Nursing Assignment: Cystic Fibrosis Review Nursing Assignment: Cystic Fibrosis Review What is Cystic Fibrosis?? Cystic Fibrosis is an inherited disorder that causes severe damage to the lungs, digestive system and other organs of the human body. Nursing Assignment: Cystic Fibrosis Review Cystic Fibrosis damages cells that are responsible for generating mucus, digestive juice and sweat. These types of secreted fluids are defined as slippery and thin; however, for people with Cystic Fibrosis, the fluids are thick and sticky. As opposed to carrying out their intended functions of lubrication, the secretion from these fluids plugs up the passageways, ducts, and tubes particularly in the pancreases and the lungs. ORDER INSTRUCTIONS-COMPLIANT NURSING Nursing Assignment: Cystic Fibrosis Review PAPERS Cystic Fibrosis Symptoms, Causes, Treatment The signs and symptoms vary depending on the severity of the disease. People with Cystic Fibrosis have high levels of salt in the sweat and mostly the signs and symptoms affect the digestive and the respiratory system. Adults diagnosed with this condition have high chances of atypical symptoms including; recurring pneumonia, infertility, and pancreatitis. Respiratory Signs and Symptoms The thick and sticky mucus linked with Cystic Fibrosis clogs the tubes carrying air to and from the lungs and is associated with the following signs and symptoms; ?Cystic Fibrosis Nursing stuffy nose or inflated nasal passage persistent lung infection Intolerance to exercise breathlessness Wheezing production of thick mucus through persistent coughing Digestive Signs and Symptoms The thick mucus also has the ability to block the tubes carrying enzymes used in the digestive process from various parts such as small intestine and pancreas. As a result, the intestines lack the capability to absorb nutrients from food and this can be identified with the following signs and symptoms:?Cystic Fibrosis Nursing severe constipation blockage of intestine particularly among the newborns poor growth and weight gain Greasy stools that may be characterized with foul-smelling Causes?Cystic Fibrosis Cystic Fibrosis is mainly caused by defection or mutation in the genes which causes alterations in the proteins responsible for regulating the movement of salts in and out of the cells.?Cystic Fibrosis Nursing This leads to sticky and thick mucus in the reproductive, digestive and respiratory systems and increased concentration of salt in the sweat.? In addition, various defects can take place in the gene which is termed as the gene mutation that is linked with the rigorousness of the disorder. For children to experience this condition, they have to inherit a copy of the gene from each parent for the disease to develop. However, in case the kid only inherits one copy, they cannot develop Cystic Fibrosis condition. Interestingly, such kids will be carries and they will possibly pass the gene to their children. Treatment of?Cystic Fibrosis Though no cure has been established for Cystic Fibrosis, there are various treatments that can be used to relieve the symptoms and minimize complication risks.?Cystic Fibrosis Nursing Some of these medications include; prescription of anti-biotic to help get rid of lung infection and prevent an attack from other infections in the future medication on muscle thinning to make muscles less stick and maintain then thinner use of Nonsteroidal anti-inflammatory drugs (NSAIDs) including; indomethacin and ibuprofen to reduce fever and pain associated with Cystic Fibrosis.?Cystic Fibrosis Nursing Use of Bronchodilators to help relax the muscles that are around the tubes carrying air to and from the lungs Bowel surgery and lung transplant. Chest physical therapy Major Cystic Fibrosis Nursing Care Plans The major nursing care plans for Cystic Fibrosis include the following; preventing complication, ensuring there is adequate nutrition, articulating the importance of sufficient dietary and fluid intake, promoting measures that will enhance of pulmonary secretions, and ensuring there is adequacy of oxygenation in the lungs. The Role of the Cystic Fibrosis Nurse Specialist Cystic fibrosis nurse specialist plays the following roles; Advocacy: due to the many demands made by the patient and the CF team, family and patient advocacy have been established to be a vital role of the nurse specialist. This ensures patient satisfaction and well-being. Clinical management: the nurse specialist must assume a central role in decision making of the patient and monitoring care. Besides the practical responsibilities, the day to day care of the nurse specialist is to ensure they are responsibly aware of the treatment modalities that are used on the management of CF by ensuring that each patient gets an optimum can that matches personal needs of the patient. Nurse specialist also acts as a link between community, family and patient services in a healthcare facility that has multi-disciplinary teams.?Cystic Fibrosis Nursing Advice and support: professional colleagues, families, and patients all benefits from support, advice, and liaison that is offered by the nurse specialist. This can be done through counseling, consistent carer, and confidante. Cystic fibrosis nurse specialist also plays a central role in enhancing effective communication since problems are well resolved more efficiently through communication pathways put in place for all parties. In addition, cystic fibrosis nurse specialist also educates patients, carers, and families and takes a central role in education research and management.? Nursing Assignment: Cystic Fibrosis Review Order Now

