Question One: The physician asked the mother of the infant if the infant's skin was salty because one of the symptoms of cystic fibrosis is having thick and heavy mucous ... and salty sweat. When the CFTR (Cystic Fibrosis Trans membrane Conductance Regulator) protein is defective, epithelial cells can't regulate the way chloride (part of the salt called sodium chloride) passes across cell membranes. This disrupts the essential balance of salt and water needed to maintain a normal thin coating of fluid and mucus inside the lungs, pancreas, and passageways in other organs.…
I already knew that asthma is a chronic disease which affects the lungs and that…
“The life expectancy of a person with CF is rising. Today some people with CF live into their 30s,…
There is no prescribed treatment to eradicate the condition but prevention of respiratory infections, malabsorption problems and maintaining good nutrition and an active lifestyle can aid individuals in living a sustainable life. The goal for all patients should be maintaining their quality of life. Since the condition is diagnosed before birth parent teaching is vital in managing cystic fibrosis. Education on medication regimen of bronchodilators, nebulizer treatments and all respiratory treatments. Administer pancreatic enzymes before all meals and snacks. Fat-soluble vitamins replacement. Identifying the signs and symptoms of infection is important; monitoring their vital signs, temperature, listening to their chest, nasal flairing, chest retraction, cyanosis color, persistent cough and wheezing. All abnormal symptoms are to be notified to the physician and child should be brought in for further evaluation. As adolescents the cystic fibrosis patient should engage in sports, activities, avoidance of drugs, smoking and alcohol. Encourage all women with the disorder to participate in genetic testing. The prognosis of Cystic fibrosis has improved. For an example the U.S Cystic Fibrosis Foundation Complies that in 2008 the life expectancy has improved to 37.4 years old and 240 American with cystic fibrosis were able to become pregnant. The Priority Nursing Diagnosis’s are: Ineffective airway clearance related to…
There is currently no tested cure for cystic fibrosis. There are 2 types of potential treatments which corrects the inherent problem behind the disease; correctors and potentiators (fig. 3). Both of these treatments show promise in improving patient standard of living. Both of these could deliver huge improvements in patients’ life, there is a long time to go before these therapies are approved for widespread usage.…
The symptoms that are associated with cystic fibrosis can be reduced through diet and exercise, support can be provided from staff at specialist centre for cystic fibrosis.…
As chronic infections reduce lung function, the ability to breathe often decreases. A person with CF may eventually begin to feel short of breath, even when resting. Despite aggressive medical therapy, lung disease develops in nearly all patients with CF and is a common cause of…
A combination of physiotherapy and medication can help control lung infections and prevent lung damage. To avoid the risk of cross-infection, it is recommended that people with CF do not come into close contact with others with Cystic Fibrosis. Cystic Fibrosis affects the pancreas, which makes it difficult for people with CF to digest food. This can cause malnutrition, which can lead to poor growth, physical weakness and delayed puberty. There is medication that can compensate for the failure of the pancreas.…
There is no cure for CF, however, some treatment can delay the progression of the disease, however, some side effects to the treatment include the strain on vital organs, especially the lungs and pancreas. Chest physiotherapy is also a treatment that a sufferer of CF can go through.…
Goals of treatment include preventing and controlling lung infections, loosening and removing mucus from the lungs, preventing and treating intestinal blockage and providing adequate diet. There are antibiotics to treat and prevent lung infections, anti- inflammatory medications to help reduce the swelling in your airways due to infections. You may need pulmonary rehabilitation such as exercise training, nutritional counseling, breathing strategies and psychological counseling or group support. They may need mucus thinning drugs to improve lung function, or a bronchodilator which opens your airways to breathe better or an oral pancreatic enzyme to help digest fats and proteins and absorb more vitamins. Once you find out you have CF you and your doctor will come up with a plan to help you handle your Cystic…
What is cystic fibrosis? Cystic fibrosis is a disease that is passed down through families, from parent to child due to a faulty gene. It currently affects both babies, children and young adults. This faulty gene controls the movement of salt and water in and out of the cells, so the lungs and digestive system become so clogged with mucus, it makes it hard to breathe and digest food.…
People can be carriers of the CF gene and not even know. Currently, it is not possible to be able to prevent Cystic Fibrosis because it is a genetic disease. However people can go through genetic counseling, where you classify and understand the risk a family may have of inheriting a genetic disease. Currently, doctors and scientist are studying new effective treatments for example the CFTR modulator, which targets a certain mutation of the faulty CF gene. There are simple ways to prevent making Cystic Fibrosis less unstable, for example, maintaining a healthy diet for a good lung function and paying attention to nutrition and fluid intake. Patients can also exercise to assist loosening up the mucus in the airways and if patients have a smoking habit, they should eliminate smoking in order to prevent worsening of the lung area. Moreover, there is no way to prevent Cystic Fibrosis because of it being a genetic disease, eventually by taking medication Cystic Fibrosis will be less threatening. Patients will be able to live almost normally if they are not…
It also does not discriminate against gender or race. In 2013, the Centers for Disease Control stated that 8.2% of the American population had asthma. That includes 18.9 million adults (What 2). Asthma in children has more than doubled since 1980 causing scientists to investigate the cause. An estimation according to the CDC is that one in every ten children has this ever-growing disease. Even though this disease can come about to anyone, it has been proven that if you have a family history of asthma, you are at higher risk of developing the disease,…
Cystic fibrosis has been a major part of not only my life , but my families’ lives too. I have two sisters , my twin Alani, and my oldest sister Adriana ,who also suffer from cystic fibrosis . Our family supports us everyday to help fight this disease .…
Cystic fibrosis is an inherited disease of the secretory glands that causes persistent lung infections and limits the ability to breathe over time. It causes cells to produce thick and sticky mucus, sweat, and digestive juices that block airways, ducts, and passageways. There is no cure, but there are ways to manage symptoms.…