Pulmonology A&P Flashcards

1
Q

What divides the upper and lower respiratory tract?

A

the larynx (below the vocal cords is lower respiratory tract)

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2
Q

Conducting Zone vs Respiratory Zone

A
  • conducting zone: transfers air to and from the lungs
    • nose, pharynx, larynx, trachea, bronchi, to terminal bronchioles
  • Respiratory Zone: site of gas exchange at alveoli
    • respiratory bronchioles, alveolar ducts, alveoli
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3
Q

Where is the trachea located

A

anterior to esophagus, extends from larynx to ~T5

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4
Q

What is located in the mediastinum?

A

heart, esophagus, trachea, great vessels

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5
Q

Location of Oblique fissures and Horizontal fissure (R lung)

A
  • oblique fissures: T3 spinous process to 6th rib mid-clavicular
  • Horizontal fissure (R lung): 4th rib anteriorly, to 5th rib at mid axillary line
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6
Q

Parietal pleura has what type of sensation?

A

pain sensation in response to injury or inflammation: Phrenic nerve (refers pain C3,C4, C5)

  • phrenic nerve also innervates mediastinal and diaphragmatic part
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7
Q

Visceral Pleura and lung tissue have what type of sensation?

A
  • have visceral sensory reflexes but no pain sensation
  • have parasympathetic innervation from Vagus nerve CNX
  • also innervated by sympathetic fibers from the sympathetic trunks
  • will have visceral reflexes such as cough and stretch reflexes
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8
Q

Type I Alveolar Cells

A

simple squamous epithelium supported by elastic basement membrane

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9
Q

Type II Alveolar Cells

A

secrete surfactant

  • surfactant: lipoproteins
    • coats the alveoli to reduce surface tension to prevent collapse of alveoli
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10
Q

Alveolar Macrophages

A

aka dust cells, mononuclear phagocytes

  • engulf debris and prepare it for removal via lymph nodes
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11
Q

Inspiration

A
  • passive (resting): diaphragm contracts
    • external intercostals contracts
  • active (forced or strained):
    • sternocleidomastoid and scalenes contract
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12
Q

Expiration

A
  • passive (resting:
    • diaphragm relaxes
  • active (forced, strained):
    • internal intercostals
    • abdominal muscles
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13
Q

Transmural Pressure Gradient

A

the difference in pressure between the pleural cavity and the atmosphere or alveoli

  • approx -4mmHg
  • normal atmospheric pressure: 760mmHg
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14
Q

High Compliance vs Low Compliance

A
  • high compliance: loose, easy inflation
    • typically destruction of airspace or decreased elasticity
      • ex: emphysema
  • Low compliance: stiff, hard to inflate
    • typically connective tissue changes or fluid build up
      • ex: fibrosis, edema, ARDS
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15
Q

PO2 deoxygenated vs oxygenated

A

Po2 deoxygenated = 40mmHg

PO2 oxygenated = 100mmHg

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16
Q

PCO2 at the tissues versus the alveoli

A

PCO2 at tissue = 46mmHg

PCO2 at alveoli = 40mmHg

17
Q

V/Q ratio

A
  • V= airflow (ventilation)
  • Q = blood flow (perfusion)
  • normal V/Q (ventilation/perfusion) ratio on average ~0.8
  • ***highest ventilation and perfusion are both highest at the base of the lungs***
18
Q

What causes high V/Q?

A

ventilation > perfusion

blockage of blood flow → no gas exchange

19
Q

What causes low V/Q?

A

ventilation

  • blockage of airway → diverted away from non-ventilated alveoli to areas of better ventilation → SHUNT
20
Q

What causes decreased hemoglobin saturation and increased oxygen unloading?

A
  • increased temp
  • increased CO2
  • increased H+ levels
  • shifts the hemoglobin saturation curve to the Right
21
Q

What causes increased saturation of the hgb and decreased oxygen unloading?

A

decreased temperature

decreased CO2 levels (ph> 7.6)

22
Q

Chloride Shift

A

HCO3- is returned to the plasma through HCO3- channels that swap Cl- for HCO3-

23
Q

When CO2 enters the blood via diffusion gradients at tissue what happens to it?

A
  • slow reaction, converts to HCO3- when it interacts with water in the plasma
  • fast reaction, converts to HCO3- quickly in RBCs due to enzyme carbonic anhydrase
  • the HCO3- rxn reverses at the lungs to release CO2 and CO2 is transported out of the plasma into the alveoli
24
Q

Central Chemoreceptors and Breathing

A
  • sense pH changes in the CSF
  • CO2 enters the CSF through the BBB
  • pH decreases when CO2 = high
  • low CSF pH = increased breathing rate
  • Note: become insensitive to chronically high levels of CO2
25
Peripheral Chemoreceptors
* directly detect pH, CO2, and O2 in the arterial circulation * low pH and high arterial CO2 = increased breathing rate * low O2 (only very low \<60mmHg) = increased breathing rate
26
Bronchiolitis obliterans
fibrotic changes permanently scar the lungs, occlude airways
27
Atelectasis
collapse of lung tissue that occurs due to a variety of conditions * _compression atelectasis_: external pressure on lungs due to tumors, pneumothorax, abdominal torsion * _absorption atelectasis_: obstructed or hypoventilated alveoli from inhalation of concentrated O2 or anasthesia * _Surfactant Impairment_: decreased production in premature infants, ARDS, anesthesia, mechanical ventilation * \*\*\*post surgical care = deep breathing, ambulation, position changes\*\*\*
28
Parenchyma
the functional tissue of an organ, excluding the connective tissue and the supportive tissue
29
First line medication for smoking cessation
varenicline (chantix) * varenicline use with nicotine replacement products should generally be avoided → can cause n/v, headaches, dizziness, GI upset
30
Smoking Cessation Options
1. varenicline (Chantix) 2. nicotine replacement products 3. antidepressants 1. bupropion 2. nortriptyline
31
Nicotine Withdrawal
a theory says that a drop in dopamine release in the brain after long periods of exposure to nicotine leads to mood disorders, cravings for tobacco, and other sxs
32
Cystic Fibrosis and Genetics
mutation in the CFTR gene autosomal recessive
33
Asthma and Genetics
* asthma runs in families * polygenic, multifactorial disorder * ADAM33, filigrin and other genes associated with atopy are associated with asthma
34
Alpha-1-antitrypsin deficiency
inherited disorder that may lead to lung and liver disease * this deficiency causes neutrophil elastase to destroy alveoli and cause lung disease (like emphysema/COPD) * the abnormal alpha-1 antitrypsin can also accumulate in the liver and cause damage * Environmental Factors: tobacco smoke, chemicals and dust can also impact the severity of this deficiency * **autosomal dominant with codominance features**
35
Sarcoidosis and genetics
both environmental and genetic factors * siblings of patients with sarcoidosis are 5x as likely of developing sarcoidosis * HLA (human leukocyte antigen) alleles have been consistently associated with sarcoidosis susceptibility