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Use of loteprednol for routine prophylaxis after photorefractive keratectomy
BACKGROUND: The purpose of this work is to report our experience using loteprednol 0.5% for routine prophylaxis after photorefractive keratectomy in an academic refractive surgery center. MATERIALS AND METHODS: Photorefractive keratectomy was performed on 579 eyes from 316 patients in this retrospec...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3346185/ https://www.ncbi.nlm.nih.gov/pubmed/22570546 http://dx.doi.org/10.2147/OPTH.S30282 |
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author | Mifflin, Mark D Leishman, Lisa L Christiansen, Steven M Sikder, Shameema Hsu, Maylon Moshirfar, Majid |
author_facet | Mifflin, Mark D Leishman, Lisa L Christiansen, Steven M Sikder, Shameema Hsu, Maylon Moshirfar, Majid |
author_sort | Mifflin, Mark D |
collection | PubMed |
description | BACKGROUND: The purpose of this work is to report our experience using loteprednol 0.5% for routine prophylaxis after photorefractive keratectomy in an academic refractive surgery center. MATERIALS AND METHODS: Photorefractive keratectomy was performed on 579 eyes from 316 patients in this retrospective chart review of patients treated postoperatively with either fluorometholone 0.1% (273 eyes) or loteprednol 0.5% (306 eyes). Primary outcome measures at 6 months included uncorrected distance visual acuity, corrected distance visual acuity, and manifest refraction spherical equivalent. Secondary outcome measures were incidence of corneal haze and increased intraocular pressure. RESULTS: There were no statistically significant differences in preoperative characteristics between the two groups when comparing age, sex, best-corrected visual acuity, spherical equivalent, or keratometry. Both groups achieved excellent visual outcomes, with a mean uncorrected distance visual acuity (logMAR) of 0.004 ± 1.4 in the fluorometholone group and −0.028 ± 1.1 in the loteprednol group (P = 0.013) at 6 months. Postoperative corneal haze and increased intraocular pressure were uncommon and not statistically different between the groups. CONCLUSION: Loteprednol 0.5% performed similarly to fluorometholone 0.1% when used for prophylaxis following photorefractive keratectomy. The incidence of haze and increased intraocular pressure were similar between the two groups. |
format | Online Article Text |
id | pubmed-3346185 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-33461852012-05-08 Use of loteprednol for routine prophylaxis after photorefractive keratectomy Mifflin, Mark D Leishman, Lisa L Christiansen, Steven M Sikder, Shameema Hsu, Maylon Moshirfar, Majid Clin Ophthalmol Original Research BACKGROUND: The purpose of this work is to report our experience using loteprednol 0.5% for routine prophylaxis after photorefractive keratectomy in an academic refractive surgery center. MATERIALS AND METHODS: Photorefractive keratectomy was performed on 579 eyes from 316 patients in this retrospective chart review of patients treated postoperatively with either fluorometholone 0.1% (273 eyes) or loteprednol 0.5% (306 eyes). Primary outcome measures at 6 months included uncorrected distance visual acuity, corrected distance visual acuity, and manifest refraction spherical equivalent. Secondary outcome measures were incidence of corneal haze and increased intraocular pressure. RESULTS: There were no statistically significant differences in preoperative characteristics between the two groups when comparing age, sex, best-corrected visual acuity, spherical equivalent, or keratometry. Both groups achieved excellent visual outcomes, with a mean uncorrected distance visual acuity (logMAR) of 0.004 ± 1.4 in the fluorometholone group and −0.028 ± 1.1 in the loteprednol group (P = 0.013) at 6 months. Postoperative corneal haze and increased intraocular pressure were uncommon and not statistically different between the groups. CONCLUSION: Loteprednol 0.5% performed similarly to fluorometholone 0.1% when used for prophylaxis following photorefractive keratectomy. The incidence of haze and increased intraocular pressure were similar between the two groups. Dove Medical Press 2012 2012-05-01 /pmc/articles/PMC3346185/ /pubmed/22570546 http://dx.doi.org/10.2147/OPTH.S30282 Text en © 2012 Mifflin et al, publisher and licensee Dove Medical Press Ltd. This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited. |
spellingShingle | Original Research Mifflin, Mark D Leishman, Lisa L Christiansen, Steven M Sikder, Shameema Hsu, Maylon Moshirfar, Majid Use of loteprednol for routine prophylaxis after photorefractive keratectomy |
title | Use of loteprednol for routine prophylaxis after photorefractive keratectomy |
title_full | Use of loteprednol for routine prophylaxis after photorefractive keratectomy |
title_fullStr | Use of loteprednol for routine prophylaxis after photorefractive keratectomy |
title_full_unstemmed | Use of loteprednol for routine prophylaxis after photorefractive keratectomy |
title_short | Use of loteprednol for routine prophylaxis after photorefractive keratectomy |
title_sort | use of loteprednol for routine prophylaxis after photorefractive keratectomy |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3346185/ https://www.ncbi.nlm.nih.gov/pubmed/22570546 http://dx.doi.org/10.2147/OPTH.S30282 |
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