What are the recommended dosing, tapering schedule, contraindications, and monitoring parameters for prednisolone in adults and children?

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Prednisolone Dosing, Tapering, Contraindications, and Monitoring

Adult Dosing by Indication

Autoimmune Hepatitis

Prednisolone 1 mg/kg daily (or prednisone 40-60 mg daily) in combination with azathioprine 1-2 mg/kg daily is the preferred first-line regimen. 1

  • Start prednisolone at 1 mg/kg daily (Europe) or prednisone 40-60 mg daily (United States) with azathioprine 50-150 mg daily 1
  • Taper prednisolone over 6-8 months to 5-10 mg daily once biochemical response is achieved by 4-8 weeks 1
  • Maintain azathioprine throughout the taper and continue as monotherapy after steroid withdrawal 1
  • Prednisone monotherapy (40-60 mg daily) is appropriate only when treatment duration is expected to be <6 months or azathioprine is contraindicated 1
  • Prolonged prednisone monotherapy, especially at doses >10 mg daily, should be avoided due to well-known drug toxicities 1

Acute Severe Ulcerative Colitis

Methylprednisolone 60 mg daily or hydrocortisone 100 mg every 6 hours intravenously is the cornerstone of treatment. 1

  • Methylprednisolone 60 mg daily has less mineralocorticoid effect than hydrocortisone and causes significantly less hypokalemia 1
  • Hydrocortisone 400 mg daily is equivalent to 80 mg methylprednisolone 1
  • Assess for clinical and biochemical response after 3 days to determine need for salvage therapy 1
  • Extending therapy beyond 7-10 days carries no additional benefit and increases toxicity 1

Asthma Exacerbations (Adults)

Prednisone 40-60 mg daily as a single morning dose or in 2 divided doses for 5-10 days without tapering is the standard outpatient regimen. 2, 3

  • For severe exacerbations requiring hospitalization, use 40-80 mg daily until peak expiratory flow reaches 70% of predicted or personal best 2
  • Oral administration is strongly preferred and equally effective as intravenous therapy when gastrointestinal absorption is intact 2
  • No tapering is necessary for courses lasting 5-10 days, especially if the patient is concurrently taking inhaled corticosteroids 2
  • Higher doses (>60 mg/day) have not shown additional benefit in severe exacerbations but increase adverse effect risk 2

Rheumatoid Arthritis

Low-dose prednisone ≤10 mg daily, often given as 5 mg twice daily, is safe and effective for long-term management. 4

  • Prednisone should be initiated as early as possible, usually with another DMARD 4
  • Supplemental calcium 800-1,000 mg/day and vitamin D 400-800 units/day should always be initiated with treatment 4
  • Taper slowly using 1 mg decrements every 2-4 weeks to the lowest effective dose 4
  • Doses ≤15 mg daily have a marked effect over placebo on joint tenderness, pain, and grip strength 5

Systemic Lupus Erythematosus

For serologically active but clinically stable SLE, prednisone 30 mg/day for 2 weeks, 20 mg/day for 1 week, then 10 mg/day for 1 week can avert severe flares. 6

  • This short-term regimen is indicated when both anti-dsDNA levels increase by 25% and C3a levels increase by 50% over previous monthly visits 6
  • This approach prevents severe flares requiring >40 mg/day prednisone or addition of immunosuppressive agents 6

Pediatric Dosing by Indication

Autoimmune Hepatitis

Prednisone 1-2 mg/kg daily (maximum 40-60 mg/day) with azathioprine 1-2 mg/kg daily is the initial regimen. 1

  • Taper prednisone over 6-8 weeks to 0.1-0.2 mg/kg daily or 5 mg daily with azathioprine 1
  • Continue until normal liver tests for 1-2 years during treatment with no flare during entire interval 1
  • Early use of azathioprine is recommended for all children without contraindications to minimize long-term corticosteroid effects on growth, bone development, and physical appearance 1

Asthma Exacerbations (Children)

Prednisone or prednisolone 1-2 mg/kg/day in 2 divided doses (maximum 60 mg/day) for 3-10 days without tapering is the standard regimen. 2, 3

