Cystic fibrosis (patient information): Difference between revisions
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* [[Immunoreactive trypsinogen]] (IRT) test is a standard newborn screening test for cystic fibrosis. A high level of IRT suggests possible cystic fibrosis and requires further testing. | * [[Immunoreactive trypsinogen]] (IRT) test is a standard newborn screening test for cystic fibrosis. A high level of IRT suggests possible cystic fibrosis and requires further testing. | ||
* [[Sweat chloride test]] is the standard diagnostic test for | * [[Sweat chloride test]] is the standard diagnostic test for cystic fibrosis. A high salt level in the patient's sweat is a sign of the disease. | ||
Other tests that identify problems that can be related to cystic fibrosis include: | Other tests that identify problems that can be related to cystic fibrosis include: | ||
* [[Chest x-ray]] or [[CT scan]] | * [[Chest x-ray]] or [[CT scan]] | ||
* | * Fecal fat test | ||
* [[Lung function tests]] | * [[Lung function tests]] | ||
* Measurement of pancreatic function | * Measurement of pancreatic function | ||
* [[Secretin stimulation test | * [[Secretin]] stimulation test | ||
* [[Trypsin]] and [[chymotrypsin]] in stool | * [[Trypsin]] and [[chymotrypsin]] in stool | ||
* [[Upper GI]] and [[small bowel series]] | * [[Upper GI]] and [[small bowel series]] | ||
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==Treatment options== | ==Treatment options== | ||
An early diagnosis of | An early diagnosis of cystic fibrosis and a comprehensive treatment plan can improve both survival and quality of life. Follow-up and monitoring are very important. If possible, patients should be cared for at cystic fibrosis specialty clinics, which can be found in many communities. When children reach adulthood, they should transfer to a cystic fibrosis specialty center for adults. | ||
Treatment for lung problems includes: | Treatment for lung problems includes: | ||
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* Inhaled medicines to help open the airways | * Inhaled medicines to help open the airways | ||
* [[DNAse enzyme replacement therapy]] to thin mucus and make it easier to cough up | * [[DNAse enzyme replacement therapy]] to thin mucus and make it easier to cough up | ||
* [[Flu vaccine]] and [[pneumococcal polysaccharide vaccine]](PPV) yearly | * [[Flu vaccine]] and [[pneumococcal polysaccharide vaccine]] (PPV) yearly | ||
* [[Lung transplant]] is an option in some cases | * [[Lung transplant]] is an option in some cases | ||
* [[Oxygen therapy]] may be needed as lung disease gets worse | * [[Oxygen therapy]] may be needed as lung disease gets worse | ||
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Most children with cystic fibrosis are fairly healthy until they reach adolescence or adulthood. They are able to participate in most activities and should be able to attend school. Many young adults with cystic fibrosis finish college or find employment. | Most children with cystic fibrosis are fairly healthy until they reach adolescence or adulthood. They are able to participate in most activities and should be able to attend school. Many young adults with cystic fibrosis finish college or find employment. | ||
Lung disease eventually worsens to the point where the person is disabled. Today, the average life span for people with | Lung disease eventually worsens to the point where the person is disabled. Today, the average life span for people with cystic fibrosis who live to adulthood is approximately 35 years, a dramatic increase over the last three decades. | ||
Death is usually caused by lung complications. | Death is usually caused by lung complications. | ||
Revision as of 14:28, 8 February 2018
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Cystic fibrosis |
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Cystic fibrosis On the Web |
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For the WikiDoc page for this topic, click here
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Assistant Editor-in-Chief: Meagan E. Doherty
Overview
Cystic fibrosis (CF) is an inherited disease of the mucus and sweat glands. It affects mostly your lungs, pancreas, liver, intestines, sinuses and sex organs. CF causes your mucus to be thick and sticky. The mucus clogs the lungs, causing breathing problems and making it easy for bacteria to grow. This can lead to problems such as repeated lung infections and lung damage.
What are the symptoms of Cystic fibrosis?
Because there are more than 1,000 mutations of the CF gene, symptoms differ from person to person.
Symptoms in newborns
- Delayed growth
- Failure to gain weight normally during childhood
- No bowel movements in first 24 to 48 hours of life
- Salty-tasting skin
- Belly pain from severe constipation
- Increased gas, bloating, or a belly that appears swollen (distended)
- Nausea and loss of appetite
- Stools that are pale or clay colored, foul smelling, have mucus or that float
- Weight loss
- Coughing or increased mucus in the sinuses or lungs
- Fatigue
- Nasal congestion caused by nasal polyps
- Recurrent episodes of pneumonia (Symptoms include fever, increased coughing, increased shortness of breath, loss of appetite, more sputum, sinus pain or pressure caused by infection or polyps)
What are the causes of Cystic fibrosis?
Cystic fibrosis CF is caused by a defective gene which causes the body to produce abnormally thick and sticky fluid, called mucus. This mucus builds up in the breathing passages of the lungs and in the pancreas, the organ that helps to break down and absorb food.
This collection of sticky mucus results in life-threatening lung infections and serious digestion problems. The disease may also affect the sweat glands and a man's reproductive system.
