J Korean Ophthalmol Soc.  2006 Sep;47(9):1394-1400.

Clinical Results of Single-Piece Hydrophilic IOL after Cataract Surgery

Affiliations
  • 1Department of Ophthalmology, University of Ulsan College of Medicine, Asan Medical Center, Seoul, Korea. hwtchah@amc.seoul.kr

Abstract

PURPOSE: To compare the clinical results of single-piece hydrophilic acrylic intraocular lenses (IOL) (Akreos AdaptTM, B&L) with those of three-piece hydrophobic acrylic IOL (Sensar(R), AMO) after cataract surgery.
METHODS
This study was a prospective case-control study in which Akreos lenses were implanted for the experimental group and Sensar lenses were implanted for the control group. All surgical procedures were performed by the same surgeon. Best corrected visual acuity (BCVA), change of anterior chamber depth, degree of posterior capsule opacification (PCO), higher-order aberration, and contrast sensitivity (CS) were examined. Measurements were performed by masked examiners prior to the surgery and at 1 week, 1 month, 3 months, and 6 months, postoperatively.
RESULTS
There were no statistically significant differences in BCVA, CS or PCO between the two groups. The Refractive error was -0.17+/-0.67D in the experimental group and -0.02+/-0.41D in the control group at 6 months, postoperatively. During the first postoperative month, forward movement of both IOLs was detected. Afterward, both IOLs moved backwards until 6 months. Fourth-order spherical aberrations were significantly higher in the Akreos group (p<0.05) at 1 month, 3 months, and 6 months, postoperatively.
CONCLUSIONS
The clinical results for Akreos IOL and Sensar IOL were similar in most aspects.

Keyword

Akreos Adapt(TM); Hydrophilic acrylic lens; Spherical aberration

MeSH Terms

Anterior Chamber
Capsule Opacification
Case-Control Studies
Cataract*
Contrast Sensitivity
Lenses, Intraocular
Masks
Prospective Studies
Refractive Errors
Visual Acuity
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