

GLAUCOMA

A
more in-depth discussion of the current status of glaucoma diagnosis
and management
A famous glaucomatologist once described the treatment of glaucoma
as "delaying the inevitable progression toward blindness".
Though pessimistic, this viewpoint was based on common clinical
experience in an age when few medications or surgeries were successful
at halting the process of glaucoma. Thankfully, recent advances
in glaucoma diagnosis and treatment have made this the exception
rather than the rule. This article will review a few of these advances.
Glaucoma is
best understood as an optic neuropathy characterized by progressive
damage to the optic nerve and typical visual field loss (loss of
peripheral vision). In the center of the optic disc (the portion
of the optic nerve that is visible inside the eye) is an excavation
or "cup" that is normally only 30% of the surface area
of the disc. The "cup-to-disc ratio" (CDR or C/R) is a
way to document the size of the cup. As nerve fibers are lost due
to progressive glaucoma damage, the CDR enlarges as more of the
nerve head is taken up with cup instead of healthy nerve tissue.
Documented enlargement of the cup is diagnostic of glaucoma, while
a large cup or asymmetry of the cups between the eyes (one cup much
larger than the other) are suggestive, but not diagnostic of glaucoma.
Nerve fibers tend to be lost first from the top and the bottom of
the optic disc resulting in specific patterns of visual field loss.
Initial glaucomatous visual field loss is often "nasal"
(on the nose side of each eye's field of vision) and so is not noticed
(less so if one's nose is big!). This gradually progresses around
and toward the center of vision until only a central island of vision
is left ("tunnel vision"). In the end stages, complete
blindness can occur.
Elevation of
the pressure inside the eye (intraocular pressure or IOP) was once
thought to cause all glaucoma, but we now know that this is only
one (if the most important) of many risk factors. In fact, up to
a third of glaucoma patients never have an abnormally high IOP (so-called
"low or normal tension" glaucoma). Recently, the first
gene causing a form of glaucoma was identified. As more genes are
identified, we may realize the exciting goal of earlier and more
accurate diagnosis, followed by therapy directed at the underlying
genetic/biochemical cause of the glaucoma, rather than at the effect
(elevated IOP).
Automated visual
field testing has undergone a revolution in the past couple of years.
Improvements in the computer software of the Humphrey perimeter
(called SITA = Swedish Interactive Testing Algorithm) have allowed
the test time to be cut in half with improved reliability, so patients
get less tired and we get better information. The machine uses a
"smart" strategy that adjusts the speed of the test based
on the patient's responses, thus reducing patient anxiety. Patients
do still need to be reminded that the test is mapping out their
side vision so they must keep their eyes looking straight ahead
and only use their side vision to "see" the lights. The
machine is trying to find the dimmest light that can be seen peripherally,
so even a normal person will not see half the lights and even the
"seen" lights may only appear as a dim glimmer. Once this
is understood, most patients do a very good job of taking the test,
improving the reliability of the results.
There are several
"hot" new visual field tests that are not yet commonly
used. SWAP (Short Wave Automated Perimetry, also known as "blue-on-yellow")
can be performed on a properly upgraded Humphrey perimeter. Unlike
standard perimetry which flashes a white spot of light onto a white
background, SWAP projects a blue light onto a yellow background.
It can catch subtle glaucoma damage earlier than standard perimetry,
which may be helpful in deciding when to treat persons with high
intraocular pressure but normal appearing optic nerves (a "glaucoma
suspect"). Another exciting new technique is called Frequency
Doubling Technology (FDT). Because the machine required for this
test is relatively small and the test only takes a couple of minutes
to perform, FDT may be very useful in screening large populations
for glaucoma.
Optic nerve
imaging is a rapidly developing technology allowing one to compare
computerized measurements of the optic disc and/or nerve fiber layer
to determine if glaucoma damage is present or has worsened. Examples
of these instruments include the GDx Nerve Fiber Analyzer, the Heidelberg
Retinal Tomograph (HRT) and Ocular Coherence Tomography (OCT). Eye
Health Northwest has recently purchased a GDx Nerve Fiber Analyzer.
