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199 Cards in this Set
- Front
- Back
2 functional parts of respiratory tree
|
conducting zone
respiratory zone |
|
conducting zone is ___
respiratory zone does ___ |
dead space
gas exchange |
|
3 parts of respiratory zone
|
respiratory bronchioles
alveolar ducts alveoli |
|
___ cells comprise 97% of alveolar surface
they are ___ (shape) the remainder is ___ cells |
type I pneumocyte
thin type II pneumocyte |
|
type II pneumocytes do ___ (2)
they are ___ (shape) and have ___ |
surfactant secretion
differentiate to type I cells cuboidal lamellar bodies |
|
___ is an index of fetal lung maturity
|
lecithin:sphingomyelin ratio
|
|
lecithin:sphingomyelin ratio of ___ indicates mature lungs
|
>2
|
|
bronchopulmonary segment has ___ (3) in center and ___ (2) peripherally
|
3' (segmental) bronchus
bronchial a. pulmonary a. veins lymphatics |
|
R lung has ___ lobes
L lung has ___ lobes |
3
2 + lingula |
|
lobe missing on L
|
middle
|
|
a peanut aspirated while standing lands in ___
|
lower R inferior lobe
|
|
a peanut aspirated while supine lands in ___
|
upper R inferior lobe
|
|
pulmonary a. is ___ with respect to R main bronchus,
and ___ with respect to L main bronchus |
anterior
superior |
|
inferior pleural border at midclavicular line
|
7th rib
|
|
inferior pleural border at midaxillary line
|
10th rib
|
|
inferior pleural border at paravertebral line
|
12th rib
|
|
for paracentesis, puncture ___ with respect to inferior pleural border
|
up to 2 ribs above
|
|
3 diaphragmatic hiatuses from superior to inferior
|
IVC
esophageal aortic |
|
superior hiatus is ___
inferior hiatus is ___ |
anterior
posterior (the 3 structures pierce the diaphragm on its posterior aspect, so more posterior = lower) |
|
IVC hiatus is at level ___
|
T8
|
|
esophageal hiatus is at level ___
|
T10
|
|
aortic hiatus is at level ___
|
T12
|
|
___ (2) go through the esophageal hiatus
|
esophagus
vagus |
|
___ (3) go through the aortic hiatus
|
aorta
thoracic duct azygos vein |
|
muscles driving inspiration at rest
muscles driving expiration at rest |
diaphragm
none |
|
3 muscles driving inspiration during exercise
|
external intercostal
scalene SCM |
|
5 muscles driving expiration during exercise
|
internal intercostal
rectus abdominis internal oblique external oblique transversus abdominis |
|
laplace's law
|
P = 2T/R
where P=collapsing pressure T=wall tension R=radius |
|
4 basic lung volumes
|
RV (residual)
ERV (expiratory reserve) V_T (tidal) IRV (inspiratory reserve) |
|
FRC is sum of ___
it is ___ |
RV
ERV volume of air in lungs after normal expirium |
|
IC is sum of ___
it is ___ |
V_T
IRV total volume which could be inspired after normal expirium |
|
VC is sum of ___
it is ___ |
ERV
V_T IRV total volume which can be inspired after maximal expirium |
|
TLC is sum of ___
it is ___ |
VC
RV total voluime of air which can be contained in lungs |
|
physiologic dead space in terms of V_T
|
V_D = V_T x (P_aCO2 - P_eCO2)/P_aCO2
where P_aCO2 = aterial P_CO2 P_eCO2 = expired P_CO2 |
|
figure showing compliance plots of chest well and lungs gives ___
this is located at ___ |
FRC
y value for which sum of lungs and chest wall pressures equals 0 |
|
2 Hb conformations
|
T (taut)
R (relaxed) |
|
Hb in T conformation has high/low O2 affinity
this is favored by low/high body temp |
low
high |
|
4 chemicals which increase probability of T conformation
|
Cl-
H+ CO2 2,3-BPG |
|
fetal Hb has high O2 affinity because ___
|
it has low 2,3-BPG affinity
|
|
met-Hb has low affnity for ___ but
high affinity for ___ |
O2
CN- |
|
