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Ranibizumab in patients with dense cataract and proliferative diabetic retinopathy with rubeosis

BACKGROUND: To evaluate the safety of ranibizumab as a surgical adjunct during cataract surgery in patients with proliferative diabetic retinopathy (PDR) with rubeosis, and to evaluate the efficacy and adverse effects of ranibizumab in treating PDR with rubeosis. MATERIALS AND METHODS: Three intravi...

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Autores principales: Tu, Yufei, Fay, Catherine, Guo, Suqin, Zarbin, Marco A., Marcus, Edward, Bhagat, Neelakshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3574511/
https://www.ncbi.nlm.nih.gov/pubmed/23439790
http://dx.doi.org/10.4103/0974-620X.106099
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author Tu, Yufei
Fay, Catherine
Guo, Suqin
Zarbin, Marco A.
Marcus, Edward
Bhagat, Neelakshi
author_facet Tu, Yufei
Fay, Catherine
Guo, Suqin
Zarbin, Marco A.
Marcus, Edward
Bhagat, Neelakshi
author_sort Tu, Yufei
collection PubMed
description BACKGROUND: To evaluate the safety of ranibizumab as a surgical adjunct during cataract surgery in patients with proliferative diabetic retinopathy (PDR) with rubeosis, and to evaluate the efficacy and adverse effects of ranibizumab in treating PDR with rubeosis. MATERIALS AND METHODS: Three intravitreal injections of 0.5 mg ranibizumab were administered on day-1, months-1 and -2 with cataract surgery 6-16 days after first injection. Retreatments with ranibizumab injections and pan-retinal photocoagulation (PRP) were given if recurrence or persistence of PDR was noted between months-3 and -11. Safety observation visits occurred at months-12, -18 and -24. Primary end points were incidence and severity of adverse events (AEs) that were related to both cataract surgery and treatment of PDR with rubeosis through month -12. RESULTS: Of six patients screened, four (mean age 61.3 years) were enrolled. No AEs were noted with either cataract surgery or treatment of PDR. Neovascularization of iris (NVI) promptly regressed by 4 days after first ranibizumab injection, prior to cataract surgery in three of four patients (one had significantly regressed NVI by post-injection day-3 visit); NVI was not noted in any patient at 2 weeks after first ranibizumab injection. Recurrence of rubeosis or NVA after 3 monthly injections was not observed in any. At month-12, PDR was not present when assessed clinically and by fluorescein angiogram (FA). Only one patient developed neovascularization of disc and neovascularization elsewhere and required retreatments at months-5 and -9. CONCLUSIONS: Multiple intravitreal injections of ranibizumab may be a safe, effective treatment adjunct for PDR and diabetes-related rubeosis.
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spelling pubmed-35745112013-02-22 Ranibizumab in patients with dense cataract and proliferative diabetic retinopathy with rubeosis Tu, Yufei Fay, Catherine Guo, Suqin Zarbin, Marco A. Marcus, Edward Bhagat, Neelakshi Oman J Ophthalmol Original Article BACKGROUND: To evaluate the safety of ranibizumab as a surgical adjunct during cataract surgery in patients with proliferative diabetic retinopathy (PDR) with rubeosis, and to evaluate the efficacy and adverse effects of ranibizumab in treating PDR with rubeosis. MATERIALS AND METHODS: Three intravitreal injections of 0.5 mg ranibizumab were administered on day-1, months-1 and -2 with cataract surgery 6-16 days after first injection. Retreatments with ranibizumab injections and pan-retinal photocoagulation (PRP) were given if recurrence or persistence of PDR was noted between months-3 and -11. Safety observation visits occurred at months-12, -18 and -24. Primary end points were incidence and severity of adverse events (AEs) that were related to both cataract surgery and treatment of PDR with rubeosis through month -12. RESULTS: Of six patients screened, four (mean age 61.3 years) were enrolled. No AEs were noted with either cataract surgery or treatment of PDR. Neovascularization of iris (NVI) promptly regressed by 4 days after first ranibizumab injection, prior to cataract surgery in three of four patients (one had significantly regressed NVI by post-injection day-3 visit); NVI was not noted in any patient at 2 weeks after first ranibizumab injection. Recurrence of rubeosis or NVA after 3 monthly injections was not observed in any. At month-12, PDR was not present when assessed clinically and by fluorescein angiogram (FA). Only one patient developed neovascularization of disc and neovascularization elsewhere and required retreatments at months-5 and -9. CONCLUSIONS: Multiple intravitreal injections of ranibizumab may be a safe, effective treatment adjunct for PDR and diabetes-related rubeosis. Medknow Publications & Media Pvt Ltd 2012 /pmc/articles/PMC3574511/ /pubmed/23439790 http://dx.doi.org/10.4103/0974-620X.106099 Text en Copyright: © 2012 Tu Y, et al. http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Original Article
Tu, Yufei
Fay, Catherine
Guo, Suqin
Zarbin, Marco A.
Marcus, Edward
Bhagat, Neelakshi
Ranibizumab in patients with dense cataract and proliferative diabetic retinopathy with rubeosis
title Ranibizumab in patients with dense cataract and proliferative diabetic retinopathy with rubeosis
title_full Ranibizumab in patients with dense cataract and proliferative diabetic retinopathy with rubeosis
title_fullStr Ranibizumab in patients with dense cataract and proliferative diabetic retinopathy with rubeosis
title_full_unstemmed Ranibizumab in patients with dense cataract and proliferative diabetic retinopathy with rubeosis
title_short Ranibizumab in patients with dense cataract and proliferative diabetic retinopathy with rubeosis
title_sort ranibizumab in patients with dense cataract and proliferative diabetic retinopathy with rubeosis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3574511/
https://www.ncbi.nlm.nih.gov/pubmed/23439790
http://dx.doi.org/10.4103/0974-620X.106099
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