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A controlled trial of photodynamic therapy of actinic keratosis comparing different red light sources.
Giehl, Kathrin A; Kriz, Martin; Grahovac, Maja; Ruzicka, Thomas; Berking, Carola.
Afiliação
  • Giehl KA; Department of Dermatology and Allergology Ludwig-Maximilian University Munich Frauenlobstr. 9-11 80337 Munich, Germany.
  • Kriz M; Department of Dermatology and Allergology Ludwig-Maximilian University Munich Frauenlobstr. 9-11 80337 Munich, Germany, Department of Dermatology and Allergology, Klinikum Augsburg, Stenglistr. 2, 86156 Augsburg, Germany.
  • Grahovac M; Department of Dermatology and Allergology Ludwig-Maximilian University Munich Frauenlobstr. 9-11 80337 Munich, Germany.
  • Ruzicka T; Department of Dermatology and Allergology Ludwig-Maximilian University Munich Frauenlobstr. 9-11 80337 Munich, Germany.
  • Berking C; Department of Dermatology and Allergology Ludwig-Maximilian University Munich Frauenlobstr. 9-11 80337 Munich, Germany.
Eur J Dermatol ; 24(3): 335-41, 2014.
Article em En | MEDLINE | ID: mdl-24876164
BACKGROUND: Photodynamic therapy (PDT) using 5-aminolevulinic acid (ALA) with red light is well established for actinic keratosis (AK). Differences have been observed concerning pain and efficacy rates with different red light sources. OBJECTIVES: To compare pain scores, short- and long-term efficacy rates of PDT of multiple AKs when employing different red light sources. MATERIAL AND METHODS: In a controlled trial, 88 patients (310 AK lesions) received ALA-PDT in combination with either visible light (VIS) + water-filtered infrared A (wIRA) light (PhotoDyn(®) 750 (PD750), 580-1400 nm) for 30 min or incoherent light (Waldmann(®) 1200L (Wa1200L), 600-720 nm) for 10-11 min. Follow-up visits were performed after 1, 3, 6, and 12 months. If there was no complete cure after 1, 3 or 6 months, a second cycle of PDT was performed. RESULTS: Pain scores were significantly lower in patients illuminated with PD750 rather than Wa1200L. Patient complete clearance rates were 85% and 91% after 1 month, 79% and 92% after 3 months, 97% and 92% after 6 months, and 69% and 85% after 12 months in the PD750 and Wa1200L groups, respectively. Lesion complete clearance rates were 94% and 92% after 1 month, 88% and 97% after 3 months, 96% and 95% after 6 months, and 81% and 89% after 12 months in the PD750 and Wa1200L group, respectively. The efficacy rates were not significantly different. CONCLUSION: A VIS + wIRA light source produced considerably less pain, while efficacy was not much affected in contrast to previously published studies, probably because the illumination time was longer in this study.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fotoquimioterapia / Fármacos Fotossensibilizantes / Ceratose Actínica / Ácido Aminolevulínico Tipo de estudo: Clinical_trials Limite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Eur J Dermatol Assunto da revista: DERMATOLOGIA Ano de publicação: 2014 Tipo de documento: Article País de afiliação: Alemanha

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fotoquimioterapia / Fármacos Fotossensibilizantes / Ceratose Actínica / Ácido Aminolevulínico Tipo de estudo: Clinical_trials Limite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Eur J Dermatol Assunto da revista: DERMATOLOGIA Ano de publicação: 2014 Tipo de documento: Article País de afiliação: Alemanha