Diagnosis

Pseudomonas Aeruginosa & Cystic Fibrosis: Learn the Facts

Pseudomonas aeruginosa is a bacteria that can cause infections in many parts of the body. It survives in most environments and is very resistant to antibiotics. Infections caused by P. aeruginosa can be life-threatening, but all have the potential to be treated.

While P. aeruginosa rarely makes healthy people sick, it is an opportunistic pathogen. This means it can be dangerous for people with a weakened immune response. If you catch an infection while in a hospital, it will most likely bePseudomonas aeruginosa.

Cystic Fibrosis & Bone Disease Complications

One possible complication of cystic fibrosis is bone disease. The digestive problems of CF cause malabsorption, meaning your body can’t take in the vitamins and minerals it needs from food.

This leads to malnutrition, where your body doesn’t have the nutrients it needs to work and stay healthy. If your body doesn’t get the resources it needs to build and maintain healthy bones, the result is bone disease.

Average Day for Adults with Cystic Fibrosis

Adults with cystic fibrosis are just like everyone else; they have jobs, hobbies, friends, and families. But they a genetic disease they need to manage. If you have CF, then your diet, exercise, and treatment are an important part of life. Here’s an opportunity to look at what it means to eat right, stay active, and keep disciplined about taking your medication in a typical day.

Cystic Fibrosis Prognosis

The cystic fibrosis prognosis used to be a very severe diagnosis that would often take the life of an infant within a few years. As you can see below, there have been a number of discoveries and advancements in the treatment of cystic fibrosis throughout recent history which have improved the quality of life and prognosis for those with cystic fibrosis.

Cystic Fibrosis & Adult Diagnosis

Cystic fibrosis is classically a pediatric disease. This means that it presents and is diagnosed in infancy. Until fairly recently, cystic fibrosis would never be considered a diagnostic option for an adult presenting CF related symptoms. This is due to the fact that historically, untreated cystic fibrosis resulted in early mortality.

However, recent occurrences have manifested where cystic fibrosis has been diagnosed in adulthood. It usually involves unique mutations of the CFTR and can present itself in a number of ways.

Cystic Fibrosis Inheritance: Are you a carrier?

Cystic fibrosis inheritance is passed on through a change in a gene on the 7th chromosome. This change results in the production of the protein CFTR(cystic fibrosis transmembrane regulator). This protein is the reason that the mucus is thick and builds up in people with cystic fibrosis.

Cystic fibrosis inheritance is passed on through autosomal recessive genes, meaning that it is necessary for a child to inherit the changed gene that produces the CFTR protein from BOTH parents in order to express the symptoms of CF.

Cystic Fibrosis Symptoms

Cystic fibrosis is related to many symptoms throughout the body. The most profoundly affected systems have problems due to the build up of thick, sticky mucus.

The Respiratory Tract is the most notably affected organ since the buildup of mucus makes it difficult to breath and must constantly be treated and coughed out. The mucus is a great environment for opportunistic bacterial lungs infections, which is the principal reason for decline in lung function of people with cystic fibrosis.

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