respiratory problems Flashcards

1
Q

bronchiolitis

A
  • bronchioles

- small bronchi

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2
Q

pathogens causing bronchiolitis

A
  • RSV
  • adenovirus
  • parainfluenza virus
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3
Q

incidence of bronchiolitis

A

<2 years old

  • winter & spring
  • one of the most frequent cause of hospitalization
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4
Q

s/s of bronchiolitis

A
  • fussy, malaise
  • URI for 1-2 days
  • low grade fever
  • elevated ESR/CRP (show infection)
  • s/s of lower respiratory obstruction
  • nasal flaring/retractions
  • prolonged expiration (wheezes, crackles)
  • pallor
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5
Q

vital signs in bronchiolitis

A
  • increased RR, HR

- low pulse ox

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6
Q

diagnosing bronchiolitis

A
  • chest xray: white mass is found (fluid or bones)
  • throat culture
  • nasopharyngeal swab (for RSV)
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7
Q

mgmt of bronchiolitis

A
  • without rx, can cause death
  • 95% can be managed at home with high humidity, adequate fluids, rest, manage fever
  • hospitalization: if tachypneic/retractions/apnea, and poor fluid intake
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8
Q

medical tx for bronchiolitis

A
  • nebulized bronchodilators/steroids
  • IV fluids, O2, antipyretics
  • antibiotics for secondary bacterial infection
  • mechanical ventilation (extreme cases)
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9
Q

meds for bronchiolitis

A
  • ribavirin

- caffiene citrate

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10
Q

high risk at bronchiolitis

A

<24 mo (BPD, CF, premature)

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11
Q

prevention of RSV

A
  • IGIVV

- synagis: antibodies to prevent serious lower resp tract disease

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12
Q

bronchopulmonary dysplasia (BPD)

A
  • usually a secondary dx
  • chronic obstructive lung disease
  • mortality rate: 10-25%
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13
Q

risk factors of BPD

A

newborns requiring mechanical ventilation

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14
Q

what has reduced the incidence of BPD

A
  • antenatal steroids: help lung maturity

- surfactant replacement tx

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15
Q

pathophysio of BPD

A
  • caused by tx of respiratory distress syndrome
  • bronchial epithelium is dmged over time
  • airway edema occurs
  • alveolar walls thicken
  • fibrotic changes occur in airways & alveoli
  • loss of ciliated cells
  • continued O2 use decreased developing alveoli
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16
Q

s/s of BPD

A
  • s/s of respiratory distress
  • adventitious breath sounds
  • failure to thrive (not growing normal bc unable to breath, eat)
  • episodes of sudden respiratory deterioration (d/t bronchospasms, mucous plugging, air trapping)
17
Q

diagnosing BPD

A

must have

    • xrays
    • s/s
  • required mechanical ventilation @ 1wk old
  • O2 dependence befyond 28 days of age
18
Q

mild O2 dependence

A

room air by 36 wks GA

19
Q

moderate O2 dependence

A

<30% FiO2 at 36 wks GA

20
Q

severe O2 dependence

A

> 30% FiO2 at 36 wks GA

21
Q

mgmt of BPD

A
  • O2
  • meds
  • limiting fluids
  • nutrition (similac 27cal/oz - more than normal)
  • chest physiotherapy
  • immunizations are important
  • trach if necessary @ home
22
Q

medications for BPD

A
  • bronchodilators
  • corticosteroids
  • diuretics
  • electrolyte supplements
  • antibiotics, ribavirin
23
Q

potential outcomes of BPD

A
  • developmental delays
  • growth retardation
  • pulmonary dysfunction in adolescents
24
Q

cystic fibrosis incidence

A
  • gender is not a factor

- more common in whites, then blacks, then asians

25
Q

cystic fibrosis

A
  • inherited autosomal recessive disorder (you can be a carrier and not have it)
  • mutation of chromosome 7
  • severity depends on the form inherited
  • *dysfunction of the exocrine glands causing alterations in mucous secretions & sweat electrolytes -> multiple system dmg
26
Q

early s/s of cystic fibrosis

A
  • newborn: meconium ileus (distended abd)
  • infants/toddlers: fecal impaction & intussusception
  • FTT
  • steatorrhea
  • rectal prolapse
  • insulin insufficiency
  • wt loss
27
Q

pulmonary s/s of cystic fibrosis

A
  • coughing, sputum production
  • chronic respiratory infections
  • hemoptysis
  • atelectasis
  • pneumothorax
  • digital clubbing (d/t chronic hypoxia)
28
Q

metabolic s/s of cystic fibrosis

A
  • “salty taste”

- level of NaCl is 2-5 times above normal perspiration

29
Q

reproductive s/s of cystic fibrosis

A

males: sterile d/t blockage of vas deferens
females: puberty delayed d/t chronic ventilation and nutritional deficiencies; difficulty conceiving d/t increased mucus secretions in the reproductive tract interfering with passage of sperm

30
Q

tests to diagnose cystic fibrosis

A
  • presence of classic symptoms
  • sweat test (easiest)
  • family hx
  • genetic testing
  • pulmonary function test (6+ yrs old)
  • chest xray
  • stool analysis for fat & enzymes
31
Q

mgmt of cystic fibrosis

A
  • maintain resp function with bronchodilators, mucolytics, chest physiotx, steroids, NSAIDs
  • managing infections: antibiotics
  • promoting nutrition, hyrdation, & exercise: pancreatic enzyme supplements; diet (200% protein, moderate fat, salt supplements); multivitamins
  • prevent GI blockage: laxatives, fluids