Pediatric Resp Flashcards

1
Q

What are some common presentations of cystic fibrosis?

A
  1. Nasal polyps/ sinusitis
  2. Persistent cough/ resp infection/ refractory asthma
  3. Fussy baby
  4. Steatorrhea
  5. Failure to thrive, malnutrition
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2
Q

Laryngomalacia

A
  1. Most common cause of chronic stridor
  2. Worse with feeding, crying
  3. Spontaneous resolution by 12-18 mo
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3
Q

Congenital tracheal lesions causing stridor

A
  1. Tracheomalacia
  2. Anterior compression (inominate artery)
  3. Vascular sling (left pulmonary artery wraps)
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4
Q

Acquired structural airway lesions causing stridor

A
  1. Granuloma
  2. Papilloma
  3. Tumours
  4. Subglottic Stenosis
  5. Vocal cord paresis
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5
Q

Croup

A
  1. Caused by parainfluenza virus
  2. 3mo to 3 years
  3. Febrile
  4. Gradual progression of barky cough to stridor
  5. May have rhinorrhea, hoarseness, conjunctivitis
  6. treat with nebulized epinephrine, systemic steroids
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6
Q

Bacterial Tracheitis

A
  1. Caused by staph aureus, group a strep
  2. 1-8 years old
  3. Sick
  4. Muffled voice, cough, tracheal tenderness
  5. Gradual progression to stridor
  6. Treatment: NPO, analgesia, antibiotics
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7
Q

When do you need to rule cystic fibrosis out?

A
  1. Bowel obstruction
  2. Rectal prolapse
  3. Family hx
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8
Q

What are concerning features of a childhood cough?

A
  1. Perceived to be ill
  2. Losing sleep
  3. Interfering with school
  4. MSK pain
  5. Associated vomiting
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9
Q

What mutation causes cystic fibrosis?

A

F508 in the CFTR protein

Actually many mutations

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10
Q

What virus causes bronciolitis?

A

RSV

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11
Q

What are the risk factors for pediatric asthma

A
  • pre or post natal tobacco exposure
  • viral infections with RSV
  • indoor/outdoor pollution
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12
Q

What signs do you NOT see in pediatric asthma?

A
  • clubbing, polyps (CF)
  • Hyperinflation
  • Hemmorrage in eye (Pertussis)
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13
Q

How is pediatric asthma treated?

A
  1. Usually first line is trial therapy of inhaled steroids
  2. Second line is leukotriene receptor antagonist (add this on if refractory)
  3. Use chamber with mask or valve depending on age
    Education is vital!
  4. Usually only do PFTs if old enough (usually around 8 years old)
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14
Q

What are the system based effects of cystic fibrosis?

A

Head/neck: chronic sinusitis, nasal polyps
Chest: lower resp tract infections
GI: pancreatic insufficiency, diabetes, liver disease, gall stones, steatorrhea
MSK: Osteoporosis, arthritis, finger clubbing
GU: male infertility

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15
Q

How do we test for cystic fibrosis

A
  1. Currently newborn screening programs in most provinces (Immune reactive trypsinogen first step, then sweat chloride, then genetic testing)
  2. May also do CXR/CT/PFTs if later
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16
Q

What are the signs of a life-threatening asthma attack?

A
  1. Silent chest
  2. Cyanosis/hypoxia
  3. Bradycardia
  4. Hypotension
  5. Hypercapnia despite effortf
17
Q

When does bronchiolitis incidence peak?

A
  1. In 2-5 month old group

2. Typically more in winter

18
Q

How do we test for OSA in children?

A
  1. Polysomnography is the only real test we can do

2. Different cutoffs: moderate=5-10/h, severe >10/h

19
Q

Epiglottitis

A
  1. Very quiet, very sick, rapid onset of airway obstruction- get stridor
  2. Drool
20
Q

Red flags with stridor

A
  1. Present since birth
  2. Biphasic
  3. Abnormal voice
  4. Poor feeding

All of these merit further investigation as may be structural