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Cortisone
Cortisone
Cortisone
1 Use Cautiously in: Chronic treatment (will lead to adrenal suppression; use low-
est possible dose for shortest period of time), unless being used to treat adrenal in-
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cortisone (kor-ti-sone) sufficiency; Stress (surgery, infections); supplemental doses may be needed; Hypo-
Cortone thyroidism; Cirrhosis; Ulcerative colitis; Potential infections may mask signs (fever,
Classification inflammation); OB: Safety not established; Pedi: Chronic use will result inpgrowth;
Therapeutic: anti-inflammatories (steroidal) use lowest possible dose for shortest period of time.
Pharmacologic: corticosteroids Adverse Reactions/Side Effects
Pregnancy Category C Adverse reactions/side effects are much more common with high-dose/long-term
therapy CNS: depression, euphoria, headache,qintracranial pressure (children
Indications only), personality changes, psychoses, restlessness. EENT: cataracts,qintraocular
Management of adrenocortical insufficiency; chronic use in other situations is lim- pressure. CV: hypertension. GI: PEPTIC ULCERATION, anorexia, nausea, vomiting.
ited because of mineralocorticoid activity. Replacement therapy in adrenal insuffi- Derm: acne,pwound healing, ecchymoses, fragility, hirsutism, petechiae. Endo:
ciency. adrenal suppression, hyperglycemia. F and E: fluid retention (long-term high
doses), hypokalemia, hypokalemic alkalosis. Hemat: THROMBOEMBOLISM, throm-
Action bophlebitis. Metab: weight gain, weight loss. MS: avascular necrosis of joints, mus-
In pharmacologic doses, suppresses inflammation and the normal immune re- cle wasting, osteoporosis, muscle pain. Misc: cushingoid appearance (moon face,
sponse. Has numerous intense metabolic effects (see Adverse Reactions and Side Ef- buffalo hump),qsusceptibility to infection.
fects). Suppresses adrenal function at chronic doses of 20 mg/day. Replaces endoge-
nous cortisol in deficiency states. Also has potent mineralocorticoid Interactions
(sodium-retaining) activity. Therapeutic Effects: Suppression of inflammation Drug-Drug: Additive hypokalemia withthiazide or loop diuretics, or ampho-
and modification of the normal immune response. Replacement therapy in adrenal tericin B. Hypokalemia mayqrisk of digoxin toxicity. Mayqrequirement for insu-
insufficiency. lins or oral hypoglycemic agents. Phenytoin, phenobarbital, and rifampin
stimulate metabolism; maypeffectiveness. Oral contraceptives maypmetabolism.
Pharmacokinetics qrisk of adverse GI effects with NSAIDs (including aspirin). At chronic doses that
Absorption: Well absorbed after oral administration. suppress adrenal function, maypantibody response to andqthe risk of adverse re-
Distribution: Widely distributed; crosses the placenta and enters breast milk. actions from live-virus vaccines.
Metabolism and Excretion: Metabolized mostly by the liver to inactive metabo-
lites. Route/Dosage
Half-life: 0.5 2 hr (plasma), 8 12 hr (tissue). PO (Adults): 25 300 mg/day in divided doses every 12 24 hr.
PO (Children): Adrenocortical insufficiency 0.7 mg/kg/day (20 25 mg/m2/
TIME/ACTION PROFILE (anti-inflammatory activity)
day) in divided doses every 8 hr. Other uses 2.5 10 mg/kg/day (75 300 mg/m2/
ROUTE ONSET PEAK DURATION day) in divided doses every 6 8 hr.
PO rapid 2 hr 1.251.5 days
NURSING IMPLICATIONS
Contraindications/Precautions Assessment
Contraindicated in: Active untreated infections (may be used in patients being Indicated for many conditions. Assess involved systems before and periodically
treated for tuberculous meningitis); Lactation: Avoid chronic use. during therapy.
Canadian drug name. Genetic Implication. CAPITALS indicate life-threatening, underlines indicate most frequent. Strikethrough Discontinued.
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