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102 Cards in this Set
- Front
- Back
conducting zone of respiratory tree
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brings air in and out, humidifies, filters air
anatomic dead space nose, pharynx, trachea, bronchi, bronchioles, and terminal bronchioles |
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respiratory zone of respiratory tree
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participates in gas exchange
consists of the respiratory bronchioles, alveolar ducts, and alveoli |
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type 1 pneumocytes
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thin squamous cells, for gas exchange
97% of alveolar surfaces |
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type 2 pneumocytes
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secrete pulmonary surfactant - decrease alveolar surface tension
cuboidal proliferate to lung damage lethacin-to-shingomyelin ratio >2 in amniotic fluid indicates lung maturity of fetus |
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lethacin-to-sphingomyelin ratio
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> 2 in amniotic fluid indicates lung maturity in fetus
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clara cells
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nonciliated columnar with secretory granules - secretes a component of surfactant (GAG), degrade toxins, act as reserve cells
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T/F goblet cells are present throughout the respiratory tract
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FALSE
found only until the terminal blronchioles |
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where do you find pseudostratified ciliated columnar epithelium?
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extend to respiratory bronchioles
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gas exchange barrier
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endothelial cell of capillary
basement membrane type 1 pneumocyte - epithelial cell |
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bronchopulmonary segment
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each has a tertiary bronchus and 2 arteries (1 bronchial and 1 pulm) in the center
arteries run with airways veins and lymphatics run along boarders |
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which lung is more common for inhaled objects?
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the right because the right main stem bronchous is more vertical and wider
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how many lobes does the right lung have? left lung?
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right - 3 lobes
left - 2 lobes + lingula - left has 2 lobes because heart takes up space, lingula represents the missing middle lobe |
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most likley location for aspirated objects while upright? supine?
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when upright - lower portion of right inferior lobe
when supine - superior portion of right inferior lobe |
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location of strictures passing through diaphragm
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T8 - IVC
T10 - esophagus + vagus nerve T12 - aorta, thoracic duct, azygous I ate (T8) ten (T10) eggs at twelve (T12) I = IVC eggs = esophagus at = aorta |
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diaphragm innervation
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C3,4,5 keeps diaphragm alive
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muscles of quiet breathing - inspiration and expiration
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inspiration - diaphragm
expiration - passive |
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muscles of breathing during exercise - inspiration and expiration
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inspiration - external intercostals, scalene muscles, sternomastoids
expiration - rectus abdominus, internal and external obliques, transverse abdominis, internal intercostals |
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collapsing pressure
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2(tension)/radius
tendency to collapse as radius decreases |
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residual volume
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air left in lung after maximal expiration
cannot be measured by spirometry |
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expiratory reserve volume
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air that can still be breathed out after normal breathing
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tidal volume (TV)
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air that moves in with each quiet inspiration
usually 500ml |
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inspiratory reserve volume (IRV)
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air in excess of tidal volume that moves into lung during MAXIMAL inspiration
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vital capacity (VC)
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everything by residual volume
TV + IRV + ERV |
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functional residual capacity (FRC)
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RV + ERV
volume in lungs after normal exhalation |
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inspiratory capacity (IC)
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IRV + TV
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total lung capacity (TLC)
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IRV + TV + ERV + RV
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physiologic dead space
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physiologic dead space = anatomical dead space in conducting airways + functional dead space in alveoli
does not take part in gas exchange Vd = Vt x (PaCO2-PeCO2)/PaCO2 Vt = tidal volume PaCO2 = arterial PCO2 PeCO2 = expired air PCO2 |
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lung and chest wall determinants
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lung has tendency to collapse
chest wall has tendency to expand at FRC they balance and system of pressure is atmospheric |
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hemoglobin T vs R state
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T state - has low affinity for O2
R state - high affinity O2 increased Cl-, H+, CO2, 2,3-BPC and temperature favor the T form (shift curve right leading to increased O2 unloading) |
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methemoglobin
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oxidized form of hemoglobin to Fe3+ (normal is Fe2+)
does not bind O2 well, has increased affinity for CN- treat with METHylene blue |
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why can methemoglobin be useful in treating cyanide poisoning
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methemoglobin has high affinity for CN-, thus competes for binding, allowing cytochrome oxidase in mitochondria to function
give nitrites to oxidize hemoglobin to methemoglobin - binds CN- then give thiosulfate to bind this -> excretion |
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carboxyhemoglobin
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hemoglobin bound to Carbon monoxide
CO has a much higher affinity for hemoglobin than O2 causes a left shift in disassociation curve decreases oxygen unloading |
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what causes a right shift in the dissociation curve?
