Exam 28: Cystic Fibrosis
Exam 1: Fetal Lung Development6 Questions
Exam 2: Fetal Gas Exchange and Circulation7 Questions
Exam 3: Antenatal Assessment and High Risk Delivery24 Questions
Exam 4: Exam and Assessment of the Neonatal and Pediatric Patient33 Questions
Exam 5: Pulmonary Function Testing and Bedside Pulmonary Mechanics18 Questions
Exam 6: Radiographic Assessment19 Questions
Exam 7: Bronchoscopy20 Questions
Exam 8: Invasive Blood Gas Analysis and Monitoring21 Questions
Exam 9: Noninvasive Monitoring in Neonatal and Pediatric Care18 Questions
Exam 10: Oxygen Administration17 Questions
Exam 11: Aerosols and Administration of Medication22 Questions
Exam 12: Airway Clearance Techniques and Lung Volume Expansion20 Questions
Exam 13: Airway Management25 Questions
Exam 14: Surfactant Replacement14 Questions
Exam 15: Non-Invasive Mechanical Ventilation and Continuous Positive Pressure of the Neonate19 Questions
Exam 16: Noninvasive Mechanical Ventilation of the Child21 Questions
Exam 17: Mechanical Ventilation of the Neonate and Pediatric Patient28 Questions
Exam 18: Administration of Gas Mixtures24 Questions
Exam 19: Extracorporeal Life Support25 Questions
Exam 20: Pharmacology20 Questions
Exam 21: Thoracic Organ Transplantation19 Questions
Exam 22: Neonatal Complications and Pulmonary Disorders26 Questions
Exam 23: Congenital and Surgical Disorders That Affect Respiratory Care20 Questions
Exam 24: Congenital Cardiac Defects24 Questions
Exam 25: Sudden Infant Death Syndrome Sleep Disorders16 Questions
Exam 26: Pediatric Airway Disorders and Pulmonary Infections24 Questions
Exam 27: Asthma22 Questions
Exam 28: Cystic Fibrosis18 Questions
Exam 29: Acute Respiratory Distress Syndrome19 Questions
Exam 30: Shock, Sepsis and Anaphylaxis21 Questions
Exam 31: Pediatric Trauma53 Questions
Exam 32: Disorders of the Pleura14 Questions
Exam 33: Neurologic and Neuromuscular Disorders15 Questions
Exam 34: Transport of Infants and Children14 Questions
Exam 35: Home Care16 Questions
Exam 36: Quality and Safety11 Questions
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Which of the following is the earliest pathologic change that causes airway dysfunction?
Free
(Multiple Choice)
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Correct Answer:
D
On pulmonary function testing,which of the following lung abnormalities is/are common in patients with severe cystic fibrosis?
I.Obstructive pattern
II.Restrictive pattern
III.Airway hyperreactivity
IV.Normal pattern when asymptomatic
Free
(Multiple Choice)
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Correct Answer:
D
Which of the following respiratory signs and symptoms should prompt the therapist for evaluation of cystic fibrosis in a child?
I.Recurrent wheezing
II.Frequent thick sputum production
III.Chronic cough
IV.Nasal polyps
Free
(Multiple Choice)
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Correct Answer:
D
What are the chances of two CFTR gene carriers having a normal child?
(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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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 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 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 microorganisms commonly colonize the airways of patients with cystic fibrosis?
I.Actinomyces israelii
II.Haemophilus influenzae
III.Pseudomonas aeruginosa
IV.Staphylococcus aureus
(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 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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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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Approximately what percentage of patients with cystic fibrosis present with pulmonary symptoms?
(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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Which of the following radiographic features is consistent with CF?
(Multiple Choice)
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Which of the following antiinflammatory agents should be considered in patients with CF to slow the progression of the lung disease?
(Multiple Choice)
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What percentage of patients with adult cystic fibrosis are chronically infected with Pseudomonas?
(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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