ArticleClinical ophthalmology (Auckland, N.Z.)2025
The Prevalence of Corneal Sensitivity Loss in Patients with and without Dry Eye Disease.
Article in Clinical ophthalmology (Auckland, N.Z.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
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Who cites it
8 citing papers in PubMed.
- Topical Insulin for Corneal Persistent Epithelial Defects: A Multicenter Retrospective Study.Ophthalmology and therapy · 2026Article
- Validation and Comparative Analysis of a Contemporary Non-Contact Corneal Aesthesiometer.Journal of clinical medicine · 2026Article
- Research progress in animal models of dry eye disease: Types, mechanisms, and application prospects.Animal models and experimental medicine · 2026Review
- Adjunctive Cryopreserved Amniotic Membrane for Recalcitrant Keratopathy: Long-Term Outcomes with Maintenance Therapy.Clinical ophthalmology (Auckland, N.Z.) · 2026Article
- Corneal Sensitivity with the Non-contact Esthesiometer as Compared to the Cotton Wisp Test in Patients with Ocular Surface Diseases.Ophthalmology and therapy · 2026Article
- Management of Stage 1 Neurotrophic Keratopathy with Shelf-Stable, Cryopreserved Amniotic Membrane: A Retrospective Study.Clinical ophthalmology (Auckland, N.Z.) · 2026Article
- Therapeutic Outcomes of Shelf-Stable, Cryopreserved Amniotic Membrane in Recalcitrant Keratopathy.Clinical ophthalmology (Auckland, N.Z.) · 2025Article
- Shelf-Stable, Cryopreserved Amniotic Membrane for the Management of Ocular Surface Disease: A Retrospective Assessment.Clinical optometry · 2025Article
Corrections and comments
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Authors and funding
1 author.
Funding
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Abstract
Purpose: To assess the prevalence of corneal sensitivity loss in consecutive patients presenting to the clinic as well as in those patients with and without dry eye disease (DED). Methods: Retrospective, single-center study of consecutive patients who presented to the eye clinic and underwent corneal sensitivity testing using a non-contact esthesiometer. Data included demographics, medical history, prior or current treatments, comorbidities, corneal sensitivity measurements, dry eye symptoms (Standard Patient Evaluation of Eye Dryness Questionnaire [SPEED] questionnaire), and corneal staining scores (Oxford scale). The primary outcome was the prevalence of corneal sensitivity loss, defined as ≥8 mbar. Secondary outcome measures included the prevalence of corneal sensitivity loss in eyes with DED (Oxford ≥2 and SPEED ≥5) and without DED (Oxford ≤1 and SPEED <5). Results: A total of 395 eyes of 198 patients were included for analysis. Average age was 67.7 ± 16.0 years, and the majority of patients (60.6%) were female. Corneal sensitivity loss was observed in 9.4% of all eyes, and 12.6% of patients had reduced corneal sensitivity in at least one eye. When assessing eyes with signs of DED (Oxford ≥2), 19.7% (13/66) had corneal sensitivity loss. This prevalence increased to 31.4% (11/35) in eyes with both signs and symptoms of DED. Conversely, the prevalence was 5.5% (12/219) in eyes without DED. Binary logistic regression demonstrated that Oxford staining score was the strongest predictor of reduced corneal sensitivity (OR: 2.0, 95% CI: 1.3-3.0, p=0.001), with other significant factors including history of DED, stroke, and herpes zoster virus. Conclusion: Reduced corneal sensation, a sign of corneal nerve damage and precursor to neurotrophic keratitis, affects nearly 10% of all eyes and 30% of eyes with signs and symptoms of DED. Routine clinical testing of corneal sensation should be implemented, particularly in patients with DED, to ensure early diagnosis and prompt treatment to prevent disease progression.
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