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Red light emitting diode as an adjuvant treatment for epidermal growth factor receptor inhibitors-induced paronychia.
Jornsamer, Chanoknan; Theerawattanawit, Chinathip; Wichayachakorn, Chanitwan; Panchaprateep, Ratchathorn; Kerr, Stephen J; Asawanonda, Pravit; Rerknimitr, Pawinee.
Afiliación
  • Jornsamer C; Department of Medicine, Faculty of Medicine, Division of Dermatology, Skin and Allergy Research Unit, Chulalongkorn University, Bangkok, Thailand.
  • Theerawattanawit C; Department of Medicine, Faculty of Medicine, Division of Dermatology, Skin and Allergy Research Unit, Chulalongkorn University, Bangkok, Thailand.
  • Wichayachakorn C; Department of Medicine, Division of Dermatology, Nail Clinic, Sclerotherapy Clinic, Dermatologic Surgery Unit, Faculty of Medicine, Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.
  • Panchaprateep R; Department of Medicine, Faculty of Medicine, Division of Dermatology, Skin and Allergy Research Unit, Chulalongkorn University, Bangkok, Thailand.
  • Kerr SJ; Center for Excellence in Biostatistics, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.
  • Asawanonda P; Department of Medicine, Faculty of Medicine, Division of Dermatology, Skin and Allergy Research Unit, Chulalongkorn University, Bangkok, Thailand.
  • Rerknimitr P; Department of Medicine, Faculty of Medicine, Division of Dermatology, Skin and Allergy Research Unit, Chulalongkorn University, Bangkok, Thailand.
J Dermatolog Treat ; 33(4): 1990-1994, 2022 Jun.
Article en En | MEDLINE | ID: mdl-33961534
We evaluated the efficacy and safety of red light LED as an adjuvant treatment for epidermal growth factor receptor inhibitor-induced paronychia. Eight patients were recruited in this randomized, single-blinded controlled trial. They were randomized to receive red-light on one hand or foot 2-3 times/week for 6 weeks while the contralateral side served as controls. The standard treatments were continued. Erythema and lesion elevation observed by Anthera® 3D, severity and pain scores were obtained at weeks 0, 2, 4, 6, and 8. The red light group showed significantly lower erythema, severity, and pain scores at weeks 4, 6, and 8. The elevation was significantly lower in the red light group at every follow-up visit. No adverse events occurred. Red light therapy may be an option as adjunctive treatment for EGFRi-induced paronychia.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Paroniquia / Fototerapia / Inhibidores de Proteínas Quinasas Tipo de estudio: Clinical_trials / Etiology_studies Límite: Humans Idioma: En Revista: J Dermatolog Treat Asunto de la revista: DERMATOLOGIA Año: 2022 Tipo del documento: Article País de afiliación: Tailandia Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Paroniquia / Fototerapia / Inhibidores de Proteínas Quinasas Tipo de estudio: Clinical_trials / Etiology_studies Límite: Humans Idioma: En Revista: J Dermatolog Treat Asunto de la revista: DERMATOLOGIA Año: 2022 Tipo del documento: Article País de afiliación: Tailandia Pais de publicación: Reino Unido