A meta-analysis of the effect of a dexamethasone intravitreal implant versus intravitreal anti-vascular endothelial growth factor treatment for diabetic macular edema
Autor: | Xin-jun Ren, Wai Ching Lam, Xiaorong Li, Ye He, Bo-jie Hu |
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Rok vydání: | 2018 |
Předmět: |
Vascular Endothelial Growth Factor A
Intraocular pressure medicine.medical_specialty Visual acuity genetic structures Anti-Inflammatory Agents Visual Acuity Angiogenesis Inhibitors Cochrane Library Dexamethasone Macular Edema law.invention 03 medical and health sciences 0302 clinical medicine lcsh:Ophthalmology Randomized controlled trial Diabetic macular edema law Ranibizumab Ophthalmology Dexamethasone Intravitreal Implant Humans Medicine Dexamethasone implant 030212 general & internal medicine Adverse effect Glucocorticoids Drug Implants Diabetic Retinopathy business.industry Anti-VEGF General Medicine eye diseases Bevacizumab Meta-analysis lcsh:RE1-994 Delayed-Action Preparations Ozurdex Intravitreal Injections 030221 ophthalmology & optometry Implant medicine.symptom business Research Article medicine.drug |
Zdroj: | BMC Ophthalmology, Vol 18, Iss 1, Pp 1-11 (2018) BMC Ophthalmology |
ISSN: | 1471-2415 |
Popis: | Background This meta-analysis evaluated the effectiveness and safety of dexamethasone (DEX) implant and intravitreal anti-vascular endothelial growth factor (VEGF) treatment for diabetic macular edema (DME). Methods The PubMed, Embase, clinicaltrials.gov website and Cochrane Library databases were comprehensively searched for studies comparing DEX implant with anti-VEGF in patients with DME. Best-corrected visual acuity (BCVA), central subfield thickness (CST) and adverse events were extracted from the final eligible studies. Review Manager (RevMan) 5.3 for Mac was used to analyze the data and GRADE profiler were used to access the quality of outcomes. Results Based on four randomized clinical trials assessing a total of 521 eyes, the DEX implant can achieve visual acuity improvement for DME at rates similar to those achieved via anti-VEGF treatment (mean difference [MD] = − 0.43, P = 0.35), with superior anatomic outcomes at 6 months (MD = − 86.71 μm, P = 0.02), while requiring fewer injections, in comparison to anti-VEGF treatment. Although the mean reduction in CST did not showed significant difference at 12 months (MD = − 33.77 μm, P = 0.21), the significant in BCVA from baseline to 12 months supported the anti-VEGF treatment (MD = − 3.26, P |
Databáze: | OpenAIRE |
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