Preview

Annoted Bibliography

Satisfactory Essays
Open Document
Open Document
251 Words
Grammar
Grammar
Plagiarism
Plagiarism
Writing
Writing
Score
Score
Annoted Bibliography
Annotated bibliography
Dasenbrook, EC.”Greater Risk of Death in People with Cystic Fibrosis and MRSA.” Journal of American Medical Association 303 (2010):2386-2392. Clinical Digest. Web. November 11, 2010.
This Journal contains information on patients with Cystic Fibrosis with MRSA.It also shows association between respiratory tract MRSA and survival in Cystic Fibrosis. I feel like the author did a great job getting this information out to the public.
Capron, Wayne. Surviving Childhood and Achieving Adulthood: Fireflies Book. Toronto, Fireflies, 2004. Print. November 11, 2010
A comprehensive guide that draws on current research to discuss symptoms, diagnosis and complications arising from the disease, treatments including lung transplants and transition to adulthood. The author has done a lot of research and has given a lot of information in this book to help Cystic Fibrosis patients.
Kulczycki, Lucas L. M.D. and Harry Schwachman M.D. “The New England Journal of Medicine.” Studies in Cystic Fibrosis of the pancreas-Occurrence of Rectal Relapse. Volume 2, 259 (2008) 409-412. Medical Journal. Web. November 11, 2010.
Our interest in rectal prolapsed was aroused in the course of a study of patients with Cystic Fibrosis. Patients have been aware of this complication for sometime know. However they think they had no appreciation of the frequency of this complication. The information in this journal is helpful to patients with Cystic Fibrosis.
Parker, James N. and Philip M. Parker, EDS. The Official Patients Sourcebook on Cystic Fibrosis: San Diego: Icon Health, 2002; November 11,
Continue Reading
View Writing Issues

You May Also Find These Documents Helpful

  • Better Essays

    Unit Project 4
    • 1226 Words
    • 5 Pages

    Unit Project 4

    Bibliography: Brand PL, van der Ent CK. The Practical Application and Interpretation of Simple Lung Function Tests in Cystic Fibrosis. J R Soc Med. 1999;92 (Suppl 37):2–12. [PMC free article] [PubMed]…

    • 1226 Words
    • 5 Pages
    Better Essays
    Read More
  • Good Essays

    Cystic Fibrosis Case Study
    • 277 Words
    • 2 Pages

    Cystic Fibrosis Case Study

    The different symptoms of cystic fibrosis include repeated infections and thick mucus secretions in the lungs, it affects you with wheezing, a chronic cough, bronchitis, asthma, weight loss, dehydration, and many more mainly affecting the lungs and stomach. Sufferers may also feel very fatigued easily.…

    • 277 Words
    • 2 Pages
    Good Essays
    Read More
  • Good Essays

    Assignment 249
    • 861 Words
    • 4 Pages

    Assignment 249

    Roger is 54 years old and has cerebral palsy with a mild learning disability, however he was fully independent, living in his own house and working part time as an office assistant at a local solicitor’s. He recently had surgery on his left leg, resulting in a reduction in his mobility. While in hospital he contracted MRSA and was…

