Phlebotomy Essentials
6th Edition
ISBN:9781451194524
Author:Ruth McCall, Cathee M. Tankersley MT(ASCP)
Publisher:Ruth McCall, Cathee M. Tankersley MT(ASCP)
Chapter1: Phlebotomy: Past And Present And The Healthcare Setting
Section: Chapter Questions
Problem 1SRQ
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Question
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Baby Sean has cystic fibrosis (CF), a life-threatening genetic disease. He inherited a defective gene from each
parent. This faulty gene adversely affects the transport of salt—sodium chloride (NaCl)—into and out of cells. As a result, thick, sticky secretions are produced in both the digestive and respiratory systems. In someone with
CF, the digestive juices produced are so thick they clog in the pancreas and cannot get into the small intestine.
Digestive juices contain enzymes that break down carbohydrates, lipids, and proteins in food so that they can be
absorbed and used by cells. Without these enzymes, Sean’s food passes right through him without being digested, leading to weight loss and fatty stools. In addition, the abnormal secretions clog the lungs, making Sean short of breath, wheezy, and susceptible to repeated lung infections. Finally, CF makes his skin taste very salty because of salt being lost in the sweat.
The diagnosis of cystic fibrosis is made with a sweat test. A sweat-producing chemical is applied to an
area of Sean’s skin, and the sweat is collected and tested for chloride concentration. Sean’s treatment starts
immediately. His parents give him digestive enzymes before each feeding so that he can absorb nutrients. Sean’s parents learn chest physical therapy: For 20–60 minutes, twice per day, they percuss (clap forcefully with a
cupped hand) and vibrate (shake with an open hand) his chest to loosen the thick mucus so he can cough it up
and out. Soon Sean gains weight and begins to thrive, but this therapy will be lifelong.
QUESTIONS:
1. What undigested substances would have made Sean’s stools greasy and foamy?
2. Why are digestive enzymes necessary for life?
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