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Journal of Ophthalmology
Volume 2018, Article ID 1329874, 8 pages
https://doi.org/10.1155/2018/1329874
Research Article

Early Results with a New Posterior Chamber Phakic Intraocular Lens in Patients with High Myopia

1Beyoğlu Eye Research and Training Hospital, Bereketzade Mah., No. 2 Beyoglu, Istanbul, Turkey
2Dr. Sadi Konuk Bakirkoy Research and Training Hospital, Zuhuratbaba Mah., Tevfik Saglam Cad., No. 21 Bakirkoy, Istanbul, Turkey

Correspondence should be addressed to Dilek Yaşa; moc.liamg@2asaykelid

Received 28 February 2018; Accepted 3 May 2018; Published 19 June 2018

Academic Editor: Suphi Taneri

Copyright © 2018 Dilek Yaşa et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Purpose. To report clinical results of a foldable, hydrophilic acrylic, single-piece, injectable, posterior chamber phakic intraocular lens (pIOL). Material and Methods. Medical records of patients who underwent posterior chamber phakic IOL (Eyecryl Phakic IOL, Biotech Vision Care, Ahmedabad, India) implantation for surgical correction of myopia were retrospectively reviewed. Only patients with at least a one-year follow-up were included. Manifest refraction, uncorrected distance visual acuity (UDVA), corrected distance visual acuity (CDVA), endothelial cell density (ECD), and pIOL vault were analyzed at 1, 3, 6, and 12 months after surgery. Complications observed during and after surgery were also recorded. Results. The study included 58 eyes of 29 patients. Mean patient age was 32 ± 7 years. Spherical equivalent of manifest refraction was −13.41 ± 3.23 D preoperatively and −0.44 ± 0.55 D postoperatively. Preoperative CDVA was 0.29 ± 0.71 logMAR. Postoperative UDVA and CDVA were 0.21 ± 0.66 and 0.15 ± 0.69 logMAR, respectively, at the 12-month visit. At the 12-month visit, the efficacy index was 1.20 and the safety index was 1.39. Mean ECD was 2713 ± 339 cells/mm2 at the preoperative visit and 2608 ± 362 cells/mm2 at the 12-month visit (3.9% loss, ). ECD loss from 3 months to 12 months was not statistically significant. No significant cataract formation, significant endothelial cell loss, glaucoma, uveitis, or any other vision-threatening complication was observed. Conclusion. Based on postoperative experience, we have found that Eyecryl Phakic IOL is safe and effective for treating high myopia.