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Acute Kidney Injury from Intravitreal Anti-vascular Endothelial Growth Factor Drugs: A Systematic Review and Meta-analysis of Randomized Controlled Trials.
- Source :
-
BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy [BioDrugs] 2023 Nov; Vol. 37 (6), pp. 843-854. Date of Electronic Publication: 2023 Sep 07. - Publication Year :
- 2023
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Abstract
- Background: Several observational studies have reported acute kidney injury from intravitreal anti-vascular endothelial growth factor (anti-VEGF) drugs for retinal diseases. However, systematic reviews and meta-analyses of randomized controlled trials on this critical topic are scant.<br />Objective: To evaluate acute kidney injury risk associated with intravitreal anti-VEGF drugs in patients with retinal diseases.<br />Methods: We searched PubMed, Embase, and the Cochrane Central Register of Controlled Trials on 12 July, 2023, and included randomized controlled trials reporting acute kidney injury between anti-VEGF drugs (e.g., aflibercept, bevacizumab, brolucizumab, and ranibizumab) and controls for retinal diseases (e.g., age-related macular degeneration, polypoidal choroidal vasculopathy, diabetic retinopathy/diabetic macular edema, retinal vein occlusion, and myopic choroidal neovascularization). Data were synthesized by a fixed-effects model for pooling odds ratios (ORs) using the Peto method.<br />Results: We included 13 randomized controlled trials (four and nine trials for aflibercept and ranibizumab, respectively) with a total of 4282 participants. The meta-analysis indicated intravitreal anti-VEGF drugs did not increase the acute kidney injury risk, compared with controls (odds ratio [OR]: 1.00, 95% confidence interval [CI] 0.49-2.04, I <superscript>2</superscript> : 0%), and no differences in the acute kidney injury risk were observed between different anti-VEGF drugs (OR: 1.10, 95% CI 0.27-4.43, I <superscript>2</superscript> : 0% for aflibercept; OR: 0.97, 95% CI 0.42-2.22, I <superscript>2</superscript> : 0% for ranibizumab) and between different retinal diseases (OR: 4.61, 95% CI 0.07-284.13, I <superscript>2</superscript> : not applicable for age-related macular degeneration; OR: 0.90, 95% CI 0.42-1.93, I <superscript>2</superscript> : 0% for diabetic retinopathy/diabetic macular edema; OR: 1.57, 95% CI 0.16-15.88, I <superscript>2</superscript> : 0% for retinal vein occlusion).<br />Conclusions: Intravitreal anti-VEGF drugs were not associated with an acute kidney injury risk, regardless of which anti-VEGF drugs (aflibercept or ranibizumab) or retinal diseases (age-related macular degeneration, diabetic retinopathy/diabetic macular edema, or retinal vein occlusion) were involved.<br />Systematic Review Protocol Registration: PROSPERO CRD42021267854.<br /> (© 2023. The Author(s), under exclusive licence to Springer Nature Switzerland AG.)
- Subjects :
- Humans
Angiogenesis Inhibitors adverse effects
Bevacizumab adverse effects
Endothelial Growth Factors therapeutic use
Intravitreal Injections
Randomized Controlled Trials as Topic
Ranibizumab adverse effects
Recombinant Fusion Proteins adverse effects
Systematic Reviews as Topic
Vascular Endothelial Growth Factor A
Vascular Endothelial Growth Factors antagonists & inhibitors
Acute Kidney Injury chemically induced
Acute Kidney Injury complications
Acute Kidney Injury drug therapy
Diabetic Retinopathy drug therapy
Diabetic Retinopathy chemically induced
Diabetic Retinopathy complications
Macular Degeneration chemically induced
Macular Degeneration complications
Macular Degeneration drug therapy
Macular Edema drug therapy
Macular Edema chemically induced
Macular Edema complications
Retinal Diseases chemically induced
Retinal Diseases complications
Retinal Diseases drug therapy
Retinal Vein Occlusion drug therapy
Retinal Vein Occlusion chemically induced
Retinal Vein Occlusion complications
Subjects
Details
- Language :
- English
- ISSN :
- 1179-190X
- Volume :
- 37
- Issue :
- 6
- Database :
- MEDLINE
- Journal :
- BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy
- Publication Type :
- Report
- Accession number :
- 37676536
- Full Text :
- https://doi.org/10.1007/s40259-023-00621-6