Cystic Fibrosis
Cystic fibrosis (CF) is an inherited disease of your mucus and sweat glands. Cystic fibrosis disease affects mostly your lungs, pancreas, liver, intestines, sinuses, and sex organs. Normally, mucus is watery. It keeps the linings of certain organs moist and prevents them from drying out or getting infected. But in fibrosis cystic, an abnormal gene causes mucus to become thick and sticky.
The mucus builds up in your lungs and blocks the airways. This makes it easy for bacteria to grow and leads to repeated serious lung infections. Over time, these infections can cause serious damage to your lungs.
The thick, sticky mucus can also block tubes, or ducts, in your pancreas. As a result, digestive enzymes that are produced by your pancreas cannot reach your small intestine. These enzymes help break down the food that you eat. Without them, your intestines cannot absorb fats and proteins fully.
As a result:
- Nutrients leave your body unused, and you can become malnourished.
- Your stools become bulky.
- You may not get enough vitamins A, D, E, and K.
- You may have intestinal gas, a swollen belly, and pain or discomfort.
Symptoms of cystic fibrosis can also cause infertility (mostly in men).
The symptoms and severity of Cystic Fibrosis vary from person to person. Some people with fibrosis cystic have serious lung and digestive problems. Other people have more mild disease that doesn't show up until they are adolescents or young adults.
Respiratory failure is the most common cause of death in people with cystic fibrosis symptoms.
Until the 1980s, most deaths from fibrosis cystic occurred in children and teenagers. Today, with improved treatments, people with cystic fibrosis symptoms live, on average, to be more than 35 years old. Research continues to look for:
- Better treatments
- A cure
- CF
- Cystic fibrosis of the pancreas
- Fibrocystic disease of the pancreas
- Mucoviscidosis
- Mucoviscidosis of the pancreas
- Pancreas fibrocystic disease
- Pancreatic cystic fibrosis
Cystic fibrosis (CF) is caused by a defect in a gene called the cystic fibrosis transmembrane conductance regulator (CFTR) gene. This gene makes a protein that controls the movement of salt and water in and out of the cells in your body. In people with fibrosis cystic, the gene does not work effectively. This causes the thick, sticky mucus and very salty sweat that are the main features of Cystic Fibrosis.
Each of us inherits two CFTR genes, one from each parent.
- Children who inherit an abnormal CFTR gene from each parent will have CF.
- Children who inherit an abnormal CFTR gene from one parent and a normal CFTR gene from the other parent will not have CF. They will be CF carriers.
- Usually have no symptoms of CF
- Live normal lives
- Can pass the abnormal CFTR gene on to their children
- One in four chance of inheriting two abnormal CFTR genes and having CF.
- One in four chance of inheriting two normal CFTR genes and not having CF or being a carrier.
- Two in four chance of inheriting one normal CFTR gene and one abnormal CFTR gene. The baby will not have CF but will be a CF carrier like its parents.
Who Is At Risk for Cystic Fibrosis
About 30,000 people in the United States have cystic fibrosis (CF).
- It affects both males and females.
- It affects people from all racial and ethnic groups but is most common among Caucasians whose ancestors came from northern Europe.
About 1 in every 3,000 babies born in the United States has Cystic Fibrosis.
Cystic Fibrosis is also common in:
- Latinos
- Native Americans, especially the Pueblo and Zuni
- African Americans
- Asian Americans
What Are the Signs and Symptoms of Cystic Fibrosis?
Most of the symptoms of cystic fibrosis (CF) are caused by the thick, sticky mucus. The most common symptoms include:
- Frequent coughing that brings up thick sputum, or phlegm (flem).
- Frequent bouts of bronchitis and pneumonia. They can lead to inflammation and permanent lung damage.
- Salty-tasting skin.
- Dehydration.
- Infertility (mostly in men).
- Ongoing diarrhea or bulky, foul-smelling, and greasy stools.
