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  • Two-year interim safety results of the 0.2ug/day FAC intravitreal implant for the treatment of DMO

Two-year interim safety results of the 0.2ug/day FAC intravitreal implant for the treatment of DMO
Reviewed by Jonathan Chan

1 December 2021 | Jonathan Chan | EYE - Vitreo-Retinal
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This is a 24-month interim prospective observational study of 95 previously steroid challenged patients (115 eyes) receiving intravitreal 0.2ug/day fluocinolone acetaid (FAC) implant for diabetic macular oedema (DMO) treatment. The mean IOP for pre- and post- FAC implants were stable, with IOP-related procedures (Pre-FAC of two cases; two trabeculoplasties and four IOP-lowering surgeries post-FAC). The mean visual acuity was stable post-FAC (mean improvement of one to three letters) and fewer DMO treatments per year post-FAC. Mean central subfield thickness (CST) was significantly reduced at 24 months post-FAC (p<0.001). The percentage of patients with CST <300um was significantly increased post-FAC compared to baseline (46.3% at 12 months, p=0.009, versus 42.2% at 24 months, p=0.041). The authors concluded that FAC implant is a valuable tool in the management of DMO for selected patients after a prior steroid challenge.

 

Two-year interim safety results of the 0.2 µg/day fluocinolone acetonide intravitreal implant for the treatment of diabetic macular oedema: the observational PALADIN study.
SE Mansour, Kiernan DF, Roth DB, et al.
BRITISH JOURNAL OF OPHTHALMOLOGY
2021;105:414-9.
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CONTRIBUTOR
Jonathan Chan

Royal Hallamshire Hospital, Sheffield, UK.

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