Please use this identifier to cite or link to this item:
|Scopus||Web of Science®||Altmetric|
|Title:||Retrospective study of an as required dosing regimen of intravitreal bevacizumab in neovascular age-related macular degeneration in an Australian population|
|Citation:||Clinical and Experimental Ophthalmology, 2010; 38(7):659-663|
|Publisher:||Blackwell Publishing Asia|
|Susie T Luu, Timothy Gray, Sunil K Warrier, Ilesh Patel, James S Muecke, Robert Casson and Jagjit S Gilhotra|
|Abstract:||<h4>Purpose</h4>To investigate the efficacy of intravitreal bevacizumab for the treatment of neovascular age-related macular degeneration (AMD) using an as required dosing regimen.<h4>Methods</h4>A retrospective study of 210 patients (231 eyes) with choroidal neovascularization resulting from neovasacular AMD. Patients were treated with 1.25 mg intravitreal bevacizumab at a vitreoretinal practice in Adelaide, South Australia. Patients were followed up at 2-4 weeks and then at 1-month intervals; repeat injections were offered in the event of recurrence. Recurrence was defined as either a decrease of best-corrected visual acuity or an increase in macular oedema, subretinal fluid or intraretinal fluid on optical coherence tomography, after complete or partial resolution in previous follow-up visits. Patient data were collected for 12 months of follow up or until the patient's treatment was changed to ranibizumab.<h4>Results</h4>Significant improvement in visual acuity and central retinal thickness was demonstrated at 1 month with an improvement of vision from logMAR equivalent 0.76 to 0.68 (P < 0.001) and a decrease of central retinal thickness from 306 µm to 244 µm (P < 0.001). This overall improvement was continued throughout the 12-month follow-up period; however, follow up was poor with 12-month data available for only a small number of patients (7.8%). Ocular and systemic side-effects were rare at 3.5% and 0.4%, respectively.<h4>Conclusion</h4>Eyes with neovascular AMD treated with intravitreal bevacizumab for up to 12 months had significant functional and anatomical improvement. Further studies need to confirm the long-term safety and efficacy of this treatment.|
|Keywords:||age-related macular degeneration|
|Rights:||© 2010 The Authors. Journal compilation © 2010 Royal Australian and New Zealand College of Ophthalmologists|
|Appears in Collections:||Aurora harvest|
Opthalmology & Visual Sciences publications
Files in This Item:
There are no files associated with this item.
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.