Cystic Fibrosis Flashcards

1
Q

What is Cystic Fibrosis?

A

A multi-organ disease affecting mainly ductal organs (lungs, pancreas, immune system)

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

What is the inheritance pattern of CF?

A

Autosomal recessive
1/2500 live births
1/25 carrier freq

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

What is the most common mutation in CF?

A

Mutation in CFTR

Chr7, pos 508, point deletion

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

What is the main effect of malfunctioning CFTR genes?

A

Abnormally thick secretions
Pancreatic insufficiency
Recurrent chest infections

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

What is the life expectancy of a CF sufferer?

A

> 30yrs

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

What are the main clinical features of CF?

A

Pulmonary effects
GI effects
Systemic effects

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

What are the pulmonary effects of CF?

A
Recurrent childhood chest infections (failure to thrive)
Breathlessness
Haemoptysis
Spontaneous pneumothorax
Chronic sinusitis w/ nasal polyps
Resp failure/cor pulmonale
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

What are the GI effects of CF?

A

Meconium ileus at birth
Steatorrhoea & malabsorption
Gallstones/peptic ulceration
Cirrhosis (10%)

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

What are the systemic effects of CF?

A

Clubbing
Infertility in males, subfertility in females
DM (10%)
Rickets/osteomalacia

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

What are the causative organisms of infections in CF?

A

S. aureus
Haemophilus influenzae
G-bacilli
Pseudomonas (later on, poor prognosis)

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

What is Allergic Bronchopulmonary Aspergillosis?

A

Body’s response to common aspergillus fumigatus fungus causes worsening breathing problems

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

What investigations are appropriate in suspected CF?

A

FBC, LFTs, U&Es, clotting
Na sweat test (>70mmol/L)
DM screening
Sputum cultures
CXR (hyperinflation, evidence of bronchiectasis)
Abdo USS (fatty liver/cirrhosis, chronic pancreatitis)
Spirometry (obstructive defects)

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

How should the pulmonary aspect of CF be managed?

A
Physiotherapy
A/b for exacerbations
Prophylactic azithromycin
Mucolytics (DNase nebulisers)
Airway clearance devices
Bronchodilators
Lung transplant
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

How should the GI aspect of CF be managed?

A

Pancreatic enzyme replacement (creon)
Fat soluble vitamin supplementation (ADEK)
Liver transplantation for cirrhosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

How should the systemic aspects of CF be managed?

A

Treatment of DM
Fertility treatment
Genetic counselling

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