Dermatology
Psoriasis
Manage psoriasis by confirming the clinical phenotype, quantifying extent and life impact, identifying psoriatic arthritis and cardiometabolic comorbidity, then selecting site-directed topical therapy, phototherapy, systemic therapy, or biologic treatment according to severity, trajectory, and treatment risk.
Initial assessment
Confirm psoriasis clinically and identify presentations requiring urgent escalation
Most plaque psoriasis does not require laboratory confirmation.
Make the diagnosis clinically when sharply demarcated scaly plaques have a typical symmetric distribution involving scalp, extensor elbows or knees, lumbosacral skin, or flexures. Document morphology and distribution before treatment because plaque psoriasis accounts for approximately 80% to 90% of cases and may coexist with nail or fold disease that changes topical formulation and potency selection. WHO+1WHO1. Application to Add Ustekinumab to the ...WHO[PDF] Application for inclusion of calcipotriol (calcipotriene)
Obtain a skin biopsy when the morphology or distribution is atypical, when an alternative papulosquamous disorder remains plausible, or when erythrodermic or pustular disease creates diagnostic uncertainty. Histopathology can complement the clinical diagnosis but is not routine for characteristic plaque psoriasis. WHO+1WHO[PDF] 29 October 2024 WHO Expert Committee on the Selection and Use ...WHO1. Application to Add Ustekinumab to the ...
Treat generalized erythroderma as an urgent dermatologic presentation. It may arise from progressive confluent plaque disease or unstable psoriasis precipitated by infection, medications, or corticosteroid withdrawal, and can cause hypothermia, hypoalbuminemia, anemia, and nutrient loss. WHOWHO[PDF] 29 October 2024 WHO Expert Committee on the Selection and Use ... Evaluate for precipitating infection or medication exposure and arrange urgent specialty management rather than escalating outpatient topical therapy alone. WHOWHO[PDF] 29 October 2024 WHO Expert Committee on the Selection and Use ...
At each flare, review potential exacerbating factors: infection, alcohol, medications, stress, and intercurrent illness. BMJBMJPsoriasis - Symptoms, diagnosis and treatment | BMJ Best Practice
Document a trauma-associated distribution when present; new lesions at sites of injury support a Koebner phenomenon. WHOWHO1. Application to Add Ustekinumab to the ...
Refer promptly for atypical, pustular, erythrodermic, or extensive disease and for failure of systemic or biologic therapy. PubMedPubMedPlaque Psoriasis - StatPearls - NCBI Bookshelf
Treatment intensity
Measure extent, site burden, and quality-of-life impact before choosing therapy
Extent alone can underestimate high-impact localized disease.
Record BSA and a reproducible activity measure such as PASI or PGA at baseline and before changing treatment. PASI incorporates plaque erythema, induration, scaling, and involved surface area across the head and neck, trunk, and upper and lower limbs; PGA, BSA, DLQI, and nail scores can complement PASI when the disease phenotype or practice workflow makes PASI less practical. WHOWHO[PDF] 29 October 2024 WHO Expert Committee on the Selection and Use ...
Use severity measures to guide, not replace, clinical judgment. A PASI of at least 10 or BSA of at least 10% with DLQI greater than 10 is a commonly used severe-disease threshold, while dermatology referral criteria also identify BSA greater than 10%, PASI greater than 10, or DLQI greater than 10 as moderate-to-severe disease. Wolters Kluwer+1Wolters KluwerBiologics and Biosimilars in Psoriasis : Indian Journal of DermatologyPubMedPlaque Psoriasis - StatPearls - NCBI Bookshelf Lesions on the scalp, face, flexures, hands, feet, genitals, or nails can justify escalation despite limited BSA when symptoms, function, or treatment feasibility are disproportionate. Site and symptom burden are explicit components of severity assessment. WHO+1WHO[PDF] 29 October 2024 WHO Expert Committee on the Selection and Use ...WHO[PDF] Application for inclusion of calcipotriol (calcipotriene)
Use topical treatment for mild or limited psoriasis, particularly when disease can be treated reliably by the patient. Topical corticosteroids and vitamin D analogues are the core first-line options for limited disease. BMJ+2BMJPsoriasis - Symptoms, diagnosis and treatment | BMJ Best Practice USBMJPsoriasis - Symptoms, diagnosis and treatment | BMJ Best Practicestaging aadPsoriasis clinical guideline If disease is extensive, cannot be practically treated with topical therapy, remains uncontrolled despite an adherent topical regimen, or produces substantial functional or quality-of-life burden, assess candidacy for phototherapy or systemic treatment. staging aad+2staging aadPsoriasis clinical guidelineaadPsoriasis clinical guideline - American Academy of DermatologyPubMedPlaque Psoriasis - StatPearls - NCBI Bookshelf
Measure DLQI when visible, genital, hand-foot, scalp, or nail disease appears discordant with BSA; impact on daily life is part of severity determination. WHO+1WHO[PDF] 29 October 2024 WHO Expert Committee on the Selection and Use ...WHO[PDF] Application for inclusion of calcipotriol (calcipotriene)
Record nail involvement because it contributes to disease burden and should heighten surveillance for musculoskeletal disease. WHO+1WHO[PDF] 29 October 2024 WHO Expert Committee on the Selection and Use ...PubMedPsoriatic Arthritis - StatPearls - NCBI Bookshelf
Use serial BSA, PASI/PGA, and patient-reported impact to determine whether a treatment is controlling disease rather than relying on a single baseline category. WHO+1WHO[PDF] 29 October 2024 WHO Expert Committee on the Selection and Use ...WHO[PDF] Application for inclusion of calcipotriol (calcipotriene)
Skin-directed therapy
Match topical vehicle and escalation to body site and treatment feasibility
Topical therapy remains foundational for mild-to-moderate plaque disease.
