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acute spasmodic laryngitis
Subglottic inflammation
-tissue below the vocal cords
etiology: viral, emotional (usually virus)
s/sx: sudden onset at net
-harsh cough, hoarseness (chief complaint)
self limiting, no LT sequelae
rx: humidity
-encourage fluids
-treat symptomatically
laryngotracheobronchitis (LTB)
inflammation of the larynx, trachea, and bronchi
-most common of the croups
the most common cause of airway obstruction in kids <5
etiology: usually viral (RSV, parainfluenza, influenza A+B)
inflammation of the mucosal lining of trachea and larynx causes airway narrowing
dx: based on history and symptoms
LTB s/sx
gradual onset following URI
sore throat, harsh cough
use of accessory muscles
agitation, restlessness, sweaty
increased RR, HR, increased respiratory difficulty leading to hypoxia
cyanosis
inflammation is usually followed by inspiratory stridor
supra/substernal and intercostal retractions
*if stridorous at rest, go to ER
LTB treatment
humidity and cool mist vaporizer to decrease mucosal edema
racemic epinephrine (usually neb)
IV fluids
continuous oxygen saturation monitor
humidification w/ blow by oxygen
nursing process for LTB
assess: continuous, vigilant observation and accurate respiratory assessment
recognize impending respiratory failure: FGR
-use of accessory muscles
-irritability, cyanosis
-increased HR, RR, POX<= 90%
diagnosis: ineffective airway clearance r/t mucosal swelling and airway obstruction
expected outcome/goal: child will breathe without difficulty, V/S WNL
evaluation: child has a RR and HR WDL, pink mucous membranes and nail beds, SpO2 > 955
interventions for LTB
continuous SpO2 monitoring
V/s hourly
high humidity, cool mist
emergency intubation equipment available
aerosolized racemic Epinephrine
maintain a calm, quiet environment
prevention of LTB
American Academy of Pediatrics recommends H. flu vaccine beginning at 12 months
eliminate passive smoking
asthma
A chronic allergic disorder characterized by episodes of severe breathing difficulty, coughing, and wheezing.
airway inflammation related to upper airway reactivity
airway hyperresponsiveness
airway obstruction
dx: History, s/s: chronic cough, expiratory wheeze
anti-inflammatory agents key
etiology of asthma
not well understood
factors:
-biochemical: irritants, smoke, strong odor
-immunologic: allergies
-infectious: cold, flu can trigger attack
-endocrine: paralleled with obesity (may share genetic determinants)
-psychologic
diagnosis of asthma
based on history and s/sx
-cough in the absence of infection and/or expiratory wheezes usually sufficient for diagnosis
labs and X-rays to r/o other diagnoses
pulmonary function tests to establish baseline
-objective measure of the severity of the illness and the response to treatment
spirometry is taught
s/sx of asthma
COUGH (nonproductive which becomes rattling with the production of frothy, clear sputum)
SOB, wheezes, crackles, coarse loud lung sounds
restlessness, apprehension
long term:
-barrel chest
-elevated shoulder
management of asthma
measure lung function
environmental control
pharmacologic therapy
education
lung function tests
Peak expiratory flow rate: pushing out as much air as quickly and forcefully as they can
Peak flow meter
RT consult
3 acceptable measures
-one that is unbroken that doesn't include coughing
environmental control of asthma
eliminating triggers
allergens, irritants, virus, cold air, exercises
non-environmental stimuli include laughing, crying, anxiety, stress, GERD
IDing asthma tirggers
obtaining a thorough history of previous asthma attacks (how long did it last, when did symptoms start, what made it worse/better, what were you doing) or skin tests
pharmacologic therapy of asthma
"PREVENTER"
-controller, anti-inflammatory'
-taken daily
-corticosteroids (most effective single LT control therapy for pts with asthma)
-Mast cell stabilizers (anti-infective)
-Long acting beta-2 agonist
-Methylxanthines (bronchodilator)
-Leukotriene modifiers (decrease frequency and severity of asthma attacks)
"RESCUE"
-bronchodilators
-quick relief
-inhaled short-acting beta 2 agonists to relax smooth muscle cause bronchodilation (Albuterol)
-anticholinergics (smooth muscle relaxants)
-systemic corticosteroids (PO/IV)
-magnesium sulfate (most sever, IV, high alert med)
the rule of 2-4-6 (asthma)
When to consider long term control for asthma in infants and preschoolers
More than 2 asthma episodes/week requiring treatment
4 or more episodes of wheeze lasting long than a day and affecting sleep in the past year
6 severe exacerbations less than 6 weeks apart requiring the use of a beta agonist
reactive airway disease (RAD)
respiratory condition characterized by wheezing, shortness of breath, and coughing after exposure to an irritant