ADDITIONAL INFORMATION 

Cystic Fibrosis

Introduction

Cystic fibrosis (CF) is a rare genetic disorder that affects the lungs and digestive system. Cystic fibrosis is the most common form of hereditary lung disease, which affects more than 30,000 people in the United States. If a person has one copy of the defective gene and one normal copy, he or she has a 50 percent chance of passing on this mutation to their children and grandchildren. However, if both parents have two copies of the defective gene, then all members of their family are at risk for developing CF even if they don’t know it yet!

The most common type of cystic fibrosis, F508del CF, occurs when a person has two abnormal CFTR genes.

The most common type of cystic fibrosis, F508del CF, occurs when a person has two abnormal CFTR genes. This form is caused by a defective gene that affects mostly the lungs, but also the pancreas and other organs.

A person must have two copies of this defective gene to develop cystic fibrosis. If you have one copy of it and your child has two copies (one from each parent), then they will not develop cystic fibrosis unless there are other factors present at birth—such as being born prematurely or having certain infections during pregnancy—that cause mutations in their DNA.

Cystic fibrosis is not an inherited disease, but rather a genetic disorder that can be passed on from parents to children. It’s caused by mutations in the CFTR gene. The mutant form of this gene causes the production of defective proteins that cause mucus buildup in the lungs and digestive system.

Cystic fibrosis is caused by a defective gene that affects mostly the lungs, but also the pancreas and other organs.

Cystic fibrosis is a genetic disease that affects the lungs, pancreas and other organs. The defective gene responsible for cystic fibrosis is called cystic fibrosis transmembrane conductance regulator (CFTR).

The CFTR protein helps move salt and water out of cells in your body by controlling chloride levels in your cells. A defective version of this protein causes thick mucus to build up in the lungs that can cause serious problems such as dehydration or infections.

The thick mucus also makes it difficult for air to pass through the lungs, which can lead to coughing and shortness of breath. The build-up of mucus causes inflammation in your pancreas that prevents the organ from producing enzymes needed for digestion.

A person must have two copies of the defective gene to develop cystic fibrosis.

You must have two copies of the defective gene to develop cystic fibrosis. Cystic fibrosis is an autosomal recessive disease, so your child may be a carrier (not have cystic fibrosis) and still transmit it to other people in his or her family. However, if both parents have one copy of the defective gene and one normal copy, they will both pass along their genetic defect to their children.

About 1 out of every 20 Caucasian babies are born with CF each year worldwide; about 90% of those babies die before reaching their first birthday because of complications related to CF lung disease itself—and another 10% die from complications caused by other conditions like malnutrition or infection that result from having CF lung disease

Cystic fibrosis is one of many conditions known as “rare diseases” that affect fewer than 200,000 people in the US.

The term “rare disease” describes an illness that affects fewer than 200,000 people in the US. It’s a condition that is so rare that it can only be treated by a specific drug or treatment that has been approved by the FDA and administered in clinical trials.

There are many different types of rare diseases, but cystic fibrosis is one of them. People who have cystic fibrosis develop thick mucus in their lungs (or airways) and digestive system—but there are no treatments available for this condition yet!

Conclusion

Cystic fibrosis is a disease that affects the lungs and digestive system. It is most common in people of European ancestry and affects half a million people worldwide. There is no cure, but treatments can help patients live longer and healthier lives.

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