met-Hb is desirable in setting of ___
it is generated by ___ing |
CN- poisoning
giving nitrites |
|
CN-met-Hb complex is bound by ___
this is cleared by ___ |
thiosulfate
kidneys |
|
CO poisoning does ___ (2) to Hb
|
left shift O2 binding curve (less unloading)
down-shift O2 binding curve (lower affinity) |
|
3 gases with perfusion limited pulmonary exchange
|
O2 (normally)
CO2 N2O |
|
2 gases with diffusion limited pulmonary exchange
|
O2 (pathological)
CO |
|
diffusion (V_gas) in terms of surface area
|
V_gas = A/T x D_k(P_1 - P_2)
where A=surface area, T = interface thickness |
|
2 situations in which O2 exchange is diffusion limited
|
emphysema
fibrosis |
|
diffusion disruption in emphysema
|
low A
|
|
diffusion disruption in fibrosis
|
high T
|
|
normal pulmonary a. pressure
pulm HTN is ___ at rest or ___ during exercise |
10--14
>25 >35 |
|
gene linked to 1' pulmonary HTN
|
BMPR2
|
|
BMPR2 does ___
|
inhibits vascular smooth muscle proliferation
|
|
3 cardiovascular causes of pulmonary HTN
3 pulmonary causes of pulmonary HTN 1 systemic cause of pulmonary HTN |
mitral stenosis
recurrent emboli L -> R shunt OSA COPD high altitude living collagen vascular disease |
|
COPD causes pulmonary HTN via ___
|
parenchymal destruction
|
|
OSA casues pulmonary HTN via ___
|
hypoxic vasoconstriction
|
|
CVD causes pulmonary HTN via ___ which causes ___
|
intimal fibrosis
medial hypertrophy |
|
ohm's law expression for pulmonary vascular resistance (PVR)
|
PVR = (P_PA - P_LA)/CO
where P_PA = pulmonary a. pressure P_LA = L atrial pressure |
|
2 parts of blood O2 content
|
Hb bound
dissolved |
|
Hb-bound O2 is determined by ___ (2)
|
binding capacity
% saturation |
|
normal binding capacity is determined by ___ (2)
|
Hb binding capacity (constant)
Hb quantity |
|
Hb O2 binding capacity
|
1.34 mL/g
|
|
normal Hb quantity in blood
|
15 g/dL
|
|
in anemia,
O2 content does ___ Hb does ___ arterial PO2 does ___ O2 sat does ___ |
falls
falls stays same stays same |
|
alveolar gas equation
|
P_AO2 = P_IO2 - P_ACO2/R
where P_AO2 is alveolar P_O2 P_IO2 is inspired P_O2 P_ACO2 is alveolar P_CO2 R is ratio of CO2 produced per O2 consumed (.8) |
|
normal approximation for alveolar gas equation
|
P_AO2 = 150 - P_ACO2/0.8
|
|
normal A-a gradient
|
10--15 mm Hg
|
|
3 kinds of oxygen deprivation problems
|
hypoxemia
hypoxia ischemia |
|
hypoxemia means ___
hypoxia means ___ ischemia means ___ |
low P_aO2
low O2 delivery to tissues low blood flow to tissues |
|
2 kinds of causes of hypoxemia
|
high A-a gradient
normal A-a gradient |
|
3 causes of hypoxemia with high A-a gradient
|
V/Q mismatch
Diffusion limitation R-L shunt (VDRL) |
|
2 causes of hypoxemia with normal A-a gradient
|
high altitude
hypoventilation |
|
5 causes of hypoxia
|
hypoxemia
ischemia anemia CO poisoning CN poisoning |
|
V/Q ratio at apex of lung
V/Q ratio at base of lung |
3
0.6 |
|
V/Q -> 0 means ___ is present
100% O2 does/doesn't help |
airway obstruction (shunt)
doesn't |
|
V/Q -> infinity means ___ is present
100% O2 does/doesn't help |
perfusion defect present
does |
|
3 ways CO2 is transported in blood
|
as HCO3-
bound to Hb dissolved CO2 |
|
HCO3- accounts for ___% of CO2 in blood
|
90
|
|
CO2 binds to ___ of Hb
___% of CO2 in blood is Hb bound |
N terminus
5 |
|
in lungs ___ does ___ to H+ affinity for Hb
this causes the rxn ___ which causes the rxn ___ the overall effect is ___ |
high O2
lowers H+ + bicarb -> H2CO3 H2CO3 -> CO2 + H2O (CA) high O2 in lungs causes CO2 unloading |
|
in tissue, ___ does ___ to O2 affinity for Hb
the overall effect is ___ |
high H+
lowers high H+ causes O2 unloading at tissues |
