Lecture 17 Flashcards

1
Q

COPD presents as a mix of two conditions, what are they ?

A
  1. Chronic bronchitis (excess mucus production + inflammatory reaction)
  2. Emphysema (destruction of lung tissue forming big gaps in alveoli, alveolar ducts and respiratory bronchioles)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What are the risk factors of COPD ?

A
  1. Infection.
  2. Age.
  3. Environment (Chemicals, Pollution, Cigarette Smoke)
  4. Genetic (AAT deficiency, AAT usually inhibits NE which is an enzyme that destroys lung architecture)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

How is diagnosis of COPD achieved ?

A

Through spirometry to assess airflow limitation (if FEV/FVC <0.7 then there is airflow limitation)

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

What is the classification system for COPD?

A

GOLD 1 to 4

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

True or false : treatment for COPD includes anti-inflammatory medication such as corticosteroids .

A

FALSE. Don’t work.

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

True or false: Asthma is mostly prevalent in underdeveloped countries.

A

FALSE. Mostly in developed countries. BUT the death rate is higher in underdeveloped countries.

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

What characterizes asthma ?

A
Chronic inflammation.
Shortness of breath
Chest tightness
Wheezing.
Variable respiratory airflow limitation.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

What is atopic asthma ?

A

Asthma caused by an allergen. Most common.

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

What is non-atopic asthma ?

A

Asthma not caused by an allergen. Usually by a pollutant or a virus.

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

What is airway hyper responsiveness (AHR) ?

A

It is a clinical presentation of asthma, whereby the airways have an exacerbated response to bronchoconstrictors.
PC(20) is the amount of bronchoconstrictor needed to cause a 20% decrease in FEV.
PC(20) = 8-16 mg -> Asthma
PC(20) >16 mg -> Normal.

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

What type of Th reactions are seen in COPD and Asthma ?

A

COPD has a th1 reaction with cigarette smoke.

Asthma has a th2 reaction with allergens.

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

What is the pathogenesis of Asthma?

A
  1. Airway remodelling (persistent effect) ->increased vasculature, thickened airways, hyperplasia/hypertrophy of smooth muscle.
  2. Inflammation (variable effect) -> th2 response
  3. Bronchoconstriction
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

True or false : both airway remodelling and inflammation contribute to AHR.

A

TRUE.

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

True or false : treatments of COPD and Asthma are the same.

A

TRUE. Both use bronchodilators + spirometer.

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

In terms of pathology, what differs in a smoking vs a non-smoking asthmatic ?

A

They have different mechanisms of inflammation.
Non-smoking asthmatic: eosinophils.
Smoking asthmatic : IL8 + neutrophils.

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

True or False : COPD considered non-reversible, while asthma is considered reversible.

A

TRUE.

17
Q

What is the progression of cystic fibrosis ?

A

Genetic mutation in CF gene -> decreased chloride secretion -> abnormal composition of mucus -> obstruction of bronchi -> bacterial infections -> inflammation -> lung insufficiency.

18
Q

Digital clubbing occurs in what respiratory diseases ?

A

COPD and Idiopathic Pulmonary Fibrosis.

19
Q

What is the pathogenesis of Idiopathic pulmonary fibrosis ?

A

There is an ongoing injury to the epithelial cells that increases TFF-B secretion, which triggers fibrosis (scarring) that is excessive.

20
Q

What are the risk factors of idiopathic pulmonary fibrosis ?

A

Smoking (main one!)
Genetic
Antibiotics
Radiation

21
Q

What is the histology of idiopathic pulmonary fibrosis?

A

Fibroblastic foci : aggregates of myofibroblasts.

Honeycombing.

22
Q

What are the treatments of idiopathic pulmonary fibrosis?

A
  1. Lung transplant.

2. Drugs : Ofev/Profenedone , which are tyrosine kinase inhibitors so the drugs stop the production of growth factors.