DILEMMAS IN GLAUCOMA
This lecture was delivered by Dr Parvez Siddique on 23 May 2010 at
a JDOS CME in Hotel Narmada Jackson 5 PM. It was a JDOS self sponsored
session.
Why is the incidence of glaucoma (in india or world) rising ?
In general, longevity of people is increasing across the globe resulting
in increase in number of old people in the world. Glaucoma being an age-related
disease is also increasing correspondingly.
For the general ophthalmologist, how do you know whether optic nerve
and RNFL damage is controlled or not ?
A base line optic disc stereo photograph should be taken and should be
compared with the patient's current status to see if change in optic nerve
hand and nerve fiber layer are occurring. One look for increase thinning
of the neuro retinal rim, disc hemorrhages and increase in the angular
extent or area of parapapillary atrophy to assess the optic disc for change.
The nerve fiber layer can also be examined with red free illumination
to look for appearance of new defect is pathological only if it extends
all the way to the disc margin.
If disc photography is not possible, detailed drawing of the disc appearance
will help.
What do edge points in the evaluation of visual fields mean ?
The edge point refer to those points on the visual field that are at
edge of the field (the most peripheral points).
They are of significance because we usually do not include the edge points
in a 30-2 printout since they could be artifact. The nasal edge point
about and below the horizontal midline are included since the nasal step
in glaucoma affects these points.
How reliable is the anderson criteria ?
The Anderson criteria is not a measure of how reliable a visual field
is. It describes a defect, which is significant and likely to be due to
glaucoma. The Glaucoma hemi field test is reported to have a specificity
of 94% for glaucoma affects these points.
Due to heavy patient attendance and being unable to screen patients
for glaucoma how should one proced so that no glaucoma ?
Glaucoma being an asymptomatic disease, the chances of missing it are
very high. At present we do not have any single test with specificity
and sensitivity. The idea way will be to do a comprehensive eye examination
for all people who seek ophthalmic check up.
Will you treat a non-progressing field defect in the absence of any
clinical optic nerve head cupping ?
If we detect a visual field defect which is consistent on repeated testing
and the optic disc appears normal it is important to rule out other pathology
on drug available clinically for neuroprotection of the optic nerve hand
in glaucoma.
At present we do not have any medication with proven neuroprotection.
However theoretically speaking, we need to assess whether visual function
and structural damage remain stable as an effect of neuroprotection.
Is there any difference in therapeutic effect amongst the various brands
of antiglaucoma drugs, for instance, travatan versus travoprost ?
The scientific evaluation of such a difference requires a randomized
clinical trial with cross over, which has not been performed for travatan
varsus Travoprost. Any drug can be used provided the clinician notes the
baseline IOP and checks that there is a drop in IOP by at least 20% for
a first-line drug such as a prostaglandin. Since cost is a major issue
affecting compliance to therapy in our population, generic brands can
be prescribed as monotherapy with a cheak on IOP lowering efficacy and
how long a bottle of the drug lasts (the number of drops in a bottle).
What should be the line of treatment for a patient having almost total
glaucomatous cupping ?
Such a patient requires a target IOP of around 12 mm Hg and should be
treated medically with a prostagladin-betablocker combination OD (provided
there are no contra-indications to beta-blockers) and brimonidine 0.1%
or dorzolamide BD. Three drugs give as three drops provide maximal IOP
lowering with potential for maintaining long-term compliance without compromising
the quality of life of the patient. If target IOP is not achieved medically
(evaluated by doing a diurnal IOP curve on medications) or there is evidence
of progression of optic neuropathy on visual fields, the patient should
be subjected to trabeculectomy with Mitomycin c and use of releasable
sutures.
What is the safest drug in juvenile glaucoma and congenital glaucoma
?
Timolol BD 0.25% with occlusion of tear duct performed by the mother
is the safest drug for congenital glaucoma. Medical therapy for juvenile
glaucoma is not different from adult POAG and can be treated with any
the drugs.
In manipulative gonioscopy is the true angle before or after manipulation?
If before, then why manipulate at all ?
The true angle is before manipulation If this is open, there is no need
to manipulate (indentation with 4 mirror lens is better). However, if
the angle is narrow or closed, indentation will tell us if the closure
is appositional (opens with indentation) or synechial. When the angle
opens, one will be able to visualize giniosynechiae and blotchy pigments
that are diagnostic of primary closure.
How do you interpret a visual field change due to glaucoma in a patient
with moderate-to-advanced cataract as well ?
The visual field analysis software is robust enough to filter out the
effect of most cataracts and the Pattern Deviation plot display the defect
after adjusting for this generalized depression. What is important is
to assess whether the visual field defect corresponds to the optic disc
changes. If it does not, and there is a localized defect that corresponds
to a localized dense posterior subcapsular or cortical cataract we could
attribute the defect to the cataractous change.
Which antiglaucoma drug should be used if you have a patient who has
silicone oil in his eyes ?
For early postoperative glaucoma, you could use beta-blockers, alpha
agonists and/ systemic carbonic anhydrase inhibitors. If high IOP is due
to an overfill, some silicone oil should be removed. For late post-operative
gloucoma, prostagladins can be used.
How would you manage a trabeculectomy-failed case who is not responding
medically ?
Failed trabeculectomy not responding to medical therapy. In the early
postoperation period, do a gonioscopy to check internal ostium. If ostium
is patent, laser suturolysis and needling of the bleb under the scleral
flap (with 5 FU) can be attempted.
In the late postoperative periods, If conjunctiva is fibrosed, a glaucoma
drainage device should be implanted.
If Visual potential is poor (inaccurate projection) a 180/270 degree
diode laser cyclophotocoagulation can be performed leaving the superior
quadrant (operated area)
When Should Viscoannulostomy Be preferred over a trabeculectomy ?
Long-term IOP control with trabeculectomy is much better then viscocannlostomy.
Trabeculectoy is more likely to achieve target IOP in eyes with moderate
to advanced glaucoma. In addition the surgical procedure is technically
much easier and takes less surgical time so at present there is no condition
where I would prefer viscocannlostomy over trabeculectomy.
In case of acute angle closure glaucoma do you intervene with SLT laser
?
SLT is contraindicated in angle closure glaucoma since SLT selectively
target the pigmented cells of the trabecular meshwork which gets obsured
in angle closure cases.
THANK YOU
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