Treatment of psoriasis

Original author: Dr Amy Stanway, 2004. Revised and fully updated by Dr Douglas Maslin, Specialist Registrar in Dermatology and Clinical Pharmacology & Therapeutics, Addenbrooke’s Hospital, Cambridge, UK. DermNet NZ Editor-in-Chief: A/Prof Amanda Oakley, Dermatologist, Hamilton, New Zealand. February 2018. 

This update was made possible with independent financial support from LEO Pharma A/S.

What is psoriasis?

Psoriasis is a common, chronic, immune-mediated skin disease with characteristic red, scaly plaques caused by excessive proliferation of skin cells.

There are a number of types of psoriasis, such as chronic plaque psoriasis, guttate psoriasis, flexural psoriasis, palmoplantar psoriasis and nail psoriasis.


Principles of treatment

Despite recent advances in our understanding of the mechanism of how psoriasis develops, psoriasis may be difficult to treat: there is currently no cure and no single treatment works for everyone.

Several treatments may need to be tried before the most suitable regime is established; and different treatments may need to be used concurrently, or in rotation, for best effect or to minimise side-effects.

Treatment of adults includes:

  • General measures
  • Topical preparations
  • Ultraviolet therapy
  • Systemic non-biologic therapy
  • Systemic biologic therapy.

Treatment choice depends on a number of factors. For example:

  • Disease pattern
  • Dsease severity: body surface area (BSA), psoriasis area and severity index (PASI)
  • Disease impact: symptoms, Dermatology Life Quality Index (DLQI) score
  • Patient preference
  • Acceptability and practicalities of treatment
  • Patient age and general health
  • Comorbidities, eg, liver or renal disease; psoriatic arthritis
  • Other medications
  • Conception plans / current pregnancy
  • Treatment goals, eg, improving nail psoriasis or aiming for PASI90 (a 90% improvement in PASI score).

More details about each treatment are found on individual topic pages.

General measures used to treat psoriasis

Avoidance of triggers 

Where possible, minimise factors that aggravate/trigger psoriasis, such as stress, streptococcal infections and certain medications (lithium, beta blockers, antimalarial drugs).

Treatment of associated conditions

Health conditions associated with psoriasis include psoriatic arthritis, sleep disturbance, and depression. Treatment for these may help the skin disease.

Due to the association between psoriasis and metabolic syndrome, weight loss, smoking cessation, moderation of alcohol intake, and blood pressure control may also lead to improvements in skin disease [1,2]. 

Sun exposure

Sun exposure (heliotherapy) may help to clear psoriasis; in many people the psoriasis improves dramatically during summer months or on sunny holidays.

Psoriasis aggravated by sun exposure


Soaking in warm water can soften the psoriatic plaques and lift the scale.

  • Soap substitutes or bath oils are useful.
  • Antiseptics are not necessary and may cause skin irritation.
  • Balneotherapy is a popular form of complementary therapy in certain demographic areas [5], although there is little or no strong evidence for benefit.


One avenue of current research is looking at the skin and gut microbiome (the bacteria living on and in the human body) and whether the alteration of this microbiome may be effective in the treatment of psoriasis [3,4]. To date, probiotics have not been found to help psoriasis.

Occlusive dressings

Relatively small, localised patches of psoriasis may improve with occlusion, for example using waterproof adhesive dressings.

Topical preparations for psoriasis


Regular use of emollients and moisturisers soften psoriasis and add moisture to the skin. This improves the dryness, scaling and irritation.

  • There are a diverse range of options of lotions (for scalp psoriasis), creams, and ointments (for dry, thick, scaly areas).
  • Thick ointments based on white soft paraffin are often recommended for chronic plaques and hand/foot disease.
  • They should be applied liberally and frequently.

Be aware of the flammability of emollients and the risk of slipping in the bath after applying these agents to the feet. Emollients can rarely irritate the skin; this is less likely with ointments than with lotions and creams.

Keratolytic agents can be useful to reduce thick scale: They may contain urea (5–40%), salicylic acid (0.5–10%) or propylene glycol (for example, propylene glycol 20% in aqueous cream).

Topical steroids 

Topical steroids are safe and relatively easy to use for  plaque psoriasisscalp psoriasis, flexural psoriasissebopsoriasis and psoriasis affecting the palms and soles. They are not very effective in nail psoriasis.

Topical steroids are available in various strengths and formulations. They are also used in combination with other agents, such as:

The selection of a suitable product depends on the site and type of psoriasis.

