Department of Ophthalmology, Shanghai Tenth People's Hospital, Tongji University School of Medicine, Shanghai, P.R. China.
Department of Ophthalmology, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, P.R. China
In Vivo. 2023 Nov-Dec;37(6):2829-2834. doi: 10.21873/invivo.13397.
BACKGROUND/AIM: To evaluate the clinical efficacy of combination therapy with diquafosol sodium and sodium hyaluronate in dry eye patients after small incision lenticule extraction (SMILE).
A prospective randomized controlled study was conducted on consecutive patients who were diagnosed with dry eye disease (DED) and ready to accept SMILE from January 2021 to December 2021. The participants were randomly allocated to either a combination with diquafosol sodium 3% and sodium hyaluronate 0.3% group (DQS group, n=40) or a sodium hyaluronate 0.3% group (HA group, n=41). Dry eye disease parameters included tear film break-up time (TBUT), Shirmer I test (SIT), corneal and conjunctival fluorescein staining score (FS score), and Ocular Surface Disease Index (OSDI); tests were conducted before surgery and at 1 week, 1 month, and 3 months after surgery.
At 1 week after surgery, there were no statistically significant overall differences in DED parameters between the 2 groups. At postoperative month 1, the FS score was significantly lower in the DQS group than in the HA group (1.20±1.06 vs. 1.83±1.41 respectively, p=0.026). At 3 months after the surgery, the DQS group was significantly superior to the HA group in OSDI (12.98±7.29 vs. 16.82±8.25, p=0.029), TBUT (5.83±2.02 vs. 4.24±0.94, p=0.0002), and SIT (7.75±3.92 vs. 5.24±3.42, p=0.003).
Our study showed that combination therapy with diquafosol and hyaluronate was beneficial for improving both signs and symptoms of dry eye patients after small incision lenticule extraction.
背景/目的:评估双氯非酸钠和透明质酸钠联合治疗在微创透镜提取(SMILE)后干眼症患者中的临床疗效。
对 2021 年 1 月至 2021 年 12 月连续诊断为干眼病(DED)并准备接受 SMILE 的患者进行前瞻性随机对照研究。将参与者随机分配至双氯非酸钠 3%和透明质酸钠 0.3%联合治疗组(DQS 组,n=40)或透明质酸钠 0.3%组(HA 组,n=41)。干眼疾病参数包括泪膜破裂时间(TBUT)、泪液分泌试验(SIT)、角膜和结膜荧光素染色评分(FS 评分)和眼表面疾病指数(OSDI);术前及术后 1 周、1 个月和 3 个月进行测试。
术后 1 周,两组 DED 参数总体无统计学差异。术后 1 个月,DQS 组 FS 评分明显低于 HA 组(分别为 1.20±1.06 和 1.83±1.41,p=0.026)。术后 3 个月,DQS 组 OSDI(12.98±7.29 对 16.82±8.25,p=0.029)、TBUT(5.83±2.02 对 4.24±0.94,p=0.0002)和 SIT(7.75±3.92 对 5.24±3.42,p=0.003)均明显优于 HA 组。
本研究表明,双氯非酸钠和透明质酸钠联合治疗有利于改善微创透镜提取术后干眼症患者的症状和体征。