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低水平光疗法治疗干眼症患者的效果:一项前瞻性、随机、观察者设盲试验。

Effect of low-level light therapy in patients with dry eye: a prospective, randomized, observer-masked trial.

机构信息

Department of Ophthalmology, Dankook University Hospital, College of Medicine, Dankook University, Cheonan, Republic of Korea.

Department of Biomedical Engineering, School of Medicine, Dankook University, Cheonan, Republic of Korea.

出版信息

Sci Rep. 2022 Mar 4;12(1):3575. doi: 10.1038/s41598-022-07427-6.

Abstract

To evaluate the efficacy of low-level light therapy (LLLT) with near-infrared light-emitting diodes (LED-LLLT) for the treatment of dry eye. 40 patients were randomly assigned with a 1:1 allocation ratio to receive LED-LLLT (LLLT group, n = 20) or placebo treatment (placebo group, n = 20). Patients in the LLLT group received LLLT twice a week for 3 weeks, for a total of 6 treatment sessions. The primary endpoint was the changes in the fluorescein corneal staining (FCS) score. The secondary endpoints were the changes in the ocular surface disease index (OSDI) score, lissamine green conjunctival staining (LGCS) scores, tear film break-up time (TBUT), Schirmer test, and the meibomian gland dysfunction (MGD) index. These were evaluated before treatment and 4 weeks after start of treatment. The mean difference of score change in primary endpoint revealed significant improvement in the LLLT group, compared to the placebo. Among secondary endpoints, LGCS, Schirmer's test, upper meibography scores showed significant improvements, while TBUT, lid debris, lid swelling, lid telangiectasia, meibomian gland secretion and expressibility scores had slight improvement without significant differences. No serious adverse events were observed. The use of LED-LLLT for the treatment of dry eye and MGD appears to be safe and beneficial.

摘要

评估近红外光发光二极管(LED-LLLT)低水平光疗治疗干眼症的疗效。40 名患者按 1:1 的比例随机分配,接受 LED-LLLT(LLLT 组,n=20)或安慰剂治疗(安慰剂组,n=20)。LLLT 组患者每周接受 LLLT 治疗 2 次,共 6 个疗程,为期 3 周。主要终点是荧光素角膜染色(FCS)评分的变化。次要终点是眼表疾病指数(OSDI)评分、丽丝胺绿结膜染色(LGCS)评分、泪膜破裂时间(TBUT)、泪液分泌试验和睑板腺功能障碍(MGD)指数的变化。这些指标在治疗前和治疗开始后 4 周进行评估。主要终点评分变化的平均差异显示,与安慰剂相比,LLLT 组有显著改善。在次要终点中,LGCS、Schirmer 测试、上睑板腺评分均有显著改善,而 TBUT、睑缘碎屑、眼睑肿胀、眼睑毛细血管扩张、睑板腺分泌和表达评分略有改善,但无显著差异。未观察到严重不良事件。LED-LLLT 治疗干眼症和 MGD 似乎是安全且有益的。

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