Respiratory: Chornic obstructive Flashcards

1
Q

What characterizes chronic obstructive disease

A

lung does not empty

-air is trapped

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2
Q

what values are changed in spirometry for obstructive lung disease

A

decrease FEV and FEV1 ( FEV1 is decreased more)

Increase TLC

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3
Q

Define chronic bronchitis

A

productive cough lasting at least 3 months over a minimum of 2 years

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4
Q

chronic bronchitis is highly associated with what habit

A

smoking

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5
Q

what characterizes chronic bronchitis

A

hypertrophy of bronchial mucinous glands

  • increased thickness of mucus glands relative to bronchial wall thickness
  • Reid index increases to greater 50%
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6
Q

what are 3 clinical features of chronic bronchitis

A
  1. productive cough with excessive mucus production
  2. cyanosis ‘blue bloaters’
  3. increase risk for infection and cor pulmonale
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7
Q

why does cyanosis ‘blue bloaters’ occur in chronic bronchitis

A

mucus plugs trap carbon dioxide

increase PaCO2 and decrease PaO2

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8
Q

Define emphysema

A

destruction of alveolar air sacs

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9
Q

what happens during exhalation in emphysema

A

loss of elastic recoil and collapse of airways

- results in obstruction and air trapping

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10
Q

In emphysema why do the alveolar air sacs collapse

A

imbalance of proteases and antiproteases

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11
Q

who and what gets released during normal inflammation of the lung

A

neutrophils and macrophages release proteases

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12
Q

what neutralizes porteases

A

alpha1-antitrypsin

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13
Q

how is the protease and antiprotease imbalanced in emphysema

A

excessive inflammation - increase protease

lack of alpha1-antitrypsin

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14
Q

what is the most common cause of emphysema

A

smoking

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15
Q

how does smoking cause emphysema

A
  • excessive inflammation

- protease mediated damage

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16
Q

what does emphysema from smoking result in

A

centriacinar emphysema

upper lobe

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17
Q

what is a rare cause of emphysema

A

A1At deficiency

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18
Q

how does A1AT cause emphysema

A
  • lack of antiprotease
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19
Q

what results from A1At emphysema

A

panacinar emphysema

lower lobes

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20
Q

what other clinical findings would you find for someone who has A1AT emphysema? why?

A

liver cirrhosis

  • A1AT deficiency due to misfolding of mutated protein
  • mutant A1At accumulates in endoplasmic reticulum of hepatocytes,
  • liver damage
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21
Q

what does biopsy of liver cirrhosis show in an A1AT deficient person

A

reveals pink, PAS-positive globules in hepatocytes

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22
Q

what is the severity of A1AT based on

A

degree of A1AT deficiency

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23
Q

what is the normal allele for A1AT

24
Q

what is the most common clinically relevant mutation in A1AT

25
What alleles are usually asymptomatic with decreased circulating levels of A1AT
PiMZ heterozygotes
26
PiMZ heterozygotes have a significant risk for emphysema if they do what
smoke!
27
what allele are at significant risk for panacinar emphysema and cirrhosis
PiZZ homozygotes
28
what are 5 clinical features of emphysema
1. dyspnea and cough with minimal sputum 2. prolonged expiration and pursed lips 3. weight loss 4. increase A/P diameter of chest ( 'barrel-chest') 5. hypoxemia and cor pulmonale ( both late complications)
29
why would hypoxemia occur in emphysema
destruction of capillaries in alveolar sac
30
What asthma and is the most likely cause
reversible airway bronchoconstriction | - allergic stimuli ( atopic asthma)
31
when does asthma usually present and what is asthma associated with
- in childhood | - allergic rhinitis, eczema, family history of atopy
32
Asthma is what type of hypersensitivity
type I hypersensitivity
33
In asthma, allergens induces what response and in what type of individuals
Th2 phenotype in CD4+ T cells | - genetically susceptible individuals
34
in Asthma, Th2 cells secrete what
IL4 IL5 IL10
35
role of IL4
mediates class switch to IgE
36
role of IL5
attracts eosinophils
37
role of IL10
stimulates Th2 cells and inhibits Th1
38
in asthma, re-exposure to allergen leads to what
IgE-mediated activation of mast cells
39
When mast cells are activated by IgE what do they release
- preformed histamine granules | - generation of leukotrienes C4, D4, E4
40
Leukotirienes C4, D4 and E4 causes what
bronchocontriction, inflammation, and edema ( early-phase reaction)
41
What is the late-phase reaction to mast cells that are activated by IgE in asthma
inflammation | -especially major basic protein derived from eosinophils, damaged cells and perpetuates bornchocontraction
42
When do clinical features present for asthma
episodic, | related to allergen exposure
43
what are clinical features of asthma
dyspnea wheezing productive cough status asthmaticus
44
describe the productive cough in asthma
spiral-shaped mucus plugs (Curschmann spirals) | eosinophil-derived crystals ( charcot-Leyden crystals)
45
what is status asthmaticus and what can it lead to
severe, unrelenting attack | can lead to death
46
what are some non-allergic causes of asthma
exercise viral infection aspirin (aspirin-intolerant asthma) occupational exposures
47
What is bronchiectasis
permanent dilatation of bronchioles and bronchi | - loss of airway tone results in air trapping
48
what is the common pathological cause for bronchiectasis
necrotizing inflammation with damage to airway
49
what are specific causes of bronchiectasis
``` cystic fibrosis Kartagener syndrome tumor or foreign body necrotizing infection allergic bronchopulmonary aspergillosis ```
50
what is Kartagener syndrome
inherited defect of dynein arm, necessary for cilliary movement
51
Kartagener syndrome is associated with what other complications
sinusitis infertility (poor motility of sperm) situs inversus (position of major organs is reversed ex. heart is on right side of thorax)
52
What is allergic bronchopulomary aspergillosis
hypersensitivity reaction to Aspergillus
53
what does bronchopulmonary aspergillosis lead to
chronic inflammatory damage
54
who is bronchopulomary aspergillosis usually seen in
asthma or cystic fibrosis
55
what are clinical features of Bronchiectasis
cough dyspnea foul-smelling sputum
56
what are complications of Bronchiectasis
hypoxemia with cor pulmonale | secondary amyloidosis