What is the psoriasis treatment protocol according to Indian guidelines?

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Psoriasis Treatment Protocol: Indian Context

Disease Severity Classification

Body Surface Area (BSA) measurement is the primary tool for severity assessment and treatment stratification in Indian clinical practice 1.

  • Mild psoriasis: <5% BSA, generally asymptomatic with minimal quality of life impact 2, 3
  • Moderate-to-severe psoriasis: ≥5% BSA OR involvement of vulnerable areas (face, hands, feet, genitals) OR symptomatic disease OR DLQI >10 2, 3
  • Special considerations: Severe scalp or palmoplantar psoriasis affecting <5% BSA may warrant systemic therapy due to significant quality of life impact 1

First-Line Treatment: Mild Psoriasis (<5% BSA)

Apply calcipotriene/betamethasone dipropionate combination product once daily for 4-8 weeks, achieving clear or almost clear status in 48-74% of patients 2, 3.

Alternative regimens:

  • Clobetasol propionate 0.05% or betamethasone dipropionate 0.05% twice daily for maximum 2-4 weeks for body plaques 2
  • For scalp psoriasis: calcipotriene foam or calcipotriene plus betamethasone dipropionate gel for 4-12 weeks 3

Critical pitfall: Avoid systemic corticosteroids, lithium, chloroquine, and mepacrine due to severe deterioration risk including erythrodermic transformation 2.

Second-Line Treatment: Moderate-to-Severe Psoriasis (≥5% BSA)

Phototherapy (First-Line for Moderate-to-Severe Disease)

Narrowband UVB phototherapy 2-3 times weekly is the preferred initial systemic approach due to efficacy, cost-effectiveness, and lack of systemic immunosuppression 1, 2, 3.

  • PUVA (psoralen plus UVA): Start at 70% of minimum phototoxic dose, given 2-3 times weekly 1
  • Treatment duration: Typically 30-40 treatments for noticeable response 1
  • Contraindications: Lupus erythematosus, porphyria, xeroderma pigmentosum, pregnancy 1
  • Monitoring: Regular full skin examination due to photocarcinogenesis risk in Caucasians after 200 treatments; risk not present for non-Caucasians 1

Third-Line Treatment: Traditional Systemic Agents

Methotrexate (Most Cost-Effective First-Line Systemic Agent)

Methotrexate is the most widely prescribed traditional systemic therapy worldwide and the most cost-effective option with longest safety data 1, 4.

  • Dosing: Start 7.5-15 mg weekly, increase gradually based on response 1
  • Response time: 2 weeks 3
  • Baseline monitoring: Complete blood count, liver function tests, hepatitis profile, serum creatinine 1, 3
  • Ongoing monitoring: CBC, LFTs, serum creatinine every 4-8 weeks 1, 3
  • Contraindications: Pregnancy (Category X), active liver disease, significant alcohol consumption, renal impairment 1
  • Critical pitfall: Avoid trimethoprim-sulfamethoxazole and other folate antagonists due to severe bone marrow suppression 1

Cyclosporine (For Rapid Response)

Cyclosporine 3-5 mg/kg/day provides the most rapid response among traditional systemic agents 2, 3, 4.

  • Duration: Limited to 3-4 months for acute flares or maximum 1 year in US guidelines 1
  • Baseline monitoring: Blood pressure, serum creatinine, lipid profile 3
  • Ongoing monitoring: Blood pressure every 2 weeks initially, then monthly; serum creatinine and lipids monthly 3
  • Contraindications: Uncontrolled hypertension, renal impairment, active infections 1
  • Critical concern: Significant glomerulosclerosis risk with long-term use (3-5 years) 1

Acitretin

Acitretin is particularly effective when combined with phototherapy, producing synergistic effects and reducing cumulative UV exposure 1.

  • Dosing: 25-50 mg daily 1
  • Monitoring: Lipid profile, liver function tests 1
  • Contraindications: Pregnancy (teratogenic for 3 years after discontinuation in women; men should avoid conception for 3 months after discontinuation) 1

Fourth-Line Treatment: Biologic Therapies

IL-17 inhibitors, IL-23 inhibitors, or IL-12/23 inhibitors are recommended for severe disease or inadequate response to traditional systemic agents 2, 3.

