4.6 Article

Risk factors for microcystic macular oedema in glaucoma

Journal

BRITISH JOURNAL OF OPHTHALMOLOGY
Volume 107, Issue 4, Pages 505-510

Publisher

BMJ PUBLISHING GROUP
DOI: 10.1136/bjophthalmol-2021-320137

Keywords

glaucoma; macula; imaging

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This retrospective cohort study aimed to identify clinical characteristics and factors associated with microcystic macular edema (MME) in patients with primary open-angle glaucoma (POAG). The study found that more severe glaucoma and younger age were associated with MME, but MME was not associated with faster global visual field decay.
Background/aims To identify clinical characteristics and factors associated with microcystic macular edema (MME) in patients with primary open-angle glaucoma (POAG). Methods We included 315 POAG eyes between 2010 and 2019 with good-quality macular volume scans that had reliable visual fields (VF) available within 6 months in this observational retrospective cohort study. Eyes with retinal pathologies except for epiretinal membrane (ERM) were excluded. The inner nuclear layer was qualitatively assessed for the presence of MME. Global mean deviation (MD) and Visual Field Index (VFI) decay rates, superior and inferior MD rates and pointwise total deviation rates of change were estimated with linear regression. Logistic regression was performed to identify baseline factors associated with the presence of MME and to determine whether MME is associated with progressive VF loss. Results 25 out of 315 eyes (7.9%) demonstrated MME. The average (+/- SD) age and MD in eyes with and without MME was 57.2 (+/- 8.7) versus 62.0 (+/- 9.9) years (p=0.02) and -9.8 (+/- 5.7) versus -4.9 (+/- 5.3) dB (p<0.001), respectively. Worse global MD at baseline (p=0.001) and younger age (p=0.02) were associated with presence of MME. ERM was not associated with the presence of MME (p=0.84) in this cohort. MME was not associated with MD and VFI decay rates (p>0.49). Conclusions More severe glaucoma and younger age were associated with MME. MME was not associated with faster global VF decay in this cohort. MME may confound monitoring of glaucoma with full macular thickness.

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