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  3. Temporal Trends in Acute Adrenal Insufficiency Events in Children With Congenital Adrenal Hyperplasia During 2019-2022.
 

Temporal Trends in Acute Adrenal Insufficiency Events in Children With Congenital Adrenal Hyperplasia During 2019-2022.

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BORIS DOI
10.48620/76186
Publisher DOI
10.1210/jendso/bvae145
PubMed ID
39258010
Description
Background
It is unclear whether targeted monitoring of acute adrenal insufficiency (AI) related adverse events (AE) such as sick day episodes (SDEs) and hospitalization rate in congenital adrenal hyperplasia (CAH) is associated with a change in the occurrence of these events.Aim
Study temporal trends of AI related AE in the I-CAH Registry.Methods
In 2022, data on the occurrence of AI-related AE in children aged <18 years with 21-hydroxylase deficiency CAH were compared to data collected in 2019.Results
In 2022, a total of 513 children from 38 centers in 21 countries with a median of 8 children (range 1-58) per center had 2470 visits evaluated over a 3-year period (2019-2022). The median SDE per patient year in 2022 was 0 (0-2.5) compared to 0.3 (0-6) in 2019 ( = .01). Despite adjustment for age, CAH phenotype and duration of study period, a difference in SDE rate was still apparent between the 2 cohorts. Of the 38 centers in the 2022 cohort, 21 had also participated in 2019 and a reduction in SDE rate was noted in 13 (62%), an increase was noted in 3 (14%), and in 5 (24%) the rate remained the same. Of the 474 SDEs reported in the 2022 cohort, 103 (22%) led to hospitalization compared to 299 of 1099 SDEs (27%) in the 2019 cohort ( = .02).Conclusion
The I-CAH Registry can be used for targeted monitoring of important clinical benchmarks in CAH. However, changes in reported benchmarks need careful interpretation and longer-term monitoring.
Date of Publication
2024-08-27
Publication Type
Article
Keyword(s)
21-hydroxylase deficiency
•
adrenal insufficiency
•
adverse events
•
benchmark
•
congenital adrenal hyperplasia
•
quality improvement
•
registry
•
sick day episodes
Language(s)
en
Contributor(s)
Tseretopoulou, Xanthippi
Ali, Salma R
Bryce, Jillian
Amin, Nadia
Atapattu, Navoda
Bachega, Tania A S S
Baronio, Federico
Ortolano, Rita
Birkebaek, Niels H
Bonfig, Walter
Cools, Martine
Davies, Justin H
Thomas, Tessy
de Vries, Liat
Elsedfy, Heba
Amr, Nermine H
Flück, Christa Eorcid-logo
Department of Paediatrics
Department for BioMedical Research, Forschungsgruppe Endokrinologie / Diabetologie / Metabolik (Pädiatrie)
Globa, Evgenia
Guran, Tulay
Yavas-Abali, Zehra
Guven, Ayla
Hannema, Sabine E
Iotova, Violeta
Konrad, Danielorcid-logo
Lenherr-Taube, Nina
Krone, Nils P
Leka-Emiri, Sofia
Vlachopapadopoulou, Elpis
Lichiardopol, Corina
Marginean, Otilia
Markosyan, Renata
Neumann, Uta
Niedziela, Marek
Banaszak-Ziemska, Magdalena
Phan-Hug, Franziska
Poyrazoglu, Sukran
Probst-Scheidegger, Ursina
Randell, Tabitha
Russo, Gianni
Salerno, Mariacarolina
Seneviratne, Sumudu
Shnorhavorian, Margarett
Thankamony, Ajay
Tadokoro-Curraro, Rieko
van den Akker, Erica
van Eck, Judith
Vieites, Ana
Wasniewska, Malgorzata
Ahmed, S Faisal
Additional Credits
Department of Paediatrics
Series
Journal of the Endocrine Society
Publisher
Oxford University Press
ISSN
2472-1972
Access(Rights)
open.access
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