2009 H1N1 FLU INFORMATION: NEW non-essential visitor policy information to help us protect our patients. Read »

Diagnosis of CF

Riley Cystic Fibrosis Center Home

Flu Update from our CF Center Director

What is CF?

Diagnosis of CF

Newborn Screening

What to Expect at a Visit

Respiratory Care

Infection Control

Nutrition Care

Medications

What to do When You're Sick

Insurance/Reimbursement

Research

Quality Initiative

School/Daycare Information on CF

Transition to Adult Care

Upcoming Events/Educational Opportunities

Photos

The diagnosis of Cystic Fibrosis (CF) is usually made after the primary care provider, usually a pediatrician or family practice physician, has concerns regarding signs and symptoms that may be suggestive of cystic fibrosis. This may include respiratory symptoms such as cough or recurrent pneumonia or gastrointestinal symptoms such as poor weight gain or diarrhea. Typically, both respiratory and nutritional concerns exist in the infant or child. The practitioner then refers the child to a Cystic Fibrosis Foundation (CFF) accredited lab for a sweat chloride test or to a CFF accredited care Center where evaluation and testing can be completed. A diagnosis of CF is possible when there are positive signs and symptoms of the disease, or a positive family history and a test that confirms the diagnosis of cystic fibrosis.

Sweat Test

The usual test for CF is a sweat test. This test done at a special lab and involves a skin test which measures the amount of chloride (one of the body’s natural salts) in a collection of sweat. The test starts with the application of a chemical called pilocarpine to the skin, followed by a small electrical current that stimulates the sweat glands. The sweat is then collected and measured. Persons with cystic fibrosis have elevated or high levels of chloride in the sweat. This test takes about an hour to complete and the results are usually available the same day.

Michelle Howenstine, 
Center Director

Michelle Howenstine
Center Director

Genetic Testing

Another possible way to diagnose CF is to send a blood sample to check for the exact genes involved in CF. This test is more expensive and may miss some patients because of the many gene mutations that can cause CF, as well as the inability to test all of these in a conventional test. It is usually ordered when the sweat chloride test is unable to give an accurate result, or at times when more specific information is needed after the diagnosis of CF is made.

Nasal Potential Difference

Rarely, a test called "nasal potential difference" is used to firmly diagnose CF in very complicated cases, but this test is generally used for research purposes. This test is available at most CF research centers and is usually possible in older children and adults. The nasal potential difference test takes several hours to complete.

US News - America's Best Children's Hospitals 2008 America's Top Doctors Parents Magazine: 25 Best Children's Hospitals

Copyright © 2000-2009
University Pediatric Associates, Inc.
Riley Hospital for Children
702 Barnhill Dr. Room 5900
Indianapolis, IN 46202

1-800-248-1199

Web Design: NetMediaOne