Psoriasis Treatment Algorithm
Initial Disease Severity Assessment
Treatment selection for psoriasis depends on disease severity, with mild disease (<5% body surface area, minimal symptoms, minimal quality of life impact) treated with topical therapy alone, while moderate-to-severe disease (≥5% BSA, symptomatic with pain/bleeding/itching, significant quality of life impact, or inadequate response to topicals) requires systemic therapy or phototherapy. 1, 2
Assessment must include:
- Body surface area (BSA) - threshold of 5% separates mild from moderate-to-severe disease 1, 2
- Symptom burden - presence of pain, bleeding, or itching 1, 3
- Quality of life impact - measured by DLQI 2
- Special site involvement - face, genitals, hands/feet, nails, scalp, or intertriginous areas warrant more aggressive treatment regardless of BSA 1
- Psoriatic arthritis screening - joint symptoms change treatment approach 1
Algorithm for Mild Psoriasis (<5% BSA)
First-Line: Combination Topical Therapy
Start with calcipotriene/betamethasone dipropionate combination product once daily for 4-8 weeks, which achieves clear or almost clear status in 48-74% of patients. 1, 3
Strength of recommendation: A 1
- Apply once daily to affected areas for initial 4-8 weeks 3
- Maximum calcipotriene use: 100g per week to avoid hypercalcemia 3
- This combination is more effective than either agent alone 1
Site-Specific Modifications
For scalp psoriasis: Use calcipotriene foam or calcipotriene plus betamethasone dipropionate gel for 4-12 weeks 1
For facial/intertriginous psoriasis: Use low-potency corticosteroids (hydrocortisone) combined with calcipotriene, OR tacalcitol ointment for 8 weeks to avoid skin atrophy 1, 3
- Never use high-potency corticosteroids on face or flexures - risk of severe atrophy and telangiectasia 3
For nail psoriasis: Calcipotriene combined with betamethasone dipropionate reduces nail thickness and onycholysis, though efficacy is limited by poor nail matrix penetration 1
- Alternative: Tazarotene 0.1% cream under occlusion for 12 weeks 1
For thick, chronic plaques on body/extremities: Use ultrahigh-potency (class 1) corticosteroids like clobetasol propionate 0.05% or halobetasol propionate 0.05% 3, 4
- Maximum continuous use: 4 weeks to prevent skin atrophy, striae, and HPA axis suppression 3
Maintenance Therapy After Initial Control
Transition to weekend-only high-potency corticosteroid application (twice daily on weekends) with weekday vitamin D analogue therapy (twice daily on weekdays) to minimize corticosteroid exposure while maintaining efficacy. 1, 3
Strength of recommendation: B 1
Alternative maintenance regimen: Apply high-potency topical corticosteroid in the morning and vitamin D analogue in the evening 1
Strength of recommendation: B 1
Second-Line Topical Options
If combination therapy inadequate:
- Tazarotene 0.1% gel once daily for 8-12 weeks, achieving treatment success in 40-51% of patients 1
- Coal tar preparations - effective but stain skin and clothing, limiting practical use 3, 5
- Anthralin - effective but causes staining 3, 5
Critical Pitfalls to Avoid
Never combine salicylic acid with calcipotriene simultaneously - the acidic pH completely inactivates calcipotriene and eliminates its effectiveness. 1
Never use systemic corticosteroids in psoriasis - they cause severe disease flare during taper. 2, 6
Algorithm for Moderate-to-Severe Psoriasis (≥5% BSA or Inadequate Response to Topicals)
First-Line Options (Choose Based on Clinical Scenario)
Option 1: Phototherapy
Narrowband UVB phototherapy 2-3 times weekly is highly effective for moderate-to-severe psoriasis and is the preferred first-line option for pregnant women. 1, 2, 7
- Requires significant time commitment (2-3 times weekly) 1
- Lacks systemic toxicities and immunosuppressive properties of systemic agents 1
- Can be combined with methotrexate or acitretin for synergistic effect, reducing treatment duration and cumulative UV exposure 1
- 308-nm excimer laser allows selective targeting of localized resistant areas like scalp and skin folds 3
PUVA (psoralen plus UVA) is an alternative phototherapy option 1, 2
