Heier J S, Topping T M, Baumann W, Dirks M S, Chern S
Ophthalmic Consultants of Boston, Boston, Massachusetts, USA.
Ophthalmology. 2000 Nov;107(11):2034-8;discussion 2039. doi: 10.1016/s0161-6420(00)00365-1.
To evaluate the efficacy of ketorolac tromethamine 0.5% ophthalmic solution, prednisolone acetate 1.0% ophthalmic solution, and ketorolac and prednisolone combination therapy in the treatment of acute, visually significant, cystoid macular edema (CME) occurring after cataract extraction surgery.
Randomized, double-masked, prospective trial.
Twenty-eight patients who had undergone cataract extraction and in whom clinical CME developed within 21 to 90 days after cataract surgery.
Patients were randomized to topical therapy with ketorolac (group K), prednisolone (group P), or ketorolac and prednisolone combination therapy (group C) four times daily. Treatment was continued until CME resolved or for 3 months, whichever occurred first. Treatment was then tapered over 3 weeks. Examinations were monthly and included Snellen visual acuity, contrast sensitivity, Amsler grid, slit-lamp examination, dilated fundus examination, and fluorescein angiography.
Twenty-six of 28 patients completed the study. Patients were enrolled an average of 48 days after surgery. The average improvements in Snellen visual acuity were as follows: 1.6 lines in group K, 1.1 lines in group P, and 3.8 lines in group C. This reached statistical significance for all visits when group C was compared with group P, and for visits 4 and 5 when group C was compared with group K. Group C reached a mean change of two lines or more by visit 2; at no time did either group K or P reach a mean two-line improvement. At no time was a significant difference detected between group K and P with regard to visual acuity or change from baseline. A two-line or more improvement in Snellen acuity was achieved in 16 of 26 patients (61%). Analysis by group revealed four of eight patients (50%) in group P, six of nine patients (67%) in group K, and eight of nine patients (89%) in group C who had achieved a two-line or more improvement. In patients who did improve two lines or more, improvement occurred an average of 2.75 months after initiating therapy in group P, 1.43 months in group K, and 1.33 months in group C. Improvements in contrast sensitivity and leakage on fluorescein angiography tended to mirror improvements in Snellen acuity.
Treatment of acute, visually significant pseudophakic CME with ketorolac and prednisolone combination therapy appears to offer benefits over monotherapy with either agent alone. Patients were more likely to experience recovery of two lines or more of visual acuity. Patients treated with combination therapy or ketorolac monotherapy responded more quickly than did patients treated with prednisolone alone.
评估0.5%酮咯酸氨丁三醇滴眼液、1.0%醋酸泼尼松龙滴眼液以及酮咯酸与泼尼松龙联合治疗对白内障摘除术后发生的急性、具有明显视力影响的黄斑囊样水肿(CME)的疗效。
随机、双盲、前瞻性试验。
28例接受了白内障摘除术且在白内障手术后21至90天内出现临床CME的患者。
患者被随机分为三组,分别接受每日四次的局部用药治疗,即酮咯酸组(K组)、泼尼松龙组(P组)或酮咯酸与泼尼松龙联合治疗组(C组)。治疗持续至CME消退或3个月,以先到者为准。然后在3周内逐渐减少用药量。每月进行检查,包括Snellen视力、对比敏感度、Amsler方格表、裂隙灯检查、散瞳眼底检查和荧光素血管造影。
28例患者中有26例完成了研究。患者平均在术后48天入组。Snellen视力的平均改善情况如下:K组为1.6行,P组为1.1行,C组为3.8行。C组与P组相比,所有随访时均具有统计学意义;C组与K组相比,在第4次和第5次随访时具有统计学意义。C组在第2次随访时平均视力变化达到或超过两行;K组和P组在任何时候均未达到平均两行的改善。K组和P组在视力或与基线相比的变化方面未检测到显著差异。26例患者中有16例(61%)Snellen视力提高了两行或更多。按组分析显示,P组8例患者中有4例(50%)、K组9例患者中有6例(67%)、C组9例患者中有8例(89%)视力提高了两行或更多。在视力提高两行或更多的患者中,P组在开始治疗后平均2.75个月出现改善,K组为1.43个月,C组为1.33个月。对比敏感度和荧光素血管造影渗漏情况的改善往往与Snellen视力的改善情况相似。
酮咯酸与泼尼松龙联合治疗急性、具有明显视力影响的人工晶状体眼CME似乎比单独使用任何一种药物的单一疗法更具优势。患者更有可能恢复两行或更多的视力。联合治疗组或酮咯酸单一治疗组的患者比单独使用泼尼松龙治疗的患者反应更快。