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Cystic fibrosis doctors report
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Cystic fibrosis is a disease many have heard of, but not many actually know what it all entails. The article “About Cystic Fibrosis,” describes it as, “a progressive, genetic disease that causes persistent lung infections and limits the ability to breathe over time” (n.d.). This causes thick mucus buildup not only in the lungs but also in other organs as well such as the pancreas. Because of this build up, bacteria becomes trapped in the patients’ airways, which leads to infections, lung damage, and can even cause respiratory failure. The occurrence in the pancreas causes certain enzymes from being released and used in the body during digestion (“About Cystic Fibrosis,” n.d.). Clearly, this is a very serious disease that requires a lot …show more content…
A person is either a carrier of the defective CF gene, not a carrier of the CF gene, or will have cystic fibrosis. If a person has cystic fibrosis that means that the defective CF gene was received from each parent. If a person does not have two defective CF genes but does have one defective CF gene then he/she is a carrier of cystic fibrosis. There are more than seventy thousand people leaving with this disease worldwide, and most are diagnosed by the age of just two (“About Cystic Fibrosis,” n.d.). That is a very large population so as a nurse it is beneficial to know what this disease is and how and why it …show more content…
Patients must have a high-calorie, high-fat diet, and take vitamin and mineral supplements along with enzyme replacement therapy in a lot of situations because they are not getting the enzymes they need to absorb nutrients. These patients need this particular kind of diet because they require more energy to breathe properly, to fight infections or prevent them, and to aid in poor digestion. Muscle mass is often lost when one has this disease so high protein is needed to maintain a normal weight and body mass index (“Getting Your Nutrients,” n.d.). Nutrition is key in keeping these clients
Infections, for example, sinusitis, bronchitis, and pneumonia add to long-term lung damage. Cystic Fibrosis also causes damage to the pancreas because the thick mucus blocks tubes, and ducts, preventing enzymes from reaching the intestines. When this happens, the digestive system is unable to ingest fundamental fats and proteins, causing diarrhea, serious constipation, and intestinal blockage. As CF worsens, more serious manifestations rise like bronchiectasis, pancreatitis, hepatopathy, and diabetes. Treatment:
b) Comprehensive diagnostic chemistry panel with significantly increased amylase (1626 with normal being 300-1100 U/L), total
CF is a chronic condition therefore the patients are either seeking medical attention or receiving (sometime involuntarily) a great deal of medical scrutiny and intervention during their lifetime.
Being diagnosed with a chronic illness is a life-altering event. During this time, life is not only difficult for the patient, but also for their loved ones. Families must learn to cope together and to work out the best options for the patient and the rest of the family. Although it may not be fair at times, things may need to be centered on or around the patient no matter what the circumstance. (Abbott, 2003) Sacrifices may have to be made during difficult times. Many factors are involved when dealing with chronic illnesses. Coping with chronic illnesses alter many different emotions for the patients and the loved ones. Many changes occur that are very different and difficult to get used to. (Abbott, 2003) It is not easy for someone to sympathize with you when they haven’t been in the situation themselves. No matter how many books they read or people they talk to, they cannot come close to understanding.
In the Shadow of Illness, the book describes different experiences of families who have or had children with cystic fibrosis (CF). CF is an inherited disease that is passed on from the mother or father who is a carrier, but doesn’t have the condition. Doctors have figured that in this scenario, the parents are likely to have a child with CF. Individuals with CF have to take Cotazymes to help the pancreas digest food. If the person does not take these enzymes, the food goes straight through them as diarrhea. Also, the person’s lungs are affected by a thick mucus that must be removed or thinned before it clogs. Doctors recommend the patient to perform daily breathing exercises that prevent the mucus from thickening; for example, swimming
Cystic fibrosis is one of the most common lethal mutations in humans. The autosomal recessive allele is carried by 1/20 Caucasians, 1/400 couples will have children with the disease, and ¼ children will be afflicted. If untreated, 95% of affected ch ildren will die before age five (Bell, 1996).
Cystic Fibrosis (CF) is a very common, potentially life threatening condition. The disease is caused by inheritance, and affects the exocrine glands of the patient. Cystic fibrosis is found primarily among Caucasians and those of European descent. Those diagnosed with Cystic Fibrosis battle daily to perform simple tasks, such as breathing, as the mucus in their bodies thickens immensely. This mucus will potentially accumulate in the patient’s vital organs, such as the lungs, pancreas, and intestines. One can determine if he/she has cystic fibrosis by analyzing certain symptoms. Cystic Fibrosis can be diagnosed according to the symptoms the patient shows, and can be treated through specific types of treatments, such as gene therapy.
