2010
DOI: 10.1016/j.ophtha.2010.02.021
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Ranibizumab for Macular Edema following Branch Retinal Vein Occlusion

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Cited by 797 publications
(779 citation statements)
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“…Research has demonstrated the benefit of anti-VEGF injections for 'centre-involved' diabetic macular oedema, 9 central retinal vein occlusion, 10 and branch retinal vein occlusion. 11 NICE has recently approved the use of ranibizumab for diabetic macular oedema and retinal vein occlusions, and this will result in even more pressure on the resources of NHS eye units across the UK. NP-delivered anti-VEGF injections is one solution to assist in meeting these extra demands and this method of service delivery has recently been endorsed by the Royal College of Ophthalmologists (Intra-ocular injections by non-medical health care professionals, Royal College of Ophthalmologists statement, 01/05/2013) and the Macular Society.…”
Section: Discussionmentioning
confidence: 99%
“…Research has demonstrated the benefit of anti-VEGF injections for 'centre-involved' diabetic macular oedema, 9 central retinal vein occlusion, 10 and branch retinal vein occlusion. 11 NICE has recently approved the use of ranibizumab for diabetic macular oedema and retinal vein occlusions, and this will result in even more pressure on the resources of NHS eye units across the UK. NP-delivered anti-VEGF injections is one solution to assist in meeting these extra demands and this method of service delivery has recently been endorsed by the Royal College of Ophthalmologists (Intra-ocular injections by non-medical health care professionals, Royal College of Ophthalmologists statement, 01/05/2013) and the Macular Society.…”
Section: Discussionmentioning
confidence: 99%
“…32 Following dexamethasone, ranibizumab (Lucentis, Genentech, Inc., South San Francisco, CA, USA; Novartis Pharma AG, Basel, Switzerland) intravitreal injection was also approved in the United States for the same indication on the basis of two multicenter, randomized, doublemasked clinical trials (BRAVO and CRUISE). 33,34 In these clinical trials, both dexamethasone and ranibizumab demonstrated clinically and statistically improved vision acuity compared with placebo. In GENEVA, 23 and 18% of patients with BRVO and CRVO, respectively, gained at least three lines (15 letters) of best-corrected visual acuity (BCVA) in the first 3 months after treatment with dexamethasone intravitreal implant, compared with 20 and 12% in the respective sham groups.…”
Section: Risk Of Vascular and Cardiovascular Complications In Rvomentioning
confidence: 99%
“…32 In BRAVO and CRUISE, after 6 months of ranibizumab therapy, between 55 and 61% of patients with BRVO gained at least three lines of BCVA (compared with 28% in the sham group) and about 48% of patients with CRVO gained at least three lines of BCVA (compared with 17% in the sham group). 33,34 Intravitreal triamcinolone acetonide has also been investigated and was shown to be superior to observation in CRVO but failed to demonstrate superiority in efficacy or safety over grid photocoagulation in BRVO in a multicenter phase III SCORE study. 35,36 Although this article was under review, the Royal College of Ophthalmologists' guidelines were updated to recommend consideration of dexamethasone intravitreal implant and ranibizumab for managing macular edema following CRVO and BRVO.…”
Section: Risk Of Vascular and Cardiovascular Complications In Rvomentioning
confidence: 99%
“…These demographic characteristics are unusual in daily medical practice and could account for differences with other published studies. [7][8][9] Furthermore, the mean age of the patients enrolled (69.3 years; ± 12.2 years) was higher (although not significantly) than those in the Geneva study group (64.7 years; range 33-90 years). 7 Mean BCVA at baseline was poor in our population (20/200 Snellen equivalent; +0.98(0.56) LogMAR; about 35 letters translated into the ETDRS grading scale) compared to 54.3, 51, and 48 letters in the Geneva study group, SCORE study and CRUISE Trial, respectively.…”
Section: Discussionmentioning
confidence: 75%
“…The BRAVO, CRUISE, and GENEVA trials are three studies that have demonstrated the efficacy of anti-VEGF agents and DEX implants, but they cannot serve as comparative studies. 7,8,10 For example, two-thirds of the patients included in the BRAVO and CRUISE (ranibizumab) studies had more recent onset macular edema (short duration ≤ 90 days) than patients in the GENEVA study (only 16% ≤ 90 days). A shorter duration of ME was associated with greater improvements in BCVA after DEX implant.…”
Section: Eyementioning
confidence: 99%