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93 Cards in this Set
- Front
- Back
FEV1/FVC
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nl is 0.8
decr in obstructive dz not decr in restrictive dz |
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Muscles of expiration
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abdominal muscles compress abdominal cavity
push diaphragm up and push air out of lungs internal intercostals: pull ribs dnwd and inwd - ex |
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transmural lung pressure
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alveolar press minus intrapleural press
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hysteresis
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inspiration follows a different curve than expiration.
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compliance of chest wall lung system
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At FRC press in lungs is equal to ATM.
Equal negative transmural press by chest wall versus the positive intramural press by lungs |
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Emphysema and compliance
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lung compliance is incr
thus at the original FRC the tendency for the lung to collapse is much less than that of the chest wall to expand. Thus a higher FRC equilibrium and a barrel chest. |
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Lung fibrosis and compliance
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Compliance is decr thus FRC will decr and chest wall smaller at equilibrium.
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Causes of decr lung compliance
(4) |
Fibrosis
Incr pulm venous press High expanding pressures Lack of surfactant |
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Causes of incr lung compliance
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Emphysema
Age |
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Law of Laplace
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P = 2T/r
T=surface tension |
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Surfactant
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Synth by Type II pneumocytes
DPPC Mature surfactant 2:1 lecithin:sphingomyelin ratio. |
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Lung volumes and airway resistance
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radial traction exerted on the airways by surrounding lung tiss
High lung vol: great traction and lower resistance (asthmatics learn to breath at high lung vol) Lower lung vol: less traction, incr airway resistance. |
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Site of highest airway resistance
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Medium sized bronchi
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Perfusion limited exchange vs diffusion limited exchange
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Perfusion limited: N20 and O2 under nl conditions. gas equilibrates early along the length of the capillary
Diffusion limited exchange: CO2 and O2 during strenuous exercise or lung fibrosis. gas does not equilibrate by the time the blood reaches the end of the pulm cap. diffusion continues as long as the partial pressure gradient is maintained. |
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Adult Hb
Fetal Hb |
Adult - alpha2/beta2
HbF - alpha2/gamma2 - higher O2 affinity because it binds 2,3 dpg less avidly. |
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O2 content
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total amount of O2 in the blood. = O2 binding capacity x % sat + dissolved O2.
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PO2 at 40mmHg (venous blood)
PO2 at 25 mmHg |
PO2 at 40 mmHg - Hb is 75% saturated - 3/4 heme groups on each Hb has O2 bound.
PO2 at 25 mmHg = P50 = Hb is only 50% saturated. |
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Hb dissociation curve shift to the right
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Hb affinity for O2 is decr, P50 increases.
Caused by incr CO2, decr pH, incr in temp (during exercise), incr 3-DPG concentration (which binds deoxy Hb) - it is part of the adaptation to chronic hypoxemia. |
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CO and Hb
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occupied O2 binding sites
decr O2 content of blood Causes a left shift bc of incr affinity for O2 in remaining binding sites. |
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Cloride shift
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90% of CO2 is carried as Bicarb in Hb.
CO2 in tissue diffuses into venous plasma then into RBC In RBC it combines with H20 to form H2CO3 which dissociates via carbonic anhydrase. HCO3- diffuses out of RBC in exchange for Cl and is transported to the lungs in the plasma. H+ remains in the RBC and is buffered by deoxyHb (much better than oxyHb. ) In the lungs: bicarb enters RBC in exchange for Cl. Recombines with H+ to form H2CCO3 -> H2O and CO2 and CO2 is expired. |
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Pulm Circ
press, resistance |
Pressures are much lower in the pulm circ mainly because the resistance is much lower than in the systemic circ.
