Real-world experience with 0.2 μg/day fluocinolone acetonide intravitreal implant (ILUVIEN) in the United Kingdom

Aims To compare safety outcomes and visual function data acquired in the real-world setting with FAME study results in eyes treated with 0.2  μ g/day fluocinolone acetonide (FAc). Methods Fourteen UK clinical sites contributed to pseudoanonymised data collected using the same electronic medical reco...

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Published inEye (London) Vol. 31; no. 12; pp. 1707 - 1715
Main Authors Bailey, C, Chakravarthy, U, Lotery, A, Menon, G, Talks, J
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 01.12.2017
Nature Publishing Group
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Summary:Aims To compare safety outcomes and visual function data acquired in the real-world setting with FAME study results in eyes treated with 0.2  μ g/day fluocinolone acetonide (FAc). Methods Fourteen UK clinical sites contributed to pseudoanonymised data collected using the same electronic medical record system. Data pertaining to eyes treated with FAc implant for diabetic macular oedema (DMO) was extracted. Intraocular pressure (IOP)-related adverse events were defined as use of IOP-lowering medication, any rise in IOP>30 mm Hg, or glaucoma surgery. Other measured outcomes included visual acuity, central subfield thickness (CSFT) changes and use of concomitant medications. Results In total, 345 eyes had a mean follow-up of 428 days. Overall, 13.9% of patients required IOP-lowering drops (included initiation, addition and switching of current drops), 7.2% had IOP elevation >30 mm Hg and 0.3% required glaucoma surgery. In patients with prior steroid exposure and no prior IOP-related event, there were no new IOP-related events. In patients without prior steroid use and without prior IOP-related events, 10.3% of eyes required IOP-lowering medication and 4.3% exhibited IOP >30 mm Hg at some point during follow-up. At 24 months, mean best-recorded visual acuity increased from 51.9 to 57.2 letters and 20.8% achieved ≥15-letter improvement. Mean CSFT reduced from 451.2 to 355.5  μ m. Conclusions While overall IOP-related emergent events were observed in similar frequency to FAME, no adverse events were seen in the subgroup with prior steroid exposure and no prior IOP events. Efficacy findings confirm that the FAc implant is a useful treatment option for chronic DMO.
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Medisoft Audit Group Contributors Dr Clare Bailey (Principal Investigator), Bristol Eye Hospital; Dr Ahmed Kamal, Aintree University Hospitals; Professor Usha Chakravarthy, Belfast Health and Social Care Trust; Dr Faruque Ghanchi, Bradford Teaching Hospitals; Dr Rehna Khan, Calderdale Royal Hospital; Professor Geeta Menon, Frimley Park Hospital; Dr Robert Johnston, Gloucestershire Hospitals; Dr Martin McKibbin, Leeds Teaching Hospitals; Dr Atul Varma, Mid Yorkshire Hospitals; Dr Bushra Mustaq, BMEC; Dr Christopher Brand, Sheffield Teaching Hospitals; Dr James Talks, Newcastle Upon Tyne Hospitals; Professor Andrew Lotery, University Hospital Southampton; Dr Nick Glover, Queen Elizabeth Birmingham.
Medisoft Audit Group contributors are listed before the references and in Supplementary Table S1
ISSN:0950-222X
1476-5454
DOI:10.1038/eye.2017.125