Asthma and Cystic Fibrosis Flashcards

1
Q

Obstructive disease

A

air gets trapped in lungs

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2
Q

Nonseptic obstructive diseases

A
  • less sputum

- emphysema, asthma, chronic bronchitis

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3
Q

Septic obstructive diseases

A
  • lots of sputum

- CF, bronchiectasis

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4
Q

Restrictive disease

A
  • loss of lung compliance and chest wall expansion

- decreased depth and increased rate of breathing

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5
Q

What is asthma?

A

reversible obstruction to airflow within the lungs

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6
Q

Risk factors of asthma?

A
  • childhood asthma
  • family history
  • atopy (allergic hypersensitivity)
  • maternal smoking
  • occupation/environmental exposures
  • secondary smoke
  • gender (women more likely)
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7
Q

Associations of asthma

A
  • increased in families with asthma or allergies
  • 1 parent: 1/3 chance
  • 2 parents: 7/10 chance
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8
Q

Signs and symptoms of asthma

A
  • wheezing: high pitched whistling sounds when breathing out

- cough, chest tightness, difficulty breathing

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9
Q

Symptoms may occur/worsen with what?

A
  • exercise
  • infection
  • animals/allergies
  • smoke
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10
Q

Pathophysiology of asthma

A
  • intermediate type hypersensitivity reaction
  • mast cells release histamine
  • cells of immune system stimulate airway
  • airway inflammation –> intermittent airflow obstruction –> bronchial hyper-responsiveness
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11
Q

Diagnosis of asthma (FEV1 and FEV1/FVC percentages)

A

Airway obstruction is episodic AND reversible

– Airway obstruction: FEV1 12% and 200 ml after short acting beta-2 agonist

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12
Q

Classification of severity of asthma: Severe persistent

A
  • Days with symptoms – continuous
  • Nights with symptoms – frequent
  • PEF or FEV1 30%
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13
Q

Classification of severity of asthma: Moderate persistent

A
  • Days with symptoms – daily
  • Nights with symptoms > or = 5/month
  • PEF or FEV1 > 60% and 30%
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14
Q

Classification of severity of asthma: Mild persistent

A
  • Days with symptoms – 3-6/week
  • Nights with symptoms – 3-4/month
  • PEF or FEV1 > or = 80%
  • PEF variability = 20-30%
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15
Q

Classification of severity of asthma: Mild intermittent

A
  • Days with symptoms or = 80%

- PEF variability

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16
Q

Common medications used to treat asthma (4)

A

a. Albuterol (B2 selective bronchodilator)
b. Atrovent (anticholinergic, prevents bronchoconstriction)
c. Salmeteral (Serovent; B2 bronchodilator)
d. Inhaled steroids (advair, flovent, symbicort)

17
Q

Persistent asthmas needs 2-step process….what is it?

A
  1. long-term control
    - - steroids, leukotriene agonists
    - - long acting beta agonist
  2. acute exacerbations
    - - albuterol or short acting beta agonist
18
Q

Asthma treatment goals

A
  • minimal symptoms day or night
  • near normal pulmonary function
  • no limitations on activity
  • aggressive treatment at first sign of worsening
  • minimal or no exacerbations
  • minimal albuterol use
  • minimal or no adverse effects of medications
19
Q

Consequences of asthma

A
  • comorbities (obesity, sinusitis, GERD, sleep apnea)
  • hyperexpansion of thorax
  • postural changes
  • decreased physical fitness/ restricted physical activity
  • increased hospitalization
20
Q

Exercise induced asthma

A

a. Airway drying –> hyperemia (increased blood flow) –> increased permeability –> swelling
b. Airway cooling –> hyperemia –> re-heat airway –> swelling

21
Q

Incidence of exercise induced asthma occurring normally and in cold weather?

A
  • Normally: 3-10%

- Cold weather: 35-50%

22
Q

Treatment for exercise induced asthma

A
  • Pre-treat with B-agonist before exercise
  • early and longer warm up
  • short exertion periods
23
Q

What is cystic fibrosis?

A

cogenital disease of exocrine glands (genetic – must inherit a gene from each parent)

24
Q

What is the gene for cystic fibrosis and what does it do?

A

CF Transmembrane Regulator (CFTR) Gene

a. Normally opens channel thru plasma membrane to allow chloride to pass thru

25
Defect of CFTR gene in people with cystic fibrosis?
Defect = faulty movement of Na+ and Cl- | -- Too much NaCl pulled into cells, leaving behind dry mucus in airways --> increased bacterial infection
26
Consequences of cystic fibrosis
1. mucus build up in airways --> severe lung infections 2. Hypoxemia (low O2 in blood) 3. Intestinal blockages (water and salt stay in cells) 4. Pancreatic enzymes do not cross cell membrane 5. Reproductive blockages
27
Common infections of cystic fibrosis
staphylococcus aureus, pseudomonas aeruginosa - - transmitted by respiratory or hand contact - - usually colonize in lungs and difficult to eradicate
28
Bronchiectasis
multiple infections in tubules of lungs = dilation/chronic stretching of bronchial walls
29
Treatment of pulmonary infections from cystic fibrosis
1. beta-agonist inhaled bronchodilator 2. mucolytics -- thins mucus (pulmozyme, guaifenesin) 3. airway clearance (autogenic drainage, active cycle breathing, percussion) 4. antibiotics (aminoglycosides, inhaled Tobramycin, azithromycin)
30
Rheumatoid diseases in patients with CF (3)
1. Cystic fibrosis arthropathy 2. Hypertrophic pulmonary osteoarthropathy 3. Osteoporosis