Abstract

Purpose: To compare the effect of latanoprost 0.005% with that of a placebo (balanced salt solution [BSS®]) applied after phacoemulsification on intraocular pressure (IOP).Setting: Pasco Eye Institute, New Port-Ritchey, Florida, USA.Methods: A group of patients having cataract extraction by phacoemulsification was randomized following surgery to receive one drop of latanoprost 0.005% (1.5 μg) or a placebo (BSS). Exclusion critefia included ocular diagnosis in addition to cataract, previous eye surgery, history of glaucoma, previous use of glaucoma medications, or vitreous loss during surgery. Standard phacoemulsification was performed through a scleral tunnel: approach and a one-piece, poly(methyl methacrylate) intraocular lens implanted in the capsular bag. Approximately 24 hours after surgery, IOP was measured with a Goldmann applanation tonometer by the surgeon. The anterior chamber reaction was qualitatively graded from 1+ to 4+.Results: The study included 103 eyes (latanoprost = 53; control = 50). Latanoprost treatment resulted in significantly lower postoperative IOP (16.4 mm Hg ± 3.7 [SD]) than preoperative IOP (17.9 ± 3.0 mm Hg) (P < .025). There was no decrease in postoperative IOP in the control group (18.2 ± 3.5 mm Hg) compared with preoperative IOP (18.3 ± 2.6 mm Hg). When the two groups were compared, postoperative IOP after treatment witti latanoprost was significantly less than control IOP (P < .01). Preoperative IOP was not significantly different in the placebo and latanoprost groups. Anterior chamber reaction was not increased by latanoprost; it averaged 1 + in both groups.Conclusions: Latanoprost may pharmcologically enhance uveoscleral outflow immediately after cataract extraction, In this study, latanoprost was a safe, effective method of reducing postoperative IOP.

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