A meta-analysis of anti-vascular endothelial growth factor remedy for macular edema secondary to central retinal vein occlusion

Central retinal vein occlusion (CRVO) associates with severe vision outcome and no proven beneficial treatment. Our meta-analysis intended to appraise the efficacy and safety of anti-vascular endothelial growth factor (anti-VEGF) agents in macular edema (ME) following CRVO. Data were collected and a...

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Veröffentlicht in:PloS one 2013-12, Vol.8 (12), p.e82454
Hauptverfasser: Huang, Peirong, Niu, Wenquan, Ni, Zhentian, Wang, Renzuo, Sun, Xiaodong
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Niu, Wenquan
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Wang, Renzuo
Sun, Xiaodong
description Central retinal vein occlusion (CRVO) associates with severe vision outcome and no proven beneficial treatment. Our meta-analysis intended to appraise the efficacy and safety of anti-vascular endothelial growth factor (anti-VEGF) agents in macular edema (ME) following CRVO. Data were collected and analyzed by Review Manager 5.2.1. We employed a random-effects model to eliminate between-study heterogeneity. Nfs (called fail-safe number) was calculated to evaluate the publication bias. We included 5 trials consisting 323 cases and 281 controls. Primary outcomes showed that overall comparison of anti-VEGF agents with placebo control yielded a 374% and 136% increased tendency for a gain of 15 letters or more on Early Treatment Diabetic Retinopathy Study (ETDRS) chart (95% confidence interval [95% CI]: 2.43-9.23; P
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Our meta-analysis intended to appraise the efficacy and safety of anti-vascular endothelial growth factor (anti-VEGF) agents in macular edema (ME) following CRVO. Data were collected and analyzed by Review Manager 5.2.1. We employed a random-effects model to eliminate between-study heterogeneity. Nfs (called fail-safe number) was calculated to evaluate the publication bias. We included 5 trials consisting 323 cases and 281 controls. Primary outcomes showed that overall comparison of anti-VEGF agents with placebo control yielded a 374% and 136% increased tendency for a gain of 15 letters or more on Early Treatment Diabetic Retinopathy Study (ETDRS) chart (95% confidence interval [95% CI]: 2.43-9.23; P&lt;0.00001; I(2) = 59%, 95% CI: 1.60-3.49; P&lt;0.0001; I(2)  = 0%, respectively) at 6 and 12 months. Secondary outcomes showed that a 90% and 77% decreased risk at 6 and 12 months for a loss of 15 letters or more. The overall mean difference showed a statistically significance in best-corrected visual acuity (BCVA) on each time point. However, changes of central retinal thickness (CRT) lost significance at 12 months after 6-month as-needed treatment. The incidence of adverse events (AEs) had no statistical difference between anti-VEGF and placebo groups. Subgroup analyses indicated that patients receiving Aflibercept got the highest tendency to gain 15 letters or more (OR = 9.78; 95% CI: 4.43-21.56; P&lt;0.00001). Age controlled analysis suggested a weaken tendency of BCVA improvement in age over 50 (MD = 12.26; 95% CI: 7.55-16.98; P&lt;0.00001). Subgroup analysis by clinical classification showed a strengthen difference of BCVA changes at 6 months in ischemic type (MD = 19.65 letters, 95% CI: 13.15 to 26.14 letters, P&lt;0.00001). Our results showed that anti-VEGF agents were superior to placebo in CRVO-ME treatment with no statistically significant AEs, especially in younger people and for ischemic type.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0082454</identifier><identifier>PMID: 24376538</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Acuity ; Aged ; Aged, 80 and over ; Angiogenesis Inhibitors - adverse effects ; Angiogenesis Inhibitors - pharmacology ; Angiogenesis Inhibitors - therapeutic use ; Clinical trials ; Comparative analysis ; Confidence intervals ; Data processing ; Diabetes ; Diabetes mellitus ; Diabetic retinopathy ; Diabetic Retinopathy - complications ; Edema ; Female ; Hospitals ; Humans ; Ischemia ; Laboratories ; Macular Edema - drug therapy ; Macular Edema - etiology ; Macular Edema - physiopathology ; Male ; Medicine ; Meta-analysis ; Middle Aged ; Occlusion ; Pharmaceuticals ; Randomized Controlled Trials as Topic ; Retina ; Retinal Vein Occlusion - complications ; Retinal Vein Occlusion - physiopathology ; Retinopathy ; Standard deviation ; Statistical analysis ; Studies ; Vascular endothelial growth factor ; Vascular Endothelial Growth Factor A - antagonists &amp; inhibitors ; Visual Acuity</subject><ispartof>PloS one, 2013-12, Vol.8 (12), p.e82454</ispartof><rights>COPYRIGHT 2013 Public Library of Science</rights><rights>2013 Huang et al. 