Cystic fibrosis research paper outline. Research Paper on Cystic Fibrosis 2022-11-15
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Cystic fibrosis (CF) is a chronic, genetic disease that affects the respiratory and digestive systems. It is caused by a mutation in the gene that encodes for the cystic fibrosis transmembrane conductance regulator (CFTR) protein, which regulates the movement of salt and water in and out of cells. As a result of the mutation, thick and sticky mucus builds up in the lungs, pancreas, and other organs, leading to a range of serious health problems, including difficulty breathing, frequent lung infections, and malnutrition.
CF is a rare disease, affecting about 30,000 people in the United States and 70,000 people worldwide. It is most common in people of Northern European ancestry, but it can affect people of any racial or ethnic background. There is currently no cure for CF, but treatments such as antibiotics, airway clearance techniques, and nutritional support can help improve quality of life and extend lifespan.
Other complications (liver disease, diabetes, infertility)
III. Diagnosis and treatment of CF
Tests and procedures used to diagnose CF (sweat test, genetic testing)
Current treatments for CF (antibiotics, airway clearance techniques, nutritional support)
Experimental treatments and potential therapies (gene therapy, CFTR modulators)
IV. The impact of CF on patients and their families
Physical and emotional challenges of living with CF
Support systems for individuals with CF and their families
Advocacy and research efforts to find a cure for CF
V. Conclusion
Recap of the main points of the essay
Reflection on the importance of ongoing research and treatment for CF
Call to action for readers to learn more about CF and support efforts to find a cure.
Home Page: Journal of Cystic Fibrosis
Sometimes a sore throat is mistaken for strep throat. In medical treatment, a doctor may subscribe antibiotics or medication that helps in mucus thinning. These fluids that are secreted are normally thin and slippery. A defective gene causes the secretions to become thick and sticky. Due to the importance of this condition, …show more content… Cystic fibrosis most commonly affects Caucasians, with a prevalence of about 1:3000 persons in Caucasian Americans. Quality of life with cystic fibrosis has been greatly improved with the current treatments offered, before the 1980s half of patients diagnosed with cystic fibrosis did not live into their 20s.
Today doctors understand the disease much better. Types of cystic fibrosis research The complications of CF caused by CFTR malfunction include Research into nonsense and rare CF mutations Early cystic fibrosis research naturally focused on treatments for the most common genetic mutations. This implies patients and their families should pay for convenience, travel costs, parking, day care and loss of Cystic Fibrosis Changed My Life 289 Words 2 Pages In my childhood I rarely took notice to the impact that Cystic Fibrosis was leaving on my life. Another major management protocol that has been found to be very efficient in managing some of the symptoms of the cystic fibrosis is the provision of hypertonic saline for the affected individual, especially those patients that are 6 years old and above Girish, 2014. Discovered in 1989, Cystic Fibrosis is the most common, fatal genetic disease in the United States. It is most common among nations in the Western world minus the exception of Finland but it is equally diagnosed between male and female.
This causes for the body to produce thick, sticky mucus that clogs up the lungs, leads to infection, blocks the pancreas, which stops the digestive enzymes from reaching the intestine. Sanfilippo type A: A person does not have a normal working form of the enzyme called heparan N-sulfatase, Sanfilippo type B: Occurs when a person Clostridium Difficile Case Study 1464 Words 6 Pages Clostridium difficile, also referred to as C. Cyanosis occurs as a result of the decrease in gas exchange through the inflamed alveolar membrane and subsequent decline in hemoglobin saturation. The variation in the clinical manifestation is usually by the age of the patient, especially the age at presentation. Patients with cystic fibrosis can be prescribed antibiotics, anti-inflammatory drugs, and mucous thinners to help. Diet with additional energy and unrestricted fat intake is important for such affected individual.
Over half the of the people with CF are over the age of 18. I did use some academic databases like NCBI. Due to the malfunction in the glands that produce mucus, the lungs tend to accumulate thick mucus that eventually leads to infection, difficulty breathing and in severe cases a lung transplant or respiratory failure. Bridges of this extra bone develops across joints which causes immobility What is FOP. The treatment protocols that are currently in use are therefore designed to address the immediate symptoms of the condition, which in many cases. There was no problem when it came to narrowing down on one particular search because I knew cystic fibrosis was one major respiratory challenge to many. Works Cited Dahl, Morten, Anne Tybjaerg-Hansen, Peter Lange and Borge Nordestgaard.
Statistics show that 30,000 people in the US have been named with this disease. Pulmonary issues or involvement is found in 90 percent of patients surviving the neonatal period. This disease also effects the …show more content… Delta F508 is the most common mutation in …show more content… REPETATIVE, CHANGE INTRO It is estimated that 1 in every 3,700 births will have cystic fibrosis placing this disease the second most common life-shortening inherited disease. This is especially found in young babies, where the intestines are blocked some few days after birth or when the kids are introduced to solid foods. Cystic fibrosis causes protean manifestations, but the most common include lung and gastrointestinal symptoms. It also maximizes the remaining capabilities and functions of an already disabled patient. With time patients develop bronchiectasis.
Reimbursement: The Role Of Ethical Issues In Healthcare 635 Words 3 Pages Healthcare ethics involves making well researched and considerate decisions about medical treatments, while taking into consideration a patient's beliefs and wishes regarding all aspects of their health. Causes The disease is primarily characterised with secretion of slippery mucus. Stanford researchers in their studies have established some form of new sweat tests for cystic fibrosis, which has been noted to lead to more treatments Becky, 2014. The secretions plug up tubes, ducts and airways in the lungs and pancreas. This can be an overwhelming experience for a parent, adult or family to persevere. This has moved the researchers closer towards finding a potential drug to manage the condition.
Fibrodysplasia Research Paper 1450 Words 6 Pages Fibrodysplasia Ossificans Progressiva which is sometimes referred to FOP is a very rare genetic disorder in which bones grow uncontrollably to the point of causing disability Fibrous Dysplasia. Although technically a rare disease, it is ranked as one of the most wide spread life-shortening genetic diseases. However, the most common and deadly lupus is Systemic Lupus Erythematosus SLE. Under chest physical therapy, a patient is supposed to lie down on their stomach. This test helps in Patients with cystic fibrosis are subjected to medical imaging examination as it helps in monitoring the disease pathologic changes. Cystic Fibrosis patients either produce uncommon CFTR protein or no CFTR protein at all.
The CFTR gene deficiency also affects some other parts of the body in various ways. A host or researches that had been done on cystic fibroids appeared ranging from systematic reviews to peer reviewed scientific journal articles appeared. In the case of CF, many potential new drugs target certain genetic mutations, such as F508del. This bacterium can also be spread through contact from healthcare workers that have not followed correct cleansing routines such as but not limited to hand washing. Nursing assistants need to know what the persons wishes are if they do pass. In turn, this affects the respiratory system, leading to difficulties in breathing efficiently Harris and Super 36.
