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强脉冲光联合局部 0.05%环孢素 A 滴眼液治疗干燥综合征相关干眼的疗效。

The effect of intense pulsed light combined with topical 0.05% Cyclosporin A eyedrops in the treatment of Sjögren's syndrome related dry eye.

机构信息

Eye Center, The Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, Zhejiang, China.

Zhejiang Provincial Key Laboratory of Ophthalmology, Hangzhou, Zhejiang, China.

出版信息

Expert Rev Clin Immunol. 2024 Oct;20(10):1261-1267. doi: 10.1080/1744666X.2024.2358157. Epub 2024 May 27.

Abstract

OBJECTIVES

This study aimed to assess the effectiveness and safety of intense pulsed light (IPL) therapy plus topical 0.05% cyclosporine A (CsA) eye drops to treat Sjögren's Syndrome-related dry eyes (SS-DE).

RESEARCH DESIGN AND METHODS

In this prospective, randomized trial included, 60 individuals with SS-DE symptoms were randomized to receive topical eye drops containing either 0.1% sodium hyaluronate (Group S) or 0.05% CsA (Group C) plus IPL therapy. Before the first treatment (baseline), and at 12, 16, and 20 weeks after treatment commencement, we assessed the best corrected visual acuity (BCVA), the Ocular Surface Disease Index (OSDI) score, the Schirmer I test (SIT), noninvasive tear breakup time (NBUT), corneal fluorescein staining (CFS), meibomian gland (MG) dropout, lid margin abnormality, MG expressibility, and meibum quality.

RESULTS

Both groups showed significant improvements in the OSDI, NBUT, CFS, MG expressibility, and meibum quality (all  < 0.05). Group C showed a greater increase in OSDI, NBUT, MG expressibility, and meibum quality (all  < 0.05). Moreover, SIT and lid margin abnormalities significantly improved in Group C (both  < 0.05), but not in Group S.

CONCLUSION

Treatment with 0.05% CsA eyedrops plus IPL therapy could significantly reduce the issues and physical discomfort of patients with SS-DE.

CLINICAL TRIAL

Registered on 20 July 2021, with the registration number ChiCTR2100049059.

摘要

目的

本研究旨在评估强脉冲光(IPL)联合局部 0.05%环孢素 A(CsA)滴眼液治疗干燥综合征相关干眼症(SS-DE)的有效性和安全性。

研究设计与方法

在这项前瞻性、随机试验中,纳入 60 例 SS-DE 症状患者,随机分为局部含 0.1%透明质酸钠(S 组)或 0.05%CsA(C 组)滴眼液联合 IPL 治疗组。在首次治疗(基线)前和治疗开始后 12、16 和 20 周,评估最佳矫正视力(BCVA)、眼表疾病指数(OSDI)评分、泪膜破裂时间(SIT)、非侵入性泪膜破裂时间(NBUT)、角膜荧光素染色(CFS)、睑板腺(MG)缺失、眼睑边缘异常、MG 分泌能力和睑脂质量。

结果

两组 OSDI、NBUT、CFS、MG 分泌能力和睑脂质量均显著改善(均  < 0.05)。C 组 OSDI、NBUT、MG 分泌能力和睑脂质量改善更为显著(均  < 0.05)。此外,C 组 SIT 和眼睑边缘异常显著改善(均  < 0.05),但 S 组无明显改善。

结论

0.05%CsA 滴眼液联合 IPL 治疗可显著减轻 SS-DE 患者的不适症状。

临床试验

于 2021 年 7 月 20 日注册,注册号 ChiCTR2100049059。

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