considered this until it is established as asthma
treatment steps for asthma (for kids <2)
1. bronchodilator and O2 prn
2. step 1 + corticosteroid x5d
3. step 2 + controller (2-3 months)
4. step 2+ controller (long term)
5. look for cause of Rx failure
-misdiagnosed
-noncompliance/poor technique
-refer to pulmonologist
patient education for asthma
help patient decide on plan and take action
discuss barriers and benefits
put plans in writing
-every pt goes one with a color coded Asthma Action Plan
-reviewed at every visit
assess patient needs at every visit
teach and review
what a caregiver should know about asthma
what may trigger an exacerbation
s/sx that warn of an exacerbation
techniques that can prevent an exacerbation
which meds the child is on and how to administer
side effects of those meds
when to call the PCP or go to the ED
assessment of asthma
history
family history
exacerbations
alleviation
parent knowledge base
management
in acute phase:
-V/S, LS, SpO2
-retractions
-LOC
-WOB
-hydration
nursing process for asthma
diagnosis: risk for suffocation r/t bronchospasm
goal: no acute asthma episode
interventions: assessment
-O2 at 2L/min, position of comfort
-NPO, IV access
-use play techniques for breathing exercises
cystic fibrosis
Chronic multisystem disorder that is genetic and ultimately lethal
exocrine glands, mucous produced is abnormally thick, causing obstruction of bronchioles, small intestine, pancreas, and bile duct
autosomal recessive trait that is genetically transmitted
average survival age in Americans is about 40 years old
more common in white people
diagnostics for cystic fibrosis
diagnosis made based on family history of CF, absence of certain pancreatic enzymes, and a sweat test
sweat test: pilocarpine iontophoresis: stimulates sweating, NaCl level positive value is >60mEq
fecal fat determination
LFT
PFT
amniocentesis: early interventions, gives better outcomes
s/sx of CF
vary widely and are system specific
-bronchial obstruction
-intestinal obstruction
-malabsorption syndrome
-portal hypertension
respiratory s/sx of CF
progresses overtime to worsening outcomes over the lifespan
-wheezing
-cough
-pneumonia
-bronchitis
-copious purulent sputum
-accessory muscle use
-dyspnea
-tachypnea
-cyanosis
-emphysema
-atelectasis
-cor pulmonale
-digital clubbing
-barrel chest
GI symptoms of CF
progresses overtime to worsening outcomes over the lifespan
-meconium ileus
-steatorrhea (frothy fatty stools because of malabsorption)
-malnutrition
-vitamin deficiencies
-protuberant abdomen
-thin extremities
-wasted buttocks
-rectal prolapse
-biliary cirrhosis
-portal hypertension
-esophageal varices
-higher incidence of diabetes
integument s/sx of CF
abnormally high NaCl in sweat
risk electrolyte imbalance
dry mouth
reproductive s/sx of CF
delayed development
difficulty conceiving
increased rate of fetal loss
sterility in men (congenital bilateral absence of the vas deferens [CBAVD] is common)
women have normal hormones but frequent reproductive issues
treatment of CF
Chest physiotherapy
-with bronchodilators and mucolytics
regular aerobic exercise may be as effective as CPT
antibiotics: pseudomonas aeruginosa
O2/steroids with caution because of CO2 retention risk and risk of pseudomonas with steroids
immunizations
-flu vaccine
ivacaftor, TOBI
calorie requirements are 1.5x normal due to increased WOB and malabsorption
-high calorie, high protein
-pancreatic enzyme replacement
-vitamin supplement
GT feeds/TPN as needed if unable to maintain weight
pancreases/pancreatin with meal
Ivacaftor
this can cure kids if they have a specific genetic mutation
TOBI
inhaled tobramycin 28 days on, 28 days off
helpful with bacteria found in half of CF and is the leading cause of lung damage
Pancrease/Pancreatin
encapsulated pancreatic enzyme powder that should be administered with every meal or snack and the dosage is adjusted based on stool formation
-constipated, decreased dose; diarrhea, increased dose)
psychological support for CF
chronic illness
-1-800-fight-cf
normal activities
birth control
genetic counseling
nursing process for CF
assessment of L/s, exp. phase, nail beds, digits, SpO2, cough (sputum color and quality), exercise tolerance, height and weight, s/s of malabsorption, ability to sleep laying down
diagnosis: ineffective airway clearance r/t increased pulmonary secretions
goal: child with be able to move secretions from airway
interventions:
-assess respiratory status q2h
-CPT q4h around the clock
-administer expectorants and bronchodilators in between
-humidified low flow O2
-increased HOB
evaluation:
-child exhibits improved breath sounds, ability to participate in usual activities, pOx >94% on RA
-parent demonstrates CPT, inhalation therapy, ability to administer meds