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خرید پکیج
تعداد آیتم قابل مشاهده باقیمانده : 3 مورد
نسخه الکترونیک
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Major adverse effects associated with systemic glucocorticoid therapy and potential interventions*

Major adverse effects associated with systemic glucocorticoid therapy and potential interventions*
System Reported relationship to prednisone dosing for adults Possible interventions
Metabolic and endocrine
Hypothalamic-pituitary-adrenal axis suppression

Typically with supraphysiologic doses (>5 mg)

Rarely reported with <5 mg/day for <4 weeks
Screen for suppression when tapering if compatible symptoms
Hyperglycemia Reported with <10 mg/day Intensify screening for type 2 diabetes
Dermatologic and appearance
Cushingoid features Rare with <5 mg/day Ask about self-image and/or bullying, especially for pediatric patients
Weight gain Typically with >5 mg/day

Monitor weight at visits

Ask about gastrointestinal symptoms leading to increased food intake

Increase intake of high-fiber foods and water to increase satiety
Skin thinning and ecchymoses Reported with <5 mg/day Encourage sun-protective measures
Acne, hirsutism, facial erythema Few data available  
Cardiovascular
Fluid retention Reported with ≥5 mg/day Monitor weight at visits
Hypertension Rare with <10 mg/day Monitor blood pressure at visits
Premature atherosclerotic disease and major cardiac events (eg, myocardial infarction, stroke) Reported with ≥7.5 mg/day Include glucocorticoid use as an additional risk factor when screening for atherosclerotic cardiovascular disease
Arrhythmias Sudden cardiac death reported in patients receiving pulse dose steroids (methylprednisolone 500 to 1000 mg/day) Use telemetry for patients with significant cardiac disease who receive pulse dose steroids
Venous thromboembolism (VTE) Reported with <20 mg/day Include glucocorticoid use as an additional VTE risk factor when deciding to use perioperative VTE prophylaxis
Possible hyperlipidemia Typically with >10 mg/day Intensify screening for hyperlipidemia
Gastrointestinal
Gastritis, peptic ulcer disease, and upper gastrointestinal bleeding Reported with <20 mg/day

Administer glucocorticoids with food

Evaluate other risk factors for gastroduodenal toxicity, particularly the coadministration of nonsteroidal antiinflammatory drugs (NSAIDs), and potential need for primary prevention

Consider pharmacologic prophylaxis for upper gastrointestinal complications in critically ill patients receiving high-dose steroids
Drug-induced steatotic liver disease Rare, few data available  
Visceral perforation Rare, few data available  
Bone and muscle effects
Osteoporosis Reported with as low as 2.5 mg/day Screen for osteoporosis in patients with >3 months of treatment and prescribe preventive therapies in those at greater risk
Osteonecrosis/avascular necrosis Rare with <15 to 20 mg/day, associated with peak dose  
Myopathy

Typically with >40 mg/day

Rare with <10 mg/day
Monitor strength examination at visits for patients on chronic glucocorticoids
Neuropsychiatric
Insomnia Reported with <5 mg/day Take in the morning or early afternoon when possible
Mood disorders, including anxiety and depression Typically with >7.5 mg/day Intensify screening for anxiety and depression, especially in patients over age 65 and/or with history of neuropsychiatric disorders
Psychosis Almost always with >20 mg/day  
Memory impairment Reported with as low as 5 mg/day for 1 year  
Ophthalmologic
Cataracts

Reported with <5 mg

Typically with >10 mg/day
Ophthalmology referral for screening in select patients
Elevated intraocular pressure/glaucoma Typically with >7.5 mg/day Ophthalmology referral for screening in select patients
Immune system
Increased risk of infections Reported with <5 mg/day

Give indicated vaccinations when anticipating a prolonged course of glucocorticoidsΔ

Avoid live vaccinations in select patientsΔ

Use Pneumocystis jirovecii pneumonia (PJP) prophylaxis in select patients on higher prolonged dosing
Decreased response to vaccinations Typically with ≥20 mg/day for ≥14 days Modify glucocorticoid dosing when possible or delay vaccination depending on glucocorticoid doseΔ
Other
Tooth hypersensitivity Reported with <20 mg/day, typically with pulse dose steroids (methylprednisolone 500 to 1000 mg/day)  
Epistaxis Typically with >5 mg/day  
Growth impairment in children Reported with 3 to 5 mg/m2/day Monitor growth
Interventions may vary depending on other patient risk factors, the anticipated dose and duration of glucocorticoids, and the acuity and complexity of the clinical situation. It may be helpful to minimize other risk factors for the adverse effect, as well as steroid dose and duration. Refer to UpToDate for additional details.

* High-dose inhaled glucocorticoid therapy can rarely cause systemic adverse effects. Refer to UpToDate content for information on local adverse effects of inhaled glucocorticoids.

¶ Signs and symptoms of hypothalamic-pituitary-adrenal axis suppression include fatigue, weakness, hypotension, confusion, anorexia, nausea, vomiting, and abdominal pain. Refer to UpToDate content on clinical manifestations of adrenal insufficiency for additional detail.

Δ Refer to UpToDate content on the effects of glucocorticoids on the immune system and immunizations in autoimmune inflammatory rheumatic disease in adults for more details.

◊ Refer to UpToDate content on causes of short stature.
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