Cystic Fibrosis Flashcards

1
Q

What is Cystic Fibrosis?

A

An inherited condition in which the lungs and digestive system become clogged with thick, sticky mucus

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2
Q

What causes Cystic Fibrosis?

A

Mutations in the CFTR gene

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3
Q

In which race is Cystic Fibrosis more common?

A

Caucasians

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4
Q

What characterises Cystic Fibrosis?

A

Chronic Bronchopulmonary infections and airway obstruction

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5
Q

What are the symptoms of Cystic Fibrosis?

A
Loose Oily Stools
Failure to thrive
Persistent Chest Infections
Malnutrition
Diabetes
Sinusitis
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6
Q

A one year old child, caucasian with loose oily stools and failure to thrive presents. They have had persistent chest infections. Cause?

A

Cystic Fibrosis

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7
Q

Management of CF?

A
  • Postural Drainage
  • Nutritional Supplements
  • Antibiotics for chest infections
  • Bronchodilators for symptoms
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8
Q

Describe the use of physiotherapy in CF?

A

Postural drainage is done
This involves tipping the body upside down so the affected lobe is uppermost
Percussion helps loosen mucus

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9
Q

Describe the use of antibiotics in CF?

A

These are given for chest infections

Given EARLY on in HIGH DOSES for LONGER than normal

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10
Q

Describe the use of Bronchodilators in CF?

A

Salbutamol to relieve symptoms

Corticosteroids to reduce inflammation

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11
Q

Describe the use of nutrition in CF?

A

Pancreatic enzymes, vitamin and high calorie diet

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12
Q

How is CF diagnosed?

A

Sweat Test

Genetic Testing

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