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Zone 1 pulm blood flow
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alveolar press>arterial press>venous press
Q way decr V decr V/Q incr |
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Zone 2 pulm blood flow
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arterial press>alveolar press>venous press
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Zone 3 pulm blood flow
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arterial press>venous press>alveolar press
Q way incr V incr V/Q decr |
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R->L shunt
L->R shunt |
R->L shunt: tet of fallot -
shunted blood leads to admix of venous blood in arterial blood. Can be estimated by having pt breath 100% O2 and measuring degree of dilution of art blood L->R shunt much more common Do no lead to a decr in art PO2, PO2 will be elevated on the right side. |
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V/Q ratios
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>1.0 at the apex
<0.8 in the base Apex: PO2 is highest and PCO2 is lowest bc gas exchange is more efficient Base: PO2 is lowest and PCO2 is highest bc gas exchange is less efficient. |
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Lung Stretch rec
Irritant Rec J rec Joint and muscle rec |
Hering Breuer Reflex: when stretch rec in smooth muscle of airways is stimulated by distention of the lungs - decr breathing freq
Irritant: btw airway epith cells - stim by noxious subs Juxtacapillary rec: alveolar walls close to caps. Engorgement of pulm caps (LVF) stimulates ->rapid shallow breathing Jt and muscle rec: activated by mvmt of limbs, stim breathing during exercise. |
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V/Q during exercise
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distribution is more even throughout lung during exercise.
->DECREASE IN DEAD SPACE |
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High Altitude adaptations
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hypoxemia ->
hyperventilation -> resp alkalosis (tx with acetazolamide) Incr EPO -> incr O2 capacity and incr O2 content 2,3 DPG incr PULMONARY VASOCONSTRICTION -> RVH |
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When the O2 dissociation curve shifts right
what happens to p50 how about O2 carrying capacity of Hb |
Shifts to the right incr P50
has no effect on carrying capacity of Hb that is determined by Hb CONCENTRATION |
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Changes and non changes during strenuous exercise
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Incr in vent ratematches incr in O2 consumption and CO2 generation - thus mean values for art PO2 and PCO2 do not change
Art pH may change bc of lactic acidosis Venous PCO2 increases |
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Chest tube
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inserted through 5th intercostal space in the anterior axillary line.
Tube penetration: skin->superficial fascia->serratus anterior-> external intercostal->internal intercostal-> innermost intercostal -> parietal pleura. |
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Pleuritis
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visceral pleuritis - no innervation
parietal pleura innervated by intercostal nerves and phrenic C3-C5. Pain may be referred to thoracic wall and root of the neck. |
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Compression of the trachea
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can occur via enlarged thyroid or an aortic arch aneurysm
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Bronchogenic ca
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Adenoca: most common type, peripheral lesions, less ass with smoking
SCC: 2nd most common, strong smoking ass, centrally located lesions, cavitation, may secr PTH Small Oat cell: Kulchitsky cells of neurocrest origin, ACTH secr, ADH secr |
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Intrathoracic spread of bronchogenic ca sequele
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Horners
Superior Vena Caval syndrome Dysphagia Hoarseness Paralysis of diagphragm Pancoast tumor (ulnar nerve pain and horners) |
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Lobar Pneumonia Stages
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Initial stage: acute congestion, intraalveolar fluid, many bacteria
Early Consolidation: Red hepatization, 2-4 days, consolidation with N/T and fibrin. Lung is red from RBC firm and airless. Late Consolidation: Gray hepatization, 4-8 days, large amounts of fibrin with decr red and white cells. Resolution in 8 days. |
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Bronchial Asthma
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extrinsic (type 1 hs) vs intrinsic
Mucus plugs whorl like accumulations of epith cells - curschmann spirals Charcot leyden crystals (crystalloids of eosinophil derived proteins) |
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Chronic Bronchitis
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Productive cough at least 3 consecutive mos over at least 2 consecutive years.