|
in exercise,
___ happens to V/Q ratio ___ happens to P_aO2 ___ happens to P_aCO2 ___ happens to venous P_CO2 |
becomes more uniform
no change no change increase |
|
2 causes of fat emboli
|
long bone fx
liposuction |
|
amniotic fluid embolism causes ___
|
DIC
|
|
2 diseases comprising COPD
|
emphysema
bronchitis |
|
classical emphysema patient is a ___
with ___ |
pink puffer
barrell chest |
|
___ is increased in emphysema
to prevent ___, pts exhale ___ly |
lung compliance
airway collapse through pursed lips |
|
2 kinds of emphysema
|
centriacinar
panacinar |
|
centriacinar emphysema is characteristic of ___
|
smokers
|
|
panacinar emphysema is characteristic of ___ (2)
|
a1 antitrypsin deficiency
cirrhosis |
|
hyperactive enzyme in emphysema
|
elastase
|
|
classical patient in chronic bronchitis
|
blue bloater
|
|
histopath derangement in chronic bronchitis
|
reid index > 0.5
|
|
reid index measures ratio of ___ to ___
|
mucosal thickness
total bronchial wall thickness |
|
chronic bronchitis definition
|
productive cough for > 3 m for >= 2 y
|
|
chronic bronchitis is a disease of large/small airways
|
small
|
|
2 histopath findings in asthma
|
Charcot-Leyden crystals
Curschmann's spirals |
|
Charcot-Leyden crystals mean ___ is present
Curschmann's spirals are ___ |
eosinophilia
shed epithelium |
|
in obstructive disease,
FEV1 is ___ FVC is ___ and FEV1/FVC is ___ (normal FEV1/FVC is ___) |
very low
low low 80% |
|
in restrictive disease,
FEV1 is ___ FVC is ___ FEV1/FVC is ___ |
low
low >80% |
|
test for asthma
|
methacholine challenge
|
|
in methacholine challenge test, drop of ___ in ___ is diagnostic
|
20%
FEV1 |
|
eosinophils have ___ nucleus
|
bilobed
|
|
size of particles which reach terminal airways
these particles can cause ___ |
1-5 uM
pneumoconioses |
|
coal miner's pneumoconiosis causes ___ (2)
|
cor pulmonale
Caplan's syndrome |
|
Caplan's syndrome has ___ (2)
|
pneumoconiosis
RA |
|
immune problem in silicosis
this may increase suscpeptibility for ___ |
defective MQs
TB |
|
CXR finding in silicosis
|
hilar eggshell calcification
|
|
histopath finding in silicosis
|
birefringent particles surrounded by fibrosis
|
|
CXR finding in asbestosis
|
normally NO hilar adenopathy
|
|
2 CXR findings in beryliosis
|
irregular opacities
hilar adenopathy possible |
|
histopath finding in beryliosis
|
noncaseating granuloma
|
|
CXR finding in organic dust pneumonitis
|
diffuse nodular infiltrates
|
|
CXR finding in lung abscess
|
AF level
|
|
3 causes of lung abscess
|
aspiration
bacterial pneumonia septicemia |
|
lecithin-sphingomyelin ratio commonly falls below ___ in NRDS
|
1.5
|
|
low P_aO2 in NRDS can cause ___,
but giving supplemental O2 can cause ___ |
PDA
retinopathy of prematurity |
|
3 RFs for NRDS
|
prematurity
maternal DM caesarian section |
|
NRDS prophylaxis
|
materal CS
|
|
NRDS tx (2)
|
artificial surfactant
T4 |
|
3 triggers for ARDS
|
neutrophilic toxins
activation of coagulation cascade ROS |
|
3 physical exam parameters for lung problems
___ (2) vary together |
breath sounds
fremitus percussion resonance breath sounds fremitus |
|
consolidation as in ___ has ___ breath sounds and fremitus,
and ___ percussion resonance |
pneumonia
louder reduced |
|
pleural effusion has ___ breath sounds and fremitus,
and ___ percussion resonance another pathology with these findings is ___ |
reduced
dull tumor |
|
atelectasis has ___ breath sounds and fremitus,
and ___ percussion resonance another finding is ___ |
reduced
dull tracheal deviation towards lesion |
|
emphysema has ___ breath sounds and fremitus,
