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72 Cards in this Set

  • Front
  • Back
Conducting zone of respiratory tree
From nose to terminal bronchioles
Anatomic dead space is equal to
Conducting zone of respiratory tree (from nose to terminal bronchioles)
Cartilage and goblet cells are found in conducting zone until which level?
End of bronchi
Pseudostratified ciliated columnar cells, smooth muscle cells extend to which level of conducting zone?
Terminal bronchioles
Respiratory zone consists of
Respiratory bronchioles, alveolar ducts, alveoli
Epithelial cell type in respiratory bronchioles
Cuboidal cells
Type I pneumocytes function
Squamous cells lining alveoli: gas exchange
Type II pneumocytes function
Secrete pulmonary surfactant to prevent atelectasis
Precursor to type I cells
Proliferate during lung damage
Clara cells function
Secretes surfactant component, degrades toxins, acts as reserve cells
Collapsing pressure formula
P = 2(surface tension)/radium
Law of Laplace
Alveoli tend to collapse with expiration as radius decreases
Components of surfactant
Lecithins - dipalmitoylphosphatidylcholine
When does surfactant synthesis begin in fetus?
Week 26; mature levels reached at week 35
Lung gross anatomy
Right lung: 3 lobes
Left lung: 2 Lobes + Lingula
Relation of pulmonary artery to bronchus in R and L hilus
RALS
R: artery anterior to hilus
L: artery superior to hilus
Structures passing through diaphragm at T8, T10, T12
T8: IVC
T10: esophagus, vagus
T12: aorta, thoracic duct, azygos vein
Nerve innervating diaphragm
Phrenic - C3, C4, C5
Location of diaphragmatic referred pain
Shoulder (C5), trapezius ridge (C3, 4)
Forced inspiration: which muscles are used
External intercostals, scalene muscles, sternocleidomastoid
Forced expiration: which muscles are used
Rectus abdominis, internal and external obliques, transversus abdominis, internal intercostals
Inspiratory reserve volume
Air that can be breathed in after normal inspiration
Tidal volume: typical amount
500 mL
Expiratory reserve volume
Air that can be breathed out following normal expiration
Residual volume
Air that is remaining in lungs after maximal expiration
*Cannot be measured on spirometry*
Inspiratory capacity
Tidal volume + Inspiratory reserve volume
Functional residual capacity
Volume of air in lungs after normal expiration
Vital capacity
TV + IRV + ERV; maximal amount of air expired after maximal inspiration
Total lung capacity - amount
6L
Largest contributor of functional dead space in lung
Apex
Lung & chest wall elastic tendencies
Lung: collapse inward
Chest wall: expand outwards
Lung-chest wall system pressure at FRC
Atmospheric; tendencies of lung and chest wall are balanced
Lung compliance is decreased in which conditions?
Pulmonary fibrosis, pneumonia, pulmonary edema
Lung compliance increased in which conditions?
Emphysema, normal aging
HbA subunits
2a2b
HbF subunits
2a2y
Methemoglobin
Oxidized form of Hb (ferric) with increased cyanide affinity
Treatment of methemoglobinemia
Methylene blue
Drug that forms methemoglobin
Nitrites
Carboxyhemoglobin
Hb-CO: decrease in O2 binding capacity, decreased O2 unloading in tissues
Factors causing right shift in O2-Hb curve
CADET:
CO2
Altitude/Acid
2,3-DPG
Exercise
Temperature
Partial pressure of O2 at which Hb is 50% saturated
26 mmHg
Decrease in PAO2 causes what change in pulmonary vessels?
Hypoxic vasoCONSTRICTION
Diffusion equation
Vgas = Area/Thickness x Dk(P1-P2)
Dk(P1-P2) = pressure difference
Perfusion limited circulation - when does gas equilibrate?
Early along length of pulm capillary (normal health)
Diffusion limited circulation seen in which conditions?
Emphysema, fibrosis
Normal pulmonary artery pressure
10-14 mmHg
Pulmonary HTN value
> 25 mmHg
Pulmonary HTN histological changes
Arteriosclerosis, medial hypertrophy, intimal fibrosis of pulm arteries
Cause of primary pulmonary HTN
BMPR2 gene mutation - loss of inhibition of vascular smooth muscle proliferation
Cause of secondary pulmonary HTN
COPD, mitral stenosis, recurrent thromboemboli, autoimmune disease, left-to-right shunt, sleep apnea, high altitude
Pulmonary vascular resistance formulas
PVR = [ P(pulm artery) - P (L atrium)] / CO
PVR = [Qx8nl]/[COx3.14r^4]
O2 content of blood calculation
O2 content = (O2 binding capacity x % sat) + dissolved O2
How much O2 is bound to 1 g Hb?
1 g Hb = 1.34 mL O2
Normal Hb amount in blood
15 g/dL
O2 binding capacity of blood
20.1 mL O2/dL
When does cyanosis result in relation to amount of deoxyHb?
When deoxygenated Hb > 5 g/dL
Oxygen delivery to blood calculation
O2 delivery = CO x O2 content of blood
Alveolar gas equation
PAO2 = PIO2 - [PaCO2/R]
which is equal to
PAO2 = 150 - PaCO2/0.8
Normal A-a oxygen gradient
= PAO2 - PaO2 = 10-15 mmHg
Hypoxemia, hypoxia, ischemia definitions
Hypoxemia: Decrease in PaO2 (arterial)
Hypoxia: decreased O2 delivery
Ischemia: loss of blood flow
Hypoxemia causes if A-a gradient is normal
High altitude
Hypoventilation
Hypoxemia causes if A-a gradient is increased
V/Q mismatch
Diffusion limited
R --> L shunts
Hypoxia causes
Decreased CO
Hypoxemia
Anemia
CO poisoning
V/Q values at apex vs. lung base
Apex: V/Q = 3 (more ventilation than perfusion)
Lung base: V/Q = 0.6 (more perfusion than ventilation)
Ventilation and perfusion at apex vs. lung base
More ventilation and perfusion take place in lung base than in apex
V/Q = 0 indicates what?
No ventilation (ie. airway obstruction)
V/Q = infinity indicates what?
No perfusion (eg. pulm embolus); physiological dead space
Carbaminohemoglobin
HbCO2 - CO2 bound to N terminus of globin, favours O2 unloading
Haldane effect + location of activity
Oxygenated Hb --> H+ dissociation from Hb --> favours CO2 release from RBCs; lungs
Bohr effect + location of activity
Increased H+ from tissues --> unloading of O2 from Hb; periphery
Physiological response to high altitudes
Hyperventilation
Increase in - EPO (rise in Hct, Hb), 2,3-DPG
Increase renal HCO3- excretion (compensate for respiratory alkalosis)
Hypoxic vasoconstriction
Physiological response to exercise
Hyperventilation
Uniform V/Q ration in all lung fields
Decrease in pH, increase in 2,3-DPG
NO changes in PaO2 and PaCO2