Linked to smoking and can lead to cor pulmonale Hyperplasia of mucus secreting submucosal glands |
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Emphysema subtypes
(4) |
Centrilobular: dilation of resp bronchioles - upper part of lobes
Panacinar: Alpha 1 antitrypsin def, dilation of entire acinus, loss of elasticity Paraseptal: subpleural blebs Irregular: inflamm, irreg involvement of acinus with scarring within walls of enlarged spaces. |
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Emphysema cause
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SMoking - brings in N/T and MP elastase
Alpha1 antritrypsin def: piZ allele - interferes with hepatic secr - liver damage homozygous piZZ allele - greatly decr activity, hepatic cirrhosis |
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Kartageners syndrome
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rare, AR
sinusitis, bronchiectas, situs inversus, male infertility. Problem with Dynein |
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Restrictive lung dz
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Interstitial lung dzs:
ARDS, pneumoconioses, Sarcoid, idiopathic pulm fibrosis, SLE, Scleroderma, wegners, goodpastures, Eosinophillic Granuloma |
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Hyaline membrane dz
cause, pulm maturity Complications |
neonatal resp distress syndrome
def of surfactant Surfactant: lecithin incr in 33rd week and sphingomyelin levels stay the same. 2:1 is pulm maturity. Complications: Bronchopulm dysplasia from ventilation PDA, IVH, necrotizing enterocolitis. |
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Coal workers pneumoconiosis
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Simple: coal macules around bronchioles, MP ingesting coal dust, inconsequeantial
Progressive massive fibrosis: fibrotic nodules, bronchiectasis, pulm HTN, resp failure or RHF |
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Silicosis
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incr risk for TB
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Abestosis
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Diffuse interstitial fibrosis
Ferruginous bodies hyalinized fibrocalcific plaques of parietal pleura Predisposes to BRONCHOGENIC CARCINOMA, and MALIGNANT MESOTHELIOMA |
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Sarcoid
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restrictive lung dz
Intersitial lung dz, enlarged hilar LN, anterior uveitis, erythema nodosum of skin, polyarthritis Polyclonal hypergammaglobinemia hypercalcemia and hypercalciuria Incr serum ACE |
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Idiopathic Pulm fibrosis
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Chronic inflamm and fibrosis of alveolar wall. Begins with alveolitis-> fibrosis-> ends in distored fibrotic lung filled with cystic spaces - HONEYCOMB lung
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Eosinophillic Granuloma
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Interstital lung dz
histiocytic cells, birbeck granules, lung or ribs Grouped with Hand-Schuller-Christian dz and Letterer-Siew synddrome as variants as histiocytosis X sydnrome |
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secondray Pulm HTN
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most often COPD
incr pulm blood flow (L->R shunt) incr resistance (emboli, vasoconstrict from hypoxia) polycythemia |
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Extrapulm TB
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TB meningitis, potts dz, paravertebral abcess, psoas abcess
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Most common lung cancer
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Cancer mets to lung
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bronchogenic Ca
survival |
Smoking
Air pollution Radiation Asbestos + Smoking Exposure to Nickel and Chromates 5yr survival < 10% |
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Chronic Bronchitis
Test? |
COPD
Marked hyperplasia of bronchial and submucosal glands and bronchial smooth muscle hypertrophy. Quantified by Reid index: ratio of glandular thickness to bronchiolar thickness |
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Most common lobar pneumonia
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Strep Pneumonia
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Distinguish btw primary and secondary TB
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cavitation only in 2'
Apical Lung - 2' 1' ghon complex near hilar LN |
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Carcinoid Syndrome
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Typically lung or GI can
Flushing, wheezing, recurrent diarrhea, carcinoid heart dz. Seratonin causing diarrhea |
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PCP
tx and path |
tx with TMP/SMX
Kills type 2 pneumocytes, damages alveolar epith serum leaks |
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Aortic Hiatus
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T12 - aorta, azygous vein, thoracic duct
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Esophageal Hiatus
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T10 - esophagus and Vagus
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Caval Hiatus
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Inferior vena cava - T8
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Bohr Effect
Haldane Effect |
Bohr Effect: incr H+ leads to peripheral O2 unloading
Haldane Effect: oxygenation of Hb in lungs unloads CO2 from Hb. |
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Blue Bloaters
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Chronic bronchitis
hypertrophy of mucus secr glands wheezing, crackles, cyanosis |
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Pink Puffers
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emphysema
dyspnea, decr breath sounds, tachycardia, |
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Treatment for Neonatal ARDS
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maternal steroids before birth
artificial surfactant for infant |
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Most common places for lung cancer mets
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Brain, bone, liver
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Lung Cancer presentation
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Cough, hemoptysis, bronchial obstruction, wheezing, Pneumonic coin lesion on xray.