  • For overweight children, calculate the dose based on ideal body weight rather than actual weight to avoid excessive steroid exposure 2
  • The maximum daily dose is 60 mg regardless of weight 2, 3
  • No tapering is required for short courses of 5-10 days 2, 3
  • Oral administration is preferred; reserve IV hydrocortisone 4 mg/kg for patients who are vomiting or severely ill 2

Nephrotic Syndrome

Prednisolone 60 mg/m²/day or 2 mg/kg/day (maximum 60 mg/day) for 4-6 weeks is the standard initial regimen. 7, 3

  • This regimen is for children under 12 years with new nephrotic syndrome without syndromic features 7
  • Glucocorticoids should be initiated without requiring a kidney biopsy first 7
  • The primary target population is children older than 1 year, as infants under 1 year are more likely to have a genetic etiology 7

Juvenile Idiopathic Arthritis-Associated Uveitis

Prednisolone acetate 1% topical drops are conditionally recommended over difluprednate for active chronic anterior uveitis. 1

  • Adding or increasing topical glucocorticoids for short-term control is preferred over adding systemic glucocorticoids 1
  • If still requiring 1-2 drops/day of prednisolone acetate 1% for at least 3 months despite systemic therapy, changing or escalating systemic therapy is recommended 1

Tapering Schedules

Short-Course Therapy (<7-10 Days)

No tapering is necessary for courses lasting less than 7-10 days, especially if patients are concurrently taking inhaled corticosteroids. 2, 3

  • Tapering short courses is unnecessary and may lead to underdosing during the critical recovery period 2
  • This applies to both adults and children 2, 3

Autoimmune Hepatitis Taper

Taper prednisone from 20 mg daily onward by 5 mg every week until 10 mg/day, then by 2.5 mg/week to 5 mg daily. 1

  • Continue maintenance regimen until resolution of disease, treatment failure, or drug intolerance 1
  • Prednisone may be discontinued completely once biochemical remission is achieved, leaving the patient on azathioprine alone 1

Rheumatoid Arthritis Taper

Taper slowly using 1 mg decrements every 2-4 weeks to the lowest effective dose. 4

  • Do not deem it a failure to hold the patient on the lowest effective dose of prednisone 4
  • The goal is to maintain doses ≤10 mg daily 4

Long-Term Therapy Discontinuation

If stopping after long-term therapy, withdraw gradually rather than abruptly. 3

  • For slightly longer courses (up to 10 days), there probably is no need to taper, especially if patients are concurrently taking inhaled corticosteroids 1

Contraindications and Precautions

Absolute Contraindications

  • Complete TPMT deficiency (for combination therapy with azathioprine) 1
  • Known azathioprine intolerance (for combination therapy) 1

Relative Contraindications for Autoimmune Hepatitis Treatment

The following conditions require careful risk-benefit assessment but are not absolute contraindications: 1

  • Brittle diabetes 1
  • Obesity 1
  • Acne 1
  • Malignancy 1
  • Emotional lability 1
  • Hypertension 1
  • Osteopenia with vertebral compression 1

Pregnancy Considerations

Prednisolone can be used during pregnancy in equivalent doses to prednisone. 1

  • In Europe, prednisolone is preferred over prednisone 1
  • Azathioprine-related adverse events have not been reported in pregnancy or baby, though risk of preterm birth is increased 1
  • Women with cirrhosis who are pregnant or plan to become pregnant should be screened for varices by endoscopy 1

Vaccination Considerations

For patients taking the equivalent of prednisone ≤10 mg daily, administering any non-live vaccinations is strongly recommended. 1

  • For prednisone >10 mg but <20 mg daily, administering any non-live attenuated vaccinations is conditionally recommended 1
  • For prednisone ≥20 mg daily, administering influenza vaccination is conditionally recommended 1
  • For prednisone ≥20 mg daily, deferring non-live attenuated vaccinations (other than influenza) until glucocorticoids are tapered to <20 mg daily is conditionally recommended 1
  • Live attenuated vaccines should be deferred in patients taking immunosuppressive medication 1