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CADET face right
CO2 Acid/Altitude DPG Exercise Temperature increases in all factors besides pH shift the curve right decreasing any of these factors except pH will shift left |
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a shift to the right for the dissociation curve means what in terms of oxygen affinity?
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decreased affinity for O2 - facilitates unloading of O2 to tissue
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Fetal Hb has higher or lower affinity for O2 than Hb A
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higher affinity - disassociation curve shifted left
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a decrease in PAO2 causes vasoconstriction or vasodilation?
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vasoconstriction
different from what you expect in systemic artery, pulmonary artery constricts if low O2 and redirects blood to well ventilated areas |
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normally O2, CO2, and N2O is perfusion or diffusion limited?
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usually perfusion limited
gas equilibrates early along length of capillary diffusion can only increase if blood flow increases |
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when does O2 become diffusion limited?
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emphysema or fibrosis
gas does not equilibrate completely before reaching end of capillary |
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cor pulmonale
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consequence of pulmonary hypertension - right ventricular heart failure
see jugular venous distension, edema, hepatomegally |
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what is normal pulmonary artery pressure? what is considered pulmonary hypertension?
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normal 10-14mmHg.
hypertension > 25mmHg or > 35 during exercise |
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consequences of pulmonary hypertension
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athlerosclerosis, medial hypertrophy, intimal fibrosis of pulmonary arteries
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primary pulmonary hypertension causes
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due to mutation in BMPR2 gene which normally inhibits vascular smooth muscle prolif
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2ndary pulmonary hypertension causes
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due to:
COPD - destruction of lung parenchyma mitral stenosis - increased resistance causes increased pressure recurrent thromboemboli - decreases crosssectional area of pulmonary vascular bed autoimmune disease - inflammation -> fibrosis -> medial hypertrophy L->R shunt - high shear stress -> endothelial injury sleep apnea - hypoxic vasoconstriction high altitude - hypoxic vasoconstriction |
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pulmonary vascular resistance
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PVR = P[pulmonaryartery] - P[L atrium]/Cardiac output
R = deltaP/Q R = 8nl/(pi)r^4 |
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cyanosis relationship to hemoglobin
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cyanosis results when deoxygenated Hb > 5g/dl
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O2 content of blood equation
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(O2 binding capacity x %sat) +dissolved O2
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T/F O2 content of arterial blood decreases as Hb, O2 sat, or arterial PO2 fall
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False: O2 content of arterial blood decreases as Hb decreases, BUT O2 sat and arterial PO2 does not
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alveolar gas equation
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PAO2 = PIO2 - PACO2/R
approximately = 150-PACO2/0.8 PAO2 = alveolar PO2 PIO2 = inspired PO2 PACO2 = alveolar PCO2 R = respiratory quotient = CO2 produced/O2 consumed use this equation in calculating A-a gradient |
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A-a gradient
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A-a gradient = PAO2 - PaO2
difference in PO2 between alveoli and arterial blood should equal 10-15mmHg increase in A-a gradient indicates hypoxemia - shunting, V/Q mismatch, fibrosis normal in hypoxemic states due to high altitude and hypoventilation |
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causes of hypoxemia
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hypoxemia is decrease in PaO2
high altitude hypoventilation V/Q mismatch Diffusion limitation R-L shunt |
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causes of hypoxia
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hypoxia is decreased O2 delivery to tissue
decreased cardiac output hypoxemia anemia cyanide poisoning carbon monoxide poisoning |
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causes of ischemia
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also causes O2 deprivation like hypoxemia and hypoxia
impeded artery flow impaired venous drain |
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V/Q mismatch
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ventilation should be matched to perfusion V/Q = 1, mismatched V/Q can be physiologic or due to pathology
normal: apex of lung V/Q = 3 (wasted ventilation) vase of lung V/Q = 0.6 (wasted perfusion) |
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what does it mean V/Q = 0
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V/Q = 0 means airway obstruction (shunt) - 100% O2 doesnt help
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what does it mean V/Q is infinity
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V/Q is infinity in blood flow obstruction (physiologic dead space)
100% O2 will improve PO2 as long as some part of the lung is perfused |
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why do you find TB in the apex of the lung more?
