Sakata Rei, Sakisaka Toshihiro, Matsuo Hiroshi, Miyata Kazunori, Aihara Makoto
1 Department of Ophthalmology, University of Tokyo School of Medicine, Tokyo, Japan .
2 Matsuo Eye Clinic, Tokyo, Japan .
J Ocul Pharmacol Ther. 2016 Jul-Aug;32(6):365-70. doi: 10.1089/jop.2015.0159. Epub 2016 Jun 13.
The main purpose was to determine whether a nonsteroidal anti-inflammatory drug (NSAID) ophthalmic solution would affect the intraocular pressure (IOP)-lowering effect of a benzalkonium chloride (BAK)-free prostaglandin analog, travoprost. The secondary purpose was to confirm the IOP-lowering effect of BAK-free travoprost on the diurnal IOP.
This was a prospective, randomized, double-blind, placebo-controlled 1-month trial. After baseline diurnal IOP was confirmed, travoprost was administered once daily to both eyes. Bromfenac sodium hydrate was then randomly assigned to one eye, while flavin adenine dinucleotide sodium was applied to the other eye as a control. Both solutions were administered twice daily. IOP was measured three times daily (8:00, 14:00, and 20:00). The IOP of both groups was compared using Student's t-test. The effect of NSAID on IOP was investigated by repeated measures analysis of variance (ANOVA).
Twenty-eight normal Japanese subjects (mean age, 36.6 years) completed the study. After the start of travoprost, remarkable IOP lowering was gained and it settled to 10-11 mmHg. The diurnal IOPs of the NSAID group showed similar tendencies to that of the control group (P = 0.69-1.0). In a 1-month period, the range of IOP reductions compared with the baseline IOP of both groups showed no significant difference (P = 0.76-0.92). NSAID did not have an influence on IOP (F-value = 0.0036, P = 0.95).
Although BAK-free travoprost showed a powerful IOP-lowering effect in diurnal and 1-month readings, even in eyes with an IOP of <13 mmHg, the NSAID ophthalmic solution did not affect its IOP-lowering effect.
主要目的是确定一种非甾体抗炎药(NSAID)眼药水是否会影响不含苯扎氯铵(BAK)的前列腺素类似物曲伏前列素降低眼压(IOP)的效果。次要目的是确认不含BAK的曲伏前列素对日间眼压的降低效果。
这是一项前瞻性、随机、双盲、安慰剂对照的1个月试验。确认基线日间眼压后,双眼每日一次给予曲伏前列素。然后将水合溴芬酸钠随机分配至一只眼,而另一只眼应用黄素腺嘌呤二核苷酸钠作为对照。两种溶液均每日给药两次。每日三次(8:00、14:00和20:00)测量眼压。使用学生t检验比较两组的眼压。通过重复测量方差分析(ANOVA)研究NSAID对眼压的影响。
28名正常日本受试者(平均年龄36.6岁)完成了研究。开始使用曲伏前列素后,眼压显著降低并稳定在10 - 11 mmHg。NSAID组的日间眼压与对照组显示出相似趋势(P = 0.69 - 1.0)。在1个月期间,两组与基线眼压相比的眼压降低范围无显著差异(P = 0.76 - 0.92)。NSAID对眼压没有影响(F值 = 0.0036,P = 0.95)。
尽管不含BAK的曲伏前列素在日间和1个月的测量中显示出强大的降眼压效果,即使在眼压<13 mmHg的眼中,NSAID眼药水也不会影响其降眼压效果。