Asthma Flashcards

1
Q

Major risk factor for asthma. (Harrison’s 19th edition, pp 1669)

A

Atopy

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

Spirometry findings in asthma. (Harrison’s 19th edition, pp 1675)

A

Confirms airflow limitation

Reduced FEV1, FEV1/FVC ratio and PEF

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

Reversibility in spirometry. (Harrison’s 19th edition, pp 1675)

A

> 12% and 200mL increase in FEV1 15 mins after an inhaled SABA
OR
2-4 week trial of OCS (prednisone or prednisolone 30-40mg daily)

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

Confirms the diurnal variations in airflow obstruction in asthma. (Harrison’s 19th edition, pp 1675)

A

Measurements of PEF twice daily

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

Parameters/components use in assessing severity and control of asthma. (Harrison’s 19th edition, pp 1679).

A
Daytime symptoms
Limitation of activities
Nocturnal symptoms or awakening
Need for reliever or rescue treatment
Lung function (PEF or FEV1)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Controlled asthma. (Harrison’s 19th edition, pp 1679)

A
No (< or = 2/week) daytime symptoms
No limitation of activities 
No nocturnal symptoms or awakening
No (< or = 2/week) Need for reliever or rescue treatment
Normal lung function (PEF or FEV1)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Partly controlled asthma. (Harrison’s 19th edition, pp 1679)

A

> 2/week daytime symptoms
Any limitation of activities
Any nocturnal symptoms or awakening
2/week need for reliever or rescue treatment
< 80% predicted or personal best lung function (PEF or FEV1)

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

Uncontrolled asthma. (Harrison’s 19th edition, pp 1679)

A

Three or more features of partly controlled

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

Intermittent asthma.

A

< or = 2 days per week daytime symptoms
< or = 2 times per month nocturnal symptoms or awakening
< or = 2 days per week need for reliever or rescue treatment
No limitation of activities
Normal FEV1 between exacerbations; FEV1 > 80%

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

Mild persistent asthma.

A

> 2 days per week daytime symptoms
3-4 times per month nocturnal symptoms or awakening
2 days per week need for reliever or rescue treatment
Minor limitation of activities
FEV1 >/= 80% of predicted; FEV1/FVC normal

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

Moderate persistent asthma.

A

daily daytime symptoms
once per week nocturnal symptoms or awakening
daily need for reliever or rescue treatment
some limitation of activities
80%> FEV1 > 60% of predicted; FEV1/FVC reduced to 5%

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

Severe persistent asthma.

A

Throughout the day symptoms
Often 7 times per week nocturnal symptoms or awakening
Several times per day need for reliever or rescue treatment
Extremely limited activities
FEV1 < 60% of predicted; FEV1/FVC reduced to > 5%

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

Treatment for mild intermittent asthma. (Harrison’s 19th edition, pp 1679)

A

Short acting B2-agonist, as needed

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

Treatment for mild persistent asthma. (Harrison’s 19th edition, pp 1679)

A

Short acting B2-agonist, as needed

+ low dose ICS

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

Treatment for moderate persistent asthma. (Harrison’s 19th edition, pp 1679)

A

Short acting B2-agonist, as needed
+ low dose ICS
+ long acting B2-agonist

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

Treatment for severe persistent asthma. (Harrison’s 19th edition, pp 1679)

A

Short acting B2-agonist, as needed
+ High dose ICS
+ long acting B2-agonist

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

Treatment for very severe persistent asthma. (Harrison’s 19th edition, pp 1679)

A

Short acting B2-agonist, as needed
+ High dose ICS
+ long acting B2-agonist
+ OCS

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

Most common reason for poor control of asthma. (Harrison’s 19th edition, pp 1679)

A

Noncompliance to medication, particularly ICS

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

Most effective controllers of asthma. (Harrison’s 19th edition, pp 1677)

A

Inhaled corticosteroids

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

The characteristic structural changes of airway remodeling in asthma. (Harrison’s 19th edition, pp 1675)

A

Increased airway smooth muscle
Fibrosis
Angiogenesis
Mucus hyperplasia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

The characteristic physiologic abnormality of asthma. (Harrison’s 19th edition, pp 1675)

A

Airway hyperresponsiveness

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
22
Q

The pathologic changes in asthma are found in?. (Harrison’s 19th edition, pp 1672)

A

In all airways

do not extend to the lung parenchyma

23
Q

Pathology in asthma. (Harrison’s 19th edition, pp 1671-1672)

A
  • Activation on eosinophils, T-lymphocytes and mast cells
  • Thickening of the basement membrane due to subepithelial collagen deposition
  • Shed/friable epithelium with reduced attachments to airway walls and increase number in lumen
  • Thickened and edematous airway
  • occlusion of the airway lumen by mucus plug
  • Vasodilation and angiogenesis
24
Q

Describes as the excessive bronchoconstrictor response to multiple inhaled triggers that would have no effect on normal airways. (Harrison’s 19th edition, pp 1675)

