Clinical Update
Glaucoma is the second leading cause
of blindness in the United States. Specifically,
open-angle glaucoma is progressive
and asymptomatic, with elevated
intraocular pressure causing a gradual
increase in cupping of the optic nerve
disc. The effect of this cupping on the retina
is the diminishment of the patient's
visual field.
There are several predisposing factors,
including family history, concurrent diabetes,
or severe myopia. Black patients
over the age of 40 and white patients
over the age of 65 also have an increased
risk of developing open-angle glaucoma.
Although elevated intraocular pressure
is considered a major risk factor, it is
not completely effective as a diagnostic
tool. Patients may have normal pressures
within the eye and still have glaucoma.
Visual field testing is the mainstay
of glaucoma diagnosis and its progressive
management.
Without treatment, open-angle glaucoma
will result in irreversible loss of vision.
Before aggressive treatments involving
lasers or surgery are employed, therapy
involves sterile ophthalmic solutions that
affect sympathetic receptors in the eye.
Brimonidine, at a 0.2% concentration, creates
changes at the alpha-receptor level
in order to reduce intraocular pressure.
Pharmacology
Reduction in intraocular pressure generally
is accomplished either by decreasing
the production of aqueous humor
entering the eye or by increasing its outflow
through the trabecular meshwork or
uveoscleral pathways. Brimonidine is a relatively
selective alpha-2 receptor agonist
and reduces intraocular pressure by both
decreasing the production of aqueous
humor and increasing its outflow through
the uveoscleral pathway. This alpha-2
receptor agonist property reduces both
elevated and normal pressure in the eye,
regardless of the presence of glaucoma.
The maximum reduction in pressure is
seen within 2 to 3 hours following the
administration of brimonidine. Overall, ophthalmic
pressure is reduced by ~25%.
Administration and Dosing
The recommended dosing of brimonidine
for open-angle glaucoma is 1 drop in
the affected eye 3 times daily, spaced at
8-hour intervals. Response to the initial
therapy should be checked after 4 weeks
and then monitored periodically to
observe effectiveness and to look for
potential side effects.
As with any sterile ophthalmic preparation,
care should be taken when handling
brimonidine solution to prevent
contamination. Patients should be
advised to wash their hands before and
after using this solution. In addition,
when using multiple ophthalmic therapies,
the patient needs to wait at least 5
minutes before the administration of
other eyedrops.
Side Effects and Drug Interactions
Adverse effects occur frequently with
brimonidine (at a rate of 10-30%) and
include localized burning, headache, the
sensation of a foreign body in the eye,
ocular pruritus, blepharitis, xerophthalmia,
tearing, corneal staining, and
blurred vision.
Although systemic effects of alpha-2
agonists may result in vasoconstriction,
the topical use of brimonidine among
adults appears to generate minimal concern
among clinicians regarding this
effect. The manufacturers do recommend
caution, however, when using brimonidine
in patients with severe cardiovascular
conditions, orthostatic hypotension,
cerebral or coronary insufficiency,
or Raynaud's phenomenon.
Although concern over systemic effects
is slight among adults, it should be
noted that ophthalmic use of brimonidine
among children under the age of 2 has
resulted in apnea and lethargy, and that,
in early studies, treatment was discontinued
in 16% of children aged 2 to 7 due to
sleepiness. Somnolence in these reports
appears to be age-and weight-related.
Therefore, the use of brimonidine requires
cautious monitoring in children
under the age of 7 and is actively discouraged
in children under the age of 2.
In general, patients have allergic reactions
to brimonidine at a rate of 10% to
20%. The high frequency of allergic reactions
to brimonidine appears to sensitize
the patient to subsequent drugs used to
treat open-angle glaucoma. A special formulation
using a Purite product as a preservative
has been introduced to the
market in an effort to reduce the rate of
allergy. This form, however, is still under
patent protection.
Outlook
The consequences of untreated glaucoma
can be devastating. Before today's
commonly available treatments, blindness
generally was inevitable. This progressive
condition can now be treated
with several agents. Although patients
with glaucoma can experience an
increased quality of life with their use, the
treatments themselves possess side
effects that require repeated assessment.
Brimonidine is available as a 0.2% sterile
ophthalmic solution from Bausch and
Lomb, Allergan, and Falcon Pharmaceuticals.
Mr. Middleton is an instructor of pharmacology
at Kellogg Community
College in Battle Creek, Mich.