- Huge appetite but poor weight gain and growth. This is called "failure to thrive." It is a result of chronic malnutrition because you do not get enough nutrients from your food.
- Stomach pain and discomfort caused by too much gas in your intestines.
- Sinusitis. The sinuses are air-filled spaces behind your eyes, nose, and forehead. They produce mucus and help keep the lining of your nose moist. When the sinuses become swollen, they get blocked with mucus and can become infected. Most people with CF develop sinusitis.
- Bronchiectasis. Bronchiectasis is a lung disease in which the bronchial tubes, or large airways in your lungs, become stretched out and flabby over time and form pockets where mucus collects. The mucus provides a breeding ground for bacteria. This leads to repeated lung infections. Each infection does more damage to the bronchial tubes. If not treated, bronchiectasis can lead to serious illness, including respiratory failure.
- Pancreatitis. Pancreatitis is inflammation in the pancreas that causes pain.
- Episodes of intestinal blockage, especially in newborns.
- Nasal polyps, or growths in your nose, that may require surgery.
- Clubbing. Clubbing is the widening and rounding of the tips of your fingers and toes. It develops because your lungs are not moving enough oxygen into your blood stream.
- Collapsed lung. This is also called pneumothorax.
- Rectal prolapse. Frequent coughing or problems passing stools may cause rectal tissue from inside you to move out of your rectum.
- Liver disease due to inflammation or blocked bile ducts.
- Diabetes.
- Gallstones.
- Low bone density because you do not get enough Vitamin D.
First, your doctor will obtain a detailed medical and family history and perform a thorough physical examination. Next, your doctor may order some tests to ensure an accurate diagnosis.
The sweat test is the most useful test for diagnosing cystic fibrosis (CF). It measures the amount of salt in your sweat. For this test, doctors rub a small amount of a chemical called pilocarpine (pi-lo-KAR-pen) on your arm or leg. They then attach an electrode to this spot. The electrode provides a mild electric current that produces sweat. This may cause tingling or a feeling of warmth. They then cover the area with a gauze pad or filter paper and wrap in plastic. After 30 to 40 minutes, they remove the plastic so the sweat that collected on the pad or paper can be analyzed. The test is usually done twice. High salt levels mean cystic fibrosis disease.
Your doctor may also do the following tests to understand more about your condition and how to treat it:
- Blood tests to look for an abnormal fibrosis cystic gene or other things that indicate CF.
- Chest x ray. A chest x ray takes a picture of your lungs. It can show scarring from inflammation in your lungs.
- Sinus x ray. This test may show signs of sinusitis.
- Lung function tests can measure:
- How much air your lungs can hold
- How quickly you can breathe air out of your lungs
- How well your lungs add oxygen to and remove carbon dioxide from your blood
- Sputum (phlegm) cultures. Doctors take a sample of your sputum to see what bacteria are growing in it.
- In amniocentesis (AM-ne-o-sen-TE-sis), your doctor inserts a hollow needle through your abdominal wall into your uterus to obtain cells from the fluid (amniotic fluid) around the baby. The fluid is then tested to see if both of the baby's CFTR genes are normal.
- In a chorionic villus biopsy (ko-re-ON-ik VIL-us BI-op-se), your doctor uses ultrasound to guide a thin tube through your vagina and cervix into your uterus and remove a tiny piece of the placenta to biopsy. The cells of the placenta are then tested to see if the baby has CF.
CF Carrier Testing
You may want to check whether you are a cystic fibrosis disease carrier, if:
- You have a family history of CF.
- You are a partner of someone with CF.
- You are a couple planning a pregnancy.
How Is Cystic Fibrosis Treated?
There still is no cure for cystic fibrosis (CF), but treatments have improved greatly in recent years. The goals of CF treatment are to:
- Prevent and control infections in your lungs.
- Loosen and remove the thick, sticky mucus from your lungs.
- Prevent blockages in your intestines.
- Provide adequate nutrition.
