectomy
MANAGEMENT
Surgery:
thyroidectomy
(surgical removal
of the thymus gland).
thymoma
(tumor of the thymus gland).
*25%
thymoma
5-10
Thymectomy
__ of people with MG have been found to have __. The surgery achieves
remission for _-_ years
Myasthenic Crisis
Cholinergic Crisis
The 2 major complications of MG are
MYASTHENIC CRISIS
Caused by undermedication or delayed medication
MYASTHENIC CRISIS
Clinical manifestations
Sudden marked rise in BP due to hypoxia
Increased heart rate
Severe respiratory distress and cyanosis
Absent cough and swallowing reflex
Increased secretions, increased diaphoresis, and increased lacrimation (tearing)
Restlessness, dysarthria
Bowel and bladder incontinence
Sudden marked rise in BP due to hypoxia
Increased heart rate
Severe respiratory distress and cyanosis
Absent cough and swallowing reflex
Increased secretions, increased diaphoresis, and increased lacrimation (tearing)
Restlessness, dysarthria
Bowel and bladder incontinence
MYASTHENIC CRISIS
Clinical manifestations 7
Increased doses of cholinergic as long as the client responds positively to edrophonium treatment
Possible mechanical ventilation of respiratory muscle paralysis is acute
Interventions for patients with Myasthenic Crisis: (2)
CHOLINERGIC CRISIS
Caused by excessive medications
CHOLINERGIC CRISIS
Clinical manifestations
Weakness with difficulty swallowing, chewing, speaking, and breathing
Apprehension, nausea and vomiting
Abdominal cramps and diarrhea
Increased salivation and secretions
Sweating, lacrimation, fasciculations, and blurred vision
Weakness with difficulty swallowing, chewing, speaking, and breathing
Apprehension, nausea and vomiting
Abdominal cramps and diarrhea
Increased salivation and secretions
Sweating, lacrimation, fasciculations, and blurred vision
CHOLINERGIC CRISIS
Clinical manifestations (5)
Discontinue all cholinergic drugs until cholinergic effects decrease
Provide adequate ventilator support
Atropine 1mg/IV may be necessary to counteract severe cholinergic reactions
Interventions for the patients with cholinergic crisis: (3)
Muscle relaxants
Barbiturates
Morphine sulfate
Tranquilizers
Neomycin
drugs should be avoided by the clients with MG: (5)
Reschedule daily task. To prevent weakness
Secure “handicapped” parking sticker
Frequent rest periods
Have alarm clock available – to take medications on time. This prevents myasthenic crisis
Patch each eye alternately for diplopia (double vision)
Start meal with cold beverage. To contract muscles of the throat and prevent aspiration
Avoid factors that affect respiratory functions
SURVIVAL GUIDE FOR CLIENTS WITH
MG (7)
Very hot or very cold weather
Aerosol, pesticides, cleaners
Alcohol, tonic water, cigarette smoke
factors that affect respiratory functions and may cause respiratory
infections: (3)
Assessment: Evaluate muscle strength, respiratory status, and the presence of symptoms.
Diagnosis: Identify nursing diagnoses such as impaired physical mobility, risk for aspiration, and ineffective breathing pattern.
Planning: Develop a care plan that includes goals for improving muscle strength, managing symptoms, and preventing complications.
Implementation: Provide medications, assist with ADLs, educate the patient and family, and monitor for signs of crisis.
Evaluation: Regularly assess the effectiveness of interventions and adjust the care plan as needed
MG (NURSING PROCESS)
Assessment
DX
Planning
Implementation
evaluation