Prednisone high dose long term


Systemic corticosteroid.
Author: Dr Amanda Oakley, Dermatologist, Hamilton, New Zealand, 1997. Updated February 2016.
What is a systemic corticosteroid?
A corticosteroid taken by mouth or given by intramuscular injection is often called a systemic steroid. Systemic steroids are synthetic derivatives of the natural steroid, cortisol, produced by the adrenal glands, and have profound anti- inflammatory effects.
Systemic (cortico)steroids are also called glucocorticoids or cortisones. They include:
Prednisone Prednisolone Methylprednisolone Beclomethasone Betamethasone Dexamethasone Hydrocortisone Triamcinolone.
Prednisone and prednisolone are equivalent, and are the most commonly prescribed oral corticosteroids for inflammatory skin diseases. Oral prednisone is the most commonly prescribed systemic steroid in New Zealand.
Fludrocortisone is predominantly a mineralocorticoid and its anti- inflammatory effects are minimal.
What is prednisone used for in dermatology ?
Prednisone is used for a few days (short-term) to indefinitely (long-term) in a wide variety of skin conditions including:
Systemic steroids are best avoided in patients with psoriasis.
How does a systemic steroid work?
Systemic steroids work in the same way as natural cortisol. Natural cortisol has important effects in the body, including regulation of:
Protein, carbohydrate, lipid and nucleic acid metabolism Inflammation and immune response Distribution and excretion of water and solutes Secretion of adrenocorticotrophic hormone (ACTH) from the pituitary gland.
How do systemic steroids differ?
Systemic steroids differ in dose, mineralocorticoid potency, half-life (duration of action) and how effectively they suppress the hyphothalamic-pituitary-adrenal (HPA) axis (suppression leads to reduced production of natural cortisol).
* Comparison of systemic corticosteroids – Vancouver Coastal Health Formulary tool. Accessed 12 July 2014.
What is the usual dose of prednisone?
Generally, a higher dose of prednisone, such as 40–60 mg daily, is prescribed at first, to gain control of the skin condition. In 2–4 weeks, the dose is reduced.
Prednisone is best taken as a single dose in the morning, which is thought to reduce steroid-induced suppression of the pituitary-adrenal axis compared to evening dosing.
The maintenance dose should be kept as low as possible to minimise adverse effects.
Steroid dose is commonly characterised as:
Low dose, eg < 10mg/day of prednisone Medium dose, eg 10–20 mg/day of prednisone High dose, eg > 20mg/day of prednisone, sometimes more than 100 mg/day.
Treatment for less than one month is considered short-term treatment. Corticosteroids for a few days or weeks are relatively safe when prescribed for acute dermatitis . Treatment continuing for more than 3 months is regarded as long term, and results in the majority of undesirable side effects.
What are the side effects and risks of short-term systemic steroid?
Side effects are rarely serious if a systemic steroid has been prescribed for one month or less. The following problems may arise, particularly when higher doses are taken:
Sleep disturbance Increased appetite Weight gain Increase in postprandial blood sugar Psychological effects, including increased or decreased energy.
Rare and potentially serious side effects of a short course of corticosteroid include:
Severe infection Mania, psychosis, delirium, depression with suicidal intent Heart failure Peptic ulceration Diabetes mellitus Avascular necrosis of the hip.
The risk of a serious side effect increases with increasing dose.
What are the side effects and risks of long-term systemic steroid?
Nearly everyone on a systemic steroid for more than a month suffers from some adverse effects, depending on daily dose and how long they have been on the drug. The main concerns are infections, hypertension , diabetes, osteoporosis, avascular necrosis , myopathy, cataracts, and glaucoma. The list that follows is incomplete.
Cutaneous adverse effects.
Cutaneous adverse effects from long-term systemic steroids may include:
Adverse effects of systemic steroids.
Effects on body fat.
Redistribution of body fat: moon face, buffalo hump, truncal obesity Weight gain: increased appetite and food intake.
Effects on the eye.
Glaucoma Posterior subcapsular cataracts; children are more susceptible than adults Eyelid oedema and exophthalmos Central serous chorioretinopathy.
Vascular disease.
Hypertension Ischaemic heart disease Stroke and transient ischaemic attack (TIA)
The effects of systemic steroids on atherosclerotic vascular disease may be due to complex metabolic changes, including:
Hyperlipidaemia Peripheral insulin resistance and hyperinsulinaemia.
Gastrointestinal tract.
Dyspepsia, gastritis, peptic ulceration and perforation of the gut, especially in patients also taking non-steroidal anti- inflammatory drugs Acute pancreatitis Fatty liver Fluid balance Sodium and fluid retention cause leg swelling and weight increase Potassium loss causes general weakness.