This new technology allows us to objectively measure the retinal
Nerve Fiber Layer (NFL), the tissue that is damaged by glaucoma.
In the past, this thin, semi-transparent tissue could only be subjectively
evaluated under magnification with the naked eye. The GDx uses the
change in birefringence as near-infrared polarized laser light passes
through the NFL to calculate the actual thickness of the NFL. The
GDx generates this measurement of the NFL in just seconds through
an undilated pupil. By comparing these results to a database of
healthy, glaucoma-free eyes and to the patient's previous exams,
we can assess whether glaucomatous damage has occurred or progressed.
The exam is objective so the patient is not required to respond
in order to have a valid and accurate result. This is an advantage
over other tests, such as the visual field, which requires a subjective
response from the patient. Also, it may be more sensitive to the
subtle changes in the NFL that occur early in the course of glaucoma.
This means better diagnostic decisions, including earlier diagnosis
and modification of therapy. This test does not eliminate the need
for regular examinations and visual field testing. It does provide
one additional and very useful means of diagnosing and monitoring
glaucoma.
Many new medications
are now available for lowering IOP. Ten years ago a patient with
uncontrolled glaucoma may have ended up on 5 medications before
proceeding to laser or surgery. Many of these medications had noxious
side effects and had to be taken several times a day. Now we have
medications with fewer side effects that can be taken only once
or twice a day (e.g., Alphagan, Xalatan, Lumigan and Travatan).
Combinations drugs are also coming out, decreasing the number of
bottles a patient needs to keep track of (e.g., Cosopt = Timoptic
+ Trusopt). This all serves to improve the quality of life of the
glaucoma patient who would otherwise be tied to a rigorous schedule
of drops. At the cutting edge of glaucoma research are medications
that seek to protect the optic nerve from pressure damage, rather
than lowering the pressure itself. Treatments aimed at the genetic
defects underlying most glaucoma may be seen in the not-too-distant
future.
Research has
shown that laser and surgical procedures can be considered much
earlier in the treatment of glaucoma and in some cases may precede
use of medications. Trabeculectomy is the most commonly performed
surgery for glaucoma. This procedure was developed in the 1950's
and the actual surgical technique has not changed much since that
time. What has changed is the use of medications and laser to modify
the eye's healing response during and after surgery. During surgery
a trap door is fashioned in the white of the eye (the sclera) to
allow the fluid in the eye to drain out under the clear covering
of the eye (the conjunctiva) where it is absorbed back into the
bloodstream. If this trapdoor heals shut, the surgery will fail
and the eye pressure will rise again. Frequent steroid drops are
used to suppress this healing and the sutures holding the trap door
down may be cut with the laser to allow more fluid out (suturelysis).
Mitomycin C (MMC) and 5-Fluorouracil (5 FU) are chemotherapy drugs
that also happen to inhibit or kill fibroblasts, the cells that
cause healing and scarring after surgery. MMC is applied to the
eye during surgery while 5 FU is given as one or more subconjunctival
injections in the days and weeks after surgery. While these techniques
do have side effects such as increased risk of infection and the
possibility of an eye pressure that is too low (hypotony), they
have greatly increased the success rate of trabeculectomy.
And finally,
that question topmost in your minds: what about marijuana? Legalization
of marijuana for medicinal use in Oregon has generated a flood of
patients interested in treating their glaucoma with it. The active
ingredient in marijuana does lower IOP, but not as well as commonly
available glaucoma medicines. Due to its short duration of action,
you must smoke a joint every 3 hours to maintain a therapeutic effect.
This is certainly an impractical treatment schedule, not to mention
the adverse effect of a life lived constantly "under the influence".
Research is underway to test an eye drop made from the active ingredient.
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