The one-month effects of topical betaxolol, dorzolamide and apraclonidine on ocular blood flow velocities in patients with newly diagnosed primary open-angle glaucoma
Am. Avunduk et al., The one-month effects of topical betaxolol, dorzolamide and apraclonidine on ocular blood flow velocities in patients with newly diagnosed primary open-angle glaucoma, OPHTHALMOLA, 215(5), 2001, pp. 361-365
Purpose: This double-masked, prospective and randomized clinical trial was
planned to investigate with color Doppler imaging the 1-month vascular effe
cts of betaxolol, dorzolamide and apraclonidine treatment on patients with
newly diagnosed primary open-angle glaucoma (POAG). Methods: 22 consecutive
patients with newly diagnosed POAG between the ages of 46 and 72 years wer
e enrolled in this study. All patients were newly diagnosed cases and had n
ot received any antiglaucoma medication before. Patients who had a systemic
vascular disease (including systemic hypertension) or were taking P-blocke
rs, nitrates or calcium channel blockers were excluded from the study. The
patients were randomly divided into three groups. Groups A and B contained
7 patients, group C contained 8 patients. Group A patients were treated wit
h topical betaxolol, group B patients received topical dorzolamide eye drop
s, and group C patients were treated with topical apraclonidine eye drops.
Peak systolic velocities (PSV), end-diastolic velocities (EDV) and resistiv
e indices (RI) in the right ophthalmic arteries (OA), central retinal arter
ies (CRA) and posterior ciliary arteries (PCA) were measured at baseline by
using color Doppler imaging on a masked basis. On days 15 and 30 of treatm
ent, the same measurements were repeated. The inter- and intragroup results
were compared statistically. Results: Compared to pretreatment measurement
s, topical betaxolol therapy significantly decreased PSV only in the PCA an
d only on day 30 of treatment (p = 0.011). On days 15 and 30, dorzolamide d
ecreased RI measurements in the PCA compared to pretreatment measurement (p
= 0.013 and p = 0.011, respectively). Apraclonidine also decreased PSV in
the OA on days 15 and 30 of treatment when compared to pretreatment values
(p = 0.013 and p = 0.012, respectively). When 15-day measurements were comp
ared between the groups, PSV in the CA were significantly higher in dorzola
mide-treated patients compared to other groups (p = 0.013 and p = 0.011). O
n day 30 of treatment, PSV in the OA was also higher in the dorzolamide-tre
ated group than the other groups (p = 0.012 and p = 0.01). Additionally, ap
raclonidine-treated patients had a significantly lower EDV in the OA than t
he other groups (p = 0.013 and p = 0.01). The RI in the OA was also signifi
cantly lower in the apraclonidine-treated group compared to the other group
s (p = 0.01 and p = 0.011). Conclusion: Our study suggests that dorzolamide
has the most advantageous 1-month effects on blood flow velocity in the re
trobulbar arterial circulation of POAG patients. Betaxolol seems superior t
o apraclonidine in this regard. Our data may help the clinician when treati
ng patients with POAG medically. Further studies using a larger population
size may clarify our results. Copyright (C) 2001 S. Karger AG, Basel.