EXAM 2 chronic respiratory Flashcards
(26 cards)
asthma overview
> 6 months
airway obstruction, bronchial irritability, edema,
asthma pathophysiology
type 1 immune response
IGE mediated. mast cells release histamine and leukotriens
manifestations of asthma
wheezing, cough, prolonged expiration, exacerbations, resp distress, rhonchi, chest tightness, sweating
nasal flaring, cyanosis, intercostal retractions=distress
exacerbation of asthma triggers
dust, pets, cold, stress, cigarette smoke, plants
asthma risk factors
age, heredity, gender, obesity, ethnicity
asthma diagnosis
medical hx, exam, lab results
pulmonary function tests are helpful, peak expiratory flow rate
PEFR guidelines
green=80-100 of personal best
yellow=50-79 of personal best
red= below 50 of personal best
asthma drug therapy-controllers
corticosteroids (Qvar, pulmicort, flovent)
long acting beta 2 adrenergic agonist
mast cell stabilizers
leukocite inhibitors: singulair
rinse mouth after corticosteroids
asthma rescue meds
short acting beta 2 adronergic agonist, bronchodilators=proventil, xopenex, albuterol
magnesium sulfate
nursing considerations for asthma
assess precipitating factors, are meds being used correctly? modify environment, encourage immunizations, prevent URI, exercises
asthma nursing interventions
high fowlers, assessment, oxygen monitoring, HR and BP
teach pt to use diaphragm to expel air, control panic, maintain calm approach, may need IV, administer rescue drugs,
Cystic fibrosis ethnicity
most common in caucasians, 30,000 people in the US
pathophys of cystic fibrosis
disrupts exocrine glands related to nacl transport via cystic fibrosis transmembrane regulator protein
impaired fluid secretions and abnormally thick exocrine secretions
multiorgan effect of cystic fibrosis
respiratory, endocrine, GI, reproductive, hepatic
girls-delay in puberty
boys-may be steril
CF pulmonary effects
repeated bronchitis, obstructive airway emphesema, wheezy cough, thick rattling, cyanosis, pna, clubbed digits
endocrine effects of CF
islet of langerhands may decrease in number as pancreatic fibrosis develops
cystic fibrosis related diabetes
gi effects of CF
small intestine=obstructions
pancreatic ducts=degenerate, diabetes,
signs: appetite changes, weight loss, tissue wasting, distended abdomen, anemia
hepatic effects of CF
bile ducts=biliary fibrosis and cirrhosis, portal hypertension
signs: ascites, gi bleeds, jaundice
major CF side effects
delayed puberty and infertility
SALTY SWEAT
diagnosis of CF
prenatal-dna analysis
newborn screening
sweat chloride test
stool for fecal test
CF prognosis
decreased life expectancy, maximize potential with pulmonary hygiene
nutrition
prevention and early infection treatment
CF medical management
CFTR modulation, pulmonary toilet, nutritional therapy, antibiotic use
respiratory management of CF
airway clearance, percussion, PEP mask, chest percussion, flutter device, postural drainage, breathing and physical exercise
CF meds
bronchodilators
mucolytics, donase alfa
chloride channel activators and sodium channel blockers
antibiotics for treatment and prevention