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heavily ventilated, by low perfusion means there is high O2 content
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how does exercise change V/Q ratio
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approaches 1 due to increased cardiac output and vasodilation of apical capillaries
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which part of the lung would you find PO2[alveolar] > PO2[arterial] > PO2[venous]
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apex (zone 1)
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how do PO2[alveoli], PO2[artery], PO2[venous] compare in zone 2 (middle of lung)
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PO2[artery] > PO2[alveoli] > PO2[venous]
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T/F the base of the lung has PO2[artery] > PO2[vein] > PO2[alveoli]
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True
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T/F the base of the lung has the lowest ventilation and highest perfusion compared to the apex of the lung
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FALSE
the base of the lung has the highest ventilation AND perfusion than the apex |
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CO2 is transported from the tissues to the lungs via: 3 mech
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1. bicarbonate (90%)
2. bound the hemoglobin at N-terminus (not on heme) - favors T form 3. dissolved in blood |
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Haldane effect
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in lungs, oxygenation of hemoglobin releases H+ from hemoglobin
H+ shifts equilibrium to formation of CO2 to be exhaled from the lung |
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Bohr effect
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in tissues, increased H+ from tissue metabolism shifts disassociation curve to the right -> unload O2 to tissues
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physiological response to high altitude
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1. Acute T in ventilation
2. Chronic T in ventilation 3. increased erythropoietin > increased hematocrit and hemoglobin (chronic hypoxia) 4. increased 2,3-DPG (binds to hemoglobin and releases O2) 5: . Cellular changes (increased mitochondria) 6. increased renal exerelion of bicarbonate to compensate for respiratory alkalosis 7. Chronic hypoxic pulmonary vasoconstriction results in RVH |
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physiological response to exerciase
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1. inc CO2 production
2. inc O2 consumption 3. inc ventilation rate to meet O2 demand 4. V/Q ratio from apex to base becomes uniform 5. inc pulmonary blood flow due to inc CO 6. dec pH (lactic acidosis) 7. no change in PaO2 and PaCO2 but increased venous CO2 |
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types of embolus
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FAT BAT
1. fat - associated with long bone fractures, liposuction 2. air 3. thrombus - most common from deep veins in leg (DVT) 4. bacteria 5. amniotic fluid - can lead to DIC 6. tumor |
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virchow's triad
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predisposes to DVT
1. stasis 2. hypercoagulability 3. endothelial damage |
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deep vein thrombosis
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birchow's triad
lead to pulmonary embolism homan's sign - dorsiflexion of foot -> tender calf muscle prevent with heparin |
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COPD
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obstruction of air flow resulting in air trapping in the lung
hallmark is decreased FVC and FEV1 thats even more decreased compared to FVC-> decreased FEV1/FVC ratio types: Chronic Bronchitis emphysema asthma brochiectasis |
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Chronic Bronchitis
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"blue bloater"
hypertrophy of mucus secreting glands in bronchioles use reid index >50% (gland depth/total thickness of bronchial wall) productive cough >3 consecutive months for > 2 years early onset cyanosis, wheezing, crackles |
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emphysema
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"pink puffer" - barrel chest
see increased elastase -> increased compliance enlargement of air spaces and decreased recoil - destruction of alverolar wall late onset hypoxemia, early onset dyspnea exhale through pursed lips to increase airway pressure centriacinar - smoking panacinar - alpha1 antitrypsin deficiency (also liver cirrhosis) paraseptal - see bullae that can rupture -> spontaneous pneumothorax (in young males) |
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asthma
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bronchial hyperresponsiveness -> bronchoconstriction
smooth muscle hypertrophy curschmann's spirals triggered by drugs, allergens, stress mucus plugging, pulsus paradoxus |
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curschmann's sprial
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shed epithelium from mucous plugs form a spiral shape - found in sputum and tracheal washing
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bronchiectasis
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chronic necrotizing infection of bronchi - permanently dialated airways, purulent sputum, recurrent infection, hemoptysis
see with cystic fibrosis, bronchial obstruction, poor ciliary motility, Kartagener's snydrome aspergillosis |
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restrictive lung disease
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restricted lung expansion decreases lung volume
decreased FVC and TLC FEV1/FVC > 80% type 1: poor breathing mechanism type 2: interstitial lung disease (ARDS, neonatal respiratory distress syndrome, and others) |
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interstitial lung disease types
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Acute respiratory distress syndrome
neonatal respiratory distress syndrome pneumoconioses (coal miner's lung, silicosis, asbestose) sarcoidosis idiopathic pulmonary fibrosis (repeated lung damage -> collagen) goodpasture's syndrome wergener's granulomatosis eosinophlic granuloma (histiocytosis X) drug tox |
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coal miner's lung
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pneumoconioses
results in cor pulmonale, caplan's syndrome upper lobes effected |
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ilicosis
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foundries, sandblasting, mines
