Prosdocimo Giovanni, Tassinari Giorgio, Sala Michele, Di Biase Arturo, Toschi Pier Giorgio, Gismondi Maurizio, Corbanese Ulisse
Department of Ophthalmology, Hospital of Conegliano, Conegliano, Italy.
J Cataract Refract Surg. 2003 Aug;29(8):1551-5. doi: 10.1016/s0886-3350(02)02051-5.
To compare the rates and morphologic features of posterior capsule opacification (PCO) after small-incision phacoemulsification and in-the-bag implantation of 2 foldable intraocular lenses (IOLs) over an 18-month follow-up.
Departments of Ophthalmology, Hospital of Conegliano, Conegliano, and Maggiore Hospital of Bologna, Bologna, Italy.
In an open clinical study, 78 cataract patients were randomly selected to have implantation of a silicone CeeOn Edge (Pharmacia) or acrylate AcrySof (Alcon) IOL after phacoemulsification cataract surgery. All the patients were operated on using a standard technique and in-the-bag IOL implantation. One eye in each patient was studied. Morphologic evaluation of PCO was performed using Evaluation of Posterior Capsule Opacification software.
At 18 months in the CeeOn Edge group, 36 eyes (90%) had a clear posterior capsule and 4 (10%) had PCO that did not affect visual acuity. In the AcrySof group, 26 eyes (68%) had a clear posterior capsule, 11 (29%) had PCO that did not affect visual acuity, and 1 (3%) had PCO with a decrease of 2 or more lines of visual acuity that required a neodymium:YAG laser capsulotomy. No eye developed Elschnig pearls or stretched folds in the bag. The postoperative best corrected visual acuity ranged from 0.8 to 1.0 in 96% in the CeeOn Edge group and in 92% in the AcrySof group. No IOL haze or discoloration was observed in the CeeOn Edge group. Mild IOL decentration and tilting occurred in 4 AcrySof eyes; however, no glistenings were found any AcrySof IOL.
Both the CeeOn Edge and AcrySof groups had a low incidence of PCO after an 18-month follow-up. The CeeOn Edge group had significantly less PCO than the AcrySof group. These results confirm that IOLs with square truncated edges create a barrier effect at the optic edge, reducing the overall incidence of PCO.
比较小切口超声乳化白内障吸除术联合两种可折叠人工晶状体(IOL)囊袋内植入术后18个月的后囊膜混浊(PCO)发生率及形态学特征。
意大利科内利亚诺医院眼科及博洛尼亚马焦雷医院眼科。
在一项开放性临床研究中,78例白内障患者在超声乳化白内障手术后被随机选择植入硅胶材质的CeeOn Edge(法玛西亚公司)或丙烯酸酯材质的AcrySof(爱尔康公司)IOL。所有患者均采用标准技术进行手术及囊袋内IOL植入。对每位患者的一只眼进行研究。使用后囊膜混浊评估软件对PCO进行形态学评估。
在CeeOn Edge组,术后18个月时,36只眼(90%)后囊膜清晰,4只眼(10%)出现不影响视力的PCO。在AcrySof组,26只眼(68%)后囊膜清晰,11只眼(29%)出现不影响视力的PCO,1只眼(3%)出现PCO且视力下降2行或更多行,需要进行钕:钇铝石榴石激光后囊膜切开术。没有眼出现Elschnig珠或囊袋内的皱襞。CeeOn Edge组96%、AcrySof组92%的患者术后最佳矫正视力在0.8至1.0之间。CeeOn Edge组未观察到IOL混浊或变色。4只植入AcrySof IOL的眼出现轻度IOL偏心和倾斜;然而,未在任何AcrySof IOL上发现闪辉现象。
CeeOn Edge组和AcrySof组在18个月随访后PCO发生率均较低。CeeOn Edge组的PCO明显少于AcrySof组。这些结果证实,边缘呈方形截短的IOL在光学边缘产生屏障效应,降低了PCO的总体发生率。