and ___ percussion resonance another pathology with these findings is ___ |
reduced
increased bronchiectasis |
|
tension pneumothorax has ___ breath sounds and fremitus,
and ___ percussion resonance another finding is ___ |
reduced
increased (hyperresonant) tracheal deviation away from lesion |
|
lung cancer is the ___th cause of cancer death
|
1
|
|
mets from lung ca commonly go to ___ (4)
|
adrenals
brain bone liver |
|
2 centrally located lung cancers
|
SCC
SCLC |
|
histopath finding in lung SCC
|
keratin pearls
|
|
electrolyte disturbance associated with lung SCC
|
hypercalcemia
|
|
SCLC is derived from ___ cells
these are located at ___ |
neuroendocrine Kulchitsky
basal layer of bronchial epithelium |
|
4 markers for SCLC cells
|
S100
neuron specific enolase synaptophysin chromogranin |
|
tx for SCLC (2)
|
chemo
rads |
|
3 conditions associated with SCLC
|
ectopic ADH
ectopic ACTH Lambert-Eaton |
|
2 peripherally located lung cancers
|
adenoca
large cell |
|
2 kinds of adenoca
|
bronchial
bronchoalveolar |
|
bronchoalveolar ca develops from ___ cells
|
type II pneumocytes
|
|
malignant bronchoalveolar ca cells don't ___
|
invade stroma
|
|
lung adenoca usually happens at ___
|
site of previous inflammation or injury
|
|
lung adenoca is the most common ____ (2)
|
NSCLC
lung cancer in non-smokers |
|
adenoca appears as single/multiple density on CXR
|
multiple
|
|
skeletal abnormality in adenoca
|
clubbing
|
|
large cell lung ca has ___ histology
tx is ___ prognosis is ___ |
anaplastic
surgery poor |
|
2 endocrine problems in large cell lung ca
|
gynecomastia
galactorrhea |
|
mesothelioma is the ___th most common cancer associated with asbestos
|
2
(bronchogenic lung ca is #1) |
|
2 pneumonia types associated with bacterial pneumonia
|
lobar
bronchopneumonia |
|
lobar pneumonia is mostly caused by ___ (2)
|
S. pneumoniae
Klebsiella |
|
bronchopneumonia is caused by ___ (4)
|
S. pyogenes
H. influenzae Klebsiella SA (SHiKSA) |
|
2 kinds of H1 blockers
|
first generation
2nd generation |
|
2nd generation H1 blockers end in ___ or are called ___
they have less ___ (2) SEs because of ___ |
adine
cetirizine antimuscarinic sedating lower CNS penetration |
|
2 beta_2 agonists for asthma
|
albuterol
salmetrol |
|
albuterol is used for ___
salmetrol is used for ___ |
acute attacks
chronic managment |
|
___s are nonselective PDEIs used in asthma
___ is the main example use is limited because of ___ (2) |
methylxanthine
theophylline cardiotoxicity neurotoxicity |
|
theophylline is metabolized by ___
|
CYP
|
|
3 cardiovascular SEs of theophylline
|
inotropism
chronotropism pressor |
|
3 kinds of complaints in theophylline toxicity
|
GI
arrhythmia seizure |
|
3 GI complaints in theophylline toxicity
|
abdominal pain
diarrhea vomiting |
|
theophylline toxicity tx
|
beta blocker
|
|
theophylline causes bronchodilation by ___ing (2)
|
potentiating cAMP dilator effect (PDEI)
blocking constrictor effect of adenosine |
|
2 phases of asthma attack
|
bronchoconstriction (early)
inflammation (late) |
|
3 drugs families which work on early asthma phase
|
beta agonists
antimuscarinics theophylline |
|
1 drug family which works on late asthma phase
|
CS
|
|
LTs do ___ (2) in asthma
|
bronchoconstriction
chemotaxis |
|
___ LTs aka ___ do bronchoconstriction
|
cysteinyl
LTC4/D4/E4 |
|
___ LTs do chemotaxis
|
LTB4
|
|
___ is a drug which inhibits LT synthesis by inhibiting ___
|
zileuton
5-lipoxygenase |
|
2 drugs which block LT receptor
they are particularly good for ___ |
zafirlukast
motelukast aspirin-induced asthma |
|
what type of cell lines respiratory tree?