macrophages release fibrogenic factors in response to silica -> fibrosis increased TB susceptability by damage to macrophage upper lobes affected see eggshell calcification of hilar lymph nodes |
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asbestosis
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shipbuilding, roofing, plumbing
ivory white calcified pleural plaques increased risk of bronchogenic carcinoma and mesothelioma asbestos bodies - golden brown fusiform rod shaped like dumbells in macrophages |
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neonatal respiratory distress syndrome
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surfactant deficiency -> increased surface tension and alveolar collapse
surfactant is produced by type II pneumocytes after 35th week gestation maternal diabetes and c-section delivery (reduced release of fetal glucocorticoids) test with lethicin-to-sphingomyelin ratio <1.5 low O2 tension increases risk of PDA giving O2 risks retinopathy of prematurity treatment: give mom steroids before birth, artificial surfactant after birth, thyroxine |
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acute respiratory distress syndrome
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diffuse alverolar damage -> increased alveolar capillary perm -> protein leaks in to alveoli
see intra-alveolar hyaline membrane many causes - most through neutrophil secretions damage, activation of coagulation cascade, or free radicals |
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restrictive vs obstructive lung disease
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both have decreased FEV1 and FVC
obstructive FEV1 is more dramatically reduced, thus a lower FEV1/FVC ratio (less than 80%) obstructive lung disease has increased lung volume (inc TLC, FRC, RV) ________ restrictive lung disease FEV1/FVC > 80%, decreased TLC |
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sleep apnea
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stop breathing for at least 10 seconds during sleep
central sleep apnea - no respiratory effort obstructive - effort against a airway obstruction obesity, loud snoring, systemic pulm htn, arrhythmia, sudden death treat with CPAP, weight loss, surgery |
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bronchial obstruction physical findings
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lack breath sounds over affected area
dec resonance and fremitus tracheal deviation to side of lesion |
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pleural effusion physical findings
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decreased breath sounds over site of effusion
dull resonance decreased fremitis |
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pneumonia physical findings
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still can have breath sounds over lesion
dull resonance increased fremitis |
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tension pneumothorax
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decreased breath sounds
hyperresonance absent fremitis tracheal deviation away from lesion |
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lung cancer complications
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SPHERE
Superior Vena Cava syndrome Pancoat's tumor Horner's Syndrome Endocrine (paraneoplastic) Recurrent laryngeal symptoms Effusion (pericardial, pleural) |
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presentation of metastases to lung vs primary cancer in lung
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metastasis is most common - presents with dyspnea
primary cancer - presents with cough look for "coin" lesion on x-ray |
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squamous cell carcinoma of lung
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linked to smoking
centrally located - mass arising from bronchus look for keratin pearls and intracellular bridges parathyroid like activity |
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adenocarcinoma of lung
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bronchial or bronchioalveolar - peripherally located
most common lung cancer in nonsmokers develops in site of prior injury can result in hypertrophic osteoarthropathy arise from/look like clara cells or type II pneumocytes |
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small cell (oat cell) carcinoma
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undifferentiated, centrally located - very aggressive
arise from enterochromafin cells (kulchitski cell) -> small dark blue cells ectopic production of ACTH or ADH lambert eton associated treat with chemo, surgery doesnt work |
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large cell carcinoma
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undifferentiated, peripherally located
pleomorphic giant cell with leukocyte fragments treat with surgery, chemo doesnt work |
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mesothelioma
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malignancy associated with asbestos
see pleural thickening and hemorrhagic pleural effusion psammoma bodies |
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carcinoid tumor of lung
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secretes serotonin - carcinoid syndrome (flushing, wheezing, diarrhea)
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pancoast tumor
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carcinoma that occurs in apex of lung and may affect sympathetic plexus -> horner's syndrome
ptosis, anhidrosis, ptosis (horny PAM) |
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lobar pneumonia
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pnemococcus most frequent, Klebsiella possible
see intra-alveolar exudate -> consolidation, may involve entire lung |
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bronchopneumonia
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s. aureus, H. influenza, Klebsiella, S. pyogenes
acute inflam infiltrate into adjacent alveoli - patchy distribution in more than 1 lobe |
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interstitial pneumonia
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viruses (RSV, adenovirus), mycoplasma, legionella, chlamydia
diffuse patchy inflam in interstitial areas multiple lobe involvement more indolent |
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lung abscess
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localized collection of pus in parenchyma - due to bronchial obstruction or aspiration
often S. aureus or anarobes |
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pleural effusion - 3 types
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transudate - low protein content due to CHF, nephrotic syndrome, hepatic cirrhosis
exudate - high protein content, cloudy, due to malignancy, pneumonia, collagen vascular disease, trauma lymphatic - milky fluid with high triglicerides |