#11: Pulmonary Disease States 3 Flashcards

1
Q

etiologies of bronchiectasis: (7)

A

1- Infx (Klebsiella, MAC, mycoplasma, Staph, TB)
2- Bronchial obstruction (tumor, FB, stenosis)
3- Aspiration
4- CF and Young Syndrome
5- allergic bronchopulmonary aspergillus
6- AAT deficiency
7- Autoimmune/CT disorders (rare causes: anatomic abnormality, primary ciliary dyskinesia, congenital immune dysfx)

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2
Q

MC epidemiology of bronchiectasis:

A
  • > 60 y.o.
  • caucasian
  • females
  • thin/slender
  • MC primary dz w/ MAC (Lady Windermere dz)
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3
Q

Pathophysiology associated w/ Bronchiectasis: (3)

A

1- permanent dilation of the proximal and medium sized bronchi (due to destruction of bronchial walls)
2- progressive inability to clear secretions and resolve colonization or repeated infx
3- Chronic airway obstructive dz

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4
Q

SXS of bronchiectasis: (8)

A
1- cough (common w/ hemoptysis)
2- dyspnea
3- daily muculopurulent sputum
4- fever
5- pleuritic CP
6- wheezing
7- weight loss
8- weakness
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5
Q

Imaging of choice in bronchiectasis:

A

HRCT with contrast

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6
Q

Mainstay tx modalities for bronchiectasis for sxs tx:

A

abx and chest physiotherapy

- others may include bronchodilators, corticosteroids, diertary supplementation, oxygen and surgery

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7
Q

Bronchiectasis defined as exacerbation and tx:

A
  • increased and more viscous sputum with foul odor

- hospital admission, IV abx and supplemental nutrition

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8
Q

surfactant production in the fetus begins at:

A

32-34 wks

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9
Q

surfactant production becomes sufficient at:

A

34-36 wks

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10
Q

Type 2 alveolar cell growth begins at:

A

20 wks

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11
Q

Fetal lung maturation can be assessed via:

A

testing amniotic fluid for lecithin levels

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12
Q

What would decrease surfactant levels: (5)

A
1- hypovolemia
2- hypothermia
3- hypoxemia
4- acidosis
5- rare genetic disorders
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13
Q

RDS risk factors: (9)

A
1- *MC: prematurity (1/3 between 28-32 wks)
2- asphyxia
3- CS w/o labor
4- caucasian
5- fetal distress
6- male
7- maternal DM
8- previous premie w/ RDS
9- 2nd of twins
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