29 hours ago · 1 Cystic Fibrosis: Findings to report to the provider 1a Cystic fibrosis is a respiratory disorder that results from inheriting a mutated gene. it is characterized by mucus glands that secrete an increase in the quantity of thick, tenacious mucus, which leads to mechanical obstruction of organs (pancreas, lungs, liver, small intestine, and reproductive … >> Go To The Portal
The impact on the sweat gland give rise to abnormally high chloride secretion; a simple analysis of sweat chloride content continues to be the gold standard for CF diagnosis.
The mother of a child with cystic fibrosis tells the nurse that her child makes “snoring” sounds when breathing. The nurse is aware that many children with cystic fibrosis have: A. Choanal atresia. B. Nasal polyps. C. Septal deviations.
1 Evidence Based Child Health Group, University of Nottingham, Nottingham, UK. 2 School of Medicine, NIHR Research Design Service for the East Midlands, University of Nottingham, Nottingham, UK. 3 Person with Cystic Fibrosis, Plymouth, UK. 4 School of Education, University of Leeds, Leeds, UK. 5 Parent of Children with CF, Nottingham, UK.
Nursing Care Planning and Goals. Main Article: 5 Cystic Fibrosis Nursing Care Plans. The major goals for the child include: Relieving immediate respiratory distress. Maintaining adequate oxygenation. Remaining free from infection. Improving nutritional status. Relieving anxiety.
Antibiotics to treat and prevent lung infections. Anti-inflammatory medications to lessen swelling in the airways in your lungs. Mucus-thinning drugs, such as hypertonic saline, to help you cough up the mucus, which can improve lung function.
To diagnose cystic fibrosis, doctors usually perform blood tests. They may test sweat for high salt content, which can indicate cystic fibrosis. If the diagnosis is confirmed, doctors may evaluate the condition with a chest x-ray, chest or abdominal CT or MRI, abdominal ultrasound, or sinus CT.
People with cystic fibrosis should have a balanced diet, although many will require more energy (calories) than someone without the condition in order to maintain a healthy body weight, which can be challenging. Nutritional needs will vary according to age, weight, height, symptoms, lung function and activity level.
Your CF nurse is your primary contact and is there to address your concerns, answer questions or direct you to the right CF care team member when discussing a specific part of your treatment plan. CF nurses also have the primary responsibility of providing CF education at initial diagnosis and throughout life.
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...•
Treatments for cystic fibrosis antibiotics to prevent and treat chest infections. medicines to make the mucus in the lungs thinner and easier to cough up. medicines to widen the airways and reduce inflammation. special techniques and devices to help clear mucus from the lungs.
Work with your child's schoolgive them time and privacy to perform airway clearance therapy.let them take medication.adjust attendance rules to let them go to medical appointments.provide extensions and help them catch up on lessons and assignments they miss due to medical appointments or illness.
“A CF social worker delivers a service by assessing their patient's emergency complex needs and supporting their rights, strengths and quality of life,” explains Suja Chandran, Senior Social Worker at Kings College Hospital.
What kind of limitations does someone with CF have? People with CF can live very full, normal lives. There are no limitations to their exercise, diet, or activities. However, due to the different lung infections that they can get, they should not meet or talk with other patients with CF in-person.
Intermediate priority nursing diagnoses involve non-emergent, non-life-threatening needs of patients. Low-priority nursing diagnoses are not always directly related to a specific illness or prognosis but affect the patient's future well-being.
People with CF need more calories than people who do not have CF, especially if they do not absorb all the food they eat. Extra calories are needed to fight infection as well. , high-fat diet, with 40 percent of total calories from fat is generally recommended.