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Intravitreal methotrexate infusion for proliferative vitreoretinopathy
PURPOSE: The purpose of this study was to evaluate intravitreal methotrexate infusion (IMI) during pars plana vitrectomy (PPV) for retinal detachment in patients with high risk for the development of proliferative vitreoretinopathy (PVR). METHODS: Patients presenting with severe recurrent PVR with t...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5034927/ https://www.ncbi.nlm.nih.gov/pubmed/27698550 http://dx.doi.org/10.2147/OPTH.S111893 |
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author | Sadaka, Ama Sisk, Robert A Osher, James M Toygar, Okan Duncan, Melinda K Riemann, Christopher D |
author_facet | Sadaka, Ama Sisk, Robert A Osher, James M Toygar, Okan Duncan, Melinda K Riemann, Christopher D |
author_sort | Sadaka, Ama |
collection | PubMed |
description | PURPOSE: The purpose of this study was to evaluate intravitreal methotrexate infusion (IMI) during pars plana vitrectomy (PPV) for retinal detachment in patients with high risk for the development of proliferative vitreoretinopathy (PVR). METHODS: Patients presenting with severe recurrent PVR with tractional retinal detachment and/or a history of severe ocular inflammation were treated with IMI. Clinical outcomes were determined from a retrospective medical chart review. RESULTS: Twenty-nine eyes presenting with either tractional retinal detachment and recurrent PVR (n=22) or a history of severe inflammation associated with high PVR risk (n=7) received IMI during PPV. Best-corrected visual acuity at 6 months was ≥20/200 in 19 of 29 eyes (66%) and remained stable or improved compared with initial presentation in 24 of 29 eyes (83%). At the last follow-up examination, the retinas of 26 of 29 eyes (90%) remained attached after IMI while three eyes required another reattachment procedure. Three additional eyes (10%) developed recurrent limited PVR without recurrent RD and were observed. No complications attributable to IMI occurred during a mean follow-up of 27 months. CONCLUSION: Eyes at high risk for PVR development due to a history of prior PVR or intraocular inflammation had a low incidence of PVR following IMI at the time of PPV for RD repair. No significant safety issues from IMI were observed in this series. |
format | Online Article Text |
id | pubmed-5034927 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-50349272016-10-03 Intravitreal methotrexate infusion for proliferative vitreoretinopathy Sadaka, Ama Sisk, Robert A Osher, James M Toygar, Okan Duncan, Melinda K Riemann, Christopher D Clin Ophthalmol Original Research PURPOSE: The purpose of this study was to evaluate intravitreal methotrexate infusion (IMI) during pars plana vitrectomy (PPV) for retinal detachment in patients with high risk for the development of proliferative vitreoretinopathy (PVR). METHODS: Patients presenting with severe recurrent PVR with tractional retinal detachment and/or a history of severe ocular inflammation were treated with IMI. Clinical outcomes were determined from a retrospective medical chart review. RESULTS: Twenty-nine eyes presenting with either tractional retinal detachment and recurrent PVR (n=22) or a history of severe inflammation associated with high PVR risk (n=7) received IMI during PPV. Best-corrected visual acuity at 6 months was ≥20/200 in 19 of 29 eyes (66%) and remained stable or improved compared with initial presentation in 24 of 29 eyes (83%). At the last follow-up examination, the retinas of 26 of 29 eyes (90%) remained attached after IMI while three eyes required another reattachment procedure. Three additional eyes (10%) developed recurrent limited PVR without recurrent RD and were observed. No complications attributable to IMI occurred during a mean follow-up of 27 months. CONCLUSION: Eyes at high risk for PVR development due to a history of prior PVR or intraocular inflammation had a low incidence of PVR following IMI at the time of PPV for RD repair. No significant safety issues from IMI were observed in this series. Dove Medical Press 2016-09-19 /pmc/articles/PMC5034927/ /pubmed/27698550 http://dx.doi.org/10.2147/OPTH.S111893 Text en © 2016 Sadaka et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Sadaka, Ama Sisk, Robert A Osher, James M Toygar, Okan Duncan, Melinda K Riemann, Christopher D Intravitreal methotrexate infusion for proliferative vitreoretinopathy |
title | Intravitreal methotrexate infusion for proliferative vitreoretinopathy |
title_full | Intravitreal methotrexate infusion for proliferative vitreoretinopathy |
title_fullStr | Intravitreal methotrexate infusion for proliferative vitreoretinopathy |
title_full_unstemmed | Intravitreal methotrexate infusion for proliferative vitreoretinopathy |
title_short | Intravitreal methotrexate infusion for proliferative vitreoretinopathy |
title_sort | intravitreal methotrexate infusion for proliferative vitreoretinopathy |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5034927/ https://www.ncbi.nlm.nih.gov/pubmed/27698550 http://dx.doi.org/10.2147/OPTH.S111893 |
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