Etiological analysis of pale optic disc and its association with six-month visual outcome in patients attending a tertiary care hospital: a prospective observational cohort study.

Authors

  • Dr. Yeshamalla Bhavana Senior Resident, Department of Ophthalmology, Government Medical College, Nalgonda, Telangana, India
  • Dr. Boddupally Soujanya Senior Resident, Department of Ophthalmology, Government Medical College, Nalgonda, Telangana, India
  • Dr. Beatrice Choppara Assistant Professor, Department of Ophthalmology, Government Medical College, Nalgonda, Telangana, India

DOI:

https://doi.org/10.51168/sjhrafrica.v7i2.2754

Keywords:

best-corrected visual acuity, optic atrophy, optic neuritis, pale optic disc, prospective cohort, traumatic optic neuropathy, visual outcome

Abstract

Background

Pale optic disc indicates established optic nerve damage caused by inflammatory, ischemic, traumatic, compressive, infectious, toxic, or metabolic disorders. Etiological identification is important because visual recovery varies substantially across causes.

Objectives

To determine the etiological spectrum of pale optic disc and assess its association with six-month best-corrected visual acuity outcome.

Methods

This prospective, hospital-based observational cohort study included 50 adults with optic disc pallor attending a tertiary-care ophthalmology department. Participants underwent standardized ocular examination, colour vision and visual field assessment, selected electrophysiology, laboratory investigations, and neuroimaging when indicated. Visual improvement was defined as a gain of at least one Snellen line at six months. Etiology and visual outcome were compared using Pearson's chi-square test and the Fisher-Freeman-Halton exact test.

Results

The mean age was 38.68 ± 12.09 years, and 56.0% were male. Traumatic optic neuropathy was the leading etiology (28.0%), followed by optic neuritis and tumor-related optic neuropathy (22.0% each) and primary optic atrophy (16.0%). Overall, 17 of 50 patients improved (34.0%; 95% CI, 22.4%-47.8%). Improvement occurred in 72.7% of optic neuritis cases (95% CI, 43.4%-90.3%), 54.5% of tumor-related cases (95% CI, 28.0%-78.7%), and 21.4% of traumatic optic neuropathy cases (95% CI, 7.6%-47.6%). Visual improvement differed significantly by etiology (Pearson χ²(9)=17.62, p=0.040; Fisher-Freeman-Halton exact p=0.011; Cramér's V=0.59).

Conclusion

Pale optic disc had heterogeneous causes and generally guarded visual outcomes. Optic neuritis showed the most favourable recovery, whereas established primary optic atrophy showed no improvement.

Recommendations

Early neuro-ophthalmic assessment, directed imaging, cause-specific treatment, and structured follow-up should be prioritized.

Author Biographies

Dr. Yeshamalla Bhavana, Senior Resident, Department of Ophthalmology, Government Medical College, Nalgonda, Telangana, India

is a Senior Resident in the Department of Ophthalmology at Government Medical College, Nalgonda, Telangana, India. She is involved in clinical ophthalmology services, outpatient evaluation, ocular surface assessment and academic activities. Her areas of interest include anterior segment disorders, pterygium, dry eye disease, ocular surface evaluation and comprehensive ophthalmic care.

Dr. Boddupally Soujanya, Senior Resident, Department of Ophthalmology, Government Medical College, Nalgonda, Telangana, India

is a Senior Resident in the Department of Ophthalmology at Government Medical College, Nalgonda, Telangana, India. She is involved in clinical ophthalmology practice, patient evaluation, ophthalmic diagnostics and academic work. Her areas of interest include ocular surface disease, tear film assessment, anterior segment disorders, pterygium and dry eye-related clinical research. ORCID iD: https://orcid.org/0009-0004-4677-2556

Dr. Beatrice Choppara, Assistant Professor, Department of Ophthalmology, Government Medical College, Nalgonda, Telangana, India

is an Assistant Professor in the Department of Ophthalmology at Government Medical College, Nalgonda, Telangana, India. She is actively involved in undergraduate teaching, clinical ophthalmology services, outpatient care and academic research. Her areas of interest include anterior segment disorders, ocular surface disease, dry eye evaluation, pterygium and patient-centred ophthalmic care.