Cystic Fibrosis is an inherited disease characterized by the buildup of thick, sticky mucous that can cause severe damage to the body’s organs. Mucous is usually a slippery substance that lubricates and protects the linings of the airway, digestive system, reproductive system and other organs and tissue. Problems with digestion can lead to diarrhea, malnutrition, poor growth, and weight-loss. Due to the abnormally thick mucous it can can clog airways, leading to breathing problems and bacterial infections in the lungs. Bacterial infections can lead to coughing, wheezing and inflammation. Overtime these infections can lead to permanent damage in the lungs including the formation of scar tissue, known as fibrosis and cysts in the lungs (Genetics Home Reference, 2013). The symptoms and signs of this disease vary but mostly include progressive damage to the respiratory system and chronic digestive system problems. An individuals’ lungs who are infected by cystic fibrosis have bacteria from an early stage. This bacteria can spread to the small airways, leading to the formation of bacterial micro-environments known as biofilms. Biofilms are difficult for antibodies to penetrate, therefore the bacteria repeatedly damage the lung and gradually remodel the airways, resulting in difficultly to eradicate the infection (Welsh, 1995). Cystic fibrosis patients may even have their airways chronically colonized be filamentous fungi and/or yeasts. Most men with cystic fibrosis have congenital bilateral absence of the vas deferens (CBAVD), a condition in which the tubes that carry sperm are blocked by mucous and do not develop properly. As well, women may experience complications in pregnancy. Either the c...
Mr. Smith achieved over 100% of his recommended daily protein. Mr. Smith's health is important for him to keep his protein intake within the recommended range because of the health effects of ingesting too much or too little protein. The effects of too much protein can cause kidney failure.(Too Much, 2006) Too little protein intake can mean low energy, low stamina, poor resistance to infection, mental depression, slow healing of wounds, and prolonged recovery from illness.
Cystic Fibrosis is a chronic non-gender biased illness which affects the digestive system and the lungs. This condition also results in the buildup of mucus, which clogs in the respiratory system as well as the pancreas. Cystic Fibrosis occurs because a defective gene causes the body to excrete excessive sticky and thick mucus that clogs the lungs leading to a life-limiting lung infections. When these thick secretions obstruct the pancreas, they prevent the digestive enzymes from reaching the intestines to aid in breaking down as well as absorbing food. However, if Cystic Fibrosis are not treated, it can be fatal as there is no cure. Research shows that each day one person dies from Cystic Fibrosis. As such, this is the most deadly condition
This couple has discussed their concerns involving the genetic possibility of their children having cystic fibrosis since a family member has this disorder.
Thomson, Anne H., and Ann Harris. Cystic Fibrosis: the Facts. Oxford: Oxford UP, 2008. Print.
and loss of appetite caused by the disease itself and by treatment with AZT and
Cystic fibrosis (CF) is an inherited disease that the affects the exocrine glands. CF is located on chromosome 7 and is made up of 250,000 DNA nucleotides. This produces a large amount of sticky mucus which blocks the pathway of the Pancreatic ducts, Bronchi, Lungs, Digestion system and the Theintestines. CF controls the movement of chloride ions in and out of cells. This is important for the salt and water balance on epithelial surfaces, such as the lungs or the pancreas. The bacteria created by the mucus causes the damage to the affected areas. This will often result in respiratory system to be infected. This leads to irreversible damage to the body.
GSD I is a genetic disease resulting from the deficiency of the enzyme glucose-6-phosphate (G-6-P) and glucose-6-phosphate translocase (Andria et al). These particular enzymes are important in enabling the liver to produce glucose from glycogen and/or generate new glucose via gluconeogenesis. The inability of the liver to produce glucose from these metabolic pathways can result in severe hypoglycemia since the liver is responsible for maintaining blood glucose for the body in periods of fasting. The reduction of glycogen breakdown can also cause the kidneys and liver to become enlarged because excess glycogen is typically stored within these two organs. The liver and kidneys can typically function normally during childhood, however because of the increas...