Randomized controlled observer-blinded treatment of chronic foot eczema with iontophoresis and bath-PUVA

The aim of this study was to investigate the effect of iontophoresis combined with local psoralen plus ultraviolet A (PUVA) therapy in chronic foot eczema. A randomized, observer-blinded, multi-centre study was conducted in 48 patients with chronic moderate-to-severe foot eczema randomized to one of 3 groups: In the iontophoresis group local bath-PUVA was preceded by iontophoresis. In the PUVA group only local PUVA was given. The corticosteroid group was treated with fluticasone. All treatments were given for 8 weeks, with an 8-week follow-up period. The primary efficacy parameter was eczema s... Mehr ...

Verfasser: Tupker, Ron A
Coenraads, Pieter Jan
Zanen, Pieter
Schuttelaar, Marielouise
Dokumenttyp: Artikel
Erscheinungsdatum: 2013
Reihe/Periodikum: Tupker , R A , Coenraads , P J , Zanen , P & Schuttelaar , M 2013 , ' Randomized controlled observer-blinded treatment of chronic foot eczema with iontophoresis and bath-PUVA ' , Acta dermato-venereologica , vol. 93 , no. 4 , pp. 456-460 . https://doi.org/10.2340/00015555-1537
Schlagwörter: Administration / Cutaneous / Adrenal Cortex Hormones / Adult / Androstadienes / Combined Modality Therapy / Eczema / Female / Ficusin / Foot Dermatoses / Humans / Iontophoresis / Male / Middle Aged / Netherlands / PUVA Therapy / Photosensitizing Agents / Quality of Life / Questionnaires / Severity of Illness Index / Time Factors / Treatment Outcome
Sprache: Englisch
Permalink: https://search.fid-benelux.de/Record/base-28780542
Datenquelle: BASE; Originalkatalog
Powered By: BASE
Link(s) : https://hdl.handle.net/11370/f6acec32-8f0c-4d8a-b578-c3044c06d46e

The aim of this study was to investigate the effect of iontophoresis combined with local psoralen plus ultraviolet A (PUVA) therapy in chronic foot eczema. A randomized, observer-blinded, multi-centre study was conducted in 48 patients with chronic moderate-to-severe foot eczema randomized to one of 3 groups: In the iontophoresis group local bath-PUVA was preceded by iontophoresis. In the PUVA group only local PUVA was given. The corticosteroid group was treated with fluticasone. All treatments were given for 8 weeks, with an 8-week follow-up period. The primary efficacy parameter was eczema score described by Rosén et al. Secondary efficacy parameters were a global impression by the patient, and the Dermatology Life Quality Index (DLQI). The eczema score and the DLQI decreased significantly over time. There were no significant differences in the decrease in eczema score (p=0.053) and DLQI values (p=0.563) between the 3 treatments. The DLQI values in our chronic foot eczema patients were high. There was no obvious advantage of local bath-PUVA with or with-out iontophoresis over local steroid therapy.