    • 861 Words
    • 4 Pages
    Good Essays
    Read More
  • Powerful Essays

    Cystic Fibrosis Research Paper
    • 1736 Words
    • 7 Pages

    Cystic Fibrosis Research Paper

    Cystic fibrosis is an autosomal (not sex linked), hereditary disease caused by a mutation in the gene called the cystic fibrosis transmembrane conductance regulator gene, or the CFTR gene. This CFTR gene belongs to a group of genes called ABC (ATP-binding cassette). These are transport molecules for molecules such as phosphate, glucose, chloride, and peptides. Specifically for the CFTR gene, the molecules transported are chloride and sodium. The CFTR protein, which is created by the CFTR gene, has a molecular weight of 168,173 daltons and in length, is 1480 amino acids long. This variation in genes is located in chromosome 7 of humans. Because most people have two of the CFTR gene which creates the CFTR proteins, a person can be completely healthy with a mutation in the gene, as long as at least one of these genes are unchanged from the normal state. Without the cystic fibrosis variation of the CFTR gene, the CFTR proteins created by the gene act as a channel protein which can be found in the membranes of cells which line the passageways of organs such as the pancreas, lungs, and intestines. The CFTR protein can be modified in numerous ways to give the host cystic fibrosis; in fact, over 1000 transformations of the CFTR gene have been recognized. One of the most common of these mutations is a deletion of a single amino acid from the long chain of 1480 in the CFTR protein. This causes a breakdown of the channel made with the missing amino acid, which means that it never transports chloride ions, like it was made to do, because it never reaches the cell membrane. This mutation is delta F508, because the deletion occurs at position 508 on the CFTR protein. These sorts of mutations work to deteriorate and destroy the efficiency of the CFTR protein by changing or replacing parts of the protein’s amino acid order. This order chooses the way that the protein is folded, and if this order is…

    • 1736 Words
    • 7 Pages
    Powerful Essays
    Read More
  • Good Essays

    Cystic Fibrosis and the Resulting Damage to the Lungs and Digestive System
    • 802 Words
    • 3 Pages

    Cystic Fibrosis and the Resulting Damage to the Lungs and Digestive System

    Cystic Fibrosis is a life threatening condition that causes severe damage to the lungs and digestive system. Developing this condition can change a person's entire life. Depending on the severity of the condition a person can be affected by mild symptoms such as shortness of breath, all the way to severe symptoms such as rectal prolapse, or even death. Screening is done on infants in all 50 states; therefore if a child has inherited Cystic Fibrosis it will be known in the first months of life. As professional staff members of a nursing community it will be necessary to help prepare the child and the family for the life of Cystic Fibrosis.…

    • 802 Words
    • 3 Pages
    Good Essays
    Read More
  • Better Essays

    Mrsa Thesis Statement
    • 837 Words
    • 4 Pages

    Mrsa Thesis Statement

    Thesis Statement: MRSA is an infection caused by a strain of Staphylococcus that has become resistant to antibiotics commonly used to treat staph infections.…

    • 837 Words
    • 4 Pages
    Better Essays
    Read More
  • Good Essays

    Cystic Fibrosis Research Paper
    • 637 Words
    • 3 Pages

    Cystic Fibrosis Research Paper

    More complications for CF are damaged airways, chronic infections, palyps, hemoptysis, pneumothorax, respiratory failure, and acute exacerbations. Cystic fibrosis does not only disturb the lungs and airways, it also attacks the digestive system. The thick mucus blocks the passageways of the pancreas stopping the enzymes from being able to reach the small intestine. Ergo the mucus plug constrains the digestion of protein and fat leading to a defect in attaining fat soluble vitamins. To add to the digestive system symptoms are poor weight gain and growth, increased risk of diabetes, intestinal blocking, severe constipation, diarrhea, malnutrition, and frequent straining can lead to rectal prolapse. Reproductive complications can occur in people with cystic fibrosis. Most men are infertile due to missing or mucus blocked vas deferens which connects the testes and prostate gland. Women have less of a chance getting pregnant but still can. Although pregnancy can worsen the signs and symptoms of cystic…

    • 637 Words
    • 3 Pages
    Good Essays
    Read More
  • Good Essays

    Case Study
    • 482 Words
    • 2 Pages

    Case Study

    As well as the individual that suffers from the disease it is also important that the direct family members and friends of this individual can receive some sort of support from a group. Family members or friends could use some practical advice or some sort of emotional and financial support. It could be a stressful time when an individual is diagnosed with cystic fibrosis.…

    • 482 Words
    • 2 Pages
    Good Essays
    Read More
  • Good Essays

    Cystic fibrosis, PKU and the Digestive system
    • 923 Words
    • 4 Pages

    Cystic fibrosis, PKU and the Digestive system

    Symptoms for cystic fibrosis include diarrhea that does not go away, foul-smelling stools, greasy stools, frequent urinating, frequent episodes of Pneumonia, persistent cough, skin tastes like salt, poor growth, chronic sinus infection.…