For limited psoriasis, select a topical corticosteroid, a vitamin D analogue, or their combination according to lesion thickness, anatomic site, cosmetic acceptability, and ability to apply treatment consistently. AAD-NPF guidance addresses topical agents and severity measurement, and BMJ Best Practice identifies topical corticosteroids and/or vitamin D analogues as treatment for mild or limited disease. BMJ+1BMJPsoriasis - Symptoms, diagnosis and treatment | BMJ Best Practice USstaging aadPsoriasis clinical guideline
For scalp psoriasis, use topical therapy in a formulation the patient can apply through hair-bearing skin. When a potent corticosteroid or vitamin D analogue used for up to 8 weeks does not achieve clearance, near-clearance, or satisfactory control, an adult can receive a very potent corticosteroid up to twice daily for 2 weeks; coal tar once or twice daily and specialist support with application technique are alternatives. nice org uknice org uk[PDF] Appendix A: Summary of evidence from surveillance | NICE Vitamin D analogue monotherapy is most appropriate when corticosteroids cannot be used at that site or for mild-to-moderate scalp disease. nice org uknice org uk[PDF] Appendix A: Summary of evidence from surveillance | NICE
Move beyond topical monotherapy when distribution makes application burdensome or when objective activity and patient-reported burden remain unacceptable despite a coherent regimen. Phototherapy is addressed in AAD-NPF psoriasis guidance and is an appropriate treatment-domain consideration before or alongside systemic options based on disease extent, access, and patient preference. BMJ+2BMJPsoriasis - Symptoms, diagnosis and treatment | BMJ Best Practicestaging aadPsoriasis clinical guidelinePubMedPlaque Psoriasis - StatPearls - NCBI Bookshelf
Choose vehicle and regimen around the involved site; lesion location is a core determinant of treatment selection. WHOWHO[PDF] Application for inclusion of calcipotriol (calcipotriene)
For scalp disease uncontrolled after the defined topical course, reassess adherence and formulation before declaring pharmacologic failure. nice org uknice org uk[PDF] Appendix A: Summary of evidence from surveillance | NICE
Use dermatology referral for phototherapy candidacy or when topical application support and alternative options are required. PubMed+1PubMedPlaque Psoriasis - StatPearls - NCBI Bookshelfnice org uk[PDF] Appendix A: Summary of evidence from surveillance | NICE
Advanced treatment
Choose systemic or biologic therapy by disease burden, comorbidity, and safety constraints
Moderate-to-severe disease requires individualized risk-benefit selection.