TNF-α Inhibitors

Adalimumab:

  • Dosing: 80 mg week 0,40 mg week 1, then 40 mg every other week subcutaneously 1
  • Efficacy: 80% achieve PASI-75 at 12 weeks; 68% at 60 weeks 1
  • Advantage: Effective for both skin and joint symptoms in psoriatic arthritis 2
  • Baseline monitoring: PPD, LFTs, CBC, hepatitis profile 1

Etanercept:

  • Dosing: 50 mg twice weekly for 12 weeks, then 50 mg once weekly 1
  • Efficacy: 49% achieve PASI-75 at 12 weeks with 50 mg twice weekly 1

Infliximab:

  • Dosing: 5 mg/kg IV at weeks 0,2,6, then every 6-8 weeks 1
  • Efficacy: 80% achieve PASI-75 at week 10; 50% improvement by week 2 1

IL-12/23 Inhibitor

Ustekinumab:

  • Dosing: 45 mg at weeks 0,4, then every 12 weeks for patients <100 kg; 90 mg same schedule for ≥100 kg 1, 5
  • Efficacy: 67% achieve PASI-75 at 12 weeks; 87% maintain response at 52 weeks 1

Combination Strategies for Enhanced Efficacy

Adding topical corticosteroids to biologic therapy significantly enhances efficacy 5.

  • Class 1 topical corticosteroids added to standard-dose etanercept for 12 weeks improves outcomes 3, 5
  • Calcipotriene/betamethasone added to adalimumab accelerates plaque clearance 5
  • Methotrexate combined with narrowband UVB or PUVA produces synergistic effects, reducing treatment duration and cumulative UV doses 1

Psoriatic Arthritis Management

Escalate treatment based on joint symptom severity 2, 3:

  1. Mild joint symptoms: NSAIDs 3
  2. Moderate-to-severe joint involvement: DMARDs (methotrexate, sulfasalazine, leflunomide) 3
  3. Inadequate response to ≥1 DMARD: TNF inhibitors (adalimumab, etanercept, infliximab, golimumab) 2, 3

Comorbidity Screening (Critical for Indian Population)

All patients with psoriasis require cardiovascular risk assessment 1:

  • Blood pressure screening: Every 3-5 years if normal (<120/80 mmHg) and age 18-39; yearly if age ≥40 or BP 130-139/85-89 mmHg 1
  • Diabetes screening: Every 3 years for adults aged 40-70 with BMI ≥25 kg/m² 1
  • Lipid screening: Every 4-6 years for adults aged 20-79 with standard risk factors 1
  • Risk score adjustment: Apply 1.5 multiplication factor for patients with BSA >10% or candidates for systemic/phototherapy 1

Dose Escalation Strategies for Biologic Failure

When current biologic therapy loses effectiveness, consider dose escalation before switching 5:

Current Regimen Dose Escalation Strategy
Ustekinumab 45 mg every 12 weeks (<100 kg) Ustekinumab 90 mg every 12 weeks [5]
Ustekinumab 90 mg every 12 weeks (>100 kg) Ustekinumab 90 mg every 8 weeks [5]
Adalimumab 40 mg every other week Adalimumab 40 mg weekly [5]
Etanercept 50 mg once weekly Etanercept 50 mg twice weekly [5]
Infliximab 5 mg/kg every 8 weeks Infliximab 5 mg/kg every 6 weeks [5]

Adjunctive Therapies

Stress reduction techniques improve psoriasis severity in some patients 1, 5:

  • Mindfulness meditation (guided) improves outcomes in moderate psoriasis qualifying for phototherapy 1
  • Cognitive behavioral therapy and guided imagery can improve severity 1
  • Oral curcumin supplementation may benefit patients as adjunctive therapy 1, 5

Gluten-free diet: Only for patients diagnosed with celiac disease; trial period of 3 months if celiac antibodies positive 1

Indian-Specific Considerations

Key challenges in Indian clinical practice 4, 6:

  • Average 7.8-month delay from symptom onset to dermatologist consultation 6
  • 44% of patients initially visit general physicians; approximately 25% use home remedies before seeking medical help 6
  • Only one-third of dermatologists use PASI for disease severity assessment 6
  • Only 35% of patients comply with current treatment 6
  • Treatment satisfaction highest for mild disease (62%), with only 52% overall patient satisfaction 6

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Psoriasis Treatment Guidelines

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Psoriasis Treatment Guidelines

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Treatment Options for Psoriasis Exacerbation

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

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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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