- Acitretin combined with PUVA suppresses development of cutaneous squamous cell carcinoma 1
Option 2: Biologic Agents (Preferred for Most Patients)
The American Academy of Dermatology-National Psoriasis Foundation guidelines recommend biologics as first-line treatment for moderate-to-severe plaque psoriasis due to superior efficacy and acceptable safety profiles. 7
TNF-α inhibitors:
IL-17 inhibitors:
IL-12/23 (p40) inhibitor:
IL-23 (p19) inhibitors:
- Guselkumab, tildrakizumab, risankizumab, mirikizumab 7
Option 3: Traditional Systemic Agents
Methotrexate - FDA-approved since 1972, competitive inhibitor of dihydrofolate reductase 3, 7
- Can be given subcutaneously to bypass liver 1
- Avoid conception in males until 3 months after discontinuation 1
- Synergistic when combined with phototherapy 1
Cyclosporine 3-5 mg/kg/day - provides rapid onset of action 1, 3, 7
- Use in short 3-4 month "interventional" courses 1, 3
- Particularly effective for erythrodermic psoriasis requiring rapid response 1, 3
Acitretin - decreases keratinocyte hyperproliferation 1, 3, 7
- Cannot be used in women of childbearing potential due to teratogenicity 1, 3
- Slower onset of action than cyclosporine 1, 3
- Effective when combined with phototherapy 1
Apremilast - oral phosphodiesterase 4 inhibitor 7
Combination Strategies to Enhance Efficacy
Adding topical therapy to systemic agents accelerates clearance and improves outcomes:
- Ultrahigh-potency corticosteroid added to etanercept for 12 weeks (Level I evidence) 3
- Calcipotriene/betamethasone added to adalimumab for 16 weeks accelerates clearance 3
- Calcipotriene added to methotrexate (Level I evidence) 3
- All topical corticosteroids can be combined with any biologic 3
Special Clinical Scenarios
Erythrodermic Psoriasis (Medical Emergency)
For systemically ill patients with erythrodermic psoriasis, initiate oral cyclosporine 4 mg/kg/day immediately for rapid control, with dramatic improvement expected within 2-3 weeks. 1, 6, 3
Treatment algorithm for erythrodermic psoriasis:
Initially for all patients:
- Appropriate wet dressings with mid-potency topical steroids 1
- Attention to fluid balance with control of ankle edema 1
- Rule out sepsis with blood cultures 1
First-line systemic options (in alphabetical order):
- Acitretin 1, 6
- Biologic agents (infliximab, adalimumab, ustekinumab) 1, 6
- Cyclosporine 3-4 month course 1, 6, 3
- Methotrexate 1, 6
Second-line combinations (if first-line inadequate):
- Acitretin + cyclosporine 1
- Acitretin + TNF blocker 1
- Cyclosporine + methotrexate 1
- Etanercept 1
- Methotrexate + TNF blocker 1
Base therapy on short-term efficacy rather than long-term considerations, then transition to maintenance therapy after acute illness improves. 3
Pustular Psoriasis
Ustekinumab at 90mg dose is recommended as monotherapy for moderate-to-severe pustular psoriasis, showing 67% clearance rate. 6
Strength of recommendation: C 6
For palmoplantar pustular psoriasis: Acitretin and oral PUVA appear to provide improvement, with combination superior to either alone 1
Guttate Psoriasis
UVB phototherapy has the most robust evidence for efficacy in treating guttate psoriasis. 6
First-line topical options: Low concentrations of coal tar and dithranol due to lower tolerance of erupting guttate psoriasis to topical treatments 6
Psoriatic Arthritis
For mild enthesitis/dactylitis: NSAIDs, physical therapy, local corticosteroid injections 1
For moderate disease: DMARDs 1
For severe disease: TNF inhibitors (infliximab, etanercept, adalimumab) 1
Strength of recommendation: A 1
Monitoring and Safety Considerations
Long-term use of high-potency corticosteroids beyond 12 weeks requires careful physician supervision to monitor for skin atrophy, striae, telangiectasia, and HPA axis suppression. 3
Phototherapy must be supervised by adequately trained personnel with regular equipment calibration. 6
Commercial sunbeds (emitting UVA) are rarely effective in psoriasis and may cause significant side effects - their use is not recommended. 6
Vitamin D analogues should be applied after phototherapy treatment to avoid inactivation by UVA and blocking of UVB radiation. 1, 3