|
pseudostratified ciliated columnar cells (to respiratory bronchioles)
|
|
what type of cells line alveoli?
|
type I pneumocytes (97% of surface area); squamous
|
|
stem cells of pneumocytes?
|
type II pneumocytes
|
|
chemical name of surfactant?
|
dipalmitoyl phosphatidylcholine
|
|
nonciliated columnar cells that degrade toxins in alvioli?
|
Clara cells
|
|
five compounds secreted by lung?
|
Surfactant, prostaglandins, histamine, angiotensis-converting enzyme, kallikrein (activates bradykinen)
|
|
what causes cyanosis?
|
more than 5 g/dL of deoxygenated Hb
|
|
where is V/Q normally >1?
|
at apex of lungs (wasted ventilation)
|
|
where is V/Q normally <1?
|
at base of lungs (wasted perfusion)
|
|
why is reactivation TB typically found in apices of lungs?
|
thrives in high O2 found at apex (due to V/Q > 1)
|
|
imaging test of choice for PE?
|
CT angiography
|
|
Virchow's triad?
|
1. Stasis, hypercoagubility, endothelial damage
|
|
Homan's sign?
|
pain in calf with dorsiflexion of foot (sign of DVT)
|
|
what type of emphysema causes spontaneous pneumothorax in young, healthy males?
|
paraseptal emphysema (associated with bullae)
|
|
what meds cause restrictive long disease?
|
bleomycin, busulfan, amiodarone
|
|
ivory white calcified pleural plaques?
|
asbestosis
|
|
golden-brown dumbbell shaped rods inside macrophages in lungs?
|
asbestos bodies
|
|
at what point in gestation is surfactant produced?
|
mostly after 35th week
|
|
what are risk factors for neonatal respiratory distress syndrome?
|
prematurity, maternal diabetes, cesarean delivery
|
|
mechanism of ARDS?
|
diffuse alveolar damage causes increased capillary permeability and protein-rich leakage into alveoli. Results in formation of intra-laveolar hyaline membrane
|
|
"coin" lesion on chest x-ray?
|
lung cancer
|
|
where in lung does squamous cell carcinoma occur?
|
central (hilar mass)
|
|
in what type of lung cancer do Clara cells differentiate into type II pneumocytes?
|
adenocarcinoma
|
|
Lambert-Eaton syndrome?
|
autoantibodies against neuromuscular junction calcium channels produced by lung small cell carcinoma; results in decreased ACh being released
|
|
lung cancer with Psammoma bodies in histology?
|
mesothelioma
|
|
types of lung cancer most likely causing Pancoast's tumor?
|
squamous cell or small cell carcinomas (peripherally located)
|
|
most common causes of interstitial (atypical) pneumonias?
|
Viruses (RSV, adenoviruses), Mycoplasma, Legionella, Chlamydia
|
|
Most common organisms causing lung abscesses?
|
S. aureus, anaerobes
|
|
mechanism of infertility associated with cystic fibrosis?
|
congenital absence of vas deferens
|
|
what happens to TLC in COPD?
|
increased due to lung hyperinflation
|
|
vitamin abnormality seen in sarcoidosis?
|
elevated vitamin D due to increased conversion from inactive form by macrophage
|