Department of Ophthalmology, Kim's Eye Hospital, Konyang University College of Medicine, 1, 34 Gil, Yeongshinro, Youngdeungpo-gu, Seoul, 07301, Republic of Korea.
Graefes Arch Clin Exp Ophthalmol. 2022 Oct;260(10):3285-3291. doi: 10.1007/s00417-022-05682-x. Epub 2022 Apr 29.
We aimed to investigate the difference in the treatment effects of 4.9% N-acetyl-aspartyl glutamic acid (NAAGA) and 0.05% cyclosporine A (CsA) eye drops in dry eye patients.
We retrospectively reviewed the medical records of 86 patients (86 eyes) who were diagnosed with dry eye and treated with NAAGA or CsA eye drops. Patients treated with NAAGA or CsA eye drops were designated as group A or B, respectively. We also calculated Ocular Surface Disease Index (OSDI), dry eye, and meibomian gland dysfunction (MGD) parameters before treatment and at 1 and 3 months after treatment. Eye drop discomfort was assessed by calculating visual analog scale (VAS) scores at 1 month and 3 months after treatment.
There were no significant differences in patients' demographics and OSDI, dry eye, and MGD parameters between the two groups. OSDI, dry eye, and MGD parameters at 1 month and 3 months after treatment were found to be improved in both groups. However, at 1 month after treatment, the dry eye and MGD parameters of group A, except for corneal fluorescein staining, showed more improvement than those of group B. Additionally, at 3 months after treatment, the lid margin abnormality score, corneal staining score, tear break-up time, and OSDI of group A were significantly lower than those of group B. VAS scores of group A at 1 and 3 months after treatment were significantly lower than those of group B.
Treatment with NAAGA eye drops was effective in dry eye patients and demonstrated faster treatment response and less discomfort during application than CsA eye drops.
本研究旨在探讨 4.9% N-乙酰天门冬氨酸谷氨酸(NAAGA)和 0.05%环孢素 A(CsA)滴眼液治疗干眼症患者的疗效差异。
回顾性分析 86 例(86 眼)干眼症患者的病历资料,患者分别接受 NAAGA 或 CsA 滴眼液治疗,将接受 NAAGA 或 CsA 滴眼液治疗的患者分别设为 A 组和 B 组。分别于治疗前及治疗后 1 个月、3 个月计算眼表疾病指数(OSDI)、干眼及睑板腺功能障碍(MGD)相关参数。于治疗后 1 个月和 3 个月采用视觉模拟评分(VAS)评估眼滴液不适。
两组患者的一般资料及 OSDI、干眼、MGD 相关参数比较,差异均无统计学意义(P>0.05)。两组治疗后 1 个月、3 个月 OSDI、干眼及 MGD 相关参数均较治疗前改善(P<0.05),但 A 组治疗后 1 个月除角膜荧光素染色外,其余干眼及 MGD 相关参数均优于 B 组,治疗后 3 个月 A 组的眼睑边缘异常评分、角膜染色评分、泪膜破裂时间、OSDI 均低于 B 组,VAS 评分均低于 B 组,差异均有统计学意义(P<0.05)。
NAAGA 滴眼液治疗干眼症的疗效确切,且起效更快,用药后不适感更低。