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The overall mean difference showed a statistically significance in best-corrected visual acuity (BCVA) on each time point. However, changes of central retinal thickness (CRT) lost significance at 12 months after 6-month as-needed treatment. The incidence of adverse events (AEs) had no statistical difference between anti-VEGF and placebo groups. Subgroup analyses indicated that patients receiving Aflibercept got the highest tendency to gain 15 letters or more (OR = 9.78; 95% CI: 4.43-21.56; P&lt;0.00001). Age controlled analysis suggested a weaken tendency of BCVA improvement in age over 50 (MD = 12.26; 95% CI: 7.55-16.98; P&lt;0.00001). Subgroup analysis by clinical classification showed a strengthen difference of BCVA changes at 6 months in ischemic type (MD = 19.65 letters, 95% CI: 13.15 to 26.14 letters, P&lt;0.00001). 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Our meta-analysis intended to appraise the efficacy and safety of anti-vascular endothelial growth factor (anti-VEGF) agents in macular edema (ME) following CRVO. Data were collected and analyzed by Review Manager 5.2.1. We employed a random-effects model to eliminate between-study heterogeneity. Nfs (called fail-safe number) was calculated to evaluate the publication bias. We included 5 trials consisting 323 cases and 281 controls. Primary outcomes showed that overall comparison of anti-VEGF agents with placebo control yielded a 374% and 136% increased tendency for a gain of 15 letters or more on Early Treatment Diabetic Retinopathy Study (ETDRS) chart (95% confidence interval [95% CI]: 2.43-9.23; P&lt;0.00001; I(2) = 59%, 95% CI: 1.60-3.49; P&lt;0.0001; I(2)  = 0%, respectively) at 6 and 12 months. Secondary outcomes showed that a 90% and 77% decreased risk at 6 and 12 months for a loss of 15 letters or more. The overall mean difference showed a statistically significance in best-corrected visual acuity (BCVA) on each time point. However, changes of central retinal thickness (CRT) lost significance at 12 months after 6-month as-needed treatment. The incidence of adverse events (AEs) had no statistical difference between anti-VEGF and placebo groups. Subgroup analyses indicated that patients receiving Aflibercept got the highest tendency to gain 15 letters or more (OR = 9.78; 95% CI: 4.43-21.56; P&lt;0.00001). Age controlled analysis suggested a weaken tendency of BCVA improvement in age over 50 (MD = 12.26; 95% CI: 7.55-16.98; P&lt;0.00001). Subgroup analysis by clinical classification showed a strengthen difference of BCVA changes at 6 months in ischemic type (MD = 19.65 letters, 95% CI: 13.15 to 26.14 letters, P&lt;0.00001). Our results showed that anti-VEGF agents were superior to placebo in CRVO-ME treatment with no statistically significant AEs, especially in younger people and for ischemic type.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>24376538</pmid><doi>10.1371/journal.pone.0082454</doi><tpages>e82454</tpages><oa>free_for_read</oa></addata></record>
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subjects Acuity
Aged
Aged, 80 and over
Angiogenesis Inhibitors - adverse effects
Angiogenesis Inhibitors - pharmacology
Angiogenesis Inhibitors - therapeutic use
Clinical trials
Comparative analysis
Confidence intervals
Data processing
Diabetes
Diabetes mellitus
Diabetic retinopathy
Diabetic Retinopathy - complications
Edema
Female
Hospitals
Humans
Ischemia
Laboratories
Macular Edema - drug therapy
Macular Edema - etiology
Macular Edema - physiopathology
Male
Medicine
Meta-analysis
Middle Aged
Occlusion
Pharmaceuticals
Randomized Controlled Trials as Topic
Retina
Retinal Vein Occlusion - complications
Retinal Vein Occlusion - physiopathology
Retinopathy
Standard deviation
Statistical analysis
Studies
Vascular endothelial growth factor
Vascular Endothelial Growth Factor A - antagonists & inhibitors
Visual Acuity
title A meta-analysis of anti-vascular endothelial growth factor remedy for macular edema secondary to central retinal vein occlusion
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