A

Airway hyperresponsiveness

25
The degree of inflammation is _____ related to disease severity of asthma. (Harrison’s 19th edition, pp 1671)
Poorly
26
In asthma, the inflammation in the respiratory mucosa is from the _____ to ______, but with predominance in the ________. (Harrison’s 19th edition, pp 1672)
Trachea, terminal bronchioles, bronchi
27
Clinical features of severe asthma. (Harrison’s 19th edition, pp 1679)
Increasing chest tightness, wheezing, and dyspnea that are often not or poorly relieved by their usual reliever inhaler
28
It maybe present in acute severe asthma but this is rarely a useful clinical sign. (Harrison’s 19th edition, pp 1679)
Pulsus paradoxus
29
Additional clinical features in severe exacerbation. (Harrison’s 19th edition, pp 1679)
Unable to complete sentences and cyanotic. | chest tightness, wheezing and dyspnea
30
These should never be given or not be used routinely in acute severe asthma. (Harrison’s 19th edition, pp 1679)
Antibiotics (unless there are signs of pneumonia) | Sedatives (may depress ventilation)
31
Mainstay of treatment in acute severe asthma. (Harrison’s 19th edition, pp 1679)
High doses of SABA
32
This has been shown to be effective when added to B2-agonists for treatment of acute severe asthma. (Harrison’s 19th edition, pp 1679)
Magnesium sulfate
33
Maybe effective in patients with acute severe asthma that who are refractory to inhaled therapies. (Harrison’s 19th edition, pp 1679)
Slow infusion of aminophylline
34
This may be indicated for patients with impending respiratory failure. (Harrison’s 19th edition, pp 1679)
Prophylactic intubation
35
Intubated patients due to respiratory failure may benefit from this drug if they have not responded to conventional bronchodilator. (Harrison’s 19th edition, pp 1679)
Halothane
36
Bronchodilator effect of theophylline. (Harrison’s 19th edition, pp 1677)
Due to inhibition of phosphodiesterases in airway smooth-muscle cells which increases cyclic cAMP
37
Mechanism of action of Anticholinergics (Ipatropium and tiotropium). (Harrison’s 19th edition, pp 1676)
Prevent cholinergic nerve-induced bronchoconstriction and increases mucus secretion
38
Used intravenously for the treatment of acute severe asthma. (Harrison’s 19th edition, pp 1679)
Corticosteroids
39
Mechanism of action of Beta-2agonist on airways. (Harrison’s 19th edition, pp 1676)
Relax airway smooth-muscle
40
Non bronchodilator effects of Beta-2 agonists. (Harrison’s 19th edition, pp 1676)
Inhibition of mast cell mediator release Reduction in plasma exudation Inhibition of sensory nerve activation
41
Anti-inflammatory effect of Beta-2 agonists. (Harrison’s 19th edition, pp 1676)
No effects on inflammatory cells | No reduction in airway hyperresponsiveness
42
Mechanism of action of Beta-2agonist on airways. (Harrison’s 19th edition, pp 1676)
Relax airway smooth-muscle
43
Non bronchodilator effects of Beta-2 agonists. (Harrison’s 19th edition, pp 1676)
Inhibition of mast cell mediator release Reduction in plasma exudation Inhibition of sensory nerve activation
44
Anti-inflammatory effect of Beta-2 agonists. (Harrison’s 19th edition, pp 1676)
No effects on inflammatory cells | No reduction in airway hyperresponsiveness
45
Short-acting B2-agonists. (Harrison’s 19th edition, pp 1676)
Albuterol | Terbutaline
46
Long-acting B2-agonists. (Harrison’s 19th edition, pp 1676)
Salmeterol | Formeterol
47
Most common side effect of Anticholinergics. (Harrison’s 19th edition, pp 1677)
Dry mouth
48
Most common side effects of B2-agonists. (Harrison’s 19th edition, pp 1676)
Muscle tremor | Palpitations
49
Approximately how many of asthmatic patients who are pregnant improve during the course of pregnancy? (Harrison’s 19th edition, pp 1680)
1/3 | 1/3 deteriorate, 1/3 unchanged
50
Drugs that are safe to use for asthmatic patients who are pregnant. (Harrison’s 19th edition, pp 1680)
SABA ICS Theophylline Prednisone
51
Rationale on using prednisone over of prednisolone for asthmatic patients who are pregnant. (Harrison’s 19th edition, pp 1680)
Prednisone cannot be converted to active prednisolone by fetal liver, thus protecting the fetus from systemic effects.
52
Drugs that are safe to use for asthmatic patients who are breast-feeding. (Harrison’s 19th edition, pp 1680)
SABA ICS Theophylline Prednisone
53
In acute severe asthma, this should be given by face mask to achieve oxygen saturation of > 90%. (Harrison’s 19th edition, pp 1680)
High concentration of oxygen