Essay On Cystic Fibrosis

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Cystic Fibrosis is a genetic disorder that results in abnormal secretions of the respiratory, digestive, reproductive tracts. Although it is a multi-organ disease, the lungs are the most affected and respiratory failure is the primary cause of death (McCance & Huether, 2014). My career in nursing has been solely focused on adult neurosurgical spine patients and to date have not cared for patients with cystic fibrosis. That being said, these patients have a significant risk for vertebral fractures. The article chosen for this discussion is: Increased whole body hydroxyproline production as assessed by a new stable isotope technique is associated with hip and spine bone mineral loss in cystic fibrosis by Engelen, Com, & Deutz, published in the Journal of Nutrition. …show more content…
Historically, evaluation of bone mineral density through conventional means (urinary OH-PRO excretion rates, serum hydroxyproline levels, and bone density scans) are time consuming and have not been entirely accurate in predicting hip and vertebral fractures (Engelen, Com, & Deutz, 2014). This is because these tests take an overall look at hydroxyproline levels and whole body density scans. The urinary test required a 24 hour collection period and the serum test required a collagen-free diet prior to testing.
This study evaluates the infusion of a stable isotope to measure actual production of hydroxyproline at the time of infusion and is not affected by acute changes in serum hydroxyproline and does not require a collagen-free diet at the time of testing (Engelen, Com, & Deutz, 2014). Fifteen cystic fibrosis patients and seventeen health patients were used in the study showed an accurate assessment of whole-body collagen breakdown as compared with previous methods of testing without the time consuming process or restrictive diets of the

Cystic fibrosis Essay

Speech Outline *Title: Cystic Fibrosis *Specific Purpose: To inform my classmates about cystic fibrosis and how severe it really is. *Thesis Statement: Cystic Fibrosis is a disease that is slowly killing our children and the question is how can we help these children in their times of need? Introduction Attention-getter: How many people love children? how would you feel if you knew that a mass majority of our youth has been born with and/or died from cystic fibrosis? Preview: Today I will be…

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Essay On Cystic Fibrosis

How do you think a person with cystic fibrosis lives? Cystic Fibrosis is a rare genetic disease that affects the digestive and respiratory system. Cystic Fibrosis is more common in caucasians than other race. They have to deal with the symptoms that come with the disease. Someone who is living with cystic fibrosis has many treatments/ therapies. Cystic Fibrosis is an inherited condition which makes a person develop a sticky mucus that makes it hard to breathe. It affects the lungs, liver, pancreas…

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Cystic Fibrosis Essay

Cystic Fibrosis Cystic Fibrosis is the most common lethal genetic disease in the U.S. that causes severe damage to the lungs and digestive system. It is an inherited disease that affects the cells that produce mucus, sweat and digestive juices. In affected individuals, the body produces mucus that is abnormally thick and sticky, so instead of acting as a lubricant, the mucus plugs up tubes, ducts and passageways, especially in the lungs and pancreas. As a result, a person living with cystic fibrosis…

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Essay On Cystic Fibrosis

breathe through it? It is not easy, right? For people with Cystic Fibrosis this is a daily occurrence. CF is a chronic disease affecting the lungs and digestive track of many people in the United States. Cystic Fibrosis is a disease that effects your genes. “An inherited condition, cystic fibrosis affects the cells that produce mucus, sweat and digestive juices. These secreted fluids are normally thin and slippery. But in cystic fibrosis, a defective gene causes the secretions to become thick and…

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Cystic Fibrosis Essay

(IPV), and physical activity and prescribed systemic exercise programmes (Rogers & Doull, 2005). Aggressive antibiotic therapy of bacterial airway infection is one of the main reasons for the dramatic increase in life expectancy of patients with cystic fibrosis. In patients infected with P. aeruginosa, antibiotic therapy is guided both by the clinical course of the…

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Cystic Fibrosis Essay

Cystic fibrosis What causes cystic fibrosis? A mutation in the cystic fibrosis transmembrane regulatory protein CFTR. What does CFTR protein do? It helps control the viscosity of mucus that lines the epithelial cells of the airways digestive and reproductive systems. If the mucus in airways is: • Too sticky- the cilia can’t beat and remove the mucus which then clogs up the airways. How does it affect the lungs? Sticky mucus builds up in the airways reducing flow of air into alveoli, lungs…

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Cystic Fibrosis Essay

Importance of Cystic Fibrosis Cystic Fibrosis a hereditary disorder affecting the exocrine glands. It causes the production of abnormally thick mucus, leading to the blockage of the pancreas ducts, intestines, and bronchi and often resulting in respiratory infections. Symptoms include difficulty breathing, life altering respiratory tract problems, sever or chronic lung infection, impaired growth or weight gain and extreme difficulty absorbing nutrients all due to this abnormally thick mucus. Healthy…

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Cystic Fibrosis Essay

Cystic Fibrosis Cystic Fibrosis is a genetic disorder and can affect many parts of your body such as your lungs, pancreas, and other essential organs by clogging them with sticky mucus. The mucus is very harmful to people with the disease because they cannot break down their food and have very troublesome time breathing. Cystic Fibrosis is a very serious disorder, because you do not live that long and there is no cure. Some symptoms of Cystic Fibrosis include very salty-tasting skin, persistent…

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Essay on CYSTIC FIBROSIS BASICS

CYSTIC FIBROSIS Word Bank: CFTR: gene that produces an integral membrane glycoprotein that acts as a CFTR channel that transports s chloride, bicarbonate and glutathione. Mucus: a slimy substance, typically not miscible with water, secreted by mucous membranes and glands for lubrication, protection. What is Cystic Fibrosis? A genetic disease resulting in abnormal secretions of the exocrine glands that influence a variety of clinical effects: chronic lung disease and pancreatic…

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Essay on Homework: Cystic Fibrosis and Social Care Services

PIES. Cystic fibrosis: Physical: The two organs most affected are the lungs and pancreas, where the thick mucus causes breathing and digestive problems. The thicker mucus has trouble moving out of the lungs, so bacteria can remain and cause infections, struggle to breathe may mean that you can’t take part in daily activities. You may also loss some self-confidence because you will experience bulky, light-coloured, foul-smelling bowel movements or diarrhoea (because food isn't being digested…

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