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Arkansas Children's Hospital
General Information 501-364-1100
Arkansas Children's Northwest
General Information 479-725-6800
The Pulmonary Clinic at Arkansas Children's provides infants and children with complete diagnosis and treatment of acute and chronic lung disease. It is the only Cystic Fibrosis Center in the state reviewed and approved by the national Cystic Fibrosis Foundation.
Get a Second Opinion: 501-364-4000
Pulmonary function tests are a series of tests, which evaluate how well your lungs are performing.
Staffed by Licensed Respiratory Care Practitioners, pulmonary 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.
Pulmonary function tests, called PFTs, are tests that see how well your lungs work. They are the most often ordered pulmonary lab tests. Our Pulmonary Clinic is staffed by Licensed Respiratory Care Practitioners and performs many tests to help physicians check a patient's lung health. To accurately diagnose and treat lung conditions in children, we offer pulmonary function tests.
A test that measures the total size of your lungs (how big they are) and how the air is distributed through the lungs.
This test shows the total amount of air in the lungs and gives a more complete picture of a patients’ breathing function.
The helium dilution study is used to evaluate lung volumes instead of the body box.
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.
A test to measure exercise-induced bronchoconstriction (EIB) or acute airway narrowing that occurs as a result of exercise.
This test is performed to determine how exercise affects your lung function.
This test is the most reliable way to diagnose cystic fibrosis is to analyze the chloride (salt) contained in sweat. It is important to have a sweat test using the method approved by the Cystic Fibrosis Foundation for both collection and analysis.
This test measures the transfer of gas from air in the lungs to the red blood cells in lung blood vessels.
The pre-post bronchodilator study uses spirometry to see if the narrowed airways caused by asthma and other respiratory diseases can be reversed.
This test monitors expiratory muscle weakness and bulbar involvement.
This challenge will test your child's baseline lung function as well as provide results on breathing tests using cold air.
A bronchoscopy consists of inserting a long, thin tube (usually through the nose) through the upper airway into the lungs and allows the physician to look at the surface of the lungs.
This challenge will test your child's baseline lung function as well as provide results on breathing tests using cold air.
A bronchoscopy consists of inserting a long, thin tube (usually through the nose) through the upper airway into the lungs and allows the physician to look at the surface of the lungs.
This test shows the total amount of air in the lungs and gives a more complete picture of a patients’ breathing function.
The pre-post bronchodilator study uses spirometry to see if the narrowed airways caused by asthma and other respiratory diseases can be reversed.
A test that measures the total size of your lungs (how big they are) and how the air is distributed through the lungs.
The helium dilution study is used to evaluate lung volumes instead of the body box.
This test monitors expiratory muscle weakness and bulbar involvement.
This test is the most reliable way to diagnose cystic fibrosis is to analyze the chloride (salt) contained in sweat. It is important to have a sweat test using the method approved by the Cystic Fibrosis Foundation for both collection and analysis.
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.
This test is performed to determine how exercise affects your lung function.
A test to measure exercise-induced bronchoconstriction (EIB) or acute airway narrowing that occurs as a result of exercise.
This test measures the transfer of gas from air in the lungs to the red blood cells in lung blood vessels.
Our chaplains are on staff to assist all patients and families from any faith background with religious and spiritual needs.
Child Life reduces stress and promotes positive coping using developmentally appropriate preparation, education, and play at Arkansas Children's.
Arkansas Children's offers on-site dining, shuttle services, and gift shops, as well as discounted hotels and RV parks nearby.
Manage your child's medical information and connect with your Arkansas Children's medical team anytime online!
Log in to MyChartOur chaplains are on staff to assist all patients and families from any faith background with religious and spiritual needs.
Child Life reduces stress and promotes positive coping using developmentally appropriate preparation, education, and play at Arkansas Children's.
Arkansas Children's offers on-site dining, shuttle services, and gift shops, as well as discounted hotels and RV parks nearby.