For adults with moderate-to-severe psoriasis, AAD-NPF guidance supports methotrexate and apremilast as systemic nonbiologic options; methotrexate is less effective for cutaneous psoriasis than adalimumab and infliximab. aadaadPsoriasis clinical guideline - American Academy of Dermatology Cyclosporine and acitretin are also addressed within systemic nonbiologic treatment guidance. PubMedPubMedJoint American Academy of Dermatology-National Psoriasis Foundation guidelines of care for the management of psoriasis with systemic nonbiologic therapies - PubMed Select among these approaches according to urgency of control, reproductive considerations, hepatic and renal risk, comorbid inflammatory disease, treatment burden, and monitoring capacity; the available guideline summary does not establish a universal sequence among systemic agents. PubMed+1PubMedJoint American Academy of Dermatology-National Psoriasis Foundation guidelines of care for the management of psoriasis with systemic nonbiologic therapies - PubMednice org uk[PDF] Psoriasis Guideline Consultation Comments Table - NICE
Biologic therapy is a treatment option for adults with moderate-to-severe psoriasis, including TNF inhibitors, IL-17 inhibitors, IL-12/23 inhibition, and IL-23 inhibitors. aad+1aadPsoriasis clinical guideline - American Academy of DermatologyPubMedBiologic Treatment Algorithms for Moderate-to-Severe Psoriasis with Comorbid Conditions and Special Populations: A Review After inadequate response to a first biologic, switching to a second biologic is a guideline-supported strategy; biologic plus methotrexate is another possible approach, although psoriasis-specific evidence for combination treatment is limited. PubMedPubMedTreatment Sequencing After Failure of the First Biologic in Cost-Effectiveness Models of Psoriasis: A Systematic Review of Published Models and Clinical Practice Guidelines - PMC
Before initiating a biologic, obtain a focused infection history and physical examination and screen for latent tuberculosis infection. PubMedPubMedBiologic Treatment Algorithms for Moderate-to-Severe Psoriasis with Comorbid Conditions and Special Populations: A Review Screen for viral infections, including HIV and hepatitis, before biologic therapy as described in psoriasis management recommendations; withhold biologic treatment during a major infection. PubMedPubMedRecommendations for Management of Childhood Psoriasis - PMC Incorporate inflammatory bowel disease, congestive heart failure, multiple sclerosis, hepatitis B, prior nonmelanoma skin cancer, lymphoma, and latent tuberculosis into biologic selection because these conditions materially alter class-specific risk assessment. PubMedPubMedBiologic Treatment Algorithms for Moderate-to-Severe Psoriasis with Comorbid Conditions and Special Populations: A Review
Use noninvasive hepatic-fibrosis assessment when monitoring methotrexate-associated hepatotoxicity, consistent with revised AAD-NPF monitoring guidance. aadaadPsoriasis clinical guideline - American Academy of Dermatology
Do not continue biologic treatment through a major infection. PubMedPubMedRecommendations for Management of Childhood Psoriasis - PMC
When biologic efficacy is inadequate, verify diagnosis, phenotype, adherence, safety, and joint disease before switching mechanism or agent. Switching to a second biologic is an accepted next step. PubMed+1PubMedTreatment Sequencing After Failure of the First Biologic in Cost-Effectiveness Models of Psoriasis: A Systematic Review of Published Models and Clinical Practice Guidelines - PMCPubMedPsoriatic Arthritis - StatPearls - NCBI Bookshelf
Interpreting infection risk during biologic treatment
Discuss infection risk in class- and patient-specific terms rather than treating all biologics as equivalent. In PSOLAR, serious-infection incidence was 0.83 per 100 patient-years with ustekinumab, 1.47 with etanercept, 1.97 with adalimumab, and 2.49 with infliximab; pneumonia and cellulitis were the most frequently reported serious infections. PubMedPubMedBiologic Treatment Algorithms for Moderate-to-Severe Psoriasis with Comorbid Conditions and Special Populations: A Review These observational rates inform counseling but do not substitute for baseline infection screening or individualized selection.
Longitudinal care
Screen actively for psoriatic arthritis and cardiometabolic disease
Cutaneous control does not exclude clinically consequential systemic disease.
Screen for psoriatic arthritis at psoriasis visits by asking about inflammatory joint pain, prolonged stiffness, swollen digits, heel or other entheseal pain, back symptoms, and functional limitation; examine for swollen joints, dactylitis, enthesitis, and nail disease. Approximately 30% of patients with cutaneous psoriasis in dermatology clinics have rheumatologist-diagnosed psoriatic arthritis. BMJBMJPsoriasis - Symptoms, diagnosis and treatment | BMJ Best Practice US Refer suspected inflammatory musculoskeletal disease to rheumatology because psoriatic arthritis is potentially debilitating and requires targeted treatment with ongoing monitoring. PubMedPubMedPsoriatic Arthritis - StatPearls - NCBI Bookshelf
Treat psoriasis as a multisystem disease and address cardiovascular risk factors rather than focusing only on plaque clearance. Psoriasis and psoriatic arthritis are epidemiologically linked to cardiovascular risk factors and increased cardiovascular disease risk, while psoriatic arthritis is associated with hypertension, metabolic syndrome, obesity, hyperlipidemia, diabetes mellitus, and cardiovascular disease. aad+2aadPsoriasis clinical guideline - American Academy of DermatologyPubMedCardiometabolic Comorbidities in Psoriasis and Psoriatic Arthritis. - AbstractPubMedPsoriatic Arthritis - StatPearls - NCBI Bookshelf Measure and manage blood pressure, weight, glycemic status, and lipids according to standard primary-care and cardiovascular-prevention pathways.
