Smith Seminars Online Cystic Fibrosis Test
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If for some reason you do not pass the test with 70% correct you will be notified by email to retake the test. Your order confirmation number will stay valid until you pass the test.
Part 1 - Your Information
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Part 2 - The Test
1) Manifestations of pancreatic insufficiency include:
A) Frequent passage of bulky, foul-smelling, oily stools
B) Poor growth pattern with increased subcutaneous tissue and muscle mass
C) Abdominal prolapse
D) Rectal protuberance
2) In cystic fibrosis, pulmonary damage is probably initiated by diffuse obstruction in the small airways by:
A) Increased glucose content of secretions
B) Abnormally thick mucus secretions
C) Decreased amount of mucus produced
D) None of the above
3) Pulmonary function testing is used to:
A) Provide evidence of pulmonary exacerbations
B) Follow progression of the disease
C) A only
D) A & B
4) The quantitative pilocarpine iontophoresis sweat test is:
A) Standard for diagnosing CF
B) Measures the amount of sodium and chloride in a person's sweat.
C) Can be performed on patients as young as four weeks of age
D) All the above
5) CF patients are at risk for zinc and vitamin deficiencies, particularly during the first year of life due to:
A) Malabsorption of fats
B) Malabsorption of proteins
C) A & B
6) Clinical signs in the CF patient that suggests chronic lung disease include:
7) In the CF patient,:
8) Forced expiratory technique include:
9) In people with CF, the DHA levels:
10) Low pressure PEP:
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Smith Seminars
PO Box 516 · Paradise · TX · 76073
Phone 866-857-2211 · Fax 972-759-9197 Email debra@smithseminars.com
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