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When Is Early Diagnosis Too Early?
Our charge in glaucoma is
profoundly simple: Keep our patients with glaucoma asymptomatic
until they die, hopefully using therapeutic options wisely to
minimally impact their quality of life. So when should we step
in therapeutically? This will vary radically from patient to
patient, and the genius, or lack thereof, of your care will not
be known for ten years or so, in retrospect!
What if we had a
device that could accurately count the individual ganglion cells?
Would we start therapy when one cell was unequivocally lost from
glaucomatous optic neuropathy? What about 10 cells, or 100, or
1,000, or 10,000? When is the “right” time to intercede therapeutically?
At what stage of optic nerve demise do image analyzers discern?
If the instrument-generated data indicates early glaucoma, is
it just physiologic variance, or indeed early glaucoma? This
technology has now evolved to the point of being clinically valuable.
It is not a perfect (i.e. 100% sensitive and specific), but
is now refined to the point of being clinically valuable for
many patients.
While we submit that the astute clinician using
applanation tonometry, corneal pachymetry, state-of-the-art static
threshold perimetry, and stereoscopic evaluation of the optic
nerve head will be able to assess risk for glaucoma development
plenty early enough to meet the goal stated in the first sentence,
we have found glaucoma imaging technology further enhances our
clinical decision making. We now recommend all doctors providing
glaucoma care acquire one of these available instruments. The
one we use is the GDx-VCC, and we are pleased with its clinical
performance.
Does it serve the overall good of humanity and public
health to presume abnormal findings on one test parameter or
result (in the absence of other confirmatory clinical findings)
to represent a disease entity for which treatment may needlessly
exact a toll of diminished quality of life? Carrying a disease
diagnosis and its attendant anxiety, expense of therapy, and
exposure to potential side effects is a step that should be taken
only when an appropriate assessment of risk or a definitive diagnosis
is made and the institution of therapy meets the wisdom of risk
versus benefit.
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