Cystic Fibrosis Diagnosis

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Newborn Screening

Exam and Test

All newborns in Virginia are screened for cystic fibrosis. This preliminary blood test measures the level of immunoreactive trypsinogen (IRT) present in the blood.

Definition of IRT

Trypsinogen is one of the secretory products of the pancreas making its level in the blood a specific marker of pancreatic function. Elevated levels of IRT indicate that a newborn may be at risk for CF.

Why is this test performed?

After many years of following patients with cystic fibrosis who had newborn screening, it was determined that growth and nutrition improved, survival improved and need for hospitalization decreased. Therefore, the Morbidity and Mortality Weekly Report in 10/15/04 stated the health benefits from screening "outweigh the risk of harm and justify newborn screening for cystic fibrosis”. Newborn screening in the Commonwealth of Virginia begin in March 2006.

How is this test performed?

This test is included with all other tests done for newborn screening and noted on the newborn screening card that your childre receives before discharge from the hospital or by your primary care physician.

What is done if your child has an abnormal test result?

If the first newborn screen test is abnormal, your primary care physician will order a repeat newborn screen test. If that second test is also abnormal, diagnostic testing is required. This test is usually a sweat chloride test.

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Wrestling With Cystic Fibrosis

Pediatric pulmonologist and director of CHKD's cystic fibrosis center Cynthia Epstein follows many local children with CF. Connor Ruddy is one of them.

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