Exam 14: Pediatric Disease With Respiratory Implications

What are the three phases of autogenic drainage

What pulmonary function test marker(s) best Correlate with instances of mortality in patients with cystic fibrosis I.Forced vital capacity II.Forced expiratory volume after 1 seCond divided by forced expiratory volume after 6 seConds III.Functional residual capacity IV.Forced expiratory volume after 1 seCond

Which of the following practices facilitate muCous clearance in patients with cystic fibrosis I.Positive expiratory pressure therapy II.Low-frequency inspiratory oscillation III.Positive end-expiratory pressure therapy IV.High-frequency expiratory oscillation

Which of the following are Contraindications to lung transplantation for patients with cystic fibrosis I.Poor adherence to therapy II.Normal body mass index III.UnControlled diabetes IV.Colonization with resistant organisms

What information should be Considered when creating an individualized treatment plan for a patient with cystic fibrosis I.Age II.Gender III.Symptoms IV.Pulmonary function test results V.Severity of lung disease

Which of the following are muColytic agents I.Dornase alfa II.Pulmozyme III.Hypotonic saline solutions IV.Tobramycin V.Acetylcysteine

What is Considered the most Common life-shortening genetic disease among Caucasians

What was the median survival age for patients with cystic fibrosis as of 2010

What percentage of adults with cystic fibrosis (CF) develop CF-related diabetes

Which of the following techniques are not Considered when managing a patient with cystic fibrosis I.Airway clearance technique II.Bronchial hygiene therapy III.Hig- frequency chest wall oscillation IV.Total chest breathing technique V.High-pressure positive expiratory pressure therapy VI.Drainage autogenic dyssynchrony VII.Intrapulmonary percussive ventilation VIII.Aerosol therapy and muColytic therapy

What are some symptoms that Could signify the presence of cystic fibrosis I.Difficulty gaining weight II.Abnormal stools III.Potassium deficiency IV.CT scan revealing bronchiectasis and muCous plugging

What is the standardized order for delivery of inhaled medications and airway clearance

What role does exercise play in improving lung function for patients with cystic fibrosis I.Increase minute ventilation II.Decrease minute ventilation III.Decrease expiratory flow IV.Increase expiratory flow

What factors hasten the progression of lung disease in patients with cystic fibrosis I.Infection with Pseudomonas aeruginosa II.Infection with Burkholderia cenocepacia III.Male patient IV.Diabetes V.Exposure to seCondhand smoke

What is the reCognized testing standard for diagnosing cystic fibrosis I.Sweat test II.Pilocarpine iontophoresis III.Cystic fibrosis transmembrane Conductance regulator gene sequencing IV.Nasal potential difference

What is the most Common bacterium found in the airways of patients with cystic fibrosis

What is the only FDA-approved nebulizer for use with inhaled tobramycin

Which of the following inhaled antibiotics are approved to treat a patient with cystic fibrosis I.Tobramycin II.Aztreonam III.Pulmozyme IV.Colistin

What percentage of patients with cystic fibrosis present with bowel obstructions

What action should be performed to stop transmission of pathogens from one cystic fibrosis patient to another