{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2023,11,22]],"date-time":"2023-11-22T16:43:37Z","timestamp":1700671417643},"reference-count":34,"publisher":"Springer Publishing Company","issue":"6","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Neonatal Network"],"published-print":{"date-parts":[[2021,11,1]]},"abstract":"<jats:p>Relative adrenal insufficiency (AI) is a disease process commonly associated with preterm birth and critical illness. Further, the incidence of AI is inversely proportional to gestational age. The incidence of AI is likely underreported; however, it is reported to occur in 150\u2013280\/1,000,000 live births worldwide. Functional development of the adrenal gland does not occur until after 30 weeks of gestation; however, advances made in neonatal care increase the survivability of infants born well before this period. Among infants with AI, the adrenal gland is transiently incapable of secreting physiologic levels of cortisol in response to stressors. Common and nonspecific signs include hypotension, poor perfusion, and dysregulation of fluid, electrolytes, and euglycemia. Recognition, diagnosis, and steroid therapy is critical, as inappropriately managed AI can lead to an adrenal crisis, shock, and death. Understanding the presentation and common risk factors for developing relative AI is crucial for quick diagnosis and timely management to prevent morbidity and mortality in this vulnerable population.<\/jats:p>","DOI":"10.1891\/11-t-703","type":"journal-article","created":{"date-parts":[[2021,11,29]],"date-time":"2021-11-29T15:50:15Z","timestamp":1638201015000},"page":"369-376","source":"Crossref","is-referenced-by-count":1,"title":["Relative Adrenal Insufficiency: Crisis Averted?"],"prefix":"10.1891","volume":"40","author":[{"given":"Lindsay Elise","family":"Holmstrom","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Amy J.","family":"Jnah","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"793","published-online":{"date-parts":[[2021,11,29]]},"reference":[{"key":"2021112907501058000_40.6.369.1","doi-asserted-by":"crossref","first-page":"425","DOI":"10.1016\/j.beem.2018.03.012","article-title":"Central adrenal insufficiency in children and adolescents","volume":"32","year":"2018","journal-title":"Best Pract Res Clin Endocrinol Metabol"},{"key":"2021112907501058000_40.6.369.2","doi-asserted-by":"crossref","first-page":"179","DOI":"10.6065\/apem.2015.20.4.179","article-title":"Endocrine and metabolic emergencies in children: Hypocalcemia, hypoglycemia, adrenal insufficiency, and metabolic acidosis, including diabetic ketoacidosis","volume":"20","year":"2015","journal-title":"Ann Pediat Endocrinol Metabol"},{"key":"2021112907501058000_40.6.369.3","doi-asserted-by":"crossref","unstructured":"Bowden SA , Henry R . 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