  • Weak topical steroids are used on sensitive sites (face, flexures and genital areas). 
  • In contrast, palmoplantar psoriasis require very potent topical steroid due to the thicker skin on hands and feet.

Potent steroids are often more effective than mild topical steroids but they have a higher risk of side effects.  They should be used with caution on large areas and for limited periods. They may cause:

Topical steroids can be used under medical supervision in pregnancy and, alongside emollients, are generally the first-line treatment of psoriasis in pregnancy.

Intralesional steroid injections may be used for a small number of thickened plaques of psoriasis and in nail psoriasis [6].

Vitamin D-like compounds

Vitamin D-like compounds for psoriasis include calcipotriol, calcitriol, and tacalcitol.

  • They are applied once or twice daily.
  • They reduce the thickness and scaliness of plaques.
  • Redness may persist.

Calcipotriol may be used for chronic plaque and scalp psoriasis, whereas calcitriol ointment is often preferred for flexural or genital psoriasis (as it is less irritating than calcipotriol).

  • If irritation occurs, reduce the frequency of application to every second day or less often for a period of time.
  • Vitamin D-like compounds may cause a facial rash, so these treatments are not usually suitable for facial psoriasis.
  • No more than 100 g should be used each week.

When combined with ultraviolet (UV) therapy, calcipotriol should be applied after to exposure to UV, because:

  • UV deactivates calcipotriol.
  • Calcipotriol acts as a sunscreen.

Vitamin D-like compounds are best avoided in children under 6 years, and during pregnancy and lactation, due to lack of data regarding their safety. 

Calcipotriol is available in combination with a very potent topical steroid, betamethasone diproprionate.

  • This is often the first line of treatment in plaque psoriasis.
  • It should not be used continuously or over large areas due to the risks associated with excessive steroid use.
Effect of calcipotriol ointment on chronic plaque psoriasis


Coal tar may be applied as solutions, lotions, creams, ointments, gels, and shampoos.

Care needs to be taken following application of coal tar treatments.

  • They can irritate the skin, particularly on initial use.
  • They can be messy (staining skin, hair and clothing), and often have an associated odour.
  • Sunlight can interact with tar on the skin to cause a sunburn-like contact phototoxic dermatitis.


Dithranol (also called anthralin) is occasionally recommended as a treatment for chronic plaque psoriasis. It can be very effective but dithranol treatment has a number of practical drawbacks and so is less frequently prescribed.

The method of application is complex: it is usually given as ‘short contact therapy’.

  • Dithranol is normally applied once a day.
  • It is applied directly to the psoriasis (avoiding normal skin) and then washed off after 10 to 60 minutes.
  • The strength of dithranol is gradually increased every few days until it is effective, or until skin irritation occurs.
  • Dithranol permanently stains fabrics and temporarily stains the skin.

Calcineurin inhibitors

The calcineurin inhibitors are tacrolimus ointment and pimecrolimus cream.

  • They are mostly used to treat atopic dermatitis, and their use for psoriasis is off-licence.
  • They are used as steroid-sparing agents on sensitive sites where the skin is thinner (face, flexures, genital areas)
  • They are not effective for treating chronic plaque psoriasis elsewhere (unless under occlusion) [7].


Tazarotene is a topical retinoid, which may be applied once daily to plaque psoriasis as a 0.05% or 0.1% cream. [8].

The most common side-effect is skin pain and local irritation. It is not currently available in New Zealand (January 2018).

Ultraviolet treatment for psoriasis

Phototherapy is the use of UV radiation to treat skin disorders, and can be very effective in the treatment of psoriasis. It is generally reserved for cases where topical therapy has been ineffective or too much of the skin surface is involved to treat psoriasis effectively with topical agents.  It is administered in cabinets at specialised centres, and a treatment course for psoriasis will usually consist of two to three treatments per week for 20–30 treatments.

The need for regular travel to a phototherapy centre can make this option difficult for some patients. The beneficial effects may be short-lived.


Narrowband UVB (311–312 nm wavelengths) is also known as TL-O1 therapy.

  • Narrowband UVB is particularly effective in thin chronic plaque and guttate psoriasis, especially in the winter months.
  • It is generally felt to be safe and well tolerated. About two-thirds of patients with plaque psoriasis experience a PASI75 compared to baseline [9].
  • UVB is felt to be safe in pregnancy. Note that UVB degrades folic acid and regular supplementation in pregnancy is needed[10,11].


Psoralens plus long wave UVA radiation, known as photochemotherapy or PUVA, can be applied to the whole body by giving an oral (tablet) psoralen two hours prior to treatment.

