PMID- 19120333 OWN - NLM STAT- MEDLINE DCOM- 20090422 LR - 20090317 IS - 1365-2133 (Electronic) IS - 0007-0963 (Linking) VI - 160 IP - 3 DP - 2009 Mar TI - Medium-dose ultraviolet (UV) A1 vs. narrowband UVB phototherapy in atopic eczema: a randomized crossover study. PG - 652-8 LID - 10.1111/j.1365-2133.2008.08984.x [doi] AB - BACKGROUND: Ultraviolet (UV) A1 and narrowband (NB)-UVB have been reported to be effective treatments for atopic eczema (AE). OBJECTIVES: We aimed to compare the efficacy of medium-dose UVA1 and NB-UVB mono-phototherapy in patients with AE. METHODS: A randomized double-blind controlled crossover trial (ClinicalTrials.gov Identifier: NCT00419406) was conducted in which patients with AE received a 6-week course of both medium-dose UVA1 and NB-UVB. Clinical efficacy was assessed using the Six Area, Six Sign, Atopic Dermatitis (SASSAD) score and a visual analogue scale for pruritus. Assessment of health-related quality of life was performed using the Skindex-29. Total immunoglobulin E (IgE) and eosinophilic cationic protein (ECP) were evaluated at baseline and after each phototherapy course. RESULTS: Twenty-eight patients who completed both UVA1 and NB-UVB phototherapy courses on an intention-to-treat basis were analysed according to the crossover design. Both interventions were associated with significant clinical improvement but there was no significant difference between treatments with respect to the mean +/- SD relative reduction (RR) of the clinical scores (SASSAD, 43.7 +/- 31.4% vs. 39.4 +/- 24.1%, P = 0.5; pruritus score, 16 +/- 61.8% vs. 25.2 +/- 30.5%, P = 0.5, respectively). There was no significant difference in the mean +/- SD RR of the Skindex-29 after UVA1 and NB-UVB phototherapy (12.7 +/- 18.8% vs. 16.5 +/- 17.6%, P = 0.1). Changes in the total IgE and ECP levels following UVA1 and NB-UVB did not differ significantly (P = 0.3 and P = 0.9, respectively). CONCLUSIONS: A 6-week course of NB-UVB and UVA1 phototherapy of AE resulted in significant clinical improvement. With regard to efficacy and tolerability, both phototherapeutic modalities may be considered comparably good. FAU - Gambichler, T AU - Gambichler T AD - Department of Dermatology, Ruhr-University of Bochum, Gudrunstr. 56, D-44791 Bochum, Germany. t.gambichler@klinikum-bochum.de FAU - Othlinghaus, N AU - Othlinghaus N FAU - Tomi, N S AU - Tomi NS FAU - Holland-Letz, T AU - Holland-Letz T FAU - Boms, S AU - Boms S FAU - Skrygan, M AU - Skrygan M FAU - Altmeyer, P AU - Altmeyer P FAU - Kreuter, A AU - Kreuter A LA - eng SI - ClinicalTrials.gov/NCT00419406 PT - Comparative Study PT - Journal Article PT - Randomized Controlled Trial DEP - 20081211 PL - England TA - Br J Dermatol JT - The British journal of dermatology JID - 0004041 RN - 37341-29-0 (Immunoglobulin E) RN - EC 3.1.27.- (Eosinophil Cationic Protein) SB - IM MH - Adolescent MH - Adult MH - Aged MH - Aged, 80 and over MH - Cross-Over Studies MH - Dermatitis, Atopic/immunology/*radiotherapy MH - Double-Blind Method MH - Eosinophil Cationic Protein/blood MH - Female MH - Humans MH - Immunoglobulin E/blood MH - Male MH - Middle Aged MH - Severity of Illness Index MH - Treatment Outcome MH - Ultraviolet Therapy/adverse effects/*methods MH - Young Adult EDAT- 2009/01/06 09:00 MHDA- 2009/04/23 09:00 CRDT- 2009/01/06 09:00 PHST- 2009/01/06 09:00 [entrez] PHST- 2009/01/06 09:00 [pubmed] PHST- 2009/04/23 09:00 [medline] AID - BJD8984 [pii] AID - 10.1111/j.1365-2133.2008.08984.x [doi] PST - ppublish SO - Br J Dermatol. 2009 Mar;160(3):652-8. doi: 10.1111/j.1365-2133.2008.08984.x. Epub 2008 Dec 11.