Cystic Fibrosis: Adults Flashcards

1
Q

What percentage of patients have recurrent pulmonary infections and pancreatic insufficiency?

A

80%

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2
Q

Why is there persistent respiratory infections in CF?

A

Decrease in mucociliary clearance

Increase in bacterial adherence

Reduce in endocytosis of bacteria

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3
Q

What is the effect of CF on bronchiectasis?

A

Causes Aggressive progressive bronchiectasis: chronic sputum production (purulent

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4
Q

What is the result of decreased mucociliary clearance?

A

Increased bacterial colonisation

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5
Q

What is the result of increased bacterial colonisation?

A

Inflammation

Mucus plugging

Airway ulceration

Airway damage

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6
Q

What is the result of Inflammation

Airway plugging

Airway ulceration

Airway Damage?

A

Bronchiectasis?

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7
Q

What is the result of bronchiectasis?

A

More

Decreased mucociliary clearance

Increased bacterial adherence

Decreased endocytosis

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8
Q

Describe the onset of bronchiectasis in CF patients?

A

Aggressive and progressive - chronic sputum production

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9
Q

What respiratory problems besides bronchiectasis do CF patients face?

A

Recurrent lower respiratory tract infections

Progressive airflow obstruction (survival rate related to FEV1)

Increase in exertional dyspnoea

Haemoptysis (associated with infection - possible embolisation)

Pneumothorax- poor prognosis

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10
Q

Describe the onset of colonisation of pseudomonas aeruginosa

A

21% colonisation under 1 year

80% colonisation over 26 years

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11
Q

Where is pseudomonas aeruginosa acquired from?

A

Environment (particularly hospitals)

Other CF patients

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12
Q

How does pseudomonas aeruginosa protect itself from host defences?

A

Once colonised, it undergoes mucoid change. It forms a biofilm - rapidly acquires antibiotic resistance

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13
Q

What is colonisation of pseudomonas aeruginosa associated with?

A

Reduced life expectancy 28 vs 39 years

Rapid decline in lung function

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14
Q

How does the body respond to the presence of a biofilm?

A

Neutrophils and macrophages release proteinases and oxidants (free radicals) produce tissue damage

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15
Q

What is treatment for first isolation of pseudomonas Aeruginosa?

A

Attempt eradication with oral ciprofloxacin & nebulised colomycin 3/12

If fails, i.v. ceftazidime & nebulised colomycin

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16
Q

Where is Burkholderia cepacia acquired from?

A

Environment

Other CF patients

17
Q

What is Colonisation of Burkholderia cepacia associated with?

A

Reduced life expectancy 16 vs 39 years

Rapid decline in lung function

Some patients ‘cepacia syndrome,’ very rapid deterioration

18
Q

What is the resistance of burkholderia cepacia?

A

Innate resistance to most antibiotics

19
Q

What does Genomovar 3 indicate (a group of Burkholderia cepacia-like organisms)?

A

Contraindication for transplantations

20
Q

Which organism is usually secondary to pseudomonas?

A

Stentrophomonas maltophila

21
Q

Which bacterium is resistant to all anti-tuberculosis chemotherapy and is a contraindication for transplantation.

A

Mycobacterium abscessus

22
Q

How do you treat recurrent respiratory tract infections?

A

Early and aggressively with antibiotics

23
Q

What bacteria would you treat with oral antibiotics?

A

Staph, Haemophilus, Pneumococcus

24
Q

Which bacteria do you treat with IV antibiotics?

A

Pseudomonas, Stenotrophomonas, Burkholderia

25
What is the format of antibiotic administration?
Two antibiotics (b-lactam + aminoglycoside) If multiply resistant, test for synergy between antibiotic combinations Large doses (increased volume of distribution, increased clearance) Two week courses
26
What is the function of the Ivacaftor?
Addresses primary defect of CTFR CTFR potentiator, binds to CTFR and improves the transport of chloride ions Improves lung function (10%) Weight gain Reduces sweat chloride Feel much better
27
What are the indications for a double lung transplant?
Rapidly deteriorating lung function FEV1 \< 30% predicted Life threatening exacerbations Estimated survival \<2 years
28
What is the likelihood of dying on the waiting list for a lung?
30-40% die on waiting list
29
What is survival rate for lung transplantation?
70-80% at 5 years 50% at 10 years Gradual attrition due to bronchiolitis obliterans