Prednisone Dosing for Rheumatoid Arthritis
For an adult with rheumatoid arthritis not currently taking glucocorticoids, initiate prednisone at 7.5–10 mg daily as bridging therapy while starting or optimizing DMARD therapy, then taper to discontinuation within 3 months. 1
Initial Dosing Strategy
Start prednisone at 7.5–10 mg daily (typically 10 mg/day for optimal anti-inflammatory effect) when initiating or escalating DMARD therapy in patients with moderate to high disease activity 1, 2
Doses ≤7.5 mg/day are discouraged because they provide insufficient anti-inflammatory effect in the acute setting 1
Doses >30 mg/day should be strongly avoided due to markedly increased risk of serious adverse events including infections, fractures, and gastrointestinal bleeding 1
Single daily morning dosing is preferred over divided doses to minimize HPA axis suppression 1
Rationale for This Approach
Glucocorticoids provide rapid symptom relief within days while DMARDs require 6–12 weeks to achieve therapeutic effect 1
Unlike NSAIDs, glucocorticoids reduce both clinical symptoms and structural joint progression, making them superior for disease control 1, 2
The CAMERA II trial (high-quality RCT with 236 participants) demonstrated that methotrexate combined with prednisone 10 mg/day achieved earlier sustained remission and required fewer additional therapies compared to methotrexate alone 1
Tapering Protocol
Taper to 5 mg/day by week 8 as the target maintenance dose 1
Reduce by 1 mg every 4 weeks once remission or low disease activity is achieved 1
Discontinue glucocorticoids entirely by 3 months to limit cumulative toxicity including osteoporosis, cardiovascular disease, and infections 1
If relapse occurs during taper, increase back to the pre-relapse dose and taper more slowly 1
Concurrent DMARD Therapy (Critical)
Glucocorticoids are NOT monotherapy—methotrexate must be started and optimized concurrently 1
Initiate methotrexate at 15 mg weekly with folic acid 1 mg daily 1
Escalate methotrexate by 5 mg each month to reach 20–25 mg weekly within 2–3 months 1
If oral methotrexate is inadequately effective at 20–25 mg weekly, switch to subcutaneous administration 1
Safety Monitoring Requirements
At every visit during glucocorticoid therapy, assess blood pressure, blood glucose, body weight, and peripheral edema 1
Provide calcium 800–1000 mg/day and vitamin D 400–800 IU/day from day 1 of glucocorticoid therapy 1, 3, 4
Prescribe a proton pump inhibitor for gastrointestinal prophylaxis, especially when combining with NSAIDs 1
Obtain bone mineral density scan if therapy exceeds 3 months at >7.5 mg/day; consider bisphosphonate therapy when bone density is low or fracture risk is high 1
Dose-Dependent Infection Risk
Daily prednisone doses ≥20 mg for ≥2 weeks cause significant immunosuppression and markedly raise the risk of serious infections 1
Even doses of 5–10 mg/day show dose-dependent increases in hospitalized infection risk: 1-year cumulative incidence increases from 8.6% (no glucocorticoids) to 11.0% at ≤5 mg/day and 14.4% at >5–10 mg/day in Medicare patients 5
Patients on chronic glucocorticoids (>3 weeks at >7.5 mg/day) should be instructed to take stress-dose steroids during acute illness or before surgery to avoid adrenal crisis 1
Alternative Routes for Special Populations
Intramuscular methylprednisolone 120 mg every 3 weeks may be considered when oral therapy is not tolerated, though long-term benefit remains uncertain 1
Intra-articular triamcinolone hexacetonide is preferred for mono- or oligoarticular disease (1–4 joints) to minimize systemic exposure 1
Common Pitfalls to Avoid
Do not use glucocorticoids as monotherapy—they serve only as bridging therapy while DMARDs take effect 1
Do not continue glucocorticoids beyond 3 months unless disease remains uncontrolled despite optimized DMARD therapy 1
Do not abruptly stop glucocorticoids after more than 1 month of use; gradual taper is required to prevent adrenal insufficiency 1
Do not use NSAIDs for disease control—reserve them only for short-term symptomatic relief of pain related to other conditions, as they do not modify disease progression 1