Cortisol Levels During Acute Illnesses in Children and Adolescents: A Systematic Review.
Journal
JAMA network open
ISSN: 2574-3805
Titre abrégé: JAMA Netw Open
Pays: United States
ID NLM: 101729235
Informations de publication
Date de publication:
01 06 2022
01 06 2022
Historique:
entrez:
22
6
2022
pubmed:
23
6
2022
medline:
25
6
2022
Statut:
epublish
Résumé
Endogenous cortisol levels in children and adolescents during acute illnesses can contribute to the evidence base required to optimize glucocorticoid (GC) stress doses for children and adolescents known to have GC deficiency. To identify endogenous cortisol levels during a range of acute illnesses in children and adolescents without GC deficiency from published evidence. CINAHL, Cochrane Library, Cochrane Database of Systematic Reviews, Embase, and MEDLINE were searched for studies published between January 1, 2000, and June 30, 2020. Two reviewers independently identified relevant studies. Differences were resolved by joint discussion. Inclusion criteria were common acute illnesses, age from 1 month to 18 years, and basal blood cortisol levels obtained within 48 hours of presentation. Studies with fewer than 5 participants and those that included participants known to have GC deficiency or a history of treatment that could affect cortisol levels were excluded from the review. Data for predefined fields were extracted and independently checked by separate pairs of reviewers. Overall weighted means and pooled SDs for cortisol levels were calculated. All 15 studies included were hospital based and included 864 unique participants: 14 studies were prospective observational studies, 1 was part of a trial, and 5 included control individuals. Mean cortisol levels were higher in all participants with an acute illness (n = 689) than in controls (n = 175) (difference in weighted means, 18.95 μg/dL; 95% CI, 16.68-21.22 μg/dL). Cortisol levels were highest in patients with bacterial meningitis (weighted mean [pooled SD], 46.42 [22.24] μg/dL) and were more than 3-fold higher in the group with severe gastroenteritis (weighted mean [pooled SD], 39.64 [21.34] μg/dL) than in the control group. Among the subgroups with sepsis, those with shock had lower cortisol levels than those without shock (weighted mean [pooled SD], 27.83 [36.39] μg/dL vs 37.00 [23.30] μg/dL), but levels in nonsurvivors did not differ from levels in survivors (weighted mean [pooled SD], 24.89 [51.65] μg/dL vs 30.53 [30.60] μg/dL). This systematic review found that, in children and adolescents without GC deficiency, circulating cortisol levels were higher during acute illnesses than those in controls and also varied across a range of acute illnesses. Whether these levels need to be achieved with exogenous GC stress doses tailored according to the nature and severity of the illness in children and adolescents with GC deficiency warrants investigation.
Identifiants
pubmed: 35731516
pii: 2793433
doi: 10.1001/jamanetworkopen.2022.17812
pmc: PMC9218852
doi:
Substances chimiques
Hydrocortisone
WI4X0X7BPJ
Types de publication
Journal Article
Observational Study
Research Support, Non-U.S. Gov't
Systematic Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
e2217812Références
J Clin Endocrinol Metab. 2000 Oct;85(10):3746-53
pubmed: 11061534
Best Pract Res Clin Endocrinol Metab. 2009 Apr;23(2):193-208
pubmed: 19500763
BMC Med Res Methodol. 2014 Dec 19;14:135
pubmed: 25524443
BMC Med Res Methodol. 2005 Apr 20;5:13
pubmed: 15840177
Nat Rev Endocrinol. 2019 Jul;15(7):417-427
pubmed: 30850749
Crit Care. 2018 Sep 29;22(1):244
pubmed: 30268145
Pediatr Crit Care Med. 2007 Nov;8(6):530-9
pubmed: 17914311
Pediatr Infect Dis J. 2002 Apr;21(4):330-6
pubmed: 12075765
Pediatrics. 2002 Sep;110(3):563-9
pubmed: 12205261
J Infect Dis. 2001 Dec 15;184(12):1532-7
pubmed: 11740728
N Engl J Med. 2013 Apr 18;368(16):1477-88
pubmed: 23506003
Pediatrics. 2005 Dec;116(6):1401-7
pubmed: 16322164
Pediatr Infect Dis J. 1989 Jan;8(1):16-20
pubmed: 2922232
N Engl J Med. 2003 Feb 20;348(8):727-34
pubmed: 12594318
Evid Based Ment Health. 2019 Nov;22(4):153-160
pubmed: 31563865
Arch Dis Child. 2017 Feb;102(2):199-205
pubmed: 27582458
BMJ. 2021 Mar 29;372:n71
pubmed: 33782057
Intensive Care Med. 2012 Oct;38(10):1689-96
pubmed: 22878348
Front Endocrinol (Lausanne). 2021 Oct 13;12:757566
pubmed: 34721304
Ann Clin Biochem. 2017 May;54(3):308-322
pubmed: 28068807
Horm Res Paediatr. 2016;86(2):94-99
pubmed: 27437687
J Clin Endocrinol Metab. 2020 Jul 1;105(7):
pubmed: 32170323
Intensive Care Med. 2004 Dec;30(12):2257-62
pubmed: 15536526
Endocrine. 2017 Jan;55(1):307-310
pubmed: 27430494
Eur J Pediatr. 2019 May;178(5):731-738
pubmed: 30806790
Pediatr Crit Care Med. 2006 Jan;7(1):74-8
pubmed: 16395079
Intensive Care Med. 2007 Sep;33(9):1609-13
pubmed: 17541546
Intensive Care Med. 2008 Jan;34(1):163-8
pubmed: 17710382
Nat Rev Endocrinol. 2019 Sep;15(9):525-534
pubmed: 31249398
Clin Endocrinol (Oxf). 2013 Mar;78(3):347-51
pubmed: 22803584
Crit Care. 2021 Feb 16;25(1):65
pubmed: 33593393
Pediatrics. 2006 May;117(5):e878-86
pubmed: 16618789
J Clin Endocrinol Metab. 2004 Mar;89(3):1410-4
pubmed: 15001642
Arch Dis Child Educ Pract Ed. 2015 Oct;100(5):272-6
pubmed: 25561746
Pediatrics. 2012 Oct;130(4):e804-11
pubmed: 23008453
Pediatr Crit Care Med. 2007 Jan;8(1):23-8
pubmed: 17251878