Abstract

BackgroundTo assess the efficacy, clinical outcomes, visual acuity (VA), incidence of adverse effects, and complications of peripheral iris fixation of 3-piece acrylic IOLs in eyes lacking capsular support. Thirteen patients who underwent implantation and peripheral iris fixation of a 3-piece foldable acrylic PC IOL for aphakia in the absence of capsular support were followed after surgery. Clinical outcomes and macular SD-OCT (Cirrus OCT; Carl Zeiss Meditec, Germany) were analyzed.FindingsThe final CDVA was 20/40 or better in 8 eyes (62%), 20/60 or better in 12 eyes (92%), and one case of 20/80 due to corneal astigmatism and mild persistent edema. No intraoperative complications were reported. There were seven cases of medically controlled ocular hypertension after surgery due to the presence of viscoelastic in the AC. There were no cases of cystoid macular edema, chronic iridocyclitis, IOL subluxation, pigment dispersion, or glaucoma. Macular edema did not develop in any case by means of SD-OCT.ConclusionsWe think that this technique for iris suture fixation provides safe and effective results. Patients had substantial improvements in UDVA and CDVA. This surgical strategy may be individualized however; age, cornea status, angle structures, iris anatomy, and glaucoma are important considerations in selecting candidates for an appropriate IOL fixation method.

Highlights

  • To assess the efficacy, clinical outcomes, visual acuity (VA), incidence of adverse effects, and complications of peripheral iris fixation of 3-piece acrylic intraocular lenses (IOLs) in eyes lacking capsular support

  • Materials and methods After obtaining local Institutional Ethics Committee approval and informed consent from the participants, thirteen patients who underwent implantation and peripheral iris fixation of a 3-piece foldable acrylic posterior chamber (PC) IOL were followed after surgery

  • A 4.2 mm clear corneal incision was made superiorly, acetylcholine (Iloc, Sophia Laboratories, Guadalajara Mexico) was placed in the Anterior chamber (AC) followed by a combination of 4% sodium chondroitin sulfate and 1.65% sodium hyaluronate Ophthalmic Viscosurgical Device (OVD)

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Summary

Objectives

The purpose of the current study is to assess the efficacy, clinical outcomes, visual acuity (VA), incidence of adverse effects, and complications of peripheral iris fixation of 3-piece acrylic IOLs in eyes lacking capsular support

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