Monitoring Parameters

Baseline Monitoring

Before initiating prednisolone therapy, obtain: 1

  • Complete blood count (FBC) 1
  • C-reactive protein (CRP) 1
  • Urea and electrolytes (U&E) 1
  • Liver function tests (LFTs) 1
  • Magnesium 1
  • Baseline bone mineral densitometry of lumbar spine and hip for patients anticipated to require long-term therapy 1

Ongoing Monitoring for Long-Term Therapy

Patients on long-term corticosteroid treatment require: 1, 7

  • Annual bone mineral densitometry of lumbar spine and hip 1
  • Laboratory testing every 3-4 months once biochemical remission is achieved 1
  • Growth velocity monitoring in children (most sensitive indicator of systemic corticosteroid exposure) 7
  • Blood pressure monitoring at each visit using age and height-specific percentiles in children 7
  • Annual screening for cataracts in children on therapy for more than 3 months 7
  • Annual DEXA scans and vitamin D monitoring for long-term use in children 7
  • Urine glucose screening and blood glucose if positive in children 7

Acute Severe Ulcerative Colitis Monitoring

During inpatient treatment, monitor: 1

  • Accurate stool chart recording frequency, consistency, and presence of blood 1
  • Repeat blood gases within 2 hours if initial PaO2 <8 kPa (60 mmHg) or if patient deteriorates 1
  • Peak expiratory flow 15-30 minutes after starting treatment for asthma exacerbations 2

Asthma Exacerbation Monitoring

Continue treatment until peak expiratory flow reaches ≥70% of predicted or personal best. 2, 3

  • Measure peak expiratory flow 15-30 minutes after starting treatment 2
  • Reassess patients after initial bronchodilator dose and after 60-90 minutes of therapy 2

Common Pitfalls and How to Avoid Them

Underdosing in Acute Exacerbations

Do not underdose systemic corticosteroids in acute asthma exacerbations, as this is a documented cause of preventable asthma deaths. 2

  • Administer systemic corticosteroids early in all moderate-to-severe exacerbations 2
  • Do not delay corticosteroid administration while repeatedly giving bronchodilators alone 2
  • Anti-inflammatory effects take 6-12 hours to become apparent, making early administration crucial 2

Unnecessary Tapering

Do not taper short courses (less than 7-10 days) of corticosteroids, as this is unnecessary and may lead to underdosing during the critical recovery period. 2, 3

  • This applies to both adults and children 2, 3
  • Tapering is especially unnecessary if patients are concurrently taking inhaled corticosteroids 2

Excessive Dosing in Children

For overweight children, calculate the dose based on ideal body weight rather than actual weight to avoid excessive steroid exposure. 2

  • Using actual body weight in significantly overweight children leads to excessive steroid exposure without additional benefit 2
  • The maximum daily dose is 60 mg regardless of weight 2, 3

Prolonged High-Dose Monotherapy

Avoid prolonged prednisone monotherapy, especially at doses >10 mg daily, due to well-known drug toxicities. 1

  • The combination regimen of prednisone and azathioprine is associated with lower occurrence of corticosteroid-related side effects than higher-dose prednisone regimen (10% versus 44%) 1
  • Cosmetic changes occur in 80% of patients after 2 years of corticosteroid treatment regardless of regimen 1
  • Severe complications (osteoporosis with vertebral compression, brittle diabetes, psychosis) usually occur after protracted therapy (>18 months) with prednisone alone at 20 mg daily 1

Inadequate Bone Protection

Always initiate supplemental calcium 800-1,000 mg/day and vitamin D 400-800 units/day with corticosteroid treatment. 4

  • Patients on long-term therapy require annual bone mineral densitometry 1
  • This is critical to prevent osteopenia and vertebral compression 1

Inappropriate Route Selection

Do not use intravenous corticosteroids when oral administration is possible, as oral therapy is equally effective and less invasive. 2

  • Reserve IV administration for patients who are vomiting, severely ill, or have impaired gastrointestinal absorption 2
  • There is no advantage to IV administration over oral therapy when GI function is intact 2

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Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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