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• Introduction to Pulmonary Clinic What to Bring with You to Clinic • Introduction to the Pulmonary Function Lab
The National Cystic Fibrosis Foundation recommends patients be followed in a CF Center clinic every 3 months. Our center is proud to provide the services of board certified pediatric pulmonologist along with an outstanding support team consisting of specialty nurses, advanced practice nurses, respiratory care practitioners, nutritionist, social worker, and pharmacist.
Location The CF Clinic at Arkansas Children’s Hospital is held during Pulmonary Clinic located in Clinic 2 in the Sturgis Building, 800 Marshall Street, Little Rock, Arkansas 72202.
What to Bring with You If you have any recent chest films or lab results from your primary care physician, always bring them to clinic with you. This may eliminate the needs for duplicate tests.
What to Expect At each visit, a clinic nurse will check vitals signs including height, weight, respiratory rate, heart rate, oxygen level, and blood pressure. If the patient is old enough, usually 6 and older, pulmonary function tests will be performed at each visit.
The CF Foundation requires each patient followed at a CF center have an “annual review” visit once each year. Performed during the clinic visit closest to the patient’s birthday, this is a longer, more involved appointment. During the annual review, every member of the CF team will meet with you to review your/your child’s care. This includes a visit with the nutritionist, respiratory therapist, social worker, pharmacist, nurse, and physician. Thorough testing during an annual review typically includes:
Although annual review visits are time consuming, they ensure everyone is working together toward the best treatment plan for each patient. The clinic keeps snack, toys, and videos to help occupy patient during periods of waiting. Please feel free to bring your own activities to help pass the time as well.
Appointments Please do not show up to clinic if you do not have an appointment because we will not have the necessary medical records for the patient’s care. There are also days when we will not be in clinic and doctors will not be available to see a patient. If you do not have an appointment, you must call prior to coming to the clinic, and we will attempt to meet your needs as best we can. The number to Clinic 2 is (501) 364-2903.
If you need to cancel or change an appointment, please contact Clinic 2 at (501) 364-2903.
If the need arises, patients with CF can be seen in the Emergency Room evenings, nights, weekends, or holidays. The main number to our hospital is (501) 364-1100 if you need contact the pulmonary physician on call emergently.
Additional Assistance If you need additional assistance, contact the Pulmonary Office at (501) 364-1006, which is open Monday-Friday 8:00 a.m. to 4:30 p.m. or pedspulmonary@uams.edu.
Medication Refill Information Refills for medications should be called into the Pulmonary Office at (501) 364-1006 allowing 24 hours to complete any refill request. (Please call prior to running out of a medication.)
Staffed by Licensed Respiratory Care Practitioners, the pulmonary lab performs many tests that help physicians evaluate a patient’s lung health. “Pulmonary function tests”, usually called PFT’s are the most frequently ordered pulmonary lab tests. Different types of PFT’s can be performed depending on the age of the child. Each test requires a certain level of cooperation for the test to be successful and accurate. Generally, PFT’s are ordered within the following guidelines:
Infant Pulmonary Function testing is done in the main pulmonary lab. When patients are old enough to cooperate, they will be testing in either the pulmonary lab located on the second floor in the main hospital or the satellite pulmonary lab, which is accessible in the Sturgis building. Other pulmonary lab procedures include sweat testing and exercise testing as ordered.
Spirometry (Note: this test does not hurt)
During Clinic: The most common PFT performed is basic “spirometry”. This test checks the volumes and flow rates the patient is capable of producing by forcing (blowing) air out of their lungs into a mouthpiece. The test results can be compared at each visit to determine if lung function is staying the same, improving, or getting worse. A nose clip is used to keep air from coming out of the nose, so all the air goes into the mouthpiece. Three consistent forced expirations are required for a good test. A respiratory therapist in the pulmonary lab area will coach and encourage the patient during the test to get the best effort. The test takes about 20 minutes. Sometimes, the test is repeated after giving a treatment with a bronchodilator (Albuterol) to see if breathing changes with the medicine. Spirometry can help evaluate if a change in therapy is needed at home.
During Admission: Patients admitted to the hospital perform PFT’s soon after admission and usually several more times before going home (depending on the length of stay in the hospital). This is one way to evaluate how well a patient is improving during the hospital stay and decide when they are well enough to go home.
Lung Volumes (Note: this test does not hurt) Around 8 years of age, patients usually are able perform a more difficult test called body plethysmography which is often called “a body box study”. This nickname comes from the appearance of the equipment, which resembles a phone booth with a bench seat inside. The patient sits inside the box and breaths on a mouthpiece. Chest movements and changes in breathing pressures are measured, so the computer can calculate lung volumes. This test shows the total amount of air in the lungs and gives a more complete picture of a patients’ breathing function. This test takes about 20 minutes and will be performed at least once a year during annual visit.
Helium Dilution (Note: this test does not hurt) In some instances, the helium dilution study is used to evaluate lung volumes instead of the body box. It requires quiet breathing on a mouthpiece for 3-5 minutes followed by a full inspiration and expiration. This test may not provide the more specific results for some patients with CF. It is usually used for:
Sweat Testing (Note some patients report feeling mild-to-moderate discomfort in an area about 1 inch square on the forearm for 5 minutes during test while others report no discomfort at all during this 5 minutes period.) The most reliable way to diagnose CF is analysis of the sweat for amount of chloride (salt) it contains. (Note: It is important to have a sweat test using the method approved by the CF foundation for both collection and analysis. “Screening tests” may be unreliable.) The patient’s forearm is thoroughly cleaned and chemical called pilocarpine is placed on the forearm. Two small, battery-powered electrodes are attached. A small current (4 mill amperes) from the electrodes forces the pilocarpine into the skin stimulating sweat glands to sweat in that spot on the forearm. Stimulation of the sweat gland takes 5 minutes. This sweat stimulation feels uncomfortable to some, but many people feel only a tingling sensation. Then a round, plastic disk is taped onto the arm and a piece of gauze is placed under it. The patient wears the gauze patch for 30 minutes to collect the sweat. The gauze is then removed and sent to the lab for analysis of the chloride content. Results of the sweat test are usually available on the date of service. Patients who are sent for a test by a physician outside of ACH must obtain the results from the ordering physician. Patients being seen in an ACH clinic can get results from ACH physician.
A sweat test result higher than 60 mEq/L is considered positive for cystic fibrosis and must be repeated before a diagnosis of CF can be made. Results between 40-60 mEq/L are considered inconclusive and must be repeated as well. Results lower than 40 mEq/L are negative and do not bear repeating.
Bronchoscopy This test is performed while a patient sedated by a pediatric pulmonologist and is not available as part of a clinic visit. A bronchoscopy consists of inserting a long, thin tube (usually through the nose) through the upper airway into the lungs. The physician can look at the surface of the lungs and take sputum specimens. This test may help find an infection or other lung problem. A CF patient may never need a bronchoscopy. It is performed only when a problem persists that cannot be identified by other means.
ACH offers a full range of pediatric specialist that might be necessary for CF care including Radiology, Gastroenterology (also called GI), Endocrine, Surgery, and Psychology. ACH also has outpatient pharmacy services available.
University of Arkansas for Medical Sciences Department of Pediatrics Section of Pediatric Pulmonology Arkansas Children's Hospital 800 Marshall Street Little Rock, AR 72202 Send Comments |
