Abstract

Aims/Purpose: Our aim is to explore the inter‐relationship of clinical PVEP and PERG measurements with each other and the optic nerve structure in children investigated for possible optic neuropathies.Methods: ISCEV Standard PVEPs and PERGs to 50′ check widths to large 30 and standard 15 degree fields were reviewed from children suspected to have optic neuropathy of various pathology. Amplitudes and peak times of PERG P50, N95, the N95:P50 amplitude ratio, the amplitude of the N95 from baseline and at 30 ms from the P50‐N95 slope were measured. Spectralis OCT RNFL sector measures and macular ganglion cell volumes were collated.Results: PERG, PVEP with OCT measurements were available for 42 patients, (83 eyes) aged 6‐17 yrs. Those with abnormal PVEPs (33 eyes) had the most severe macular RGC volume loss (mean 0.26 mm3 in 3.45 mm) with mean LogMAR VA 0.52 (range − 0.01 to 1.00). These patients had inherited optic neuropathies, optic neuritis associated with MOGAD and RMMS. In contrast, patients with papilledema, such as associated with IIH, or presenting with headache and reduced vision and full discs had normal PVEPs. Mean VA LogMAR 0.23 (range − 1.0 to 0.9), and mean macular RGC volume 0.45 mm3 in 3.45 mm circle. N95:P50 amplitude ratios ranged from 1.83 to 0.44 in 30 degree fields and 2.16 to 0.36 in 15 degree fields. The N95:P50 amplitude ratios, slope at 30 ms and N95 from baseline correlated with macular RGC volume, but the best PERG discriminator (AUC 0.83) in the large field was the N95 slope measured at 30 ms. RNFL values were confounded by disc oedema in many cases.Conclusions: Pattern reversal VEPs were abnormal in all patients with severe RGC volume loss. The PERG measures correlate with macular RGC volume. RNFL was confounded by disc oedema, but was helpful in highlighting temporal sector thinning in optic neuritis and inherited optic atrophy such as LHOA.

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