Objectives: Individuals with adrenal insufficiency (AI) are at risk of acute adrenal crisis and death, particularly during illness or trauma, and may require rapid treatment with parenteral glucocorticoid such as hydrocortisone (HC) to manage a crisis. Current guidelines recommend timely self-injection in an evolving crisis. Little is known about the patient experience with emergency injections. We surveyed people with adrenal insufficiency regarding success with emergency injections.
Methods: In 2022 a survey was conducted through the National Adrenal Diseases Foundation website of individuals with AI or their caregivers about experience with managing an adrenal crisis. They reported on adrenal crisis events that required an emergency cortisol injection and the success or failure of the injection, context of the event and reasons for failure, RESULTS: Nearly half (41%) of adrenal insufficient patients were unable to self-administer an emergency glucocorticoid injection, citing effects of their crisis-associated illness and confusion as major barriers. Failed injections led to bad outcomes (sicker, need for hospitalization, or death) in 36% of cases.
Conclusions: Effective, timely, management of an impending adrenal crisis can prevent progression to hospitalization, multisystem failure requiring ICU care, and death. Reliance solely on patient self-injection may result in worse outcomes. Treating physicians should include patient education about injections and specific practical instruction in the technique, as well as the potential need for assistance in a crisis. FDA approval of a glucocorticoid auto injector, greater engagement with EMS clinicians, hospital emergency staff, and other healthcare professionals, are key for future success in managing adrenal crises.
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http://dx.doi.org/10.1016/j.eprac.2025.02.017 | DOI Listing |
J Endocr Soc
March 2025
Department of Internal Medicine IV, University Hospital Munich, Munich 80336, Germany.
Context: European and German consensus guidelines advocate preoperative therapy with α-adrenoreceptor antagonists in symptomatic patients with catecholamine-producing pheochromocytomas and paragangliomas (PPGLs) to avoid hypertensive crisis during adrenalectomy. This practice has been questioned recently.
Objective: This work aimed to assess current preoperative management of PPGLs across disciplines.
Endocr Pract
March 2025
Division of Rheumatology, Department of Medicine, National Jewish Health, Denver CO. USA. Electronic address:
Objectives: Individuals with adrenal insufficiency (AI) are at risk of acute adrenal crisis and death, particularly during illness or trauma, and may require rapid treatment with parenteral glucocorticoid such as hydrocortisone (HC) to manage a crisis. Current guidelines recommend timely self-injection in an evolving crisis. Little is known about the patient experience with emergency injections.
View Article and Find Full Text PDFHorm Metab Res
March 2025
Endocrinology, Endocrinology in Charlottenburg, Berlin, Germany.
Shift work causes a disruption between the circadian system and the external light-dark cycle, but also a misalignment between various levels of the circadian system. There is no information on patients with adrenal insufficiency (AI) who are working shifts. The objective of the study was to analyze the hormone replacement therapy with hydrocortisone (HC) and the adaptation scheme in patients with AI on shifts.
View Article and Find Full Text PDFCureus
January 2025
Pediatrics, Centro Hospitalar Universitário de São João, Porto, PRT.
Adrenal insufficiency can be life-threatening and results from inadequate secretion of hormones by the adrenal cortex. In pediatric patients, the most common cause is congenital adrenal hyperplasia due to 21-hydroxylase deficiency. We present a clinical case of a 17-year-old male.
View Article and Find Full Text PDFBMJ Case Rep
February 2025
Neonatology, Bharati Vidyapeeth University, Pune, Maharashtra, India
Familial glucocorticoid deficiency (FGD) is a rare inherited cause of primary adrenal insufficiency, characterised by cortisol deficiency, without mineralocorticoid involvement. Affected patients commonly present in infancy or early childhood with hypoglycaemia, seizures, generalised hyperpigmentation and failure to thrive. Late diagnosis may lead to adverse neurological outcomes, usually resulting from repeated hypoglycaemic episodes.
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