    • 923 Words
    • 4 Pages
    Good Essays
    Read More
  • Powerful Essays

    The Calgary Family Assessment Model
    • 3153 Words
    • 9 Pages

    The Calgary Family Assessment Model

    Ruder, K., (2007, November). Cystic Fibrosis and Diabetes. Diabetes Forecast, 60(12), 28,31. Retrieved February 11, 2008, from ProQuest Nursing & Allied Health Source database. (Document ID: 1380669491).…

    • 3153 Words
    • 9 Pages
    Powerful Essays
    Read More
  • Good Essays

    Cystic Fibrosis
    • 569 Words
    • 3 Pages

    Cystic Fibrosis

    Cystic fibrous causes many effects on the body, but it mainly affects the digestive system, pancreas and the lungs. Inside the lungs, the mucus can clog the airways and trap bacteria. This more often leads to infections, lung damage and eventually, respiratory failure. Inside the pancreas, the mucus stops the release of digestive enzymes that allow the body to break down food and absorb vital nutrients, which can sometimes lead to inflammation of the pancreas. Cystic fibrosis can also affect other parts of the body, that includes the liver, the reproductive system, the sweat glands and the sinuses.…

    • 569 Words
    • 3 Pages
    Good Essays
    Read More
  • Good Essays

    Analysis Of Cystic Fibrosis
    • 989 Words
    • 4 Pages

    Analysis Of Cystic Fibrosis

    In 1938 Dr. Dorothy Andersen distinguished Cystic Fibrosis from Celiac Disease. While both diseases affect the digestive system, Cystic Fibrosis mainly affects the Respiratory system. When CF was first acknowledged, a pathological…

    • 989 Words
    • 4 Pages
    Good Essays
    Read More
  • Good Essays

    Essay On Cystic Fibrosis
    • 604 Words
    • 3 Pages

    Essay On Cystic Fibrosis

    Some symptoms of Cystic fibrosis are very salty sweat, abnormal bowel movements (your waste looks different), multiple lung infections such as pneumonia or bronchitis, as well as difficulty to gain weight. There is also many ways to treat those symptoms, Some common treatments are airway clearance with a vest you put on a vest that is connected to a machine and it vibrates very quickly loosening the mucus inside the lungs. People also use inhalers to get aerosol medicine straight to the lungs. A less common way of treating the disease is to undergo a lung transplant. Although a lung transplant seems as it would be the most effective way to cure the disease lung transplants are very expensive and you would be put on a very long wait…

    • 604 Words
    • 3 Pages
    Good Essays
    Read More
  • Good Essays

    Essay On Yersinia Pestis
    • 988 Words
    • 4 Pages

    Essay On Yersinia Pestis

    The most common pathogen isolated from the airway of Cystic Fibrosis patients is Pseudomonas aeruginosa. Phenotypic changes in the bacteria have shown that some have undergone a mutation…

    • 988 Words
    • 4 Pages
    Good Essays
    Read More
  • Good Essays

    Cystic Disorders: Cystic Fibrosis
    • 325 Words
    • 2 Pages

    Cystic Disorders: Cystic Fibrosis

    Cystic fibrosis (CF) is the most common inherited disorder which results from mutation of cystic fibrosis transmembrane regulator (CFTR) gene. It occurs approximately in one of every 2500 live births in the white population(1) ; and characterized by abnormal thick viscous secretions in the respiratory, gastrointestinal and genitourinary tracts together with chronic suppurative endobronchial infection(2), resulting in death or lung transplantation in more than 500 patients every year in the United States(3). Incidence of CF is lower among African Americans (1in 15000)(4)and Asians (1in 32000)(5).…

    • 325 Words
    • 2 Pages
    Good Essays
    Read More

Related Topics