Pediatric Resp Flashcards
What are some common presentations of cystic fibrosis?
- Nasal polyps/ sinusitis
- Persistent cough/ resp infection/ refractory asthma
- Fussy baby
- Steatorrhea
- Failure to thrive, malnutrition
Laryngomalacia
- Most common cause of chronic stridor
- Worse with feeding, crying
- Spontaneous resolution by 12-18 mo
Congenital tracheal lesions causing stridor
- Tracheomalacia
- Anterior compression (inominate artery)
- Vascular sling (left pulmonary artery wraps)
Acquired structural airway lesions causing stridor
- Granuloma
- Papilloma
- Tumours
- Subglottic Stenosis
- Vocal cord paresis
Croup
- Caused by parainfluenza virus
- 3mo to 3 years
- Febrile
- Gradual progression of barky cough to stridor
- May have rhinorrhea, hoarseness, conjunctivitis
- treat with nebulized epinephrine, systemic steroids
Bacterial Tracheitis
- Caused by staph aureus, group a strep
- 1-8 years old
- Sick
- Muffled voice, cough, tracheal tenderness
- Gradual progression to stridor
- Treatment: NPO, analgesia, antibiotics
When do you need to rule cystic fibrosis out?
- Bowel obstruction
- Rectal prolapse
- Family hx
What are concerning features of a childhood cough?
- Perceived to be ill
- Losing sleep
- Interfering with school
- MSK pain
- Associated vomiting
What mutation causes cystic fibrosis?
F508 in the CFTR protein
Actually many mutations
What virus causes bronciolitis?
RSV
What are the risk factors for pediatric asthma
- pre or post natal tobacco exposure
- viral infections with RSV
- indoor/outdoor pollution
What signs do you NOT see in pediatric asthma?
- clubbing, polyps (CF)
- Hyperinflation
- Hemmorrage in eye (Pertussis)
How is pediatric asthma treated?
- Usually first line is trial therapy of inhaled steroids
- Second line is leukotriene receptor antagonist (add this on if refractory)
- Use chamber with mask or valve depending on age
Education is vital! - Usually only do PFTs if old enough (usually around 8 years old)
What are the system based effects of cystic fibrosis?
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
How do we test for cystic fibrosis
- Currently newborn screening programs in most provinces (Immune reactive trypsinogen first step, then sweat chloride, then genetic testing)
- May also do CXR/CT/PFTs if later