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Lasik as a Solution for High Hypermetropia

AIM: To evaluate safety and efficacy of Laser in situ Keratomileusis (LASIK) procedure for the correction of high hypermetropia. METHODS: Retrospective study of 160 patients (266 eyes) who underwent LASIK procedure for the correction of hypermetropia between +3.00 and +7.00 diopters(D) and cylinder...

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Autores principales: Biscevic, Alma, Pidro, Ajla, Pjano, Melisa Ahmedbegovic, Grisevic, Senad, Ziga, Nina, Bohac, Maja
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Academy of Medical Sciences of Bosnia and Herzegovina 2019
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6643362/
https://www.ncbi.nlm.nih.gov/pubmed/31402804
http://dx.doi.org/10.5455/medarh.2019.73.191-194
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author Biscevic, Alma
Pidro, Ajla
Pjano, Melisa Ahmedbegovic
Grisevic, Senad
Ziga, Nina
Bohac, Maja
author_facet Biscevic, Alma
Pidro, Ajla
Pjano, Melisa Ahmedbegovic
Grisevic, Senad
Ziga, Nina
Bohac, Maja
author_sort Biscevic, Alma
collection PubMed
description AIM: To evaluate safety and efficacy of Laser in situ Keratomileusis (LASIK) procedure for the correction of high hypermetropia. METHODS: Retrospective study of 160 patients (266 eyes) who underwent LASIK procedure for the correction of hypermetropia between +3.00 and +7.00 diopters(D) and cylinder up to 2.00D from January 2013 and August 2015. All ablations were performed with Wavelight Allegretto Eye-Q400Hzexcimer laser (Alcon, Forth Worth, TX, USA) with aberration free module and were centered on a corneal vertex. All flaps were made with Moria M2 (Moria, Antony, France) mechanical microkeratome (90μm head). Preoperative and postoperative uncorrected and corrected distant visual acuity (UDVA, CDVA), spherical equivalent (SE) and a berrometry for 5mm pupil were measured. Measurements were taken at 1 week, 1,3,6 and 12 months after the surgery. Wilcoxon Signed Ranks Test was used for statistical analysis. RESULTS: Postoperative UDVA was lower than preoperative CDVA at 1 week(p=0.001), at 1 month there was no difference (p=0.099), and at 3,6 and 12 months UDVA was better (p<0.0001). Preoperative SE was 4.69±1.20D (+3.75 to +7.50D). At 1 week SE was 0.03±0.67D (-0.50 to +0.63D), while at 1 year regressed to 0.58±0.56D (+0.25 to +0.88D). Sphere shifted from negative values targeted in treatment planning to compensate for regression to positive values. There was significant difference in SE at every time point (p<0.0005). There was a significant increase in coma (p<0.0001), trefoil (p<0.0001, p=0.0006) and spherical aberration (p=0.022, p=0.0052) at 1 week and 1 month postoperatively, without change throughout the rest of follow up. CONCLUSION: LASIK for high hypermetropia showed satisfactory results in postoperative refraction with reasonable regression without significant loss of lines of visual acuity. However, more test are necessary to asses optical quality.
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spelling pubmed-66433622019-08-09 Lasik as a Solution for High Hypermetropia Biscevic, Alma Pidro, Ajla Pjano, Melisa Ahmedbegovic Grisevic, Senad Ziga, Nina Bohac, Maja Med Arch Original Paper AIM: To evaluate safety and efficacy of Laser in situ Keratomileusis (LASIK) procedure for the correction of high hypermetropia. METHODS: Retrospective study of 160 patients (266 eyes) who underwent LASIK procedure for the correction of hypermetropia between +3.00 and +7.00 diopters(D) and cylinder up to 2.00D from January 2013 and August 2015. All ablations were performed with Wavelight Allegretto Eye-Q400Hzexcimer laser (Alcon, Forth Worth, TX, USA) with aberration free module and were centered on a corneal vertex. All flaps were made with Moria M2 (Moria, Antony, France) mechanical microkeratome (90μm head). Preoperative and postoperative uncorrected and corrected distant visual acuity (UDVA, CDVA), spherical equivalent (SE) and a berrometry for 5mm pupil were measured. Measurements were taken at 1 week, 1,3,6 and 12 months after the surgery. Wilcoxon Signed Ranks Test was used for statistical analysis. RESULTS: Postoperative UDVA was lower than preoperative CDVA at 1 week(p=0.001), at 1 month there was no difference (p=0.099), and at 3,6 and 12 months UDVA was better (p<0.0001). Preoperative SE was 4.69±1.20D (+3.75 to +7.50D). At 1 week SE was 0.03±0.67D (-0.50 to +0.63D), while at 1 year regressed to 0.58±0.56D (+0.25 to +0.88D). Sphere shifted from negative values targeted in treatment planning to compensate for regression to positive values. There was significant difference in SE at every time point (p<0.0005). There was a significant increase in coma (p<0.0001), trefoil (p<0.0001, p=0.0006) and spherical aberration (p=0.022, p=0.0052) at 1 week and 1 month postoperatively, without change throughout the rest of follow up. CONCLUSION: LASIK for high hypermetropia showed satisfactory results in postoperative refraction with reasonable regression without significant loss of lines of visual acuity. However, more test are necessary to asses optical quality. Academy of Medical Sciences of Bosnia and Herzegovina 2019-06 /pmc/articles/PMC6643362/ /pubmed/31402804 http://dx.doi.org/10.5455/medarh.2019.73.191-194 Text en © 2019 Alma Biscevic, Ajla Pidro, Melisa Ahmedbegovic Pjano, Senad Grisevic, Nina Ziga, Maja Bohac http://creativecommons.org/licenses/by-nc/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Paper
Biscevic, Alma
Pidro, Ajla
Pjano, Melisa Ahmedbegovic
Grisevic, Senad
Ziga, Nina
Bohac, Maja
Lasik as a Solution for High Hypermetropia
title Lasik as a Solution for High Hypermetropia
title_full Lasik as a Solution for High Hypermetropia
title_fullStr Lasik as a Solution for High Hypermetropia
title_full_unstemmed Lasik as a Solution for High Hypermetropia
title_short Lasik as a Solution for High Hypermetropia
title_sort lasik as a solution for high hypermetropia
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6643362/
https://www.ncbi.nlm.nih.gov/pubmed/31402804
http://dx.doi.org/10.5455/medarh.2019.73.191-194
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