What factors affect life expectancy with cystic fibrosis?

The main factors that affect life expectancy with cystic fibrosis are improved medical treatment of the disease and early diagnosis. Cystic fibrosis, genetic disease, tends to have a low life expectancy, but medical scientists continue to discover ways to help patients with cystic fibrosis longer and with better quality of life. People with cystic fibrosis must be vigilant in the treatment of their illness and have to eat the right diet. Medical treatment dates back to drugs to surgery. The reason why life expectancy with cystic fibrosis tends to be low, is that the complications of the disease are often fatal. Cystic fibrosis results in a reinforced hock and digestive secretion. Strong mucus, which accumulates in the lungs, represents a high risk of infection to the respiratory system. In the pancreas of strong secretion, the organ prevents the organization of the necessary enzymes to spend food, resulting in malnutrition.

Cyst diagnosticsIic fibrosis can be performed in infants through a procedure that tests a high level of salt in their sweat. The sooner the disease is diagnosed, earlier treatment can begin and proper treatment, clinical and at home, is the key to improving life expectancy with cystic fibrosis. Symptoms of cystic fibrosis concentrate in the respiratory and digestive system. Because the disease causes strong mucus to disrupt normal lung function, the expectation of life with cystic fibrosis may be endangered by recurrent respiratory infections. Patients also suffer from digestive problems that include constipation, poor nutrient absorption and weight loss.

Life expectancy with cystic fibrosis can be improved with diet. Patients should eat healthy nutrient -rich foods and consider the use of supplements to provide other calories and nutrition. Intake fluid is also essential because drinking a lot of water helps reduce mucus thickness in the lungs of patients, thus increasing the cough more productive. Patients with cystic fibrosis shouldMedicize smoking or breathing a second -hand smoke. They should also try to get regular exercise because physical exertion improves respiratory functions and promotes the movement of sticky mucus.

Although there is no medicine for this disease, the prognosis for cystic fibrosis may be better through drugs that help control infection and other possible complications. Antibiotics are prescribed for patients with cystic fibrosis to prevent respiratory infection. Other medicines work on thin mucus in the patient's lungs and alleviate the malignant effects of the disease on the respiratory system. If the patient is seriously malnutrition, his life expectancy may be increased by a feed tube so that he can receive key nutrients and calories. Cystic fibrosis progression may require surgery as a lung transplant or an emergency procedure to solve the intestines.