This multicenter retrospective cohort study compared the effectiveness and safety of long-term tafluprost, travoprost, or latanoprost in patients with primary open-angle glaucoma (POAG) or normal-tension glaucoma (NTG). Data were extracted from electronic medical records of 300 patients treated with tafluprost, travoprost, or latanoprost for >6 months. Propensity matching for age and sex was used for effectiveness and safety comparisons. The primary endpoint was visual field (VF) progression via mean deviation (MD) slope. Secondary endpoints were change of MD, intraocular pressure, pattern standard deviation, VF index, and advanced glaucoma intervention study score. Treatment-related adverse events (AEs) were also compared between groups. O...
Background: Topical beta blockers, Timolol and the prostaglandin F2α analogue Latanoprost are the mo...
Background: Raised intraocular pressure (IOP) is a strong risk factor for development of glaucoma. I...
Purpose: To assess the safety and efficacy of transitioning patients whose intraocular pressure (IOP...
This multicenter retrospective cohort study compared the effectiveness and safety of long-term taflu...
Background: This prospective, open, randomized, parallel-group, comparative study is to evaluate the...
In this study, we investigated the effect of preservative-free (PF) 0.0015% tafluprost (TA), to the ...
Edmund P FarrisNew York University, New York, NY; Manhattan Veterans Administration Hospital, New Yo...
Objective: The objective of this study was to compare the safety of BAK-preserved latanoprost versus...
Aim: To evaluate the therapeutic efficacy, safety and tolerability of newly developed preservative-f...
. Purpose. To compare the ocular hypotensive effect of tafluprost with prostaglandin analogues (PGAs...
AbstractBackground: A 2005 meta-analysis suggests that lowering intraocular pressure (IOP) in patien...
The aim of the study was to evaluate the long-term 24-hour intraocular pressure (IOP) efficacy of tr...
Objective To compare a fixed combination of 0.03% bimatoprost and 0.5% timolol (BTFC) with latanopro...
Background: Prospective, observational studies that enroll large numbers of patients with few exclus...
Background: The purpose of this study was to compare and evaluate the clinical efficacy of topically...
Background: Topical beta blockers, Timolol and the prostaglandin F2α analogue Latanoprost are the mo...
Background: Raised intraocular pressure (IOP) is a strong risk factor for development of glaucoma. I...
Purpose: To assess the safety and efficacy of transitioning patients whose intraocular pressure (IOP...
This multicenter retrospective cohort study compared the effectiveness and safety of long-term taflu...
Background: This prospective, open, randomized, parallel-group, comparative study is to evaluate the...
In this study, we investigated the effect of preservative-free (PF) 0.0015% tafluprost (TA), to the ...
Edmund P FarrisNew York University, New York, NY; Manhattan Veterans Administration Hospital, New Yo...
Objective: The objective of this study was to compare the safety of BAK-preserved latanoprost versus...
Aim: To evaluate the therapeutic efficacy, safety and tolerability of newly developed preservative-f...
. Purpose. To compare the ocular hypotensive effect of tafluprost with prostaglandin analogues (PGAs...
AbstractBackground: A 2005 meta-analysis suggests that lowering intraocular pressure (IOP) in patien...
The aim of the study was to evaluate the long-term 24-hour intraocular pressure (IOP) efficacy of tr...
Objective To compare a fixed combination of 0.03% bimatoprost and 0.5% timolol (BTFC) with latanopro...
Background: Prospective, observational studies that enroll large numbers of patients with few exclus...
Background: The purpose of this study was to compare and evaluate the clinical efficacy of topically...
Background: Topical beta blockers, Timolol and the prostaglandin F2α analogue Latanoprost are the mo...
Background: Raised intraocular pressure (IOP) is a strong risk factor for development of glaucoma. I...
Purpose: To assess the safety and efficacy of transitioning patients whose intraocular pressure (IOP...