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Association of ganglion cell-inner plexiform layer thinning with visual function in pediatric papilledema
Andrew H Malem1, Y Arun Reginald2, Michael J Wan2
1Eye institute, Cleveland Clinic Abu Dhabi, Abu Dhabi, United Arab Emirates; Department of Ophthalmology, Cleveland Clinic Lerner College of Medicine of Case Western Reserve University, Cleveland, Ohio.
Insights
Pediatric papilledema can lead to vision loss. In children with papilledema, reduced macula ganglion cell-inner plexiform layer thickness (GCT) is associated with visual impairment.
Area of Science:
- Ophthalmology
- Neuro-ophthalmology
- Pediatric Neurology
Background:
- Papilledema, often caused by increased intracranial pressure, can lead to vision loss in children.
- The macula ganglion cell-inner plexiform layer (GCT) is a key indicator of retinal health.
- Understanding the relationship between GCT and visual outcomes in pediatric papilledema is crucial for early detection and management.
Purpose of the Study:
- To investigate the association between macula ganglion cell-inner plexiform layer thickness (GCT) and visual loss in pediatric patients diagnosed with papilledema.
Main Methods:
- Retrospective review of medical records for pediatric patients (<18 years) with papilledema from 2012-2022.
- Data collected included demographics, lumbar puncture opening pressure, etiology, visual acuity, retinal nerve fiber layer (RNFL) thickness, and GCT.
- Comparison of clinical characteristics between patients with and without visual loss.
Main Results:
- A total of 80 patients (160 eyes) were analyzed; 14% experienced visual loss.
- Patients with visual loss had higher lumbar puncture opening pressure and initial RNFL thickness.
- Significantly reduced final mean and minimum GCT were observed in eyes with visual loss compared to those without.
Conclusions:
- Final macula ganglion cell-inner plexiform layer thickness (GCT) is significantly diminished in pediatric patients with papilledema who experience visual loss.
- GCT may serve as a valuable biomarker for monitoring visual function in children with papilledema.
Purpose:
To characterize the association between macula ganglion cell-inner plexiform layer thickness (GCT) and visual loss in children with papilledema.
Method:
The medical records of pediatric patients (<18 years of age) presenting with papilledema at a single institution between 2012 and 2022 were reviewed retrospectively. Presenting age, sex, lumbar puncture opening pressure, and etiology were recorded in addition to initial and final best-corrected visual acuity, average peripapillary circumferential retinal nerve fiber layer (RNFL) thickness, and GCT. Clinical characteristics were compared between those with and without visual loss, defined as logMAR best-corrected visual acuity ≥0.3, Humphrey visual field mean deviation < -3.0, or abnormal Goldmann visual field.
Results:
A total of 160 eyes of 80 patients (53 female [67%]) were included. Mean patient age was 11.5 years (range, 4-18). Mean follow-up was 19.5 months. Primary pseudotumor cerebri was the diagnosis in 68 cases (85%); secondary, in 12 (15%). Of the 160 eyes, 22 (14%) experienced visual loss (visual acuity, 14; visual fields, 8). Those with visual loss had a significantly higher lumbar puncture opening pressure (41 vs 46 cm H2O [P = 0.01]) and higher initial RNFL (242 μm vs 187 μm [P = 0.04]) on univariate analysis. No difference between groups was found for baseline GCT, age, sex or etiology. Average final mean GCT was 73 μm versus 83 μm (P < 0.001) in those with vision loss versus those without, respectively; average final minimum GCT was 68 μm versus 81 μm (P < 0.001) in those with vision loss versus those without, respectively.
Conclusions:
In this cohort, final GCT was significantly reduced in pediatric patients with papilledema associated with visual loss compared with those without.
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