光动力疗法光":通过将激光辅助低辐照度光动力疗法与缩短日光光动力疗法相结合,改进了光化性角化病的治疗方案,使疼痛最小,临床疗效最佳。

Martin T Braun, Kelly Del Tredici, Anna Wölling, Luitgard Wiest
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引用次数: 0

摘要

背景:2003 年至 2016 年间,我们诊所有 546 名患者因无法忍受疼痛而中断了使用传统光动力疗法(PDT)对光化性角化病(AKs)的门诊治疗,因此有必要使用一种痛苦较小的治疗方法。因此,我们开发了一种新颖的标签外光动力疗法方案--"光动力疗法光":方法:方法:从 2014 年开始进行激光辅助低辐照度 PDT(li-PDT)治疗。2018年,剂量逐渐降低到8-12 J/cm²,这样我们在保持相当疗效的同时,疼痛也大大减轻了。从2018年起,通过将li-PDT的优势与日光PDT(DLPDT)相结合,进一步显著减轻了疼痛,从而在2018年形成了新技术 "光PDT"。AK奥尔森1级或2级和视野癌化的患者首先接受轻度分次CO2激光预处理,然后在闭塞状态下进行1.5-3小时的MAL-孵育(氨基乙酰乙酸甲酯,Metvix ®)。然后,用Aktilite-LED对患者进行平均1.02分钟的照射,并在照射区域涂上紫外线屏后,将患者送出日光下照射1小时:在 2019 年 3 月至 11 月期间,我们使用增强型 "PDT 光 "程序成功治疗了 152 例患者,其中 137 例患者在随访 1 期(平均 8.14 个月后)达到良好至卓越的清除率(CLA 和 CLB 合计 90%),不良反应极少:新颖的 "PDT 光 "方案被证明是一种出色且几乎无痛的方法,平均视觉模拟量表(VAS)评分为 1.19。与单独使用 DLPDT 相比,该疗法还具有照明时间短、门诊停留时间短、不良反应少、患者依从性好等优点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Photodynamic therapy light': An enhanced treatment protocol for actinic keratoses with minimal pain and optimal clinical outcome by combining laser-assisted low irradiance PDT with shortened daylight PDT.

Background: Between 2003 and 2016, 546 patients in our clinic discontinued outpatient treatment for actinic keratoses (AKs) using conventional photodynamic therapy (PDT) because of intolerable pain, thereby necessitating the use of a less painful procedure. Therefore, we developed a novel off-label PDT protocol: 'PDT light'.

Methods: Laser-assisted low irradiance PDT (li-PDT) was performed beginning in 2014. The dosage was gradually lowered to 8-12 J/cm² in 2018, so that we achieved considerable pain reduction while maintaining comparable therapeutic efficacy. A further considerable reduction in pain was achieved from 2018 onwards by combining the advantages of li-PDT with daylight PDT (DLPDT), thereby resulting in 2018 in the new technique 'PDT light'. Patients with AK Olsen grades 1 or 2 and field cancerization initially received a mild-fractionated CO2 laser pretreatment prior to MAL-incubation (methyl aminolaevulinate, Metvix ®) under occlusion for 1.5-3 h. Then, patients were illuminated on average for 1.02 min with the Aktilite-LED and, after application of an UV-screen on the illuminated area, sent out into daylight for 1 h.

Results: Between March and November 2019, we successfully treated 152 cases using the enhanced 'PDT light' procedure, with 137 cases achieving at follow-up 1 (on average after 8.14 months) good-to-excellent clearance rates (CLA and CLB together 90%) and minimal adverse effects.

Conclusions: The novel 'PDT light' protocol proved to be an excellent and nearly painless method with an average visual-analogue scale (VAS) score of 1.19. Additional advantages included reduced illumination time, shorter outpatient stays in the clinic, fewer adverse effects, and better patient compliance than with DLPDT alone.

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