Treatments for Lung Conditions in Cystic Fibrosis Sufferers
FOCUS: “Treatments for lung conditions Cystic Fibrosis sufferers contend with”
Word Count: 1461
This essay will aim to explore the different ideas and concepts of using several types of medication for cystic fibrosis sufferers. Cystic fibrosis is a genetic disorder that affects thousands of children and adults across the United Kingdom; it mainly affects Caucasian beings and is a well-known disease throughout the world, but has no cure only treatments to ensure a better quality of life (Jagannath VA, Asokan GV, Fedorowicz Z, Singaram JS, Lee TWR, 2010). Cystic Fibrosis affects mainly the lungs and pancreas, the glands within the human body that produce mucus, sweat and intestinal secretions do not work properly and over compensate this leaves the lungs with a thick lining of mucus, affecting breathing and increasing risk of infection, making the sufferer ill without sufficient treatment. (Høiby 2000). The severity of the illness can differ between each suffer, there is no known cure for the disease but there are significant treatments that support and improve the quality of life. Cystic fibrosis sufferers can be subjected to long hospitalisation periods meaning medication and other treatments cannot be managed at home as efficiently, especially the use of intravenous medication which requires administering a drug directly into the blood rather than orally. This Essay will aim to target the conflicting ideas on the treatments available for Cystic Fibrosis sufferers for their lung condition. Many treatments are available, ranging from drug interventions, simple relaxation therapy techniques and a more abrasive method of using suction to remove the secretions from the lung manually (Jefferson 2006). When gathering research from the internet, there are several sites that can provide inaccurate and misguided information, to minimise these errors occurring medical databases are available to browse through. This allows medical professionals and
Word Count: 1461
This essay will aim to explore the different ideas and concepts of using several types of medication for cystic fibrosis sufferers. Cystic fibrosis is a genetic disorder that affects thousands of children and adults across the United Kingdom; it mainly affects Caucasian beings and is a well-known disease throughout the world, but has no cure only treatments to ensure a better quality of life (Jagannath VA, Asokan GV, Fedorowicz Z, Singaram JS, Lee TWR, 2010). Cystic Fibrosis affects mainly the lungs and pancreas, the glands within the human body that produce mucus, sweat and intestinal secretions do not work properly and over compensate this leaves the lungs with a thick lining of mucus, affecting breathing and increasing risk of infection, making the sufferer ill without sufficient treatment. (Høiby 2000). The severity of the illness can differ between each suffer, there is no known cure for the disease but there are significant treatments that support and improve the quality of life. Cystic fibrosis sufferers can be subjected to long hospitalisation periods meaning medication and other treatments cannot be managed at home as efficiently, especially the use of intravenous medication which requires administering a drug directly into the blood rather than orally. This Essay will aim to target the conflicting ideas on the treatments available for Cystic Fibrosis sufferers for their lung condition. Many treatments are available, ranging from drug interventions, simple relaxation therapy techniques and a more abrasive method of using suction to remove the secretions from the lung manually (Jefferson 2006). When gathering research from the internet, there are several sites that can provide inaccurate and misguided information, to minimise these errors occurring medical databases are available to browse through. This allows medical professionals and