Bevacizumab vs ranibizumab for neovascular age-related macular degeneration in Chinese patients
AIM:To compare the clinical efficacy of intravitreal injections of bevacizumab and ranibizumab for treating Chinese patients with neovascular age-related macular degeneration (AMD). METHODS: Among 60 Chinese patients with exudative AMD (60 eyes), 28 received intravitreal bevacizumab injections (1...
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Format: | Article |
Language: | English |
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Press of International Journal of Ophthalmology (IJO PRESS)
2013-04-01
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Series: | International Journal of Ophthalmology |
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Online Access: | http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3633755/ |
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author | Zhe-Li Liu Feng Gu Peng Sun Han Zhang Jun Li |
author_facet | Zhe-Li Liu Feng Gu Peng Sun Han Zhang Jun Li |
author_sort | Zhe-Li Liu |
collection | DOAJ |
description | AIM:To compare the clinical efficacy of intravitreal injections of bevacizumab and ranibizumab for treating Chinese patients with neovascular age-related macular degeneration (AMD). METHODS: Among 60 Chinese patients with exudative AMD (60 eyes), 28 received intravitreal bevacizumab injections (1.25mg) and 32 received intravitreal ranibizumab injections (0.5mg), once a month for 3 months and were followed for a total of 6 months. Monthly optical coherence tomography (OCT) was used to determine whether the patients received additional treatments during the follow-up. We compared the baseline and 6-month follow-up values of mean best-corrected visual acuity (BCVA) and central retinal thickness (CRT) in both groups of patients. We also compared the occurrence of adverse events. RESULTS:At the 6-month follow-up, the mean BCVA (logMAR) of the bevacizumab and ranibizumab treatment groups improved from the baseline measurements of 0.72±0.23 and 0.73±0.22 to 0.47±0.14 and 0.45±0.20, respectively (P<0.05 for both groups). However, the change was not significantly different between the two groups. As evaluated by OCT, CRT decreased from 366.71±34.72μm and 352±36.9μm at baseline to 250.86±41.51μm and 243.22±41.38μm in the bevacizumab and ranibizumab groups, respectively (P<0.05 for both groups). However, the change was not significantly different between the two groups. There were no severe local adverse reactions or systemic adverse events. CONCLUSION:Intravitreal bevacizumab and ranibizumab have equivalent effects on BCVA and CRT and appeare safe over the short-term. |
first_indexed | 2024-04-13T14:56:46Z |
format | Article |
id | doaj.art-13f5cb67a9544e45a980524a858f3b9b |
institution | Directory Open Access Journal |
issn | 2222-3959 2227-4898 |
language | English |
last_indexed | 2024-04-13T14:56:46Z |
publishDate | 2013-04-01 |
publisher | Press of International Journal of Ophthalmology (IJO PRESS) |
record_format | Article |
series | International Journal of Ophthalmology |
spelling | doaj.art-13f5cb67a9544e45a980524a858f3b9b2022-12-22T02:42:25ZengPress of International Journal of Ophthalmology (IJO PRESS)International Journal of Ophthalmology2222-39592227-48982013-04-016216917310.3980/j.issn.2222-3959.2013.02.12Bevacizumab vs ranibizumab for neovascular age-related macular degeneration in Chinese patientsZhe-Li LiuFeng GuPeng SunHan ZhangJun LiAIM:To compare the clinical efficacy of intravitreal injections of bevacizumab and ranibizumab for treating Chinese patients with neovascular age-related macular degeneration (AMD). METHODS: Among 60 Chinese patients with exudative AMD (60 eyes), 28 received intravitreal bevacizumab injections (1.25mg) and 32 received intravitreal ranibizumab injections (0.5mg), once a month for 3 months and were followed for a total of 6 months. Monthly optical coherence tomography (OCT) was used to determine whether the patients received additional treatments during the follow-up. We compared the baseline and 6-month follow-up values of mean best-corrected visual acuity (BCVA) and central retinal thickness (CRT) in both groups of patients. We also compared the occurrence of adverse events. RESULTS:At the 6-month follow-up, the mean BCVA (logMAR) of the bevacizumab and ranibizumab treatment groups improved from the baseline measurements of 0.72±0.23 and 0.73±0.22 to 0.47±0.14 and 0.45±0.20, respectively (P<0.05 for both groups). However, the change was not significantly different between the two groups. As evaluated by OCT, CRT decreased from 366.71±34.72μm and 352±36.9μm at baseline to 250.86±41.51μm and 243.22±41.38μm in the bevacizumab and ranibizumab groups, respectively (P<0.05 for both groups). However, the change was not significantly different between the two groups. There were no severe local adverse reactions or systemic adverse events. CONCLUSION:Intravitreal bevacizumab and ranibizumab have equivalent effects on BCVA and CRT and appeare safe over the short-term.http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3633755/age-related macular degenerationchoroidal neovascularizationbevacizumab (avastin)ranibizumab (lucentis) |
spellingShingle | Zhe-Li Liu Feng Gu Peng Sun Han Zhang Jun Li Bevacizumab vs ranibizumab for neovascular age-related macular degeneration in Chinese patients International Journal of Ophthalmology age-related macular degeneration choroidal neovascularization bevacizumab (avastin) ranibizumab (lucentis) |
title | Bevacizumab vs ranibizumab for neovascular age-related macular degeneration in Chinese patients |
title_full | Bevacizumab vs ranibizumab for neovascular age-related macular degeneration in Chinese patients |
title_fullStr | Bevacizumab vs ranibizumab for neovascular age-related macular degeneration in Chinese patients |
title_full_unstemmed | Bevacizumab vs ranibizumab for neovascular age-related macular degeneration in Chinese patients |
title_short | Bevacizumab vs ranibizumab for neovascular age-related macular degeneration in Chinese patients |
title_sort | bevacizumab vs ranibizumab for neovascular age related macular degeneration in chinese patients |
topic | age-related macular degeneration choroidal neovascularization bevacizumab (avastin) ranibizumab (lucentis) |
url | http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3633755/ |
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