Bronchiectasis/Cystic Fibrosis Flashcards

1
Q

What causes half of the cases of bronchiectasis?

A

Cystic Fibrosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Most common organism that causes in bronchiectasis in non- cystic fibrosis patients?

A

H. Influenza

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

bronchiectasis clinical presentation

A
  1. Cough
  2. Daily copious amounts of mucopurulent sputum lasting months to years
  3. Hemoptysis
  4. Pleuritic chest pain
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

bronchiectasis physical exam findings

A
  1. Crackles/Rhonchi
  2. Scattered wheezing
  3. Clubbing
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

What would you expect to find on the sputum analysis that is specific to bronchiectasis?

A

Dittrich plugs-small white/yellow concentrations

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

CXR findings in bronchiectasis

A
  1. Mucus plugging
  2. Tram lines: Dilated and thickened airways
  3. Increased pulmonary markings
  4. Ring-like structures
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

What is gold standard imaging for bronchiectasis?

A

High Resolution CT (HRCT)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

CBC findings in bronchiectasis

A
  1. leukocytosis with left shift

2. Polycythemia- due to chronic hypoxia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What conditions do you want to r/o in bronchiectasis? What labs would you order?

A
  1. alpha1-antitrypsin deficiency: Quantitative serum

2. Cystic Fibrosis: Pilocarpine iontophoresis= Sweat test

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

bronchiectasis diagnostic

A

Spirometry

-Obstructive pattern

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

bronchiectasis treatment

A
  1. Abx & chest physiotherapy
  2. Bronchodilators
  3. Corticosteroids
  4. Smoking cessation!
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Cystic Fibrosis etiology

A
  • Autosomal recessive genetic disorder

- Dz of EXOCRINE gland function

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What does the defect in the CFTR gene result in?

A

Abnormal chloride transport channels

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

CF clinical presentation

A
  1. Chronic hacking cough
  2. GI manifestations: Meconium ileus, obstruction, malabsorption
  3. Infertility in males, undescended testes
  4. Sinus infection
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

CF diagnosis

A

Clinical presentation + Genetic finding

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What is the primary test for Dx of CF?

A

Sweat chloride test

17
Q

CF management

A
  1. Vaccines: Influenza and Pneumonia
  2. Bronchodilators
  3. Agents to promote clearance of secretions (enzymes)
  4. Chest physiotherapy
  5. Anti-inflammatory + Abx
  6. Negative partial pressure ventilator (NPPV)
  7. Transplant