Quick Answer: What Is A Complication Of Cystic Fibrosis?

What’s the oldest someone has lived with cystic fibrosis?

Senior citizens with cystic fibrosis The oldest person diagnosed with CF for the first time in the U.S.

was 82, in Ireland was 76, and in the United Kingdom was 79..

What are the signs and symptoms of cystic fibrosis quizlet?

Terms in this set (48)chronic sinus infections.polyps in the sinus cavity.shortness of breath.cough with sputum production.digital clubbing (in older patients)

What happens to the body during cystic fibrosis?

Cystic fibrosis (CF) is an inherited disorder that causes severe damage to the lungs, digestive system and other organs in the body. Cystic fibrosis affects the cells that produce mucus, sweat and digestive juices. These secreted fluids are normally thin and slippery.

What are some of the complications associated with cystic fibrosis?

Possible ComplicationsBowel problems, such as gallstones, intestinal blockage, and rectal prolapse.Coughing up blood.Chronic respiratory failure.Diabetes.Infertility.Liver disease or liver failure, pancreatitis, biliary cirrhosis.Malnutrition.Nasal polyps and sinusitis.More items…•

What is the main symptom of cystic fibrosis?

Symptoms of CF Frequent lung infections including pneumonia or bronchitis. Wheezing or shortness of breath. Poor growth or weight gain in spite of a good appetite. Frequent greasy, bulky stools or difficulty with bowel movements.

What are the long term effects of cystic fibrosis?

These symptoms include poor lung function, frequent and persistent lung infections and the inability to effectively digest food, particularly fats. Additional complications include CF-related diabetes, bone disease and infertility. Find out more about the symptoms of cystic fibrosis.

What triggers cystic fibrosis?

Cystic Fibrosis Causes Cystic fibrosis is caused by a change, or mutation, in a gene called CFTR (cystic fibrosis transmembrane conductance regulator). This gene controls the flow of salt and fluids in and out of your cells. If the CFTR gene doesn’t work the way it should, a sticky mucus builds up in your body.

What is a complication of cystic fibrosis quizlet?

Respiratory Complications. Children who have cystic fibrosis are at increased risk for hospitalization related to. pulmonary complications (respiratory infection, acute respiratory distress). Nursing Actions: Promptly treat respiratory infections with antibiotic therapy.

What is the cause of cystic fibrosis quizlet?

Cystic fibrosis is caused by a genetic mutation; specifically a mutation in a gene called CFTR. A genetic mutation is when the instructions found in all living cells become scrambled in some way, meaning that one or more of the processes of the body do not work in the way they should.

What gender is cystic fibrosis most common in?

Cystic fibrosis affects both males and females; approximately 30,000 people in the United States have been diagnosed with the condition.

Can you recover from cystic fibrosis?

There is no cure for cystic fibrosis, but treatment can ease symptoms, reduce complications and improve quality of life. Close monitoring and early, aggressive intervention is recommended to slow the progression of CF , which can lead to a longer life.

Can you get cystic fibrosis later in life?

While cystic fibrosis is usually diagnosed in childhood, adults with no symptoms (or mild symptoms) during their youth can still be found to have the disease.

What is the most common mutation responsible for cystic fibrosis?

F508delThe most common CF mutation, F508del, is primarily considered to be a processing mutation. The F508del mutation removes a single amino acid from the CFTR protein.

At what age is cystic fibrosis usually diagnosed?

Most children are now screened for CF at birth through newborn screening and the majority are diagnosed by age 2. However, some people with CF are diagnosed as adults. A doctor who sees the symptoms of CF will order a sweat test and a genetic test to confirm the diagnosis.

What organs are affected by cystic fibrosis?

This is how most cases are diagnosed. CF causes thick mucus that clogs certain organs, such as the lungs, pancreas, and intestines. This may cause malnutrition, poor growth, frequent respiratory infections, breathing problems, and chronic lung disease.