2017
DOI: 10.1177/1203475417736278
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An Approach to Minimising Risk of Adrenal Insufficiency When Discontinuing Oral Glucocorticoids

Abstract: Oral glucocorticoids are commonly used across every field of medicine; however, discontinuing them in patients can be challenging. The risk of acute adrenal crises secondary to glucocorticoid withdrawal can be fatal and arises from chronic suppression of the adrenal glands. Identifying risk factors for adrenal suppression in dermatological patients, such as doses greater than 5 to 7.5 mg of prednisone equivalent, duration of glucocorticoid use greater than 3 weeks, certain medications, and comorbidities, can h… Show more

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Cited by 9 publications
(14 citation statements)
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“…22 For courses less than 2 weeks, tapering is not necessary as the risk of rebound inflammation and adrenal suppression is low. 23 In our cohort, tapering was undertaken to reduce the total steroid dose (median 31.2 mg/per day for 10 days) and potential side-effects. The most commonly reported side-effects in our cohort were poor sleep, gastroesophageal reflux, and mood disturbance.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…22 For courses less than 2 weeks, tapering is not necessary as the risk of rebound inflammation and adrenal suppression is low. 23 In our cohort, tapering was undertaken to reduce the total steroid dose (median 31.2 mg/per day for 10 days) and potential side-effects. The most commonly reported side-effects in our cohort were poor sleep, gastroesophageal reflux, and mood disturbance.…”
Section: Discussionmentioning
confidence: 99%
“…The current dose was extrapolated from the effective prednisolone dose guidelines for asthma exacerbations, of 30 to 50 mg daily (approximately 0.5 mg/kg/day) for 5 to 10 days 22 . For courses less than 2 weeks, tapering is not necessary as the risk of rebound inflammation and adrenal suppression is low 23 . In our cohort, tapering was undertaken to reduce the total steroid dose (median 31.2 mg/per day for 10 days) and potential side‐effects.…”
Section: Discussionmentioning
confidence: 99%
“…Signs and symptoms of AI and hydrocortisone use, if prescribed, were documented at least 1 year after the end of hormonal treatment, because patients who had glucocorticoids for prolonged periods are considered at risk of AI up to 12 months after withdrawal 16,17 . Tests were morning cortisol level, with a diagnostic cutoff of <60 nmol·L –1 (2.2 μg/dl), and ACTH stimulation test, with a positive diagnostic peak value of <500 nmol·L –1 (18 μg/dl) 16,18,19 . The value of 60 nmol·L –1 was chosen as cutoff because it was the local laboratory standard and was more restrictive than the most restrictive value of 80 nmol·L –1 (3 μg/dl) in review articles 19,20 .…”
Section: Methodsmentioning
confidence: 99%
“…Random cortisol was not necessary to establish the diagnosis but was noted if present. Risk factors of AI were defined as molecule potency, duration of therapy, concomitant medication, illness or physical stress, and interindividual susceptibility 16,19 . Concomitant medication noted were medications that affect corticosteroid potency and those independently carrying a risk of AI 19 .…”
Section: Methodsmentioning
confidence: 99%
“…The true prevalence of AI in asthma is difficult to determine, in part, because of limited studies, as well as a shortage of reliable interstudy comparisons [ 13 , 34 ]. In one meta‐analysis, 48.7% of patients were diagnosed with AI after OCS use.…”
Section: Asthma Oral Corticosteroids and Adrenal Insufficiencymentioning
confidence: 99%