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40 Cards in this Set

  • Front
  • Back
epiglottitis is
an inflammation of the airway from the epiglottis up
epiglottis is most commonly caused by
H.flu (but several other bacteria can cause it too)
age group primarily affected by epiglottitis
2-7 year olds, but is increasing in adults and decreasing in children due to the H. flu vaccine
key symptoms of epiglottitis
4 D's - drooling, dyspnea, dysphonia, dysphagia
tripod position
toxic presentation
treatment for epiglottitis
keep patient calm, secure airway, be prepared for emergency airway, broad spectrum antibiotics and cultures
croup is
a viral infection of the upper respiratory tract - but is actually the antigen reaction to the infection, not the infection that is causing the problem
croup typically affects what age groups
6 months to 6 years (most common under 2)
croup is aka
laryngotracheobronchitits
croup is most commonly caused by
parainfluenze virus type one (but many other viruses can cause it like RSV)
croup affects what part of the airway
subglottic
signs and symptoms of croup
steeple sign on xray
cold like symptoms
harsh, barking cough
treatment for croup
cool mist?
heliox?
racemic epi
steroids
anesthetic implications for croup and epiglottitis
possible emergency airway needed,
sevo
use a smaller ETT than normal
extubate only when certain swelling is resolved
is cystic fibrosis an obstructive or restrictive lung disease
both
cystic fibrosis is caused by
a gene that causes a defective chloride ion channel leading to decreased sodium and water transport and affects bicarb transport, dehydration, thick viscous secretion, lung scarring
symptoms of CF
meconium in newborns, clugging, barrel chest, constipation, foul stools, cough, etc
CF affects what organ systems
reproductive, GI, cardiovascular, endocrine (as well as the obvious respiratory)
respiratory complications of CF
dyspnea, tachypnea, pneumothorax, nasal polyps, respiratory acidosis, cyanosis, bronchiecstasis, emphysema
cardiovascular complications of CF
right ventricle hypertrophy, pa dilation
GI complications of CF
GERD, pancreatitis, ulcers, bowel obstruction, splenomegaly, hepatomegaly, malabsorption, biliary cirrhosis
endocrine complication
salty skin, electrolyte imbalances, decreased vitamin K, a, d e absorption, Metabolic Alkalosis
treatments for CF
medications, antibiotics, mucus thinning drugs, chest physiotherapy, bronchodilators, lung transplant
anesthetic concerns wih CF
continuation of meds, PFTs, coagulopathies, possible pneumothorax, hypoxemia, air trapping, etc.
anesthetic management of CF patient
small tidal volume, large FRC, preop oxygentation, volatile anesthetics, locals are good, V:Q mismatch - many of the drugs we give are affected by the disease or the other meds they are on, so know that onset or duration may change, hydrate patient, freq suctioning, possible high dose steroid regime
one anesthetic NO-NO with CF patient
no nitrous because will leak and expand and POP
a drug that shows promise in treating CF
mannitol
drugs to avoid in a patient with CF
desflurane, ketamine, nitrous oxide
characteristics of sarcoidosis
non-caseating epithelial granulomas affecting lung, reticuloendothelial system, skin, eyes, myocardium
ACE is produced in higher quantities
is sarcoidosis restrictive or obstructive
it is an intrinsic chronic restrictive disease, although sometimes obstructive characteristics can occur at the same time from fibrosis or endobronchial disease
sarcoidosis is most common in what population
african american
pts with sarcoidosis present with
no symptoms (most often discovered because chest xray for other purpose - shows bilateral hilar lymphadenopathy)
cough
hypercalcemia
fever, night sweats, fatigue, weight loss, anorexia
pt outcomes with sarcoidosis
60 - 70% recover after a couple years with no complications
20% have some loss of lung function or visual impairment
10 - 15% die from cardiac, lung, or neurological impairment from disease
treatments for sarcoidosis
typically high dose, long term steroids (not known if actually improves outcomes and has lots of side effects),
also trying anti-inflammatories, antimalarials, radiation, immunosuppressive agents
time - spontaneous permanent remission in 50% of patients
anesthetic implications for sarcoidosis
preop lung and system assessment for degree of involvement, PFTs and ABGs
intraop - uptake of gases may be faster
smaller tidal volumes, faster rate
spO2 - 88 - 92% (oxygen is toxic)
decreased FRC, FEV1, FVC
V:Q mismatching
laryngeal sarcoidosis could restrict ETT placement
sarcoidosis summary of article
although many patients asymptomatic, if undergo all the PFT's and other tests, will show a sign somewhere that it is a restrictive disease (and lots had obstructive components too)
NPPE (type I) occurs when
spontaneous respiration against an obstructed airway causes increased negative intrathoracic pressure which when released causes influx of fluid into the lungs
NPPE (type II) occurs when
a chronic partial obstruction of the airway is removed causing patient to suddenly exhale much more effectively leading to more negative intrathoracic pressure and increased venous return and pulmonary flow before heart can compensate causing fluid to move out of pulmonary circulation and into the lungs
risk factors for NPPE
young health men, or any condition that will predispose someone to developing an obstruction
symptoms of NPPE
Hypoxemia
Cough
Frothy sputum (sometimes pink)
Tachycardia
Crackles on ausculation
Decreased lung compliance
Pulmonary infiltrates on chest x-ray
Wheezing, Stridor
Increased RR
Decreased SpO2
Agitation
treatment of NPPE
PPV
maintain airway
steroids?
diuretics?
morphine