Department of Paediatrics, Farhat Hached University Hospital, Sousse, Tunisia
Faculty of Medicine of Sousse, University of Sousse, Tunisia
Department of Endocrinology, Farhat Hached University Hospital, Sousse, Tunisia
Laboratory of Physiology and Hormonal Exploration, LR 19 ES 09, Farhat Hached University Hospital, Sousse, Tunisia
Pediatr Endocrinol Diabetes Metab 2026; 32 (4):
Prolonged corticosteroid therapy is a common paediatric intervention but is associated with serious complications, most notably adrenal insufficiency (AI). This study aimed to identify the risk factors for AI in children receiving long-term corticosteroid treatment.
We conducted a one-year prospective study of children receiving prolonged oral or inhaled corticosteroid (ICS) therapy at supra-physiological doses. Differences between subgroups were analysed using Student’s t-tests for continuous data and chi-square tests for categorical variables.
The study included 71 patients, divided into two groups based on the presence (G1) or absence (G2) of AI. A significant age difference was observed between the two groups (p = 0.027), identifying prolonged exposure as a clinical risk factor for the development of AI. While the overall duration of treatment was significantly longer in the AI group (p = 0.002), sub-analysis by administration route revealed that prolonged duration of ICS therapy was significantly associated with AI (p = 0.012), whereas treatment duration for oral corticosteroids did not reach statistical significance. These findings are consistent with a possible protective effect of the systematic tapering of oral corticosteroids following prolonged use, rather than a true difference in inherent risk between routes. Given the limited statistical power in the oral subgroup (n = 27, p = 0.09), this interpretation should be regarded as a hypothesis requiring confirmation in larger powered sample.
Secondary AI is a significant, underdiagnosed risk in children, closely linked to cumulative corticosteroid exposure and treatment duration. We hypothesise that the lack of systematic tapering, rather than the administration route itself, drives this risk.
risk factors, paediatrics, adrenal insufficiency, corticotherapy, Synacthen