Ask about inflammatory bowel symptoms and ocular symptoms when musculoskeletal disease is present. Inflammatory bowel disease, particularly Crohn disease, is associated with increased risk of psoriatic arthritis, and uveitis requires ophthalmologic evaluation and treatment. PubMedPubMedPsoriatic Arthritis - StatPearls - NCBI Bookshelf These findings should influence biologic-class selection and coordination with gastroenterology, rheumatology, or ophthalmology. PubMed+1PubMedBiologic Treatment Algorithms for Moderate-to-Severe Psoriasis with Comorbid Conditions and Special Populations: A ReviewPubMedPsoriatic Arthritis - StatPearls - NCBI Bookshelf
Trigger rheumatology referral for swollen joints, dactylitis, enthesitis, inflammatory axial symptoms, or persistent functional limitation suggestive of psoriatic arthritis. PubMedPubMedPsoriatic Arthritis - StatPearls - NCBI Bookshelf
In patients with psoriatic arthritis, screen for obesity, hypertension, dyslipidemia, diabetes, and cardiovascular disease. PubMedPubMedPsoriatic Arthritis - StatPearls - NCBI Bookshelf
Refer uveitis for ophthalmologic evaluation rather than managing ocular inflammation solely through dermatologic therapy. PubMedPubMedPsoriatic Arthritis - StatPearls - NCBI Bookshelf
References
- Psoriasis - Symptoms, diagnosis and treatment | BMJ Best Practice US — bestpractice.bmj.com · bestpractice.bmj.com
- Psoriasis - Symptoms, diagnosis and treatment | BMJ Best Practice — bestpractice.bmj.com · bestpractice.bmj.com
- Guidelines for the Diagnosis and Treatment of Psoriasis in China — journals.lww.com · journals.lww.com
- 22nd PANLAR Congress: Miami, FL, August 12-15 2020 : JCR - Ovid — journals.lww.com · journals.lww.com
- Biologics and Biosimilars in Psoriasis : Indian Journal of Dermatology — journals.lww.com · journals.lww.com
- Systemic Management of Psoriasis Patients in Indian Scenario - Ovid — journals.lww.com · journals.lww.com
- Psoriasis clinical guideline — staging.aad.org · staging.aad.org
- Treatment Sequencing After Failure of the First Biologic in Cost-Effectiveness Models of Psoriasis: A Systematic Review of Published Models and Clinical Practice Guidelines - PMC — pmc.ncbi.nlm.nih.gov · pmc.ncbi.nlm.nih.gov
- Psoriasis clinical guideline - American Academy of Dermatology — www.aad.org · www.aad.org
- Risk of psoriasis in people with hidradenitis suppurativa: A systematic review and meta-analysis - PMC — pmc.ncbi.nlm.nih.gov · pmc.ncbi.nlm.nih.gov
- Biologic Treatment Algorithms for Moderate-to-Severe Psoriasis with Comorbid Conditions and Special Populations: A Review — pmc.ncbi.nlm.nih.gov · pmc.ncbi.nlm.nih.gov
- Recommendations for Management of Childhood Psoriasis - PMC — pmc.ncbi.nlm.nih.gov · pmc.ncbi.nlm.nih.gov
- Joint American Academy of Dermatology-National Psoriasis Foundation guidelines of care for the management of psoriasis with systemic nonbiologic therapies - PubMed — www.ncbi.nlm.nih.gov · www.ncbi.nlm.nih.gov
- Plaque Psoriasis - StatPearls - NCBI Bookshelf — www.ncbi.nlm.nih.gov · www.ncbi.nlm.nih.gov
- [PDF] 29 October 2024 WHO Expert Committee on the Selection and Use ... — cdn.who.int · cdn.who.int
- 1. Application to Add Ustekinumab to the ... — cdn.who.int · cdn.who.int
- [PDF] Application for inclusion of calcipotriol (calcipotriene) — cdn.who.int · cdn.who.int
- Book of abstracts — cdn.who.int · cdn.who.int
- [PDF] Appendix A: Summary of evidence from surveillance | NICE — www.nice.org.uk · www.nice.org.uk
- [PDF] Psoriasis Guideline Consultation Comments Table - NICE — www.nice.org.uk · www.nice.org.uk
- Roflumilast (Zoryve) - NCBI Bookshelf — www.ncbi.nlm.nih.gov · www.ncbi.nlm.nih.gov
- Systemic pharmacological treatments for chronic plaque psoriasis — www.cochranelibrary.com · www.cochranelibrary.com
- Cardiometabolic Comorbidities in Psoriasis and Psoriatic Arthritis. - Abstract — pubmed.ncbi.nlm.nih.gov · pubmed.ncbi.nlm.nih.gov
- Psoriatic Arthritis - StatPearls - NCBI Bookshelf — www.ncbi.nlm.nih.gov · www.ncbi.nlm.nih.gov