  • Treatment can be localised to the hands and/or feet by using psoralen bath soaks or topical psoralens prior to treatment.
  • Localised treatment is commonly used to treat thick plaques or moderate/severe hand and/or foot psoriasis; including palmoplantar pustulosis.
  • Photosensitivity persists for some hours following oral psoralen treatment, therefore patients are advised to avoid sun exposure, including wearing of wrap-around sunglasses on the day of treatment.
  • PUVA is more likely than narrowband UVB treatment to cause skin cancer, especially squamous cell carcinoma, and is usually limited to a maximum of 100–200 lifetime treatments.
  • Psoralens (and therefore PUVA) is not recommended during pregnancy or breastfeeding.

Systemic non-biologic medication for psoriasis

Systemic (oral or injectable) medication may be required to treat psoriasis when:

  • Topical therapy is ineffective, and
  • Psoriasis is impacting on physical, social, or psychological health, and
  • Psoriasis is severe; or phototherapy is ineffective/contraindicated [12].

Selection of the appropriate medication is specific to each individual patient, as each agent carries its own risks and benefits:


Methotrexate is an immune modulatory and anti-inflammatory treatment used to treat psoriasis, psoriatic arthritis and Crohn disease.

  • Methotrexate is usually given once a week.
  • Oral tablets or subcutaneous injections may be selected.
  • Folic acid supplementation is often added.

The dose of methotrexate is often adjusted over the first few weeks or months of treatment. There are various regimens.

  • It can be given long term if there are no significant side effects.
  • 45% of patients treated with methotrexate for 12–16 weeks experience PASI75 [75% improvement of baseline PASI score] [13].
  • Regular blood tests should monitor liver function, and blood count while on methotrexate.
  • Excess alcohol should be avoided.
  • Methotrexate can cause fetal harm so women should not become pregnant while taking methotrexate and for three months after stopping it.

Side effects of methotrexate include nausea, tiredness, mouth ulcers and diarrhoea. 


Ciclosporin is an immune suppressant used short-term to treat atopic eczema and psoriasis.

  • Ciclosporin capsules are usually taken twice daily.
  • The dose is individualised according to patient weight, efficacy and adverse effects (2.5–5.0 mg/kg/day). 

Ciclosporin has a rapid onset of action, making it useful in severe plaque or pustular psoriasis] .

  • Due to side effects and risks, ciclosporin is usually prescribed for courses of 8–12 weeks.
  • 50–80% patients treated with ciclosporin for 8–12 weeks achieve PASI75 [14].
  • Regular blood tests should monitor at least blood pressure and renal function.
  • There is no evidence that ciclosporin causes fetal harm but doses should be kept low in pregnancy or it should be discontinued due to hypertension.
  • It must not be taken when breast feeding.

Important side effects of ciclosporin include hypertension, renal failure, susceptibility to infection and increased risk of skin cancer


Acitretin is a vitamin A-like compound or retinoid that is particularly effective for palmoplantar psoriasis].

  • Acitretin capsules are usually taken once daily.
  • Dose varies from 10 mg three times weekly to 50 mg daily.
  • Acitretin is often combined with phototherapy
  • 20-40% of patients treated with acitretin in full dose achieve PASI75 by week 16 [14].
  • Regular blood tests should monitor liver function and blood fats.
  • Pregnancy must be strictly avoided whilst on acitretin and for at least two years afterwards because it is associated with serious birth deformities (US pregnancy category X). Acitretin is therefore rarely given to women of childbearing age.
  • The risk does not apply to men, as acitretin does not affect sperm.

Dose-related side-effects of acitretin include dry lips, peeling palms and soles, thinning hair, tiredness and muscle pains.


Apremilast is a phosphodiesterase-4 inhibitor used to treat psoriasis and psoriatic arthritis. It is not funded in New Zealand (February 2018).

  • Dosing of apremilast is titrated for the first five days, and then given as a fixed dose twice daily.
  • Treatment may be given long-term, and does not require drug screening or monitoring.
  • 29–33% of patients treated with apremilast achieve PASI75 at week 16 [14].
  • Apremilast is thought to be harmful to a developing fetus and so it should not be given in pregnancy (US pregnancy category C). 

Side effects of apremilast include nausea and diarrhoea. There have also been reports of suicidal behaviour.

Fumaric acid esters

Fumaric acid esters are immune suppressants. They are not available or funded in New Zealand.

  • The dose of fumaric acid is slowly escalated.
  • Several different preparations are available.
  • Dose is usually gradually increased to achieve effect. PASI75 is 38% at week 16.
  • Blood tests should monitor kidney, liver, and white blood cells. 

