Exam 15: Cystic Fibrosis
Exam 1: The Patient Interview13 Questions
Exam 2: The Physical Examination and Its Basis in Physiology13 Questions
Exam 3: Pulmonary Function Study Assessments13 Questions
Exam 4: Arterial Blood Gas Assessments13 Questions
Exam 5: Oxygenation Assessments13 Questions
Exam 6: Cardiovascular System Assessments13 Questions
Exam 7: Radiologic Examination of the Chest13 Questions
Exam 8: Other Important Tests and Procedures13 Questions
Exam 9: The Therapist-Driven Protocol Program and the Role of the Respiratory Therapist11 Questions
Exam 10: Respiratory Failure and the Mechanical Ventilation Protocol6 Questions
Exam 11: Recording Skills: The Basis for Data Collection, Organization, Assessment Skill10 Questions
Exam 12: Chronic Obstructive Pulmonary Disease (COPD), Chronic Bronchitis, and Emphysema17 Questions
Exam 13: Asthma15 Questions
Exam 14: Bronchiectasis18 Questions
Exam 15: Cystic Fibrosis19 Questions
Exam 16: Pneumonia12 Questions
Exam 17: Lung Abscess13 Questions
Exam 18: Tuberculosis18 Questions
Exam 19: Fungal Diseases of the Lung18 Questions
Exam 20: Pulmonary Edema18 Questions
Exam 21: Pulmonary Vascular Disease: Pulmonary Embolism and Pulmonary Hypertension18 Questions
Exam 22: Flail Chest16 Questions
Exam 23: Pneumothorax17 Questions
Exam 24: Pleural Effusion and Empyema14 Questions
Exam 25: Kyphoscoliosis16 Questions
Exam 26: Interstitial Lung Diseases17 Questions
Exam 27: Cancer of the Lung15 Questions
Exam 28: Acute Respiratory Distress Syndrome16 Questions
Exam 29: Guillain-Barré Syndrome17 Questions
Exam 30: Myasthenia Gravis19 Questions
Exam 31: Sleep Apnea16 Questions
Exam 32: Clinical Manifestations Common with Newborn and Early Childhood Respiratory Dis17 Questions
Exam 33: Meconium Aspiration Syndrome16 Questions
Exam 34: Transient Tachypnea of the Newborn17 Questions
Exam 35: Respiratory Distress Syndrome18 Questions
Exam 36: Pulmonary Air Leak Syndromes16 Questions
Exam 37: Respiratory Syncytial Virus (Bronchiolitis or Pneumonitis)15 Questions
Exam 38: Bronchopulmonary Dysplasia17 Questions
Exam 39: Congenital Diaphragmatic Hernia17 Questions
Exam 40: Congenital Heart Diseases10 Questions
Exam 41: Croup Syndrome: Laryngotracheobronchitis and Acute Epiglottitis17 Questions
Exam 42: Near Drowning/Wet Drowning17 Questions
Exam 43: Smoke Inhalation, Thermal Injuries, and Carbon Monoxide Intoxication18 Questions
Exam 44: Atelectasis18 Questions
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All of the following can be used in the diagnosis of cystic fibrosis EXCEPT:
Free
(Multiple Choice)
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Correct Answer:
A
Which of the following is NOT recommended in children with cystic fibrosis?
Free
(Multiple Choice)
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Correct Answer:
A
What complicating pulmonary problem is likely to happen to a patient with cystic fibrosis?
Free
(Multiple Choice)
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Correct Answer:
C
A patient has a lung infection with Pseudomonas aeruginosa. What antibiotic should be used against it?
(Multiple Choice)
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During the advanced stages of cystic fibrosis, the anatomic alterations cause the patient to have:
(Multiple Choice)
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Which of the following may be recommended to reduce bronchial inflammation in a 12-year-old child with cystic fibrosis?
(Multiple Choice)
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The major pathologic or structural changes associated with cystic fibrosis include:
1) partial airway obstruction leading to hyperinflation.
2) bronchospasm.
3) thick, tenacious mucus.
4) total airway obstruction leading to atelectasis.
(Multiple Choice)
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A cystic fibrosis patient in generally good condition may be a candidate for which of the following?
(Multiple Choice)
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Which of the following are commonly cultured from the mucus in the tracheobronchial tree of a patient with cystic fibrosis?
1) Klebsiella
2) Pseudomonas aeruginosa
3) Haemophilus influenzae
4) Staphylococcus aureus
(Multiple Choice)
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Men with cystic fibrosis have difficulty reproducing because the:
(Multiple Choice)
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All of the following chest assessment findings may be seen in a patient with cystic fibrosis EXCEPT:
(Multiple Choice)
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How can the genetic mutation found with cystic fibrosis (CF) be characterized?
1) There are many variations in the mutation.
2) CF is the most common fatal childhood inherited disorder.
3) The mutation is a dominant trait.
4) The mutation stops ciliary function.
(Multiple Choice)
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If both the mother and the father are carriers for the cystic fibrosis gene, what are the chances that their child will be a cystic fibrosis carrier?
(Multiple Choice)
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Which of the following are commonly used in the management of cystic fibrosis?
1) Pancreatic enzymes and vitamins
2) Antibiotics
3) Postural drainage
4) Expectorants
(Multiple Choice)
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A common nonrespiratory clinical manifestation of cystic fibrosis is:
(Multiple Choice)
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Which ethnic group has the greatest number of people with cystic fibrosis?
(Multiple Choice)
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Cystic fibrosis patients can have all of the following EXCEPT:
(Multiple Choice)
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Common chest assessment findings in a patient with cystic fibrosis include:
1) tracheal deviation.
2) breath sounds reveal crackles and rhonchi.
3) dull percussion note.
4) hyperresonant percussion note.
(Multiple Choice)
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All of the following pulmonary function findings would be expected in a patient with moderate to severe cystic fibrosis EXCEPT:
(Multiple Choice)
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