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This is often done by manually clapping with cupped hands on the front and back of the chest -- a procedure that's best performed with the person's head over the edge of the bed so that gravity helps clear the secretions.
Mucus-thinning drugs: make it easier to cough up the mucus; prescriptive or non-prescriptive drugs, which are used to lessen or reduce the stiffness of mucus, ameliorate lung function.
Medications: Antibiotics are prescribed to treat and prevent any lung infections. They may be swallowed in pill form, inhaled in a mist or delivered intravenously.
Bronchodilators: albuterol is applied through an inhaler or a nebulizer; this relaxes the muscles around the bronchial tubes in order to help keep the airways open.
*Most severe cases: Lung transplantation is an acute surgical operation and may lead to more excessive complications than the initial symptoms could merit, especially post-surgical infections, so this is frequently seen as a last resort. However, chancing this operation is far better than death.
Lung transplant: under an extremely severe circumstances (i.e., increasing resistance to antibiotics ascribed to treat lung infections, severe breathing problems, life-threatening pulmonary complications, etc. ), a doctor may suggest lung transplantation. Both lungs will likely need to be replaced since...
Cystic fibrosis interferes with digestion, so you can't absorb nutrients from food very well. Your doctor may suggest using a feeding tube to deliver extra nutrition while you sleep. This tube may be threaded through your nose to your stomach, or surgically implanted.
The initial material is under this line:
Part Two: Cystic Fibrosis
Introduction
As the economy rebounds, hospitals and other medical businesses are investing in technology, further advanced medicines, alongside generalized technological medical advancement to increase efficiency and gain a competitive edge. In making these high-cost investments, many companies fail to consider the
cystic fibrosis. There are eleven references used for this paper. There are a number of fatal diseases which a person can be born with in the world today. One of the most debilitating is Cystic Fibrosis. It is important to examine its history, symptoms, diagnostic procedures, treatments and prognosis in order to gain a better understanding of this disease. Cystic fibrosis is a "recessive disorder common among Caucasians. Although the disease
Cff.org/will each be the source of information and professional peer reviewed articles will be cited from these sources and identified by source as they cited. There is a wealth of available information, data and studies on CF. What it all means to the patients who suffer from this debilitating and life-threatening disease will be understood as this essay proceeds. Chapter One Diagnosis and the Anatomy and Physiology of a Life Threatening Disease: Cystic
Cystic Fibrosis Impact on Lungs Introduction Cystic Fibrosis (CF) is a genetic and possible genetically inherited disease that affects lungs. It is characterized by buildup of thick and stick mucus that is had to cough out of the lungs. With the accumulation of the thick and sticky mucus, it can result to difficulty in breathing and can lead to other complications including lung infections, liver disease, and diabetes[endnoteRef:1]. CF has also been
Cystic Fibrosis is an inherited disorder which affects the secreting abilities of various glands in the body. These glands are the ones that are considered with both mucus and sweat made in the made. This disease presents with many different symptoms as it affects the lungs, intestines, liver, pancreas, sinuses and the genitals. This paper will go on to talk about the basic etiology of Cystic fibrosis. After the discussing
Treatment History Of Cystic Fibrosis The field of pediatric nursing is a particularly large one in which its members may find themselves having to counsel both young patients and their families suffering from a myriad of diseases. Cystic fibrosis (CF), in particular, is a debilitating disease that strikes many young people. In the first years following its discovery, many children could not expect to make it to their teen years. Today,
We conceivably create children who are perfect genetically -- but never have another Einstein, a man who had weaknesses as well as strengths. Hidden in such notions is the idea that people with any kind of difference or disability are somehow defective. In the United States we have put a lot of time and effort into creating a country that gives people with disabilities access to a normal or near-normal