Luminescence of favipiravir in skin appendages and sclera. A controlled study and literature review.

IF 2.5 4区 医学 Q2 DERMATOLOGY Photodermatology, photoimmunology & photomedicine Pub Date : 2024-01-01 Epub Date: 2023-10-26 DOI:10.1111/phpp.12919
Deniz Demircioğlu, Emel Öztürk Durmaz
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Abstract

Background/objectives: Favipiravir is an antiviral agent, recently used for COVID-19 infections. Several reports associate favipiravir intake with Wood's lamp fluorescence of hair, nails, and sclera. The present study was designed to elucidate the positivity rates, and sites of favipiravir-related fluorescence and to unravel the site-specific changes in fluorescence positivity rates by a function of time past exposure.

Methods: The study population comprised 50 patients and 50 control individuals. All patients in the patient group had received a full dose of favipiravir for COVID-19 infection. Fifty volunteers served as the control group. Wood's lamp examination was performed in a completely darkened room, and the positivity rate, extent, pattern, and distribution of fluorescence were recorded.

Results: Wood's light revealed fluorescence of the fingernails, toenails, sclera, and hair in 35 (70%), 35 (70%), 22 (44%), and 8 (16%) patients, respectively. No control individual tested positive by Wood's lamp. Statistical analysis revealed significant differences between patient and control groups in terms of Wood's light luminescence in the fingernails (p = .000), toenails (p = .000), sclera (p = .000) and hair (p = .003). Although fingernail, toenail, and hair fluorescence positivity rates declined or ceased at or after 91 days of favipiravir exposure, ocular fluorescence positivity rates were prolonged up to 188 days.

Conclusions: These findings confirm that favipiravir may produce fluorescence of nails, sclera, and hair, detectable by Wood's light starting from the initial month and peaking at second- and third months following exposure to the medication. Although nail and hair fluorescence tend to abate after 3 months, ocular fluorescence may persist even longer than 6 months after cessation of the medication.

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法匹拉韦在皮肤附属物和巩膜中的发光。对照研究和文献综述。
背景/目的:法维匹拉韦是一种抗病毒药物,最近用于治疗新冠肺炎感染。一些报告将法匹拉韦的摄入与头发、指甲和巩膜的Wood灯荧光联系起来。本研究旨在阐明阳性率和法匹拉韦相关荧光的位点,并通过过去暴露时间的函数揭示荧光阳性率的位点特异性变化。方法:研究人群包括50名患者和50名对照者。患者组中的所有患者均接受了全剂量法匹拉韦治疗新冠肺炎感染。50名志愿者作为对照组。Wood的灯检查是在一个完全黑暗的房间里进行的,并记录阳性率、范围、模式和荧光分布。结果:Wood光分别显示35例(70%)、35例(70%)、22例(44%)和8例(16%)患者的指甲、脚趾甲、巩膜和头发的荧光。Wood灯检测无阳性对照个体。统计分析显示,患者和对照组在指甲中的Wood发光方面存在显著差异(p = .000)、脚趾甲(p = .000)、巩膜(p = .000)和头发(p = .003)。尽管指甲、脚趾甲和头发的荧光阳性率在91岁或之后下降或停止 法匹拉韦暴露天数,眼部荧光阳性率延长至188 天。结论:这些发现证实了法匹拉韦可能会在指甲、巩膜和头发上产生荧光,从最初的一个月开始就可以被Wood的光检测到,并在暴露于药物后的第二个月和第三个月达到峰值。尽管指甲和头发的荧光在3天后趋于减弱 几个月后,眼部荧光可能会持续6个月以上 停药后数月。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
4.40
自引率
7.70%
发文量
85
审稿时长
6-12 weeks
期刊介绍: The journal is a forum for new information about the direct and distant effects of electromagnetic radiation (ultraviolet, visible and infrared) mediated through skin. The divisions of the editorial board reflect areas of specific interest: aging, carcinogenesis, immunology, instrumentation and optics, lasers, photodynamic therapy, photosensitivity, pigmentation and therapy. Photodermatology, Photoimmunology & Photomedicine includes original articles, reviews, communications and editorials. Original articles may include the investigation of experimental or pathological processes in humans or animals in vivo or the investigation of radiation effects in cells or tissues in vitro. Methodology need have no limitation; rather, it should be appropriate to the question addressed.
期刊最新文献
Subjective and objective assessment of color match of universal tinted sunscreens in Fitzpatrick skin phototypes I-VI. Immunofluorescence findings in a reactivating lichenoid photoallergic chronic dermatitis (actinic reticuloid). Sunscreens prescribed to patients with skin of color and/or with melasma: A survey of 221 dermatologists and dermatology residents in Spain. Phototherapy for the treatment of cutaneous graft-versus-host disease: A systematic review. KGF-2 ameliorates UVB-triggered skin photodamage in mice by attenuating DNA damage and inflammatory response and mitochondrial dysfunction.
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