研究目的
To test the efficacy of the intravitreal dexamethasone (DEX) implant in patients with retinal vein occlusions (RVOs) who have failed multiple anti-vascular endothelial growth factor (anti-VEGF) treatments.
研究成果
DEX should be considered as a treatment option in patients with RVOs who have failed anti-VEGF therapy, as the results of this study demonstrated an improvement in retinal morphology and macular function. Cataract progression did occur following multiple consecutive injections; however, steroid-induced glaucoma was not a limiting factor.
研究不足
The study is limited by its size; with only ten patients, strong conclusions are difficult to establish. In addition, the failure of a positive response in one of our primary outcomes, MP, is another limitation. Given the severity of cataract progression, it is difficult to draw strong conclusions from either the MP or VA results.
1:Experimental Design and Method Selection:
A randomized exploratory study was performed on ten patients with branch RVO or central RVO who received at least two previous anti-VEGF treatments and had persistent or unresponsive cystoid macular edema. Treatment with the DEX implant was either every 4 months or pro re nata (PRN) depending on their group assignment for 1 year.
2:Sample Selection and Data Sources:
Patients were required to have a central foveal thickness of at least 275 μm on OCT studies and best-corrected visual acuity (BCVA) between 3 and 72 letters based on the early treatment of diabetic retinopathy study (ETDRS) at screening visit.
3:List of Experimental Equipment and Materials:
Multifocal electroretinography (mfERG), microperimetry (MP), and optical coherence tomography (OCT) were used.
4:Experimental Procedures and Operational Workflow:
Patients were followed-up for 1 year at 4-month intervals, receiving a maximum of three DEX injections. For the PRN group, decision to treat was made at the 4-month interval visits only.
5:Data Analysis Methods:
Data analysis for OCT and MP studies under certain circumstances and for patients lost to follow-up were handled using a last observation carried forward technique.
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