| Literature DB >> 33430389 |
Laurent Kodjikian1,2, Stephanie Baillif3, Catherine Creuzot-Garcher4,5, Marie-Noëlle Delyfer6,7, Frédéric Matonti8,9, Michel Weber10,11, Thibaud Mathis1,2.
Abstract
To assess real-world outcomes of fluocinolone acetonide (FAc) implant in treating diabetic macular edema (DME), a systematic literature review was conducted on PubMed in order to identify publications assessing the efficacy and safety of the FAc implant in DME in daily practice. Case reports and randomized controlled trials were excluded. Twenty-two observational real-world studies analyzing a total of 1880 eyes were included. Mean peak visual gain was +8.7 letters (11.3 months post-FAc injection) and was greater for lower baseline best corrected visual acuity (BCVA) and for more recent DME. Mean central retinal thickness (CRT) decreased 34.3% from baseline. 77.0% of the analyzed studies reported both BCVA improvement of at least five letters and a CRT decrease by 20% or more. Rescue therapy was needed more frequently when FAc was administered for chronic DME. FAc-induced ocular hypertension was reported in 20.1% of patients but only 0.6% needed surgery. Cataract extraction was performed in 43.2% of phakic patients. Adequate patient selection is essential for optimal FAc response and better safety profile. Currently positioned as second- or third-line treatment in the management algorithm, FAc implant decreases treatment burden and provides better letter gain when administered for more recent DME.Entities:
Keywords: DME; FAc; diabetic macular edema; efficacy; fluocinolone acetonide; real-world; safety
Year: 2021 PMID: 33430389 PMCID: PMC7827527 DOI: 10.3390/pharmaceutics13010072
Source DB: PubMed Journal: Pharmaceutics ISSN: 1999-4923 Impact factor: 6.321