Authors: Steve A. Arshinoff, MD, FRCSC, Ilan Hofmann, PhD
Journal: J Cataract Refract Surg. 1998;24;814-820
Purpose: To compare the safety and efficacy of two sodium hyaluronate
viscoelastics -- I-Visc®Plus and Healon®GV -- in routine phacoemulsification and evaluate whether these more viscous and cohesive agents offer benefits compared to viscoelastics of standard viscosity and cohesion.
Setting: York Finch Eye Associates and York Finch General Hospital,
Toronto, Canada.
Methods: An unmasked, randomized, prospective clinical trial of 100 eyes of 100 patients having routine phacoemulisification with intraocular lens implantation was conducted comparing the safety and efficacy of I-Visc®Plus with those of Healon® GV. Preoperative and 6 hour, 1 and 5 days and 1 and 6 month postoperative assessments including acuity, corneal thickness, intraocular pressure, and surgeon assessment of the task-facilitating efficacy of the viscoelastics. Results were compared with those of a similar trial of I-Visc® and Healon®
Results: There were no statistically significant differences between the two treatment groups at any follow-up. The surgeon judged the two viscoelastics equivalent, although somewhat different in facilitating surgery. There was significantly less transient postoperative corneal thickening in the Healon®GV vs I-Visc®Plus group than in the Healon® vs I-Visc® group.
Conclusions: Healon® GV and I-Visc® Plus were safe and provided equal
outcomes based on the parameters assessed. I-Visc® Plus's higher zero-shear viscosity caused it to behave slightly differently than Healon® GV during surgery. More viscous, cohesive viscoelastics may increase surgical safety. |