Correction of High Myopia with Foldable Artiflex Phakic Intraocular Lenses: 1 Year Follow-up Results

To assess the one year results of Artiflex Phakic intraocular lens (IOL) implantation in the treatment of high myopia. In this non-random interventional study, myopic patients with spherical equivalent worse than -5.0 diopters (D) who were not eligible for laser surgery were assessed. All patients...

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Main Authors: Hassan Hashemi, Mansour Taherzadeh, Mehdi Khabazkhoob
Format: Article
Language:English
Published: Tehran University of Medical Sciences 2013-09-01
Series:Acta Medica Iranica
Subjects:
Online Access:https://acta.tums.ac.ir/index.php/acta/article/view/4364
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spelling doaj-5b3c18f20e2c4ea4a05c433e08ab45042020-11-25T03:42:50ZengTehran University of Medical SciencesActa Medica Iranica0044-60251735-96942013-09-015194317Correction of High Myopia with Foldable Artiflex Phakic Intraocular Lenses: 1 Year Follow-up ResultsHassan Hashemi0Mansour Taherzadeh1Mehdi Khabazkhoob2Noor Ophthalmology Research Center, Noor Eye Hospital, Tehran, Iran.Noor Ophthalmology Research Center, Noor Eye Hospital, Tehran, Iran.Dezful University of Medical Sciences, Dezful, Iran. To assess the one year results of Artiflex Phakic intraocular lens (IOL) implantation in the treatment of high myopia. In this non-random interventional study, myopic patients with spherical equivalent worse than -5.0 diopters (D) who were not eligible for laser surgery were assessed. All patients had refraction, uncorrected and best corrected visual acuity tests (UCVA and BCVA), endothelial cell count (ECC), and measurement of the anterior chamber depth and intraocular pressure before surgery and at 1, 3, 6, and 12 months after surgery. Main outcome measures of this study were refractive stability, refractive predictability, safety, and efficacy after implanting Artiflex IOLs. We studied 53 eyes of 20 female and 8 male patients. The mean preoperative spherical equivalent was -10.22±3.02 D which reached -0.69±1.08 D one year after surgery (P<0.001). On the last follow-up visit, 75% of the eyes were within +0.5 D of emmetropia, 2 eyes had lost one line of BCVA, 18.75% had gained one line and 31.25% had gained 2 or more lines of BCVA. Others showed no change in BCVA. At one year after surgery, 72.2% of the eyes had 20/25 vision or better. The safety and efficacy indices were 1.16 and 1.05, respectively. ECC showed 3.04% decrease (P=0.176). In cases where laser surgery is not an option for myopic patients, use of Artiflex IOLs can have good results with acceptable safety and efficacy. https://acta.tums.ac.ir/index.php/acta/article/view/4364ArtiflexMyopiaPhakic intraocular lenses
collection DOAJ
language English
format Article
sources DOAJ
author Hassan Hashemi
Mansour Taherzadeh
Mehdi Khabazkhoob
spellingShingle Hassan Hashemi
Mansour Taherzadeh
Mehdi Khabazkhoob
Correction of High Myopia with Foldable Artiflex Phakic Intraocular Lenses: 1 Year Follow-up Results
Acta Medica Iranica
Artiflex
Myopia
Phakic intraocular lenses
author_facet Hassan Hashemi
Mansour Taherzadeh
Mehdi Khabazkhoob
author_sort Hassan Hashemi
title Correction of High Myopia with Foldable Artiflex Phakic Intraocular Lenses: 1 Year Follow-up Results
title_short Correction of High Myopia with Foldable Artiflex Phakic Intraocular Lenses: 1 Year Follow-up Results
title_full Correction of High Myopia with Foldable Artiflex Phakic Intraocular Lenses: 1 Year Follow-up Results
title_fullStr Correction of High Myopia with Foldable Artiflex Phakic Intraocular Lenses: 1 Year Follow-up Results
title_full_unstemmed Correction of High Myopia with Foldable Artiflex Phakic Intraocular Lenses: 1 Year Follow-up Results
title_sort correction of high myopia with foldable artiflex phakic intraocular lenses: 1 year follow-up results
publisher Tehran University of Medical Sciences
series Acta Medica Iranica
issn 0044-6025
1735-9694
publishDate 2013-09-01
description To assess the one year results of Artiflex Phakic intraocular lens (IOL) implantation in the treatment of high myopia. In this non-random interventional study, myopic patients with spherical equivalent worse than -5.0 diopters (D) who were not eligible for laser surgery were assessed. All patients had refraction, uncorrected and best corrected visual acuity tests (UCVA and BCVA), endothelial cell count (ECC), and measurement of the anterior chamber depth and intraocular pressure before surgery and at 1, 3, 6, and 12 months after surgery. Main outcome measures of this study were refractive stability, refractive predictability, safety, and efficacy after implanting Artiflex IOLs. We studied 53 eyes of 20 female and 8 male patients. The mean preoperative spherical equivalent was -10.22±3.02 D which reached -0.69±1.08 D one year after surgery (P<0.001). On the last follow-up visit, 75% of the eyes were within +0.5 D of emmetropia, 2 eyes had lost one line of BCVA, 18.75% had gained one line and 31.25% had gained 2 or more lines of BCVA. Others showed no change in BCVA. At one year after surgery, 72.2% of the eyes had 20/25 vision or better. The safety and efficacy indices were 1.16 and 1.05, respectively. ECC showed 3.04% decrease (P=0.176). In cases where laser surgery is not an option for myopic patients, use of Artiflex IOLs can have good results with acceptable safety and efficacy.
topic Artiflex
Myopia
Phakic intraocular lenses
url https://acta.tums.ac.ir/index.php/acta/article/view/4364
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AT mansourtaherzadeh correctionofhighmyopiawithfoldableartiflexphakicintraocularlenses1yearfollowupresults
AT mehdikhabazkhoob correctionofhighmyopiawithfoldableartiflexphakicintraocularlenses1yearfollowupresults
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