Acute Kidney Injury from Intravitreal Anti-vascular Endothelial Growth Factor Drugs: A Systematic Review and Meta-analysis of Randomized Controlled Trials

Yu Chien Tsao, Ting Ying Chen, Li An Wang, Chia Chun Lee, Wan Ju Annabelle Lee, Sheng Min Hsu, Chi Chun Lai, Shih Chieh Shao*, Jia Horung Hung*, Edward Chia Cheng Lai

*Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

9 Scopus citations

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. Objective: To evaluate acute kidney injury risk associated with intravitreal anti-VEGF drugs in patients with retinal diseases. 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. 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 2: 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 2: 0% for aflibercept; OR: 0.97, 95% CI 0.42–2.22, I 2: 0% for ranibizumab) and between different retinal diseases (OR: 4.61, 95% CI 0.07–284.13, I 2: not applicable for age-related macular degeneration; OR: 0.90, 95% CI 0.42–1.93, I 2: 0% for diabetic retinopathy/diabetic macular edema; OR: 1.57, 95% CI 0.16–15.88, I 2: 0% for retinal vein occlusion). 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. Systematic Review Protocol Registration: PROSPERO CRD42021267854.

Original languageEnglish
Pages (from-to)843-854
Number of pages12
JournalBioDrugs
Volume37
Issue number6
DOIs
StatePublished - 11 2023
Externally publishedYes

Bibliographical note

© 2023. The Author(s), under exclusive licence to Springer Nature Switzerland AG.

Keywords

  • Humans
  • Acute Kidney Injury/chemically induced
  • Angiogenesis Inhibitors/adverse effects
  • Bevacizumab/adverse effects
  • Diabetic Retinopathy/drug therapy
  • Endothelial Growth Factors/therapeutic use
  • Intravitreal Injections
  • Macular Degeneration/chemically induced
  • Macular Edema/drug therapy
  • Randomized Controlled Trials as Topic
  • Ranibizumab/adverse effects
  • Recombinant Fusion Proteins/adverse effects
  • Retinal Diseases/chemically induced
  • Retinal Vein Occlusion/drug therapy
  • Systematic Reviews as Topic
  • Vascular Endothelial Growth Factor A
  • Vascular Endothelial Growth Factors/antagonists & inhibitors

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