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Diagnosis of cystic fibrosis after newborn screening: The Australasian experience - Twenty years and five million babies later: A consensus statement from the Australasian Paediatric Respiratory Group

journal contribution
posted on 2005-05-01, 00:00 authored by J Massie, B Clements, H Allen, D Armstrong, I Asher, Y Belessis, C Byrnes, A Chang, G Cooper, P Cooper, C Dakin, N Dore, E Edwards, P Field, D Fitzgerald, P Francis, N Freezer, L Gauld, J Gillies, M Haifer, M Harris, R Henry, J Hilton, A Isles, A Kemp, D Kennedy, L Landau, P LeSouef, J Martin, B Masters, C Mellis, J Morton, G Nixon, A Numa, T Olinsky, P Pattemore, P Phelan, S Ranganathan, C Robertson, P Robinson, R Roseby, S Sawyer, H Selvadurai, P Sly, Peter Sly, R Staugas, S Stick, P Van Asperen, C Wainwright, K Waters, B Whitehead, A Wilson
Newborn screening for cystic fibrosis has been used in Australia and New Zealand for over 20 years. In that time, considerable experience has been developed regarding the early diagnosis of cystic fibrosis after newborn screening. To date, there has not been a consensus on the process of screening and clinical evaluation leading to the diagnosis of cystic fibrosis in infants, many of whom are not symptomatic at time of notification of the screening result. The aim of this paper is to provide some consensus on the important issues of a cystic fibrosis diagnosis arising from newborn screening, based on the experience gained in Australia and New Zealand over the last 20 years. © 2005 Wiley-Liss, Inc.

History

Journal

Pediatric Pulmonology

Volume

39

Issue

5

Pagination

440 - 446

ISSN

8755-6863