Department of Biomedical and Surgical Sciences, Ophthalmology Section, University of Perugia , Perugia, Italy.
Curr Eye Res. 2020 Sep;45(9):1089-1093. doi: 10.1080/02713683.2020.1725061. Epub 2020 Feb 4.
To compare, using laser flare meter (LFM), the efficacy of topical nepafenac 0.1, % and diclofenac 0.1% ophthalmic solution in the control of anterior chamber inflammation after uncomplicated cataract surgery.
Patients undergoing phacoemulsification for age-related cataract were recruited. Complete evaluation with visual acuity, slit-lamp examination, endothelial cell density, intraocular pressure, retinal tomography and anterior chamber flare evaluation was performed before surgery and 1, 15, 30 and 60 days after surgery. Patients were randomly assigned to receive topical diclofenac 0.1% 4 times a day for four weeks or nepafenac 0.1% 3 times a day for three weeks in addition to topical steroids and antibiotic.
64 (31 males, mean age 77.3 ± 5.9) patients were enrolled. Half of them were randomly assigned to group A (diclofenac 0.1%) and half to group B (nepafenac 0.1%). There was a statistically significant visual acuity improvement postoperatively in both groups, with no statistical difference between the groups. Intraocular pressure, corneal thickness, endothelial cells count and macular thickness parameters didn't significantly vary between before and after surgery. One-day after surgery, aqueous flare was significantly higher (22,27 ± 9,25 ph/ms in group A and 22,36 ± 7,47 in group B) than before surgery (14,59 ± 7,16 ph/ms in group A and 11,84 ± 4,44 in group B) in both groups, then declining in the first month and reaching preoperative levels again by 2 months in both groups. In group B, LFM values at 15 and 30 days after surgery were significantly lower (13,59 ± 4,80 and 14,07 ± 5,01) than in group A (17,00 ± 6,97 and 16,96 ± 6,13).
Nepafenac ensured a better inflammation control than diclofenac during the first month.
使用激光前房闪烁仪(LFM)比较局部应用奈帕芬酸 0.1%和双氯芬酸钠 0.1%滴眼液在控制单纯白内障术后前房炎症方面的疗效。
招募接受超声乳化白内障吸除术的年龄相关性白内障患者。在手术前和手术后 1、15、30 和 60 天进行视力、裂隙灯检查、内皮细胞密度、眼压、视网膜断层扫描和前房闪烁评估的完整评估。患者被随机分配接受局部应用双氯芬酸钠 0.1%,每天 4 次,持续 4 周,或奈帕芬酸 0.1%,每天 3 次,持续 3 周,同时使用局部皮质类固醇和抗生素。
共纳入 64 名(31 名男性,平均年龄 77.3±5.9 岁)患者。其中一半患者被随机分配至 A 组(双氯芬酸钠 0.1%),另一半患者被分配至 B 组(奈帕芬酸 0.1%)。两组患者术后视力均有显著提高,两组间无统计学差异。术后眼压、角膜厚度、内皮细胞计数和黄斑厚度参数与术前相比均无显著差异。术后第 1 天,两组房水闪烁均明显升高(A 组为 22.27±9.25 个/ph/ms,B 组为 22.36±7.47 个/ph/ms),高于术前(A 组为 14.59±7.16 个/ph/ms,B 组为 11.84±4.44 个/ph/ms),然后在第 1 个月下降,两组均在 2 个月时恢复到术前水平。B 组术后 15 天和 30 天的 LFM 值明显低于 A 组(13.59±4.80 和 14.07±5.01)。
奈帕芬酸在术后 1 个月内的炎症控制效果优于双氯芬酸钠。