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40 Cards in this Set
- Front
- Back
epiglottitis is
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an inflammation of the airway from the epiglottis up
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epiglottis is most commonly caused by
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H.flu (but several other bacteria can cause it too)
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age group primarily affected by epiglottitis
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2-7 year olds, but is increasing in adults and decreasing in children due to the H. flu vaccine
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key symptoms of epiglottitis
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4 D's - drooling, dyspnea, dysphonia, dysphagia
tripod position toxic presentation |
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treatment for epiglottitis
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keep patient calm, secure airway, be prepared for emergency airway, broad spectrum antibiotics and cultures
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croup is
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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
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croup typically affects what age groups
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6 months to 6 years (most common under 2)
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croup is aka
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laryngotracheobronchitits
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croup is most commonly caused by
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parainfluenze virus type one (but many other viruses can cause it like RSV)
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croup affects what part of the airway
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subglottic
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signs and symptoms of croup
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steeple sign on xray
cold like symptoms harsh, barking cough |
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treatment for croup
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cool mist?
heliox? racemic epi steroids |
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anesthetic implications for croup and epiglottitis
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possible emergency airway needed,
sevo use a smaller ETT than normal extubate only when certain swelling is resolved |
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is cystic fibrosis an obstructive or restrictive lung disease
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both
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cystic fibrosis is caused by
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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
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symptoms of CF
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meconium in newborns, clugging, barrel chest, constipation, foul stools, cough, etc
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CF affects what organ systems
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reproductive, GI, cardiovascular, endocrine (as well as the obvious respiratory)
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respiratory complications of CF
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dyspnea, tachypnea, pneumothorax, nasal polyps, respiratory acidosis, cyanosis, bronchiecstasis, emphysema
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cardiovascular complications of CF
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right ventricle hypertrophy, pa dilation
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GI complications of CF
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GERD, pancreatitis, ulcers, bowel obstruction, splenomegaly, hepatomegaly, malabsorption, biliary cirrhosis
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endocrine complication
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salty skin, electrolyte imbalances, decreased vitamin K, a, d e absorption, Metabolic Alkalosis
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treatments for CF
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medications, antibiotics, mucus thinning drugs, chest physiotherapy, bronchodilators, lung transplant
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anesthetic concerns wih CF
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continuation of meds, PFTs, coagulopathies, possible pneumothorax, hypoxemia, air trapping, etc.
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anesthetic management of CF patient
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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
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one anesthetic NO-NO with CF patient
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no nitrous because will leak and expand and POP
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a drug that shows promise in treating CF
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mannitol
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drugs to avoid in a patient with CF
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desflurane, ketamine, nitrous oxide
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characteristics of sarcoidosis
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non-caseating epithelial granulomas affecting lung, reticuloendothelial system, skin, eyes, myocardium
ACE is produced in higher quantities |
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is sarcoidosis restrictive or obstructive
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it is an intrinsic chronic restrictive disease, although sometimes obstructive characteristics can occur at the same time from fibrosis or endobronchial disease
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sarcoidosis is most common in what population
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african american
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pts with sarcoidosis present with
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no symptoms (most often discovered because chest xray for other purpose - shows bilateral hilar lymphadenopathy)
cough hypercalcemia fever, night sweats, fatigue, weight loss, anorexia |
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pt outcomes with sarcoidosis
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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 |
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treatments for sarcoidosis
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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 |
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anesthetic implications for sarcoidosis
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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 |
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sarcoidosis summary of article
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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)
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NPPE (type I) occurs when
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spontaneous respiration against an obstructed airway causes increased negative intrathoracic pressure which when released causes influx of fluid into the lungs
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NPPE (type II) occurs when
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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
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risk factors for NPPE
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young health men, or any condition that will predispose someone to developing an obstruction
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symptoms of NPPE
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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 |
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treatment of NPPE
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PPV
maintain airway steroids? diuretics? morphine |