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Pancoast tumor
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Carcinoma that affects apex of lung - affecting cervical sympathetic plexus -> HORNERS SYNDROME
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Lobar
Bronchopneumonia Interstitial |
Lobar: Intraalveolar exudate, consolidation
S. Pneumococcus Broncho: Acute inflamm infiltrate from bronchioles into adjacent alveoli S. Aureus, H. Flu, Klebsiella, S. Pyogenes Interstitial (atypical):diffuse patchy infiltrate: Mycoplasma, RSV, adenovirus, legionella, chlamydia, coxiella burnetti |
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PGI
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prostacyclin
decr: platelet aggregation vasc tone bronchial tone uterine tone |
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PGE, PGF
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prostaglandins
Incr uterine tone Decr vasc tone + bronchial tone |
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TXA
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thromboxane
incr platelet aggregation incr vasc tone incr bronchial tone |
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1st gen H1 blocker
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Diphenhydramine, dimenhydrinate, chlorpheniramine
Tox - sedation, antimuscarinic, anti-alpha-adrenergic |
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2nd gen H1 block
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Loratadine, fexofenadine, desloratadine
less sedation |
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Bronchial tone
(+) (-) |
Bronchial dilation:
incr cAMP Bronchoconstriction: Ach + Adenosine |
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Most common cause of laryngeal cancer
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SCC
cigarette smoking is the most important risk factor |
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Lymphoepithelioma
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SCC that most freq occurs in the nasopharynx, less commonly in larynx.
Rich in lymphs Common in China and Africa - EBV |
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Sqaumous papilloma
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benign laryngeal neoplasm by HPV 6 +11.
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Old age and lungs
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age leads to higher compliance of lungs. Decr elastic recoil.
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How much can O2 can art blood nl carry?
1gm of Hb 100 ml blood |
1 gm Hb carries 1.34 g O2
100 ml art blood - carries about 20 ml of O2 at nl Hb of 15g/dl. |
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Esophageal Atresia
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post deviation of the tracheoesophageal septum.
Feeding causes fluid to spill into trachea and leads to aspiration pneumonia. |
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Strep Pneumoniae virulence
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Acidic polysacharide capsule. Antibody to specific capsule is necessary for resolution of infection. There are many capsule types.
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Bordet Gengou Augar
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used for isolation of Bordatella Pertussis
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Exudative effusion characteristics
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one or more of the following:
1. pleural fluid protein/serum protein >0.5 2. PLeural fluid LDH /Serum LDH >0.6 3. Pleural fluid LDH more than 2/3 nl upper limit for serum. |
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Alveolar Ventilation eqn
and what happens to Alveolar PCO2 if you hyperventilate x 4 |
VA= VCO2/PACO2
VA = alveolar ventilation VCO2 = CO2 production PACO2 = alveolar PCO2 PACO2 = goes down to 10 mmHG |
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Monoclonal antibody for RSV
|
Palivizumab
directed against the fusion protein of RSV preventing infection |
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Radial traction
restrictive dz vs obstructive |
When lung vol decr radial traction decrs -> airway diameter decr.
In interstitial fibrosis the airways are tethered more strongly to lung parenchyma thus airways held open to a greater extent at each lung vol. -incr radial traction. |
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Morbid obesity and respirations
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peripheral hypoventilation
Pickwickian Syndrome Press of fatty neck causes intermittant airway obstruction. |
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Rx that binds IgE to inhibit mast cell and basophil rxn
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Omalizumab - monoclonal abs
Inhibits binding of IgE to high affinity Fc rec on surface of mast and basophils. Indicated in 12+, moderate to severe persistant asthma Administered subQ every 2-4 wks |
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Incr surfactant
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Thyroxine, prolactin, cortisol
|
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Gestational Diabetes
|
leads to incr insulin production from baby - decrs surfactant
|
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Peripheral hypoventiation causes
vs Central Hypovent |
Fatty neck, submersion, suffocation, skeletal abnl (broken rib), trauma, phrenic nerve paralysis, polio, tetanus
Central Hypoven: barbs, opioids, benzos |