The main treatments for lung problems in people with cystic fibrosis symptoms are:
- Antibiotics for infections of the airways
- Chest physical therapy
- Exercise
- Other medications
Most people with cystic fibrosis disease have ongoing, low-grade lung infections. Sometimes, these infections become so serious that you may need to be hospitalized. Antibiotics are the primary treatment.
You may be given several different types of antibiotics. The choice of antibiotics depends on:
- The strains of bacteria involved
- How serious your condition is
- Your previous history of antibiotic use
- Oral antibiotics for relatively mild airway infections.
- Inhaled antibiotics, such as tobramycin (to-bra-MI-sin). They may be used alone or with oral antibiotics.
- Intravenous antibiotics for severe infections or when none of the oral antibiotics work.
- Antibiotics, such as azithromycin (az-ith-roe-MYE-sin), that also reduce inflammation.
Chest physical therapy (CPT) is also called chest clapping or percussion. It involves pounding your chest and back over and over again to dislodge the mucus from your lungs so that you can cough up the mucus. CPT for cystic fibrosis should be done three to four times each day.
CPT is also often referred to as postural drainage. This involves your sitting or lying on your stomach with your head down while you do CPT. This allows gravity to help drain the mucus from your lungs.
Because CPT is hard or uncomfortable for some people, several devices have been developed recently that may help with CPT. The devices include:
- An electric chest clapper, known as a mechanical percussor.
- An inflatable therapy vest that uses high-frequency air waves to force the mucus out of your lungs.
- A "flutter" device, a small hand-held device that you breathe out through. It causes vibrations that dislodge the mucus.
- A positive expiratory pressure (PEP) mask that creates vibrations that help break the mucus loose from the airway walls.
- Forced expiration technique (FET)—forcing out a couple of breaths or huffs and then doing relaxed breathing
- Active cycle breathing (ACB)—FET with deep breathing exercises that can loosen the mucus in your lungs and help open your airways
Aerobic exercise helps:
- Loosen the mucus
- Encourage coughing to clear the mucus
- Improve your overall physical condition
Other medications
- Anti-inflammatory medications may help reduce the inflammation in your lungs that is caused by ongoing infections. These medications include:
- Inhaled or, sometimes, oral steroids. Steroids are the most effective anti-inflammatory medicines.
- Ibuprofen, a type of nonsteroidal, anti-inflammatory medicine. It may slow the progress of CF in young children with mild symptoms.
- Bronchodilators, which are inhaled drugs that relax the muscles around the airways so that the airways can open up. They should be taken just before CPT to help clear mucus.
- Human DNase (Dornase Alfa), a drug that loosens the mucus in your lungs. It may lead to shorter hospital stays.
- Acetylcysteine and saline.
- Saline washes of your nasal passages, which may help clear your sinuses.
If the level of oxygen in your blood is too low, you may need oxygen therapy. Oxygen is usually given through nasal prongs or a mask.
Lung Transplantation
Surgery to replace one or both of your lungs with healthy lungs from a human donor may help you. Some of the factors that determine whether you can undergo lung transplantation include:
- The type of bacteria in your lungs
- Your age and weight
- The medications you are taking
- Whether you have other medical conditions, including osteoporosis
- How well your lungs are functioning
If you have cystic fibrosis (CF), you should learn as much as you can about the disease and work closely with your doctors to learn how to manage it.
Ongoing medical care is important. You should seek treatment from a team of doctors, nurses, and respiratory therapists who specialize in treatment for cystic fibrosis. These specialists are often located at CF Foundation Centers in major medical centers.
Good self-care includes:
- Eating a healthy diet
- Avoiding tobacco smoke
- Washing your hands often to reduce your chances of infection
- Exercising frequently
- Drinking lots of fluids
- Doing chest physical therapy every day
- Having annual flu and other appropriate vaccinations
- Taking your medicines as prescribed
If you are a parent of someone with cystic fibrosis disease, do not feel guilty about passing it on to your child. And do not be overprotective; encourage your child to be active and self-reliant.
Information Obtained From National Institute Of Health