How is cystic fibrosis treated?

Although there is no cure for cystic fibrosis, the disease can be treated, which extends the lives of those that they have touched them. In fact, progress in medical treatments allows individuals with cystic fibrosis to live into adulthood. This is not a small act, because individuals with cystic fibrosis usually died as infants at the beginning of the 20th century.

treatment for cystic fibrosis should help prevent and control lung infections. The treatment is also used to release thick mucus and its removal from the lungs, prevent intestinal locking and help the patient absorb the corresponding level of nutrition. For this purpose, antibiotics are often prescribed, as well as exercise, physical therapies and other medicines.

Often individuals living with cystic fibrosis infections contrast. In some cases, infections are sufficiently serious to require hospitalization. Antibiotics are used as the first defense line to combat these lung infections. There are several types of antibiotics usedCH to treat patients with cystic fibrosis. The type used in any case depends on the type of bacteria that cause infection, the severity of the patient's condition and the medical history of the patient with antibiotics.

Physical chest therapy (CPT) is also used to treat cystic fibrosis. This treatment involves repeatedly pounding on the chest and back of the patient in an effort to release mucus from the lungs, which makes the patient easier. This procedure is usually performed several times a day. CPT can be difficult and unpleasant for some patients with cystic fibrosis. To make it easier, several devices have been developed to help with the technique.

Breathing techniques can also be used to release mucus from the lungs. One technique called the technique of forced expiration (FET) includes forced breaths followed by relaxed breathing. Active Brazg cycle (ACB), other commonly used technique, combines fet with deep breathing, helps to release HLena and clean the airways.

aerobic exercise is also useful in the treatment of cystic fibrosis. In fact, those who practice regularly require less CPT. However, a decrease in CPT without consulting a doctor may have serious health consequences.

As part of treatment, individuals with cystic fibrosis must monitor a high calorie diet. This is usually supplemented with vitamins and medicines that help the body absorb nutrients. In fact, some patients with cystic fibrosis consume more than 20 vitamins and medicines a day. In addition, a number of drugs are taken to prevent infections, facilitate breathing, thin mucus and reduce inflammation. If the oxygen level is too low, it may also have oxygen.

Since those affected by cystic fibrosis ages, infections usually increase severity and are more difficult to treat. The dam in the lungs deteriorates. Sadly, lung infections causing damage are the primary cause of death on cystic fibrosis.