PUVA

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PatientPlus articles are written by UK doctors and are based on research evidence, UK and European Guidelines. They are designed for health professionals to use, so you may find the language more technical than the condition leaflets.

See also: Vitiligo written for patients

PUVA stands for psoralen combined with ultraviolet A (UVA) treatment. Psoralens are found in plants and can be sensitised when taken either orally or when applied topically. Interestingly, they were used for this purpose in ancient Egypt but have only been commercially manufactured in the last four to five decades. When used with UVA (long-wave radiation) they allow for a lower dose of UVA.

PUVASOL is the use of psoralens with natural sunlight in areas such as India - research so far suggests it may be as good as conventional therapy.

It remains a mystery as to why psoralens with UVA work in the above conditions but it has been postulated to relate to modulation of the skins immune system.[1]

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  • Psoralen is taken orally one hour before UVA treatment.
  • If the patient is unable to tolerate oral psoralens some hospitals provide a bathing system or topical psoralens - eg, gel-based preparations.
  • Topical therapy with psoralens is not associated with adverse effects such as nausea and vomiting seen with oral psoralens.
  • During sessions patients need to wear protective goggles, and UVA protective goggles must be worn for 24 hours following the treatment.
  • Clothes only need to be removed from the area to be treated, but groin protection is required.
  • UVA treatment is given 2-3 times per week for about 12 weeks - in a light box.
  • Once the course has finished, the patient may need maintenance therapy with one session per week.
  • Avoid exposure to sunlight for 24 hours after the session.
  • Eye protection - wear goggles.
  • Groin protection - wear protective shield/garment.
  • Skin and eye protection for 24 hours following the session of PUVA.

Adverse effects from oral psoralen

  • Nausea and vomiting - caused by psoralens and reduced if taken with food; this is a common reason for stopping treatment.
  • Headache and dizziness.

Adverse effects from PUVA

  • Sunburn (phytotoxic erythema) and blistering - occurs 2-3 days after treatment and more often in fair-skinned patients.
  • Dryness of skin with itching.
  • Tanning - lasts months (all patients).
  • Keratitis - the eyes need to be shielded during therapy.
  • Malignancy - some reports of increased risk of non-melanoma skin cancer.[2]

Adverse effects resulting from recurrent treatments

  • Enhancement of ageing changes of the skin - this includes freckling and wrinkling and occurs with extensive or prolonged treatments.
  • Increased skin neoplasia risk - eg, melanoma and non-melanoma; again, the risk is higher with extensive and prolonged treatments.

Psoriasis

  • Used in older patients and those with severe psoriasis.
  • Chronic plaque-type psoriasis is associated with up to 100% clearance.
  • Efficacy is enhanced when combined with ultraviolet B (UVB) or medications such as methotrexate (especially pustular and erythrodermic forms).
  • PUVA therapy has been compared with narrow-band UVB therapy in a randomised controlled trial which reported that the former is more effective.[3]
  • Home phototherapy is likely to become an option for selected patients.[4][5]

Eczema or dermatitis

  • Moderate-to-severe eczema only - clearance in up to 75%.

Mycosis fungoides

  • This is a rare form of cutaneous T-cell lymphoma.
  • PUVA can clear the disease but recurrence occurs in half of patients - with 30-50% remaining free of neoplasia at ten years.[6]
  • It requires ongoing treatment over many years and thus may be associated with skin damage and neoplasia.[6]

Vitiligo

PUVA can lead to repigmentation in areas where there is complete loss of pigmentation - but results are variable. A recent Cochrane study suggests that combination therapy regimens where light therapy is used are most likely to produce beneficial work, but more studies are needed.[7]

Further reading & references

  1. Wolf P, Nghiem DX, Walterscheid JP, et al; Platelet-activating factor is crucial in psoralen and ultraviolet A-induced immune suppression, inflammation, and apoptosis. Am J Pathol. 2006 Sep;169(3):795-805.
  2. Naldi L; Malignancy concerns with psoriasis treatments using phototherapy, methotrexate, Clin Dermatol. 2010 Jan-Feb;28(1):88-92.
  3. Yones SS, Palmer RA, Garibaldinos TT, et al; Randomized double-blind trial of the treatment of chronic plaque psoriasis: efficacy of psoralen-UV-A therapy vs narrowband UV-B therapy. Arch Dermatol. 2006 Jul;142(7):836-42.
  4. Nolan BV, Yentzer BA, Feldman SR; A review of home phototherapy for psoriasis. Dermatol Online J. 2010 Feb 15;16(2):1.
  5. Lee DA, Miller SJ; Nonmelanoma skin cancer. Facial Plast Surg Clin North Am. 2009 Aug;17(3):309-24.
  6. Querfeld C, Rosen ST, Kuzel TM, et al; Long-term follow-up of patients with early-stage cutaneous T-cell lymphoma who achieved complete remission with psoralen plus UV-A monotherapy. Arch Dermatol. 2005 Mar;141(3):305-11.
  7. Whitton ME, Pinart M, Batchelor J, et al; Interventions for vitiligo. Cochrane Database Syst Rev. 2010 Jan 20;(1):CD003263.

Disclaimer: This article is for information only and should not be used for the diagnosis or treatment of medical conditions. EMIS has used all reasonable care in compiling the information but make no warranty as to its accuracy. Consult a doctor or other health care professional for diagnosis and treatment of medical conditions. For details see our conditions.

Original Author:
Dr Gurvinder Rull
Current Version:
Peer Reviewer:
Dr Helen Huins
Document ID:
2688 (v24)
Last Checked:
20/06/2014
Next Review:
19/06/2019

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