Pulm Flashcards

1
Q

CP of obesity hypoventilation syndrome (OHS)

A
  • chronic fatigue
  • dyspnea
  • difficulty concentrating
  • INC partial pressure of CO2 (PaCO2)
  • setting of obesity
  • nml alveolar to arterial gradient
    • along w/: neuromuscular d/o and high altitude (low inspired fraction of oxygen)
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2
Q

OSA vs. OHS vs. narcolepsy

A
  • OSA:
    • PP: relaxed pharyngeal mu=AW closure
    • CP: loud snoring with periods of apnea
    • s/s:
      • daytime somnolence, non-restorative sleep w/ freq awakenings, morning HA, affective and cognitive s/s
    • sequelae: systemic HTN, pulm HTN+RHF
  • Narcolepsy:
    • poorly regulated REM
    • xs daytime sleepiness
    • cataplexy, sleep attacks, hypnagogic/hypnopompic hallucinations, sleep paralysis
  • OHS:
    • restricted CW expansion d/t severe obesity
    • hypoventilation with chronically elevated PCO2 and reduced PO2
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3
Q

CF vs. Kartagener syndrome (primary ciliary dyskinesia)

A
  • CF:
    • mc GI d/o: pancreatic insufficiency
      • thick, viscous secretions in pancreas lumens=obstruction, inflamm, friboris
      • CP: steatorrhea, FTT, deficiency of fat soluble vitamins
    • can have MISSING VAS DEFERENS=infertility in men
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4
Q

CF of CF

A
  • RESPIRATORY
    • obstructive lung dz–>bronchiectasis
    • recurrent pneumonia
    • chronic rhinosinusitis
  • GI
    • obstruction
      • meconium ileus
      • distal intestinal obstruction syndrome
    • pancreatic dz
      • exocrine pancreatic insufficiency
      • CF-related diabetes
    • biliary cirrhosis
  • REPRO
    • infertility…MISSING VAS DEFERENS
  • MUSCULOSKELETAL
    • osteopenia–>fractures
    • kyphoscoliosis
    • digital clubbing
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5
Q

pulm hemorrhage syndromes termed

A
  • who are they??:
    • anti-GBM Ab dz
    • vasculitis-associated hemorrhage
    • idiopathic pulmonary hemosiderosis
  • what do we see??
    • focal. necrosis. of. alveolar walls. with associated. intra-alveolar. hemorrhage
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6
Q

neutrophil-RICH alveolar EX-udate termed

A

early histologic manifestation of acute bacterial or aspiration pneumonia

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7
Q

mono-nuclear interstitial pulmonary infiltrates termed

A

early in the course of a variety of interstitial lung diseases

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8
Q

fat embolism triad

A
  • setting: pt with severe long bone and/or pelvic fractures
  • acute-onset euro abnormalities
  • hypoxemia
  • petechial rash
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9
Q

pulm embolism

A
  • CP: (sudden onset) tachnypnea, tachycardia, cough, PLEURITIC CHEST PAIN
  • pts at risk: hospitalized and postop (**ortho)
    • RF: immobilization causes venous stasis
    • RF: recent sx causes inflamm which induces a hypercoaguable state
  • hypoxemia (low PaO2) develops in pts with PE d/t ventilation/perfusion
  • thrombi originate in deep veins of pelvis and lower extremities before embolizing to lungs
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10
Q

ship between thrombotic occlusion and V/Q

A
  • thrombotic occlusion of pulm circulation leads to INC blood flow to remainder of the lung=V/Q mismatch
  • ischemic injury causes inflamm=surfactant deficiency and atelectasis in surrounding lung regions
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11
Q

what are the main causes of INC A-a gradient hypoxemia (DEC PaO2)

A
  • V/Q mismatch (pulm embolism)
  • diffusion impairment (less common, occurs in pts with end-stage interstitial lung dzL pulm fibrosis, hyaline membrane dz)
  • R-to-L shunt (high vol of deoxy blood traverses poorly ventilated lung regions)
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12
Q

atelectasis chest xray

A
  • atelectasis=diminished air vol in pt of the lung
    • most commonly d/t obstruction of corresponding bronchus or bronchiole
  • chest xray: opacification (collapse) of corresponding lobe/lobule
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13
Q

decompensated LV failure CXR

A
  • cardiomegaly (heart > 1 hemi-thorax in size)
  • pulm edema
  • pleural effusion
  • enlarged pulm vessels
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14
Q

COPD CXR

A
  • lung HYPER-inflation w/ diaphragmatic flattening
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15
Q

pulm HTN CXR

A
  • enlargement of pulm arteries (circular blobs on left and right) and RV
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16
Q

pulm fibrosis CXR

A
  • CP: gradually progressive dyspnea and bilat reticulonodular opacities
  • PFT: restrictive pattern
  • lung bx: patchy interstitial lymphocytic inflamm and fibrosis of the alveolar walls
17
Q

Cheyne-Stokes vs. Kussmaul breathing

A
  • CS: cyclic breathing
    • apnea followed by gradually INC then DEC total volumes until next apneic period
    • seen in setting of advanced CHF
  • Kussmau: deep and labored pattern
    • assoc with severe metabolic acidosis (espec DKA**)
      • also dt: uremia, sepsis, salicylates, methanol, aldehydes, LA
  • in obstructive sleep apnea breathing there is thoracic/abdo mvmt but intersperesed absence of airflow
18
Q

ABPA (allergic bronchopulmonary aspergillosis)

A
  • who? pts with asthma or CF
  • CP: recurrent asthma exacerbations
    • also: fever, maliase, expectoration of brown mucus plugs
  • CXR: infiltrates or evidence of proximal bronchiectasis
19
Q

HOT cheese up front..jk HOT T-BONE st..EAK

A
  • IL1: fever (HOT)
  • IL2: stimulates T cells
  • IL3: stimulates BONE marrow
  • IL4: stimulates IgE production
  • IL5: stimulates IgA production
  • IL6: stimulated aKute-phase protein production and fever

also: IL-8=major chemotactic factor for neutrophils