Skip to main content
. Author manuscript; available in PMC: 2024 Mar 18.
Published in final edited form as: J AAPOS. 2022 Jul 8;26(4):187.e1–187.e6. doi: 10.1016/j.jaapos.2022.05.001

Table 2.

Examination findings

Study parameter No. (%)

Fundus examinations 283
Abnormal fundus examinations (possibly related) 44 (15.5)
 Not attributable to vigabatrin 40 (14.1)
 Inconclusive 4(1.4)
 Attributable to vigabatrin 0 (0)
ERG 37
Abnormal ERG 12 (32.4)
 Not attributable to vigabatrin 10 (27.0)
 Inconclusive 0 (0)
 Attributable to vigabatrin 2 (5.4)
OCT 19
Abnormal OCT 3 (15.8)
 Not attributable to vigabatrin 3 (15.8)
 Inconclusive 0 (0)
 Attributable to vigabatrin 0 (0)
Visual Fields 6
Abnormal Visual Fields 2 (33.3)
 Not attributable to vigabatrin 2 (33.3)
 Inconclusive 0(0)
 Attributable to vigabatrin 0 (0)
Examination findings UNRELATED to vigabatrin 283
 Cortical visual impairment 81 (28.6)
 Strabismus 63 (22.3)
 Non-medication-related retinal lesionsa 31 (10.9)
 Optic atrophy 37 (13.1)
 Optic nerve hypoplasia 10 (3.5)
 Other optic nerve 6(2.1)
 VF deficit 9 (3.2)
 Otherb 38 (13.4)
 No abnormality 37 (13.1)

ERG, electroretinogram; OCT, optical coherence tomography.

a

Retinal changes included: lacunae, hamartoma, congenital hypertrophy of the retinal pigment epithelium (CHRPE), bear tracks, astrocytoma, laser scars, retinal detachment, fungal chorioretinitis, non-medication-related retinal pigment changes.

b

Other included nystagmus, pigment, cataract, microphthalmos, nasolacrimal duct obstruction, corneal abrasion or ulcer, corneal scar or opacity, exposure keratopathy, anisocoria, retrolental membrane, subconjunctival hemorrhage, glaucoma, persistent fetal vasculature, iris hypopigmentation, iris coloboma.