Corticosteroid Equivalent Dosing
The standard equivalent doses are: hydrocortisone 20 mg = prednisolone/prednisone 5 mg = methylprednisolone 4 mg = dexamethasone 0.75 mg. 1, 2, 3
Core Conversion Ratios
Relative Potency to Hydrocortisone
- Hydrocortisone: 1x (baseline reference) 1
- Prednisolone/Prednisone: 4x more potent than hydrocortisone 2
- Methylprednisolone: 5x more potent than hydrocortisone 2
- Dexamethasone: 25x more potent than hydrocortisone 1, 2
Direct Conversion Table
- Hydrocortisone 20 mg = Prednisolone 5 mg 1
- Prednisone 5 mg = Methylprednisolone 4 mg 1, 4
- Prednisone 5 mg = Dexamethasone 0.75-1 mg 2, 3
- Prednisone 20 mg = Dexamethasone 4 mg 2
- Prednisone 60 mg = Methylprednisolone 48 mg 2
- Prednisone 60 mg = Dexamethasone 10 mg 2
FDA-Approved Equivalencies
The FDA drug label for prednisolone specifies that 15 mg prednisolone base equals: 3
- Cortisone 75 mg
- Hydrocortisone 60 mg
- Prednisone 15 mg
- Methylprednisolone 12 mg
- Triamcinolone 12 mg
- Dexamethasone 2.25 mg
- Betamethasone 2.25 mg
Clinical Application Guidelines
Perioperative Dosing
For patients on chronic corticosteroids undergoing surgery, continue equivalent dosing intravenously until oral intake resumes. 1 Specifically:
- Prednisolone 5 mg oral = Hydrocortisone 20 mg IV 1
- No evidence supports routine stress-dose supplementation beyond therapeutic replacement 1
- Dexamethasone 8 mg IV provides equivalent coverage to hydrocortisone 200 mg for 24 hours 1
Critical caveat: Dexamethasone lacks mineralocorticoid activity and is inadequate for primary adrenal insufficiency stress coverage 1
Acute Graft-versus-Host Disease
Use methylprednisolone 1-2 mg/kg/day (or prednisone dose equivalent) for grade 2-4 acute GVHD. 1 The conversion is straightforward:
- Methylprednisolone dose = Prednisone dose (essentially 1:1 for practical purposes) 1
- No benefit to escalating methylprednisolone above 2 mg/kg/day 1
Inflammatory Bowel Disease Surgery
Patients on corticosteroids at time of IBD surgery should receive IV hydrocortisone in equivalent dosage until oral prednisolone can resume. 1 The conversion:
Immune Checkpoint Inhibitor Toxicities
For grade 2+ pneumonitis, use prednisone 1 mg/kg/day or IV methylprednisolone equivalent. 1 The practical conversion is 1:1 between oral prednisone and IV methylprednisolone for this indication 1
Important Pharmacokinetic Considerations
Bioavailability and Absorption
- All oral corticosteroids (hydrocortisone, prednisolone, methylprednisolone, dexamethasone) have excellent oral bioavailability and rapid absorption 1
- Prednisolone shows dose-dependent pharmacokinetics with saturable protein binding at higher doses, making dose predictions less reliable 5
- Methylprednisolone demonstrates linear, predictable pharmacokinetics without dose or time dependency 5
Half-Life and Duration
- Hydrocortisone plasma elimination half-life: approximately 90 minutes 1
- Half-life may be shorter with CYP3A4 inducers or hyperthyroidism, longer in critically ill patients 1
- Dexamethasone provides longer duration of action despite similar absorption 1
Route-Specific Considerations
IV infusion is superior to IM injection for maintaining physiologic cortisol concentrations during stress. 1 However, IM administration remains safe and effective when IV access is impractical 1
Critical warning: The dose equivalencies listed apply only to oral or IV administration—intramuscular or intra-articular injection significantly alters relative potencies 3
Mineralocorticoid Activity
Hydrocortisone possesses mineralocorticoid activity; synthetic corticosteroids (prednisolone, methylprednisolone, dexamethasone) have progressively less. 6 Specifically:
- Methylprednisolone causes significantly less hypokalemia than hydrocortisone at equivalent anti-inflammatory doses 6
- Dexamethasone has no mineralocorticoid activity 1
- For primary adrenal insufficiency, hydrocortisone or addition of fludrocortisone is required 1
Dosing Pitfalls to Avoid
Common Errors
- Do not confuse methylprednisolone with methylprednisone—they are different compounds 2
- Conversions assume normal hepatic function; adjust for CYP3A4 inducers or inhibitors 1
- Higher doses of prednisolone (>40 mg) show non-linear kinetics due to protein binding saturation 5