References

Ahmad SS, Blair K, Kanukollu VM. Optic Atrophy. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2024. PMID: 32644556.

Behbehani R. Clinical approach to optic neuropathies. Clin Ophthalmol. 2007;1(3):233-246. PMID: 19668477; PMCID: PMC2701125.

Biousse V, Newman NJ. Diagnosis and clinical features of common optic neuropathies. Lancet Neurol. 2016;15(13):1355-1367. doi: 10.1016/S1474-4422(16)30237-X. PMID: 27839652. https://doi.org/10.1016/S1474-4422(16)30237-X

Beck RW, Cleary PA, Anderson MM Jr, Keltner JL, Shults WT, Kaufman DI, Buckley EG, et al. A randomized, controlled trial of corticosteroids in the treatment of acute optic neuritis. N Engl J Med. 1992;326(9):581-588. PMID: 1734247. https://doi.org/10.1056/NEJM199202273260901

Beck RW, Cleary PA. Optic neuritis treatment trial. One-year follow-up results. Arch Ophthalmol. 1993;111(6):773-775. doi: 10.1001/archopht.1993.01090060061023. PMID: 8512477. https://doi.org/10.1001/archopht.1993.01090060061023

Gal RL, Vedula SS, Beck R. Corticosteroids for treating optic neuritis. Cochrane Database Syst Rev. 2015;(8):CD001430. doi: 10.1002/14651858.CD001430.pub4. PMID: 26273799. https://doi.org/10.1002/14651858.CD001430.pub4

Levin LA, Beck RW, Joseph MP, Seiff S, Kraker R. The treatment of traumatic optic neuropathy: the International Optic Nerve Trauma Study. Ophthalmology. 1999;106(7):1268-1277. doi: 10.1016/S0161-6420(99)00707-1. PMID: 10406604. https://doi.org/10.1016/S0161-6420(99)00707-1

Cook MW, Levin LA, Joseph MP, Pinczower EF. Traumatic optic neuropathy. A meta-analysis. Arch Otolaryngol Head Neck Surg. 1996;122(4):389-392. PMID: 8600923. https://doi.org/10.1001/archotol.1996.01890160031006

Liu A, Craver EC, Bhatti MT, Chen JJ. Population-Based Incidence and Outcomes of Compressive Optic Neuropathy. Am J Ophthalmol. 2022;236:130-135. doi: 10.1016/j.ajo.2021.10.018. PMID: 34695397. https://doi.org/10.1016/j.ajo.2021.10.018

Chuenkongkaew W, Samsen P, Thanasombatsakul N. Ethambutol and optic neuropathy. J Med Assoc Thai. 2003;86(7):622-625. PMID: 12948256.

Grzybowski A, Zulsdorff M, Wilhelm H, Tonagel F. Toxic optic neuropathies: an updated review. Acta Ophthalmol. 2015;93(5):402-410. doi: 10.1111/aos.12515. PMID: 25159832. https://doi.org/10.1111/aos.12515

Jung JJ, Baek SH, Kim US. Analysis of the causes of optic disc swelling. Korean J Ophthalmol. 2011;25(1):33-36. doi: 10.3341/kjo.2011.25.1.33. PMID: 21350692; PMCID: PMC3039192. https://doi.org/10.3341/kjo.2011.25.1.33

Kerr NM, Chew SSL, Danesh-Meyer HV. Non-arteritic anterior ischaemic optic neuropathy: a review and update. J Clin Neurosci. 2009;16(8):994-1000. doi: 10.1016/j.jocn.2009.04.002. PMID: 19596112. https://doi.org/10.1016/j.jocn.2009.04.002

Biousse V, Newman NJ. Ischemic Optic Neuropathies. N Engl J Med. 2015;372(25):2428-2436. doi: 10.1056/NEJMra1413352. PMID: 26083207. https://doi.org/10.1056/NEJMra1413352

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Published

2026-06-30

How to Cite

Yeshamalla Bhavana, Boddupally Soujanya, & Beatrice Choppara. (2026). Etiological analysis of pale optic disc and its association with six-month visual outcome in patients attending a tertiary care hospital: a prospective observational cohort study. Student’s Journal of Health Research Africa, 7(2), 12. https://doi.org/10.51168/sjhrafrica.v7i2.2754

Issue

Section

Section of Ophthalmology Research