ObjectiveTo investigate the clinical and spectral-domain optical coherence tomography (SD-OCT) biomarkers correlating with pre-injection visual acuity (VA), post-injection VA, and the likelihood of macular oedema (MO) regression after dexamethasone (DEX) implant injection in patients with non-infectious uveitic (NIU).
MethodsPatients' data were collected on the date of DEX injection (pre-injection visit), and after three months (post-injection visit). Qualitative and quantitative features were assessed on pre-injection SD-OCT scans.
ResultsData from 173 DEX were analyzed, obtained from 103 eyes of 80 patients; 38 eyes (37%) received repeated DEX. Absent ellipsoid zone (EZ) layer and disorganization of the inner retinal layers (DRIL) were associated with worse pre-(+ 0.19 LogMAR, 95% CI 0.01-0.38, p = 0.06, and + 0.10 LogMAR, 95% CI 0.02-0.21, p = 0.01) and post-injection VA (+ 0.33 LogMAR, 95% CI 0.08-0.57, p = 0.01, and + 0.17 LogMAR, 95% CI 0.01-0.32, p = 0.04). EZ disruption and DRIL increased (p = 0.01 and p = 0.04) and the chance of gaining ≥ 5 letters decreased in eyes undergoing repeated DEX (p = 0.002). The rate of MO regression after each DEX was 67%. Longer MO duration (OR = 0.75 for year, p = 0.02) was associated with lower chance of MO regression. Subretinal uid was associated with higher rate of MO regression (OR = 6.09, p = 0.01).
ConclusionIntegrity of the inner and outer retina is associated with better visual response to DEX. Long-standing or recurrent MO is associated with less chance of both visual and anatomic response. Timely treatment is necessary to maximize the outcomes of MO in NIU patients. fold higher chance of visual improvement than sham treatment. 4 Subsequent real-world studies showed that functional and anatomic responses to DEX are not always favourable, 5 and MO may persist in up to 50% of cases. [6][7][8][9][10] There is a knowledge gap regarding the clinical and morphologic factors predicting the response to intravitreal DEX in NIU MO patients.Optical coherence tomography (OCT) allows a repeatable evaluation of central macular thickness (CRT) and retinal layers' integrity. 11 Previous studies showed only a moderate correlation between visual acuity (VA) and CRT; 12 thus, alternative biomarkers explaining VA variability in NIU MO patients must be identi ed. Ellipsoid zone (EZ) damage, hyperre ective foci (HRF), disorganization of retinal inner layers (DRIL), cystoid spaces in the outer (ONL) or inner nuclear layer (INL), subretinal uid (SF), and presence of vitreoretinal abnormalities, such as an epiretinal membrane (ERM), have been evaluated in other macular diseases. 13 A comprehensive analysis in NIU MO is lacking.This study investigates the clinical and spectral-domain OCT (SD-OCT) features correlating with preinjection VA, post-injection VA, and the likelihood of MO regression after DEX in patients with NIU MO. This analysis may assist general ophthalmologists and uveitis specialists forecast the prognosis of NIU patients undergoing intravitreal treatment for MO.
Methods