Pulmonary- Obstructive disease Flashcards

1
Q

What is COPD?

A
  • Airflow obstruction due to chronic bronchitis or emphysema
  • airflow obstruction is generally progressive
  • may be accompanied by airway hyper-reactivity
  • may be partially reversible in asthma, but NOT in progressive COPD
  • Obstruction is worse on expiration
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2
Q

What are the common obstructive disorders?

Signs and symptoms?

A
  • common disorders:
    • asthma
    • emphysema
    • chronic bronchitis
  • Signs/Symptoms
    • Dyspnea
    • wheezing
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3
Q

What is Asthma?

A
  • Chronic inflammatory disorder of the airways
  • The inflammation causes:
    • recurrent episodes of wheezing
    • breathlessness
    • chest tightness, cough (especially at night an in early morning)
    • hyper-responsive to stimuli
  • Widespread but variable obstruction that is often reversible
  • **A. normal, B. emphysema, C. bronchitis, D. Asthma
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4
Q

Asthma is an atopic disorder. What does this mean?

A
  • Atopy- a genetic predisposition for the development of an IgE mediated response to common aeroallergens
  • This is the strongest identifiable predisposing factor for developing asthma
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5
Q

What are some stimuli that provoke asthma?

A
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6
Q

What are the risk factors for asthma?

A
  • Atopy
    • increased serum IgE
  • Family history of allergic diseases
  • maternal smoking during pregnancy
  • viral infections
    • especially RSV and rhino as an infant
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7
Q

How is Asthma diagnosed?

What are the differences in severity?

What dictates how the asthma is managed?

A
  • Diagnosis based on flow-volume curves
  • FEV1 and FEV1/FVC ratio decreased
  • Management dictated by FEV1
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8
Q

What is the pathophysiology of Asthma?

(chart)

A
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9
Q

What are the characteristics of COPD?

A
  • deterioration in elasticity or recoil which normally maintains the airways in open position
  • decreased rigidity of bronchiolar wall
    • collapse during exhalation
  • Increase in gas flow velocity in the narrowed bronchioli, which lowers the pressure inside the bronchioli and favors collapse
  • Increased secretions that cause bronchospasm
  • destruction of lung parenchyma, causing enlarged air sacs and developing into emphysema
  • **A. normal, B. emphysema, C. bronchitis, D. Asthma
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10
Q

What are the risk factors of COPD

A
  • Cigarette smoking
  • passive smoking- increases airway reactivity
  • chronic infections
  • occupational factors
    • coal mining, textile factories, dentists?
  • Genetic
    • Alpha-1-antitrypsin deficiency
    • only known genetic abnormality that leads to COPD
      • Accounts for less than 1% of cases
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11
Q

What causes air trapping?

A
  • During inspiration the airways are pulled open so air is able to enter
  • Upon expiration, due to loss of recoil in the airways, they will collapse and prevent normal expiratory flow
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12
Q

How is COPD diagnosed?

A
  • Chronic productive cough
  • airflow obstruction
  • pulmonary function tests
    • FEV1/FVC ratio decreased
    • significant decrease in FEF 25-75%
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13
Q

How do the lung volumes compare between a person with COPD and a person with healthy lungs?

A
  • COPD
    • Larger total lung capacity (TLC)
    • Larger residual volume (RV) because they cannot get as much air out of their lungs
    • decreased expiratory reserve volume (ERV)
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14
Q

How is COPD staged?

A
  • **All stages have FEV1:FEV ratio <70%
  • 0: At risk
    • normal spirometry but chronic cough or sputum
  • 1: Mild COPD
    • FEV1 >80%
  • 2: Moderate COPD
    • 50% 1 <80%
  • 3: Severe COPD
    • 30% < FEV1 <50%
  • 4: Very severe COPD
    • FEV1 < 30%
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15
Q

What is chronic bronchitis?

A
  • Hypersecretion of mucus and chronic productive cough that lasts for at least 3 months of the year and for at least 2 consecutive years
  • inspired irritants increase mucus production as well as the size and number of mucus glands
  • mucus is thicker than normal
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16
Q

What is emphysema?

What are the different classifications of emphysema?

A
  • abnormal permanent enlargement of the gas exchange airways with destruction of alveolar walls but no obvious fibrosis
  • loss of elastic recoil
  • Classifications
    • Centriacinar- dilation initially affects the respiratory bronchioles
    • Panacinar- dilation initially affects the alveolus and alveolar duct
17
Q

What is the difference between pure chronic bronchitis and pure emphysema?

(pic)

A
18
Q

What do anti-proteases do?

A
  • Antiproteases prevent the breakdown of tissue proteins
  • alpha1- anti-trypsin deficiency is a genetic disorder where the person doesnt have the anti-proteases so their tissue proteins get broken down faster than normal
19
Q

How does smoking cause emphysema?

A
  • Tobacco introduces free radicals into lungs
  • the free radicals inactivate the antiproteases
    • causing a “functional” alpha-1 antitrypsin deficiency
  • This increases neutrophil response and neutrophil elastase
    • neutrophil and macrophage elastases cause damage to the tissue
20
Q

What is the pathophysiology of COPD?

(Chart)

A
21
Q

What is absorption atelectasis?

A
  • Caused when inhaled volumes are not big enough to open the pores of kohn
    • make sure TV is set large enough
    • encourage post op deep breathing
22
Q

What is Bronchiectasis?

How is it diagnosed?

A
  • Localized irreversible dilation of the bronchus caused by bacterial infections (air polutants too?)
  • Destroys airways leading to airway collapse, airflow obstruction, and inability to clear secretions
    • pooling mucus
    • bacterial superinfection is tough to eradicate
  • Diagnosis-
    • chronic purulent cough
    • clubbing of fingers (not characteristic of COPD)
    • hemoptysis
    • dyspnea/wheezing
23
Q

What is cystic fibrosis?

A
  • Caused by mutation in a single gene on chromosome 7
    • with this mutation, they lack a protein that helps move Na and H2O in and out of cells (Cl- is affected too)
  • Decreased Cl- transport results in
    • results in an abnormally thick mucus outside of epithelial cells
    • destruction and scarring of various glands and tissues, causing damage to lungs, pancreas, liver, GI, & reproductive organs
  • Primary cause of M&M of pts with CF is chronic pulmonary infection
24
Q

How id CF diagnosed?

A
  • diagnosed by sweat Cl higher than 70 mEq/L