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Two‐year pilot study of newborn screening for congenital adrenal hyperlasia in New South Wales compared with nationwide case surveillance in Australia
Author(s) -
Gleeson Helena K,
Wiley Veronica,
Wilcken Bridget,
Elliott Elizabeth,
Cowell Christopher,
Thonsett Michael,
Byrne Geoffrey,
Ambler Geoffrey
Publication year - 2008
Publication title -
journal of paediatrics and child health
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.631
H-Index - 76
eISSN - 1440-1754
pISSN - 1034-4810
DOI - 10.1111/j.1440-1754.2008.01383.x
Subject(s) - medicine , congenital adrenal hyperplasia , population , pediatrics , incidence (geometry) , newborn screening , environmental health , physics , optics
Aim: To assess the benefits and practicalities of setting up a newborn screening (NBS) program in Australia for congenital adrenal hyperplasia (CAH) through a 2 year pilot screening in ACT/NSW and comparing with case surveillance in other states. Methods: The pilot newborn screening occurred between 1/10/95 and 30/9/97 in NSW/ACT. Concurrently, case reporting for all new CAH cases occurred through the Australian Paediatric Surveillance Unit (APSU) across Australia. Details of clinical presentation, re‐sampling and laboratory performance were assessed. Results: 185,854 newborn infants were screened for CAH in NSW/ACT. Concurrently, 30 cases of CAH were reported to APSU, twelve of which were from NSW/ACT. CAH incidence was 1 in 15 488 (screened population) vs 1 in 18,034 births (unscreened) (difference not significant). Median age of initial notification was day 8 with confirmed diagnosis at 13(5–23) days in the screened population vs 16(7–37) days in the unscreened population (not significant). Of the 5 clinically unsuspected males in the screened population, one had mild salt‐wasting by the time of notification, compared with salt‐wasting crisis in all 6 males from the unscreened population. 96% of results were reported by day 10. Resampling was requested in 637 (0.4%) and median re‐sampling delay was 11(0–28) days with higher resample rates in males (p < 0.0001). The within‐laboratory cost per case of clinically unsuspected cases was A$42 717. Conclusion: There seems good justification for NBS for CAH based on clear prevention of salt‐wasting crises and their potential long‐term consequences. Also, prospects exist for enhancing screening performance.