Article

Glaucoma-a diagnostic dilemma

A challenging decision for ophthalmologists is deciding when a patient transitions from suspected glaucoma to having early glaucoma. Years ago, clinical decisions were more closely linked to elevated IOP, but now the disease-defining characteristics of retinal nerve fiber layer loss and optic nerve cupping with or without functional visual field loss are measurable making the diagnosis of glaucoma more complex. Clinicians confront questions regarding what constitutes glaucomatous optic nerve damage and at what point normal aging-related axonal loss becomes glaucomatous axonal loss.

Key Points

Twenty years ago, clinical decisions were more closely linked to elevated IOP, but with tools now available to measure the disease-defining characteristics of retinal nerve fiber layer loss and optic nerve cupping with or without functional visual field loss, the diagnosis of glaucoma has become far more complex. Clinicians find themselves confronted with questions regarding what constitutes glaucomatous optic nerve damage and at what point normal aging-related axonal loss becomes glaucomatous axonal loss.

Such diagnostic dilemmas are not unique to the management of glaucoma. Even in seemingly straightforward medical settings such as those involving infectious diseases, at what point is a patient infected? Should a clinical threshold be based on measurable levels of infectious markers in the bloodstream or when there is a host inflammatory reaction? Regarding glaucoma, does it make a difference in health outcomes to diagnose the disease earlier, prior to visual field loss? Or is it better to wait for definite visual field loss?

I see no alternative to physicians acting on their informed clinical judgments even in the face of the risk that a chronic disease diagnosis would be perceived by patients as a setback. Still, given the complexity of diagnosing glaucoma and inherent uncertainty surrounding individual cases of early glaucoma, it is important to pay close attention to the components of our doctor-patient communication. Beyond the basic underpinnings of good communication, there is room for research on varying degrees of patient involvement in clinical decision-making. We should not automatically assume that more patient involvement is better, but as health professionals who have genuine expertise, neither should we be shy about sharing that expertise nor be afraid to engage patients in the decisions that have real implications in their lives.

Ultimately, the diagnosis rests on our knowledge, and the acceptance of the diagnosis and engagement of a patient in the treatment plan depends on our skills as communicators and educators.

Anne Louise Coleman, MD, PhD is the Frances and Ray Stark Professor of Ophthalmology and professor of epidemiology, Jules Stein Eye Institute, University of California, Los Angeles.

Newsletter

Don’t miss out—get Ophthalmology Times updates on the latest clinical advancements and expert interviews, straight to your inbox.

Related Videos
(Image credit: Ophthalmology Times) From MIGS to gene therapy: Inder Paul Singh, MD, celebrates the past and future of glaucoma care
(Image credit: Ophthalmology Times) NeuroOp Guru: Using OCT to forecast outcomes in ethambutol optic neuropathy
(Image credit: Ophthalmology Times) Inside NYEE’s new refractive solutions center with Kira Manusis, MD
(Image credit: Ophthalmology Times) Dilsher Dhoot, MD, on the evolution of geographic atrophy therapy: where are we now?
(Image credit: Ophthalmology Times Europe) Anat Loewenstein, MD, shares insights on the real-world results of remote retinal imaging
(Image credit: Ophthalmology Times) Two-wavelength autofluorescence for macular xanthophyll carotenoids with Christine Curcio, PhD
(Image credit: Ophthalmology Times) FLIO and the brain: Making the invisible visible with Robert Sergott, MD
(Image credit: Ophthalmology Times) Structure-function correlates using high-res OCT images with Karl Csaky, MD, PhD
(Image credit: Ophthalmology Times) SriniVas Sadda, MD, on high-res OCT of atrophic and precursor lesions in AMD
© 2025 MJH Life Sciences

All rights reserved.