Topically administered beta blockers are the preferred medical therapy
for glaucoma. These agents reduce intraocular pressure (IOP), thereby
preventing damage to the optic nerve and the subsequent loss of visio
n. Timolol, betaxolol, levobunolol, metipranolol, and carteolol are th
e topical beta blockers available in the U.S. They have similar IOP-lo
wering efficacy, but differ in other pharmacological properties. Topic
ally administered beta blockers are generally well tolerated. They und
ergo systemic absorption, however, and can adversely affect cardiovasc
ular and bronchopulmonary function in patients with existing diseases
such as heart failure, sinus bradycardia, chronic obstructive airways
disease, or asthma. Betaxolol, which is beta1-selective, and carteolol
, which has intrinsic sympathomimetic activity (ISA), may have systemi
c tolerability profiles superior to the traditional nonselective, non-
ISA beta blockers. These hypotheses require confirmation in controlled
clinical trials. Local adverse effects associated with beta blockers
include stinging, burning, red eye, itching, tearing and loss of corne
al sensitivity. Stinging upon instillation is a particularly frequent
finding with betaxolol (up to 30% to 40% of patients). Preliminary evi
dence suggests that carteolol has the best local tolerability profile
of these drugs.