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Testbank For Neonatal And Pediatric Respiratory Care 6Th Edition By Walsh/All Chapters Complete 1-36

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TESTBANK FOR NEONATAL AND PEDIATRIC RESPIRATORY CARE 6TH EDITION BY WALSH/ALL CHAPTERS COMPLETE 1-36

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,Neonatal and Pediatric Respiratory Care, 6th Edition, Brian K. Walsh Test Bank
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Table of Contents
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Chapter 1. Fetal Lung Development
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Chapter 2. Fetal Gas Exchange and Circulation
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Chapter 3. Antenatal Assessment and High-Risk Delivery
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Chapter 4. Examination and Assessment of the Neonatal and Pediatric Patient
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Chapter 5. Pulmonary Function Testing and Bedside Pulmonary Mechanics
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Chapter 6. Radiographic Assessment
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Chapter 7. Pediatric Flexible Bronchoscopy
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Chapter 8. Invasive Blood Gas Analysis and Cardiovascular Monitoring
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Chapter 9. Noninvasive Monitoring in Neonatal and Pediatric Care
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Chapter 10. Oxygen Administration
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Chapter 11. Aerosols and Administration of Inhaled Medications
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Chapter 12. Airway Clearance Techniques and Hyperinflation Therapy
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Chapter 13. Airway Management
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Chapter 14. Surfactant Replacement Therapy
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Chapter 15. Noninvasive Mechanical Ventilation and Continuous Positive Pressure of the Neonate
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Chapter 16. Noninvasive Mechanical Ventilation of the Infant and Child
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Chapter 17. Invasive Mechanical Ventilation of the Neonate and Pediatric Patient
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Chapter 18. Administration of Gas Mixtures
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Chapter 19. Extracorporeal Membrane Oxygenation
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Chapter 20. Pharmacology
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Chapter 21. Thoracic Organ Transplantation
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Chapter 22. Neonatal Pulmonary Disorders
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Chapter 23. Surgical Disorders in Childhood that Affect Respiratory Care
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Chapter 24. Congenital Cardiac Defects
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Chapter 25. Pediatric Sleep-Disordered Breathing
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Chapter 26. Pediatric Airway Disorders and Parenchymal Lung Diseases
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Chapter 27. Asthma
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Chapter 28. Cystic Fibrosis
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Chapter 29. Acute Respiratory Distress Syndrome
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Chapter 30. Shock
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Chapter 31. Pediatric Trauma
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Chapter 32. Disorders of the Pleura
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Chapter 33. Neurological and Neuromuscular Disorders
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Chapter 34. Pediatric Emergencies
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Chapter 35. Home Care of the Postpartum Family
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Chapter 36. Quality and Safety
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,Chapter 1: Fetal Lung Development
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Walsh: Neonatal & Pediatric Respiratory Care 5th Edition Test Bank (2020)
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MULTIPLE CHOICE %




1. Which of the following phases of human lung development is characterized by the formatio
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n of a capillary network around airway passages?
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a. Pseudoglandular
b. Saccular
c. Alveolar
d. Canalicular

ANS: D %


The canalicular phase follows the pseudoglandular phase, lasting from approximately 17 we
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eks to 26 weeks of gestation. This phase is so named because of the appearance of vascular c
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hannels, or capillaries, which begin to grow by forming a capillary network around the air p
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assages. During the pseudoglandular stage, which begins at day 52 and extends to week 16
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of gestation, the airway system subdivides extensively and the conducting airway system de
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velops, ending with the terminal bronchioles. The saccular stage of development, which take
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s place from weeks 29 to 36 of gestation, is characterized by the development of sacs that lat
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er become alveoli. During the saccular phase, a tremendous increase in the potential gas-
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%exchanging surface area occurs. The distinction between the saccular stage and the alveolar
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%stage is arbitrary. The alveolar stage stretches from 39 weeks of gestation to term. This stag
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e is represented by the establishment of alveoli.
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REF: pp. 3-5 % %




2. Regarding postnatal lung growth, by approximately what age do most of the alveoli that wil
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l be present in the lungs for life develop?
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a. 6 months %


b. 1 year %


c. 1.5 years %


d. 2 years %




ANS: C %


Most of the postnatal formation of alveoli in the infant occurs over the first 1.5 years of life.
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%At 2 years of age, the number of alveoli varies substantially among individuals. After 2 year
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s of age, males have more alveoli than do females. After alveolar multiplication ends, the al
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veoli continue to increase in size until thoracic growth is completed.
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REF: p. 6 % %




3. The respiratory therapist is evaluating a newborn with mild respiratory distress due to trachea
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l stenosis. During which period of lung development did this problem develop?
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, a. Embryonal
b. Saccular
c. Canalicular
d. Alveolar
ANS: A %


The initial structures of the pulmonary tree develop during the embryonal stage. Errors in de
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velopment during this time may result in laryngeal, tracheal, or esophageal atresia or stenosi
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s. Pulmonary hypoplasia, an incomplete development of the lungs characterized by an abnor
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mally low number and/or size of bronchopulmonary segments and/or alveoli, can develop d
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uring the pseudoglandular phase. If the fetus is born during the canalicular phase (i.e., prem
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aturely), severe respiratory distress can be expected because the inadequately developed air
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ways, along with insufficient and immature surfactant production by alveolar type II cells, g
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ives rise to the constellation of problems known as infant respiratory distress syndrome.
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REF: p. 6 %% %




4. Which of the following mechanisms is (are) responsible for the possible association betwee
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n oligohydramnios and lung hypoplasia?
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I. Abnormal carbohydrate metabolism % %


II. Mechanical restriction of the chest wall % % % % %



III. Interference with fetal breathing % % %



IV. Failure to produce fetal lung liquid
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a. I and III only
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b. II and III only
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c. I, II, and IV only
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d. II, III, and IV only
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ANS: D %


Oligohydramnios, a reduced quantity of amniotic fluid present for an extended period of time
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, with or without renal anomalies, is associated with lung hypoplasia. The mechanisms by w
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hich amniotic fluid volume influences lung growth remain unclear. Possible explanations for r
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educed quantity of amniotic fluid include mechanical restriction of the chest wall, interferenc
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e with fetal breathing, or failure to produce fetal lung liquid. These clinical and experimental
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%observations possibly point to a common denominator, lung stretch, as being a major growt
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h stimulant.
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REF: pp. 6-7 % %




5. What is the purpose of the substance secreted by the type II pneumocyte?
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a. To increase the gas exchange surface area
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b. To reduce surface tension
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c. To maintain lung elasticity
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d. To preserve the volume of the amniotic fluid
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Publisher: Unknown ISBN: 9780323793094 Edition: Unknown

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