Psoriasis Plan of Care
For patients with psoriasis, initiate treatment based on disease severity: mild disease (affecting <5% body surface area) should be managed with topical corticosteroids combined with vitamin D analogues, while moderate-to-severe disease (≥5% BSA or significant quality of life impairment) requires systemic therapy with biologics as first-line treatment, specifically IL-17 or IL-23 inhibitors, which demonstrate superior efficacy to traditional agents. 1, 2, 3
Initial Assessment
Severity Determination
- Assess body surface area (BSA) involvement to stratify disease severity: <5% BSA indicates mild disease, 5-10% BSA indicates moderate disease, and >10% BSA indicates severe disease 1, 4
- Evaluate patient-reported disability and quality of life impact, as subjective burden may not correlate with objective disease extent 1
- Screen for psoriatic arthritis by asking about joint pain, stiffness, and swelling, as 30% of psoriasis patients develop inflammatory arthritis requiring rheumatology referral 1, 5
Comorbidity Screening
- Check blood pressure according to national guidelines, referring patients with BP ≥140/90 mmHg to primary care for hypertension management 1
- Order fasting lipid panel and glucose/HbA1c to screen for metabolic syndrome, as psoriasis patients have significantly elevated cardiovascular risk 1, 4, 3
- Screen for depression and suicide ideation using validated tools, as psychiatric comorbidity is substantially increased in psoriasis 1, 6
Medication Review
- Immediately discontinue or avoid lithium, chloroquine, mepacrine, beta-blockers, and NSAIDs, as these medications can precipitate severe, life-threatening psoriasis flares 1, 7
- Never prescribe systemic corticosteroids for psoriasis, as withdrawal precipitates erythrodermic or generalized pustular psoriasis 1, 7, 8
Treatment Algorithm by Severity
Mild Psoriasis (<5% BSA)
First-Line Topical Therapy
- Apply betamethasone dipropionate 0.05% combined with calcipotriene (vitamin D analogue) once daily for 4-8 weeks, as this combination represents the most effective first-line topical therapy 1, 2, 7
- Limit moderately potent corticosteroids (BNF grade III) to ≤100g per month with mandatory clinical review every 4 weeks and no unsupervised refills 1
- Implement corticosteroid-free periods annually by rotating to alternative agents to prevent tachyphylaxis and skin atrophy 1
Second-Line Options for Topical Failure
- Escalate to clobetasol propionate 0.05% (ultra-high potency) twice daily for maximum 2-4 weeks if medium-potency corticosteroids fail, achieving 68-92% clearance rates 2
- Add coal tar preparations starting at 0.5-1.0% crude coal tar in petroleum jelly, increasing concentration every few days to maximum 10% as an extremely safe, cost-effective alternative 1, 2
- Consider dithranol (anthralin) 0.1-0.25% in short-contact mode (15-45 minutes daily), doubling concentration as tolerated, though expect skin staining and irritation 1, 2
Moderate-to-Severe Psoriasis (≥5% BSA or Significant QOL Impairment)
First-Line Systemic Therapy
- Prescribe IL-17 inhibitors (secukinumab, ixekizumab, brodalumab) or IL-23 inhibitors (guselkumab, risankizumab, tildrakizumab) as first-line biologics for moderate-to-severe plaque psoriasis, per American Academy of Dermatology-National Psoriasis Foundation guidelines 3, 9
- Consider TNF-α inhibitors (adalimumab, etanercept, infliximab, certolizumab) as alternative first-line biologics, particularly if concurrent psoriatic arthritis is present 10, 3
- Adalimumab 40mg subcutaneously every other week achieves 59% PASI-75 response at 24 weeks and is FDA-approved for both psoriasis and psoriatic arthritis 10
Alternative Systemic Options
- Initiate methotrexate as the most cost-effective systemic option for self-pay patients, though requires weekly monitoring of liver function tests and carries teratogenicity risk 1, 2, 3
- Consider phototherapy (narrowband UVB or PUVA) as the least toxic systemic intervention, starting PUVA at 70% of minimum phototoxic dose and increasing by 40% if no erythema develops 7, 3, 9
- Prescribe apremilast (phosphodiesterase-4 inhibitor) as an oral option for patients declining biologics or phototherapy 3, 9
Special Populations
Psoriatic Arthritis
- Refer immediately to rheumatology for any patient with joint symptoms, as early treatment prevents irreversible structural damage 1, 5
- Prioritize TNF-α inhibitors, IL-17 inhibitors, or IL-12/23 inhibitors as these biologics treat both skin and joint manifestations 10, 3
Guttate Psoriasis
- Manage most cases in primary care with topical therapy, as guttate psoriasis often self-resolves within weeks to months 1
Pregnant or Breastfeeding Patients
- Avoid methotrexate entirely due to teratogenicity, requiring contraception during treatment and for ≥1 menstrual cycle after discontinuation 1
- Avoid retinoids (acitretin) with mandatory contraception for 2 years after treatment completion due to prolonged teratogenic risk 1
Monitoring Requirements
During Active Treatment
- Conduct clinical review every 4 weeks to assess treatment response using BSA or PASI scoring and monitor for adverse effects 1, 2, 7
- Perform laboratory monitoring based on chosen therapy: weekly liver function tests for methotrexate, biweekly creatinine/blood pressure for cyclosporine 1
- Never provide unsupervised repeat prescriptions for high-potency topical corticosteroids 1, 2
Long-Term Management
- Reassess cardiovascular risk factors annually including blood pressure, lipids, glucose, and body weight 1
- Screen for depression at each visit using standardized tools, as biologic therapy improves both skin disease and psychiatric symptoms concurrently 1
- Monitor for treatment failure defined as <50% improvement in PASI or BSA after 12-16 weeks of systemic therapy 1
Adjunctive Therapies
Lifestyle Modifications
- Recommend weight loss for obese patients, as bariatric surgery should be considered for BMI >40 kg/m² when standard weight loss measures fail 1
- Advise smoking cessation and alcohol limitation, as both worsen psoriasis severity 1
- Encourage stress reduction techniques including mindfulness meditation and cognitive behavioral therapy, which improve disease severity 1
Complementary Approaches
- Consider oral curcumin supplementation as adjunctive therapy, though evidence is limited 1
- Implement gluten-free diet only for patients with confirmed celiac disease after positive antibody testing and gastroenterology consultation 1
- Do not recommend vitamin D or zinc supplementation for psoriasis treatment, as oral supplementation does not improve disease activity 1
Critical Pitfalls to Avoid
- Never combine salicylic acid with calcipotriene, as salicylic acid inactivates the vitamin D analogue 2
- Never use ultra-high potency corticosteroids beyond 4 weeks continuously due to skin atrophy, striae, and systemic absorption risk 2
- Never attribute treatment failure to "tachyphylaxis" without first addressing adherence, as perceived corticosteroid resistance is usually poor compliance 7
- Never delay systemic therapy referral for patients with ≥5% BSA involvement or significant quality of life impairment despite adequate topical therapy 2, 7