Quick Answer: Which Complication Is Appropriate In The Child With Cystic Fibrosis?

Can people with CF have kids?

While 97-98 percent of men with cystic fibrosis are infertile, they can still enjoy normal, healthy sex lives and have biological children with the help of assisted reproductive technology (ART)..

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.

Can you live a long life with cystic fibrosis?

Based on the 2018 Registry data, if your child with cystic fibrosis is born between 2014 and 2018, you can expect them to live at least till 44 years. If your child is born in 2018, they have 50% chances to live till 47 years or more.

What complication is likely to occur with cystic fibrosis?

The most common complication is chronic respiratory infection. Other complications include: Bowel problems, such as gallstones, intestinal blockage, and rectal prolapse. Coughing up blood.

What are the effects of cystic fibrosis on a child?

A child may have very thick phlegm (sputum). Infants and young children often swallow what they cough up, however, so parents may not be aware of it. Some people with cystic fibrosis develop growths (polyps) in their nasal passages. They may experience severe or chronic sinusitis, which is inflammation of the sinuses.

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 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’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.

Which complication is appropriate in the child with cystic fibrosis quizlet?

Which complication is appropriate in the child with cystic fibrosis? Prolapse of the rectum occurs in infancy and childhood and is related to large, bulky stools; malnutrition; and increased abdominal pressure secondary to paroxysmal cough.

What condition is likely to present in a newborn with cystic fibrosis?

Babies with CF are often sick with infections and need a lot of medical care. CF can cause these problems for babies: Lung and breathing problems. When the mucus builds up in the lungs, it blocks airways (tubes that carry air in and out of the lungs) and causes breathing problems and infections.

What are the primary characteristics of cystic fibrosis?

The main signs and symptoms of cystic fibrosis are salty-tasting skin, poor growth and poor weight gain despite normal food intake, accumulation of thick, sticky mucus, frequent chest infections, and coughing or shortness of breath. Males can be infertile due to congenital absence of the vas deferens.

How many types of cystic fibrosis are there?

Scientists have found more than 1,700 different mutations in the CFTR gene that can cause CF. (A mutation can be a very tiny change; a switch of one single letter to another letter, or a deletion of one or more letters.)