Koch D D, Liu J F, Glasser D B, Merin L M, Haft E
Cullen Eye Institute, Department of Ophthalmology, Baylor College of Medicine, Houston, Texas.
Am J Ophthalmol. 1993 Feb 15;115(2):188-201. doi: 10.1016/s0002-9394(14)73923-6.
We conducted a prospective, randomized trial comparing the endothelial protective effects of Healon (Kabi Pharmacia Ophthalmics, Inc., Monrovia, California) and Viscoat (Alcon Surgical, Inc., Ft. Worth, Texas) in 59 eyes of 59 patients undergoing iris-plane or posterior-chamber phacoemulsification with posterior-chamber lens implantation. We evaluated postoperative central and superior changes in corneal thickness and corneal endothelial cell density, coefficient of variation in cell size, and percentage of hexagons. In the overall series, at one day postoperatively, corneal thickness increased 17% centrally and superiorly in eyes receiving Healon compared to 12% centrally and 11% superiorly in eyes receiving Viscoat (P < .05). Sixteen weeks postoperatively, superior endothelial cell loss was 11.6% in eyes receiving Healon compared to 2.1% in eyes receiving Viscoat (P < .01). In the iris-plane phacoemulsification group, superior cell loss at week 16 was 13.8% in eyes receiving Healon and 0.5% in eyes receiving Viscoat (P < .04). In the posterior-chamber phacoemulsification group, there were no significant differences between the Healon and Viscoat subgroups. Comparing the surgical techniques, in the Healon group, central cell loss at week 16 was 13.8% in the iris-plane phacoemulsification subgroup and 0.6% in the posterior-chamber phacoemulsification subgroup (P < .03), and coefficient of variation in cell size increased 3.7% in the iris-plane subgroup and decreased 6.8% in the posterior-chamber subgroup (P < .04). In the Viscoat group, there were no significant differences between surgical techniques at week 16. Viscoat provided greater corneal endothelial protection than Healon during iris-plane phacoemulsification. In eyes receiving Healon, posterior-chamber phacoemulsification resulted in less corneal endothelial trauma than the iris-plane technique.
我们进行了一项前瞻性随机试验,比较了Healon(加利福尼亚州蒙罗维亚的卡比制药眼科公司)和Viscoat(得克萨斯州沃思堡的爱尔康外科公司)对59例接受虹膜平面或后房型超声乳化联合后房型人工晶状体植入术患者的59只眼睛的内皮保护作用。我们评估了术后角膜厚度、角膜内皮细胞密度、细胞大小变异系数和六边形细胞百分比在中央和上方的变化。在整个系列中,术后一天,接受Healon的眼睛中央角膜厚度增加17%,上方增加17%,而接受Viscoat的眼睛中央增加12%,上方增加11%(P<.05)。术后16周,接受Healon的眼睛上方内皮细胞损失为11.6%,而接受Viscoat的眼睛为2.1%(P<.01)。在虹膜平面超声乳化组中,术后16周接受Healon的眼睛上方细胞损失为13.8%,接受Viscoat的眼睛为0.5%(P<.04)。在后房型超声乳化组中,Healon和Viscoat亚组之间没有显著差异。比较手术技术,在Healon组中,术后16周虹膜平面超声乳化亚组中央细胞损失为13.8%,后房型超声乳化亚组为0.6%(P<.03),虹膜平面亚组细胞大小变异系数增加3.7%,后房型亚组减少6.8%(P<.04)。在Viscoat组中,术后16周手术技术之间没有显著差异。在虹膜平面超声乳化过程中,Viscoat比Healon提供了更好的角膜内皮保护。在接受Healon的眼睛中,后房型超声乳化比虹膜平面技术导致的角膜内皮损伤更少。