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5 Written Questions

5 Matching Questions

  1. bronchiectasis (cause)
  2. bronchiectasis (clinical)
  3. diffuse panbronchiolitis
  4. bronchiolar disorders (diagnosis)
  5. CTFR mutation
  1. a bacterial, viral, allergic bronchopulmonary aspergillosis
  2. b HRCT (tree-in-bud opacities)
  3. c chronic cough, foul-smelling sputum
  4. d defective chloride transport, ↑Na absorp (airway, thick mucus) exocrine dysfunction
  5. e in Japan, cough w/ purulent sputum

5 Multiple Choice Questions

  1. hyperplasia/trophy smooth m cells, deposition collagen type I/III (thickening)
  2. patchy inflammation/epithelial injury, fibrosis of bronchioles (noncartilaginous)
  3. triad (wheezing, chronic episodic dyspnea, chronic cough), pulsus paradoxus
  4. cystic fibrosis, primary ciliary dyskinesia
  5. clinical triad (sinusitis, situs inversus, infertility)

5 True/False Questions

  1. asthma (hallmark)diaphoretic↓FEV1, bronchoprovocation challenge (methacholine, cold-air)

          

  2. cystic fibrosis (treatment)pancreatic enzy replacement, antibiotics, bronchodilators, dornase alfa (sputum), inhaled tobramycin (pseudomal)

          

  3. cystic fibrosis (clinical)meconium ileus, steatorrhea, salty-tasting skin, pancreatic insufficiency, malasborption, azoospermia

          

  4. cystic fibrosisautosomal recessive, multi-organ (lung, pancrease, repro), CFTR defect

          

  5. bronchiolitis obliterans syndrome (treatment)Azithromycin

          

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