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Steroid sick-day rules explain how patients at risk of adrenal insufficiency should adjust glucocorticoid treatment during acute illness, injury or a medical procedure.
During physical stress, a healthy adrenal gland increases cortisol secretion. A patient with adrenal insufficiency—or suppression of the hypothalamic–pituitary–adrenal axis from prolonged corticosteroid treatment—may be unable to mount this response. Without additional glucocorticoid cover, severe illness may precipitate an adrenal crisis.
Cortisol supports vascular tone, blood pressure, glucose availability and the physiological response to infection or injury. Exogenous corticosteroids suppress hypothalamic corticotropin-releasing hormone and pituitary ACTH secretion. Prolonged treatment may therefore cause adrenal cortical atrophy and an inadequate endogenous cortisol response when the patient becomes unwell.
Adults taking approximately prednisolone 5 mg or more daily for four weeks or longer, or an equivalent glucocorticoid dose, may have clinically important adrenal suppression. The precise risk depends on dose, duration, timing, individual susceptibility and recent steroid exposure.
No additional steroid is usually required for a trivial illness without systemic upset, such as:
The patient should continue their normal prescribed dose and monitor their symptoms.
Sick-day dosing is generally required for an illness causing physiological stress, including:
Patients taking physiological replacement doses should usually double their normal oral glucocorticoid dose, ensuring a minimum total daily dose equivalent to approximately hydrocortisone 30–40 mg.
The increased dose is continued while the patient is systemically unwell—usually for 48 hours or until recovery—then the usual replacement dose can generally be resumed without tapering. Local endocrine plans may differ and should take precedence.
The correct adjustment depends on the patient’s existing dose:
Further increases may still be needed if required to treat the underlying inflammatory illness—for example, a severe asthma exacerbation—but that is treatment of the disease, not routine adrenal sick-day replacement. UK guidance therefore advises considering both the existing steroid dose and the clinical reason for which it is prescribed.
If the patient vomits once shortly after taking their steroid:
If vomiting recurs, tablets cannot be retained, or there is severe diarrhoea, oral absorption cannot be relied upon. The patient should:
Repeated vomiting in a steroid-dependent patient should be treated as an impending adrenal crisis rather than managed by repeatedly attempting oral doses.
Clinical features may include:
Do not delay treatment while awaiting biochemical confirmation.
Immediate management includes:
Hydrocortisone is safe in this emergency; the danger lies in delaying treatment.
Patients with adrenal insufficiency or significant adrenal suppression must inform the surgical, anaesthetic and dental teams in advance. Major surgery, general anaesthesia, significant trauma and invasive procedures may require parenteral hydrocortisone rather than oral sick-day dosing.
Minor dental surgery under local anaesthetic may require an additional pre-procedure dose and temporary doubling afterwards, whereas major dental surgery or general anaesthesia may require hydrocortisone 100 mg IM or IV. The precise regimen should follow local perioperative guidance.
Patients at risk should:
The Steroid Emergency Card helps clinicians recognise patients who may require urgent glucocorticoid treatment during illness, surgery or emergency care.
A 46-year-old woman with Addison’s disease takes hydrocortisone 10 mg on waking, 5 mg at lunchtime and 5 mg in the late afternoon. She develops influenza with fever and myalgia but can eat, drink and retain tablets.
Management: She increases her total hydrocortisone dose according to her sick-day plan—usually doubling the dose or taking at least 30–40 mg daily in divided doses—maintains fluid intake and monitors her symptoms.
Reasoning: Her normal 20 mg dose is physiological replacement and does not provide the additional cortisol normally produced during significant illness.
A 72-year-old man has taken prednisolone 5 mg daily for polymyalgia rheumatica for eight months. He develops a febrile urinary tract infection requiring antibiotics.
Management: His total prednisolone dose is temporarily increased to approximately 10 mg daily while systemically unwell, according to local guidance, before returning to 5 mg once recovered.
Reasoning: His hypothalamic–pituitary–adrenal axis may be suppressed, and his normal 5 mg dose may not provide sufficient stress coverage.
A 58-year-old woman is taking prednisolone 25 mg daily for active vasculitis. She develops an uncomplicated urinary infection but remains haemodynamically stable and can take oral medication.
Management: She continues prednisolone 25 mg daily. It should not automatically be increased to 50 mg as routine adrenal sick-day cover.
Reasoning: Prednisolone 25 mg is already substantially above the usual physiological stress dose. A higher dose would only be indicated if required for her vasculitis or another specific clinical reason.
A 64-year-old man with pituitary adrenal insufficiency takes prednisolone replacement. He develops gastroenteritis and repeatedly vomits his tablets. He becomes dizzy and hypotensive.
Management: Give hydrocortisone 100 mg IM immediately using the emergency kit, call emergency services and arrange urgent hospital assessment.
Reasoning: Oral dosing cannot be relied upon, and hypotension suggests evolving adrenal crisis.
Steroid sick-day rules aim to reproduce the increased cortisol secretion required during physiological stress. Patients taking low replacement doses usually need additional glucocorticoid, whereas those already taking prednisolone 10 mg or more daily may already have sufficient routine stress coverage. Severe illness, persistent vomiting, trauma or haemodynamic instability requires urgent parenteral hydrocortisone and assessment for adrenal crisis.