Aguilar Alejandro J, Marquez Maria I, Albera Paula A, Tredicce Jorge L, Berra Alejandro
Universidad de Buenos Aires, Buenos Aires, Argentina.
Clin Ophthalmol. 2014 Nov 25;8:2365-72. doi: 10.2147/OPTH.S70623. eCollection 2014.
To evaluate the ability of Systane(®) Balance (SYSB) administered four times per day for 4 weeks to increase noninvasive tear film break-up time (NITFBUT) over baseline compared with a saline (SAL) control in patients with lipid-deficient dry eye (DE).
Patients aged ≥18 years with DE and evidence of meibomian gland dysfunction (ie, abnormal gland expression and missing meibomian glands) were included in this randomized, parallel-group, controlled, investigator-masked comparison study. Patients were randomized to SYSB or SAL four times daily for 4 weeks. The primary efficacy variable was mean change in NITFBUT from baseline at week 4. Ocular surface staining, goblet cell density, and meibomian gland expression were also assessed. Safety assessments included adverse events (AEs), best-corrected visual acuity, and ocular signs.
A total of 49 patients received study treatments (SYSB, n=25; SAL, n=24). Most patients were women (67.4%) and Caucasian (63.3%); mean ± standard deviation (SD) age was 44±19 years. DE characteristics at baseline were similar between groups. After 4 weeks of treatment, the mean ± SD NITFBUT increase from baseline was significantly greater with SYSB (2.83±0.74 seconds) compared with SAL (0.66±0.55 seconds; P<0.001, t-test). Improvements in conjunctival and corneal staining, percentage of patients with increased goblet cell density, and meibomian gland expression were also observed with 4 weeks of SYSB over SAL. No AEs were reported for either treatment group; best-corrected visual acuity and ocular signs remained stable or improved compared with baseline.
SYSB restored tear film stability, improved ocular surface healing, and improved meibomian gland functionality after 4 weeks of use in patients with lipid-deficient DE. No AEs were reported with either SYSB or SAL.
评估每天给药4次、持续4周的思然平衡滴眼液(Systane Balance,SYSB)与生理盐水对照(SAL)相比,能否使脂质缺乏型干眼症(DE)患者的无创泪膜破裂时间(NITFBUT)较基线水平增加。
年龄≥18岁、患有DE且有睑板腺功能障碍证据(即腺体表达异常和睑板腺缺失)的患者纳入了这项随机、平行组、对照、研究者设盲的比较研究。患者被随机分为SYSB组或SAL组,每天给药4次,持续4周。主要疗效变量是第4周时NITFBUT相对于基线的平均变化。还评估了眼表染色、杯状细胞密度和睑板腺表达。安全性评估包括不良事件(AE)、最佳矫正视力和眼部体征。
共有49例患者接受了研究治疗(SYSB组,n = 25;SAL组,n = 24)。大多数患者为女性(67.4%)和白种人(63.3%);平均±标准差(SD)年龄为44±19岁。两组基线时的DE特征相似。治疗4周后,与SAL组(0.66±0.55秒;P<0.001,t检验)相比,SYSB组NITFBUT相对于基线的平均±SD增加显著更大(2.83±0.74秒)。与SAL组相比,使用SYSB 4周后,结膜和角膜染色、杯状细胞密度增加的患者百分比以及睑板腺表达也有改善。两个治疗组均未报告AE;与基线相比,最佳矫正视力和眼部体征保持稳定或有所改善。
脂质缺乏型DE患者使用SYSB 4周后,泪膜稳定性得到恢复,眼表愈合得到改善,睑板腺功能得到改善。SYSB组和SAL组均未报告AE。