Exam 28: Cystic Fibrosis
Exam 1: Fetal Lung Development8 Questions
Exam 2: Fetal Gas Exchange and Circulation9 Questions
Exam 3: Antenatal Assessment and High-Risk Delivery23 Questions
Exam 4: Examination and Assessment of the Neonatal and Pediatric Patient33 Questions
Exam 5: Pulmonary Function Testing and Bedside Pulmonary Mechanics19 Questions
Exam 6: Radiographic Assessment20 Questions
Exam 7: Pediatric Flexible Bronchoscopy20 Questions
Exam 8: Invasive Blood Gas Analysis and Cardiovascular Monitoring21 Questions
Exam 9: Noninvasive Monitoring in Neonatal and Pediatric Care16 Questions
Exam 10: Oxygen Administration17 Questions
Exam 11: Aerosols and Administration of Inhaled Medications23 Questions
Exam 12: Airway Clearance Techniques and Hyperinflation Therapy18 Questions
Exam 13: Airway Management26 Questions
Exam 14: Surfactant Replacement Therapy14 Questions
Exam 15: Noninvasive Mechanical Ventilation and Continuous Positive Pressure of the Neonate20 Questions
Exam 16: Noninvasive Mechanical Ventilation of the Infant and Child21 Questions
Exam 17: Invasive Mechanical Ventilation of the Neonate and Pediatric Patient28 Questions
Exam 18: Administration of Gas Mixtures22 Questions
Exam 19: Extracorporeal Membrane Oxygenation26 Questions
Exam 20: Pharmacology20 Questions
Exam 21: Thoracic Organ Transplantation18 Questions
Exam 22: Neonatal Pulmonary Disorders28 Questions
Exam 23: Surgical Disorders in Childhood That Affect Respiratory Care20 Questions
Exam 24: Congenital Cardiac Defects24 Questions
Exam 25: Pediatric Sleep-Disordered Breathing17 Questions
Exam 26: Pediatric Airway Disorders and Parenchymal Lung Diseases25 Questions
Exam 27: Asthma22 Questions
Exam 28: Cystic Fibrosis19 Questions
Exam 29: Acute Respiratory Distress Syndrome19 Questions
Exam 30: Shock20 Questions
Exam 31: Pediatric Trauma33 Questions
Exam 32: Disorders of the Pleura14 Questions
Exam 33: Neurological and Neuromuscular Disorders16 Questions
Exam 34: Transport of Infants and Children14 Questions
Exam 35: Home Care16 Questions
Exam 36: Quality and Safety12 Questions
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Which of the following radiographic features is consistent with CF?
Free
(Multiple Choice)
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Correct Answer:
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
Free
(Multiple Choice)
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Correct Answer:
D
What percentage of patients with adult cystic fibrosis are chronically infected with Pseudomonas?
Free
(Multiple Choice)
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Correct Answer:
D
Which of the following aerosolized antibiotics is nebulized to treat infections caused by Pseudomonas aeruginosa in patients with CF?
(Multiple Choice)
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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?
(Multiple Choice)
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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?
(Multiple Choice)
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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?
(Multiple Choice)
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Which of the following is the earliest pathologic change that causes airway dysfunction?
(Multiple Choice)
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Which of the following methods is the most commonly recommended for newborn screening?
(Multiple Choice)
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Which of the following therapeutic interventions should be the focus of the treatment of patients with cystic fibrosis?
(Multiple Choice)
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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
(Multiple Choice)
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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
(Multiple Choice)
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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
(Multiple Choice)
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Approximately what percentage of patients with cystic fibrosis present with pulmonary symptoms?
(Multiple Choice)
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What are the chances of two CFTR gene carriers having a child with two normal alleles?
(Multiple Choice)
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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?
(Multiple Choice)
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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
(Multiple Choice)
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Which of the following drugs should the therapist give before administering nebulized 7% saline to a patient with CF?
(Multiple Choice)
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Which of the following is a common nonpulmonary effect of CF?
(Multiple Choice)
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