Side effects include nausea, diarrhoea, stomach cramps, flushing and headaches. A rare but serious side effect is a nervous system viral infection (progressive multifocal leukoencephalopathy).

Fumaric acid esters are not to be used during pregnancy due to fetal harm.

Other non-biological medications

Other oral medications used less commonly for psoriasis include:

Biological therapies

Biological therapies or biologics are monoclonal antibodies targeted at specific components of the immune system. They are often very effective treatments for psoriasis.

  • The risk of serious side effects relates to their effect on immunity.
  • They are very expensive and prescription is tightly regulated.  
  • They are used for moderate to severe psoriasis that has failed topical and systemic options or when these are contraindicated.

Each available biologic has individual risks and benefits.  Novel biologic therapies are under development.

The biologics for psoriasis are given by subcutaneous injection, with the exception of infliximab, which is administered intravenously.

Biosimilars are drugs that are nearly identical to an original biologic medication that has come off patent [15], and are available at a reduced cost. Biosimilars are available for infliximab and etanercept and others are under development (February 2018).

Effect of adalimumab on psoriasis 


Related Information


  1. Jensen P, Zachariae C, Christensen R, Geiker N, Schaadt B, Stender S et al. Effect of Weight Loss on the Severity of Psoriasis. JAMA Dermatology. 2013;149(7):795. PubMed.
  2. Hayes J, Koo J. Psoriasis: depression, anxiety, smoking, and drinking habits. Dermatologic Therapy. 2010;23(2):174-180. PubMed.
  3. Langan E, Griffiths C, Solbach W, Knobloch J, Zillikens D, Thaçi D. The role of the microbiome in psoriasis: moving from disease description to treatment prediction?. British Journal of Dermatology. 2017. Journal.
  4. Yan D, Issa N, Afifi L, Jeon C, Chang H, Liao W. The Role of the Skin and Gut Microbiome in Psoriatic Disease. Current Dermatology Reports. 2017;6(2):94-103. PubMed.
  5. Peroni A, Gisondi P, Zanoni M, Girolomoni G. Balneotherapy for chronic plaque psoriasis at Comano spa in Trentino, Italy. Dermatologic Therapy. 2008;21:S31-S38. PubMed.
  6. De Berker, Lawrence. A simplified protocol of steroid injection for psoriatic nail dystrophy. British Journal of Dermatology. 1998;138(1):90-95. PubMed.
  7. Menter A, Korman N, Elmets C, Feldman S, Gelfand J, Gordon K et al. Guidelines of care for the management of psoriasis and psoriatic arthritis. Journal of the American Academy of Dermatology. 2009;60(4):643-659. PubMed.
  8. Lebwohl M, Ast E, Callen J, Cullen S, Hong S, Kulp-Shorten C et al. Once-daily tazarotene gel versus twice-daily fluocinonide cream in the treatment of plaque psoriasis. Journal of the American Academy of Dermatology. 1998;38(5):705-711. Journal.
  9. Almutawa F, Alnomair N, Wang Y, Hamzavi I, Lim H. Systematic Review of UV-Based Therapy for Psoriasis. American Journal of Clinical Dermatology. 2013;14(2):87-109. PubMed.
  10. El-Saie L, Rabie A, Kamel M, Seddeik A, Elsaie M. Effect of narrowband ultraviolet B phototherapy on serum folic acid levels in patients with psoriasis. Lasers in Medical Science. 2011;26(4):481-485.
  11. Zhang M, Goyert G, Lim H. Folate and phototherapy: What should we inform our patients?. Journal of the American Academy of Dermatology. 2017;77(5):958-964. Journal.
  12. Clinical Guideline. Psoriasis. The assessment and management of psoriasis. CG153. October 2012. Prescriber. 2012;23(22):42-43. Journal.
  13. West J, Ogston S, Foerster J. Safety and Efficacy of Methotrexate in Psoriasis: A Meta-Analysis of Published Trials. PLOS ONE. 2016;11(5):e0153740. Journal.
  14. Gisondi P, Altomare G, Ayala F, Bardazzi F, Bianchi L, Chiricozzi A et al. Italian guidelines on the systemic treatments of moderate-to-severe plaque psoriasis. Journal of the European Academy of Dermatology and Venereology. 2017;31(5):774-790. PubMed.
  15. Cohen A, Wu J, Puig L, Chimenti S, Vender R, Rajagopalan M et al. Biosimilars for Psoriasis: Worldwide Overview of Regulatory Guidelines, Uptake and Implications for Dermatology Clinical Practice. British Journal of Dermatology. 2017. PubMed.

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