Exam 28: Cystic Fibrosis

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Which of the following radiographic features is consistent with CF?

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C

Which of the following microorganisms commonly colonize the airways of patients with cystic fibrosis? I. Actinomyces israelii II. Haemophilus influenzae III. Pseudomonas aeruginosa IV. Staphylococcus aureus

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D

What percentage of patients with adult cystic fibrosis are chronically infected with Pseudomonas?

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D

Which of the following aerosolized antibiotics is nebulized to treat infections caused by Pseudomonas aeruginosa in patients with CF?

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A sweat chloride test and CFTR mutation analysis performed in a 10-year-old child with signs and symptoms consistent with CF are inconclusive. Which of the following tests should the therapist suggest at this time?

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A sweat chloride test is performed in a 14-year-old child who has adrenal insufficiency. What effect can this condition have on the results of this diagnostic test?

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Which of the following anti-inflammatory agents should be considered in patients with CF to slow the progression of the lung disease?

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Which of the following is the earliest pathologic change that causes airway dysfunction?

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Which of the following methods is the most commonly recommended for newborn screening?

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Which of the following therapeutic interventions should be the focus of the treatment of patients with cystic fibrosis?

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Which of the following medications should the therapist routinely administer during the management of hospitalized patients with cystic fibrosis? I. Albuterol II. Hypertonic saline III. DNAse IV. Salmeterol

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Which of the following respiratory signs and symptoms should prompt the therapist for the evaluation of cystic fibrosis in a child? I. Seasonal wheezing II. Frequent thick sputum production III. Chronic cough IV. Nasal polyps

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On pulmonary function testing, which of the following lung abnormalities are common in patients with severe cystic fibrosis? I. Obstructive pattern II. Restrictive pattern III. Airway hyperreactivity IV. Normal pattern when asymptomatic

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Approximately what percentage of patients with cystic fibrosis present with pulmonary symptoms?

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What are the chances of two CFTR gene carriers having a child with two normal alleles?

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A 10-year-old child has had two sweat tests, each indicating a sweat chloride concentration of 30 mEq/L. How should the therapist interpret these data?

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What are the primary characteristics of cystic fibrosis? I. Chronic obstruction and inflammation of the airways II. Exocrine pancreatic insufficiency III. Malabsorption and small bowel obstruction IV. Decreased sweat chloride concentration

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Which of the following drugs should the therapist give before administering nebulized 7% saline to a patient with CF?

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Which of the following is a common nonpulmonary effect of CF?

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