Millions of Americans carry the defective CF gene, but do not have any symptoms. That's because a person with CF must inherit two defective CF genes, one from each parent. An estimated 1 in 29 Caucasian Americans have the CF gene. The disease is the most common, deadly, inherited disorder affecting Caucasians in the United States. It's more common among those of Northern or Central European descent.
Most children with CF are diagnosed by age 2. A small number, however, are not diagnosed until age 18 or older. These patients usually have a milder form of the disease.
Who is at highest risk?
People who's parents are carriers of the cystic fibrosis gene are at risk of inheriting the disease.
Diagnosis
A blood test is available to help detect cystic fibrosis. The test looks for variations in a gene known to cause the disease.
Other tests use to diagnose CF include:
- Immunoreactive trypsinogen (IRT) test is a standard newborn screening test for cystic fibrosis. A high level of IRT suggests possible cystic fibrosis and requires further testing.
- Sweat chloride test is the standard diagnostic test for cystic fibrosis. A high salt level in the patient's sweat is a sign of the disease.
Other tests that identify problems that can be related to cystic fibrosis include:
- Chest x-ray or CT scan
- Fecal fat test
- Lung function tests
- Measurement of pancreatic function
- Secretin stimulation test
- Trypsin and chymotrypsin in stool
- Upper GI and small bowel series
Diseases with similar symptoms
When to seek urgent medical care?
Call your health care provider if an infant or child has symptoms of cystic fibrosis.
Call your health care provider if a person with cystic fibrosis develops new symptoms or if symptoms get worse, particularly severe breathing difficulty or coughing up blood.
Call your health care provider if you or your child experiences:
- Fever, increased coughing, changes in sputum or blood in sputum, loss of appetite, or other signs of pneumonia
- Increased weight loss
- More frequent bowel movements or stools that are foul-smelling or have more mucus
- Swollen belly or increased bloating
Treatment options
An early diagnosis of cystic fibrosis and a comprehensive treatment plan can improve both survival and quality of life. Follow-up and monitoring are very important. If possible, patients should be cared for at cystic fibrosis specialty clinics, which can be found in many communities. When children reach adulthood, they should transfer to a cystic fibrosis specialty center for adults.
Treatment for lung problems includes:
- Antibiotics to prevent and treat lung and sinus infections. They may be taken by mouth, or given in the veins or by breathing treatments. People with cystic fibrosis may take antibiotics only when needed, or all the time. Doses are usually higher than normal.
- Inhaled medicines to help open the airways
- DNAse enzyme replacement therapy to thin mucus and make it easier to cough up
- Flu vaccine and pneumococcal polysaccharide vaccine (PPV) yearly
- Lung transplant is an option in some cases
- Oxygen therapy may be needed as lung disease gets worse
Treatment for bowel and nutritional problems may include:
- A special diet high in protein and calories for older children and adults
- Pancreatic enzymes to help absorb fats and protein
- Vitamin supplements, especially vitamins A, D, E, and K
- Your doctor can suggest other treatments if you have very hard stools
Care and monitoring at home should include:
- Avoiding smoke, dust, dirt, fumes, household chemicals, fireplace smoke, and mold or mildew
- Clearing or bringing up mucus or secretions from the airways. This must be done one to fours times each day. Patients, families, and caregivers must learn about doing chest percussion and postural drainage to help keep the airways clear
- Drinking plenty of fluids. This is particularly true for infants, children, in hot weather, when there is diarrhea or loose stools, or during extra physical activity
- Exercising two or three times each week. Swimming, jogging, and cycling are good options. Avoid contact sports, scuba diving, and endurance activities such as marathons
Where to find medical care for Cystic fibrosis?
Directions to Hospitals Treating Cystic fibrosis
Prevention of Cystic fibrosis
There is no way to prevent cystic fibrosis. Screening those with a family history of the disease may detect the cystic fibrosis gene in 60 - 90% of carriers, depending on the test used.
What to expect (Outlook/Prognosis)?
Most children with cystic fibrosis are fairly healthy until they reach adolescence or adulthood. They are able to participate in most activities and should be able to attend school. Many young adults with cystic fibrosis finish college or find employment.
Lung disease eventually worsens to the point where the person is disabled. Today, the average life span for people with cystic fibrosis who live to adulthood is approximately 35 years, a dramatic increase over the last three decades.
Death is usually caused by lung complications.
Possible complications
The most common complication is chronic respiratory infection.
- Bowel problems, such as gallstones, intestinal obstruction, and rectal prolapse
- Coughing up blood
- Chronic respiratory failure
- Diabetes
- Infertility
- Liver disease or liver failure, pancreatitis, biliary cirrhosis
- Malnutrition
- Nasal polyps and sinusitis
- Osteoporosis and arthritis
- Pneumonia, recurrent
- Pneumothorax
- Right-sided heart failure (cor pulmonale)
Sources
http://www.nlm.nih.gov/medlineplus/cysticfibrosis.html
http://www.nlm.nih.gov/medlineplus/ency/article/000107.htm