UVA1 phototherapy for cutaneous diseases
Type:Uv phototherapy Time:2016-11-02 16:01:01Medium-dose UVA1 cold-light phototherapy in the treatment of severe atopic dermatitis (Citations: 33)
G. von Kobyletzki, C. Pieck, K. Hoffmann, M. Freitag, P. Altmeyer
Background: Recently, conventional high-dose UVA1 phototherapy
(340-400 nm) has been shown to be more effective than combined UVA-UVB
therapy in the treatment of severe atopic dermatitis (AD). However,
there are limitations of this treatment, such as intense sweating caused
by the immense heat load during therapy and the high cumulative UVA1
doses that are required. For this reason, lavish UVA1 equipment was
developed containing an advanced filtering and cooling system resulting
in almost complete absence of heat load and sweating during therapy.
Objective: In this study we compared the monotherapeutic efficacy of
conventional medium-dose UVA1, medium-dose UVA1 cold-light, and combined
UVA-UVB phototherapy in the treatment of severe AD. Method: The study
involved 120 patients with severe AD. Fifty patients each received
conventional UVA1 or UVA1 cold-light phototherapy (15 days, 50
J/cm2/day), and 20 patients were treated with combined UVA-UVB (15 days,
minimal erythema dose dependent). Severity of AD was scored by means of
the SCORAD score, and clinical improvement was additionally monitored
by serologic cytokine markers. Results: Six (12%) of 50 patients treated
with UVA1, 2 (4%) of 50 patients treated with UVA1 cold-light therapy,
and 4 (20%) of 20 patients treated with combined UVA-UVB therapy
discontinued treatment prematurely because of an unsatisfactory clinical
outcome or adverse reactions. Skin status improved or even cleared
completely in 77.3% of the patients treated for 3 weeks with
conventional UVA1 therapy and in 85.4% of the patients treated for 3
weeks with UVA1 cold-light therapy, resulting in a significant decrease
in the SCORAD score in both UVA1 groups (P < .05 each). In the group
treated with combined UVA-UVB, the SCORAD score also decreased but
significantly less than in both groups treated with UVA1 photo-therapy
(P < .05 each). At follow-up after 4 weeks, the patients treated with
UVA1 displayed a more prolonged therapeutic benefit than the patients
treated with UVA-UVB therapy. Plasma levels of soluble interleukin 2
receptors and soluble interleukin 4 receptors significantly decreased
under both UVA1 and UVA1 cold-light phototherapy but not under combined
UVA-UVB phototherapy. Conclusion: Our study demonstrates that
medium-dose UVA1 cold-light phototherapy displays advantages compared
with conventional UVA1 phototherapy caused by the almost complete
absence of heat load and intense sweating and is more effective than
UVA-UVB phototherapy in the treatment of severe AD. (J Am Acad Dermatol
1999;41:931-7.)
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