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- W2795508719 abstract "PURPOSE: To evaluate the efficacy, predictability and safety of myopic phakic angle-supportedintraocular lens for correction of moderate to high myopia.METHODS: In a prospective non comparative interventional case series, outcomes in 42eyes, with a preoperative mean spherical equivalent of -11.00 diopters (D) ± 2.79, wereanalyzed 12 months after the implantation of the AcrySof Cachet. They comprised uncorrectedvisual acuity (UCVA), best corrected visual acuity (BCVA), slit-lamp examination,refraction, endothelial cell count, IOL rotation and position.RESULTS: The mean UCVA and BCVA after AcrySof Cachet implantation were 0.80±0.25and 0.92±0.18, respectively (efficacy index: 0.94). No eyes lost ≥1 lines, 16 eyes did notchange after surgery, 11 eyes gained 1 line and 15 eyes gained ≥ 1 lines of visual acuity.(safety index: 1.08). All eyes were within ±1.00D of the desired refraction and 83.3%within ±0.50D. The mean postoperative spherical equivalent was -0.24±0.36D. The meanpercentage change in central endothelial cell density from the preoperative visit to 1 yearpost-surgery was -6.16±4.29%. The mean value of misalignment was 3.97±2.91 degrees.OCT Visante showed a mean central lens-endothelium value of 2.09±0.26 mm, a centrallens-anterior crystalline lens capsule value of 0.91±0.18 mm and a lens edge-endotheliumof 1.16±0.31 mm. No pupil ovalization, pupillary block, or retinal detachment events wereobserved.CONCLUSIONS: The AcrySof phakic angle-supported lens implantation was a safe, effective,and predictable procedure for the correction of moderate and high myopia" @default.
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- W2795508719 date "2012-01-01" @default.
- W2795508719 modified "2023-09-24" @default.
- W2795508719 title "AcrySof Phakic IOL for Correction of Moderate-to-High Myopia: 1 Year Results" @default.
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