Reproductive system.
Irregular menstruation Hirsutism Lowered fertility in men and women Possible fetal growth retardation in women taking prolonged courses of steroids during pregnancy Breast feeding can usually continue but infant should be monitored for adrenal suppression if mother on > 40 mg prednisone daily.
Musculoskeletal system.
Bone fracture Osteoporosis Osteonecrosis, especially hip Myopathy affecting shoulders and thighs Tendon rupture Growth restriction in children.
Osteoporosis is particularly common in smokers, postmenopausal women, the elderly, underweight or immobile, and patients with diabetes or lung problems. Osteoporosis may result in fractures of the spine, ribs or hip joint with minimal trauma. These occur after the first year in 10–20% of patients treated with more than 7.5 mg prednisone daily. It is estimated that up to 50% of patients on long-term prednisone will develop bone fractures. Vertebral fractures are more common in patients on steroids, even in those with normal bone density.
Nervous system.
Psychological effects: mood changes, increased energy, excitement, euphoria, agitation Less often: hypomania, psychosis, delirium, memory loss, depression, anxiety, personality change Insomnia and sleep disturbance Shakiness and tremor Headaches.
Metabolic effects.
Transient or persistent diabetes in previously non-diabetic patients Higher blood sugar levels in patients with diabetes mellitus Cushing syndrome.
Immune response.
Raised neutrophil and total white cell count are usual on prednisone Impaired innate and acquired immunity Increased susceptibility to tuberculosis Increased severity of measles, varicella Reduced efficacy and increased risk of vaccines.
Live vaccines such as polio or MMR (measles, mumps, rubella) should not be given to patients taking ≥ 20 mg prednisone daily. It is safe and advisable to have other routine immunisations, such as annual influenza vaccination.
Risks during intercurrent illness or surgery.
Significant intercurrent illness, trauma, or surgical procedure requires a temporary increase in corticosteroid dose, or if already stopped, a temporary re-introduction of corticosteroid treatment for up to twelve months after the steroids are stopped.
Patients who have taken ≥10 mg prednisone daily within 3 months of surgery requiring a general anaesthetic are advised to tell their anaesthetist so that intraoperative intravenous hydrocortisone can be added.
Effects of reducing the dose of systemic steroid.
No tapering is necessary if a course of prednisone has been for less than one to two weeks. Steroid should be withdrawn slowly after longer courses, to avoid acute adrenal insufficiency, particularly if the medication has been taken for several months or longer.
Side effects from reducing prednisone may include:
Fever Hypotension Tiredness Headaches Muscle and joint aches Weight loss Depression Rhinitis Conjunctivitis Painful itchy skin nodules .
Hypopituitary-pituitary-adrenal (HPA) axis suppression can persist for months or years after steroids are stopped.
Monitoring during steroid treatment.
Regular monitoring during treatment with systemic steroid may include:
Patients on prednisone should be advised to avoid non-steroidal anti- inflammatory drugs and licorice.
Prevention of osteoporosis.
Bone density scans should be considered for patients that have taken or are expected to take 7.5 mg or more of prednisone each day for three months or longer. Baseline fracture risk can be estimated from T-scores.
Current recommendations are:
Bisphosphonate therapy (alendronate, etidronate, zolidronic acid) for individuals with femoral T-scores <-2.5. It reduces fracture risk by half. Smoking cessation Balanced diet, aiming for healthy body weight Minimal alcohol Regular weight-bearing exercise Consider risk of falling and its mitigation.
Calcium, vitamin D and oestrogen are no longer recommended for prophylaxis of osteoporosis, as adverse events outweigh benefit.
Related Information.
Glucocorticoid therapy – New Zealand Formulary Reid IR. Short-term and long-term effects of osteoporosis therapies. Nat Rev Endocrinol. 2015 Jul;11(7):418-28. doi: 10.1038/nrendo.2015.71. Epub 2015 May 12. Review. PubMed PMID: 25963272. The Risk of Hyperglycaemia with Systemic Glucocorticoids. Prescriber Update 39(1): 3. Medsafe. March 2018.
On DermNet NZ.
Other websites.
FRAX® WHO Fracture Risk Assessment Tool Consumer medicine information and data sheets – Medsafe Drugs, Herbs and Supplements – MedlinePlus Medsafe on osteoporosis due to systemic steroids Oral treatment with corticosteroids – British Association of Dermatologists Prednisone – New Zealand Formulary Patient Information.
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© 2018 DermNet New Zealand Trust.
© 2018 DermNet New Zealand Trust.
DermNet NZ does not provide an online consultation service. If you have any concerns with your skin or its treatment, see a dermatologist for advice.

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