2015
DOI: 10.1016/j.ophtha.2014.08.048
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Long-term Effects of Therapy with Ranibizumab on Diabetic Retinopathy Severity and Baseline Risk Factors for Worsening Retinopathy

Abstract: Ranibizumab, as administered to patients with DME for 12 to 36 months in these studies, can both improve DR severity and prevent worsening. Prolonged delays in initiation of ranibizumab therapy may limit this therapeutic effect. Although uncommon, the development of PDR still occurs in a small percentage of eyes undergoing anti-vascular endothelial growth factor therapy and may be related to the presence of macular nonperfusion.

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Cited by 166 publications
(129 citation statements)
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“…3 We believe that once our findings have been validated in larger prospective trials, clinicians will monitor DMI with OCT angiography rather than conventional FA.…”
Section: Discussionmentioning
confidence: 79%
See 2 more Smart Citations
“…3 We believe that once our findings have been validated in larger prospective trials, clinicians will monitor DMI with OCT angiography rather than conventional FA.…”
Section: Discussionmentioning
confidence: 79%
“…2 More recently, an analysis of the RIDE and RISE trials showed that patients with DMI at baseline progressed earlier to neovascular complications of DR during intravitreal ranibizumab treatment than those with normal perfusion at baseline. 3 Therefore, baseline assessment of DMI when initiating ranibizumab therapy for diabetic macular edema (DME) has clinical implications and may be of practical importance to patients and physicians when planning review schedules for reassessment of peripheral retinopathy grades for patients receiving injections.…”
Section: Iabetic Macular Ischemia (Dmi) Is An Important Clinical Fementioning
confidence: 99%
See 1 more Smart Citation
“…1-5 In the age of antivascular endothelial growth factor therapy for DR, the assessment of macular ischemia may become more important because the effects of antivascular endothelial growth factor therapy can obscure clinical findings that predict the risk of progression. 23 Fluorescein angiography has been the primary method for evaluating macular ischemia, but it has limitations. The contrast varies with the timing of dye injection, the degree of pigmentation, and media opacity.…”
Section: Discussionmentioning
confidence: 99%
“…Aflibercept (Eylea, Regeneron-Bayer HealthCare), a new, fully human recombinant fusion protein designed to bind all isoforms of VEGF-A as well as placental growth factor, thereby inhibiting the binding and activation of VEGF receptors, has been also approved for AMD and DMO treatment 8. Recently, the potential for anti-VEGF agents to reduce DR severity has been demonstrated;9 these agents are being evaluated for the treatment of vitreous haemorrhage due to proliferative DR (PDR) 10…”
Section: Introductionmentioning
confidence: 99%