ESPE Abstracts (2021) 94 P2-24

Adrenals and HPA Axis

The incidence and presentation of congenital adrenal hyperplasia in an unscreened population

Tracey Anne Conlon1,2, Colin Patrick Hawkes3,4,5, Jennifer Brady6 & Nuala Patricia Murphy1,2


1Department of Endocrinology, CHI at Temple Street, Dublin, Ireland; 2School of Medicine, University College Dublin, Dublin, Ireland; 3Department of Paediatrics and Child Health, University College Cork, Cork, Ireland; 4Perelman School of Medicine, University of Pennsylvania, Philadelphia, USA; 5Division of Endocrinology and Diabetes, The Children’s Hospital of Philadelphia, Philadelphia, USA; 6Department of Clinical Biochemistry, CHI at Temple Street, Dublin, Ireland

Background: Newborn screening for congenital adrenal hyperplasia (CAH) has been shown to reduce time to diagnosis, and thus morbidity and mortality. Internationally, newborn screening for CAH continues to expand and screening techniques have improved, with the implementation of second-tier testing and use of gestational age stratification. The aim of this study was to examine the incidence and spectrum of early clinical presentations of CAH in an unscreened population, in order to determine the case for newborn screening.

Methods: A national retrospective observational study was undertaken to identify all children diagnosed with CAH in the Republic of Ireland, between January 2005 and December 2019. Reporting clinicians completed anonymised clinical questionnaires.

Results: There were 103 cases of CAH reported and 69 cases met the study inclusion criteria. The estimated annualised incidence of CAH in the Republic of Ireland was 1: 14,754 or 0.07 cases per 1000 live births. Forty-seven children presented clinically in the first six months of life, but only 17 of these had a confirmed diagnosis by day 10. Of these early presentations, there were 28 infants with salt-wasting, 15 females presented with virilised genitalia and four infants were detected due to a family history of CAH. Female infants presented at a median age of 0 days [IQR 0-1] and males at 14 days [IQR 9-21]. Seventy-eight percent of salt-wasting presentations occurred after day 10. Delays in clinical presentation, biochemical diagnosis and treatment initiation were identified.

Conclusions: The incidence of CAH is higher in Ireland than in other unscreened populations. In the absence of screening, clinicians should be aware of the possibility of CAH and appropriate investigations should be urgently requested. Life-threatening salt-wasting is the most frequent clinical presentation and many cases could be detected prior to decompensation if newborn screening were introduced. Consideration should be given to adding CAH to the Irish National Newborn Screening Programme, in line with best practice.

Volume 94

59th Annual ESPE (ESPE 2021 Online)

22 Sep 2021 - 26 Sep 2021

European Society for Paediatric Endocrinology 

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