Bimatoprost/timolol fixed combination (BTFC) in patients with primary open angle glaucoma or ocular hypertension in Greece

AIM: To evaluate the efficacy and tolerability of the fixed combination of bimatoprost 0.03% and timolol 0.5% (BTFC) in patients in Greece with primary open angle glaucoma (POAG) or ocular hypertension (OHT) whose previous therapy provided insufficient lowering of intraocular pressure (IOP). METHOD...

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Main Authors: Tryfon G. Rotsos, Vasso G. Kliafa, Kevin J. Asher, Dimitrios Papaconstantinou
Format: Article
Language:English
Published: Press of International Journal of Ophthalmology (IJO PRESS) 2016-01-01
Series:International Journal of Ophthalmology
Subjects:
Online Access:http://www.ijo.cn/en_publish/2016/1/20160112.pdf
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spelling doaj-7060d2205ce04879a2283f21e9011d4f2020-11-25T02:42:29ZengPress of International Journal of Ophthalmology (IJO PRESS)International Journal of Ophthalmology2222-39592227-48982016-01-0191697510.18240/ijo.2016.01.12Bimatoprost/timolol fixed combination (BTFC) in patients with primary open angle glaucoma or ocular hypertension in GreeceTryfon G. Rotsos0Vasso G. Kliafa1Kevin J. Asher2Dimitrios Papaconstantinou3st Department of Ophthalmology, University of Athens, Athens 11527, GreeceDepartment of Regulatory Affairs, Nexus Medicals S.A., Pikermi 19009, GreeceDepartment of Regional Scientific Services, Allergan Holdings Limited, Marlow SL7 1YL, UKst Department of Ophthalmology, University of Athens, Athens 11527, GreeceAIM: To evaluate the efficacy and tolerability of the fixed combination of bimatoprost 0.03% and timolol 0.5% (BTFC) in patients in Greece with primary open angle glaucoma (POAG) or ocular hypertension (OHT) whose previous therapy provided insufficient lowering of intraocular pressure (IOP). METHODS: A multicenter, prospective, open-label, non-interventional, observational study of the use of BTFC in clinical practice was conducted at 41 sites in Greece. The primary endpoint was the reduction in IOP from baseline at study end, approximately 12wk after initiation of BTFC therapy. RESULTS: A total of 785 eligible patients were enrolled in the study and 97.6% completed the study. The mean±SD IOP reduction from baseline at 12wk after initiation of BTFC was 6.3±2.8 mm Hg (n=764; P<0.001). In patients (n=680) who replaced their previous IOP-lowering monotherapy (a single drug, or a fixed combination of 2 drugs in a single ophthalmic drop) with once-daily BTFC, the mean±SD IOP reduction from baseline at 12wk was 6.2±2.8 mm Hg (P<0.001). IOP was reduced from baseline in 99.2% of patients, and 58.0% of patients reached or exceeded their target IOP. Substantial mean IOP reductions were observed regardless of the previous therapy. BTFC was well tolerated, with 96.0% of patients who completed the study rating the tolerability of BTFC as “good” or “very good.” Adverse events were reported in 8.3% of patients; only 0.6% of patients discontinued the study due to adverse events. CONCLUSION: In clinical practice in Greece, BTFC is well tolerated and effectively lower the IOP in patients with POAG or OHT who requires additional IOP lowering on their previous therapy.http://www.ijo.cn/en_publish/2016/1/20160112.pdffixed combinationglaucomaintraocular pressureocular hypertensionprimary open angle glaucomaprostaglandinprostamidetimolol
collection DOAJ
language English
format Article
sources DOAJ
author Tryfon G. Rotsos
Vasso G. Kliafa
Kevin J. Asher
Dimitrios Papaconstantinou
spellingShingle Tryfon G. Rotsos
Vasso G. Kliafa
Kevin J. Asher
Dimitrios Papaconstantinou
Bimatoprost/timolol fixed combination (BTFC) in patients with primary open angle glaucoma or ocular hypertension in Greece
International Journal of Ophthalmology
fixed combination
glaucoma
intraocular pressure
ocular hypertension
primary open angle glaucoma
prostaglandin
prostamide
timolol
author_facet Tryfon G. Rotsos
Vasso G. Kliafa
Kevin J. Asher
Dimitrios Papaconstantinou
author_sort Tryfon G. Rotsos
title Bimatoprost/timolol fixed combination (BTFC) in patients with primary open angle glaucoma or ocular hypertension in Greece
title_short Bimatoprost/timolol fixed combination (BTFC) in patients with primary open angle glaucoma or ocular hypertension in Greece
title_full Bimatoprost/timolol fixed combination (BTFC) in patients with primary open angle glaucoma or ocular hypertension in Greece
title_fullStr Bimatoprost/timolol fixed combination (BTFC) in patients with primary open angle glaucoma or ocular hypertension in Greece
title_full_unstemmed Bimatoprost/timolol fixed combination (BTFC) in patients with primary open angle glaucoma or ocular hypertension in Greece
title_sort bimatoprost/timolol fixed combination (btfc) in patients with primary open angle glaucoma or ocular hypertension in greece
publisher Press of International Journal of Ophthalmology (IJO PRESS)
series International Journal of Ophthalmology
issn 2222-3959
2227-4898
publishDate 2016-01-01
description AIM: To evaluate the efficacy and tolerability of the fixed combination of bimatoprost 0.03% and timolol 0.5% (BTFC) in patients in Greece with primary open angle glaucoma (POAG) or ocular hypertension (OHT) whose previous therapy provided insufficient lowering of intraocular pressure (IOP). METHODS: A multicenter, prospective, open-label, non-interventional, observational study of the use of BTFC in clinical practice was conducted at 41 sites in Greece. The primary endpoint was the reduction in IOP from baseline at study end, approximately 12wk after initiation of BTFC therapy. RESULTS: A total of 785 eligible patients were enrolled in the study and 97.6% completed the study. The mean±SD IOP reduction from baseline at 12wk after initiation of BTFC was 6.3±2.8 mm Hg (n=764; P<0.001). In patients (n=680) who replaced their previous IOP-lowering monotherapy (a single drug, or a fixed combination of 2 drugs in a single ophthalmic drop) with once-daily BTFC, the mean±SD IOP reduction from baseline at 12wk was 6.2±2.8 mm Hg (P<0.001). IOP was reduced from baseline in 99.2% of patients, and 58.0% of patients reached or exceeded their target IOP. Substantial mean IOP reductions were observed regardless of the previous therapy. BTFC was well tolerated, with 96.0% of patients who completed the study rating the tolerability of BTFC as “good” or “very good.” Adverse events were reported in 8.3% of patients; only 0.6% of patients discontinued the study due to adverse events. CONCLUSION: In clinical practice in Greece, BTFC is well tolerated and effectively lower the IOP in patients with POAG or OHT who requires additional IOP lowering on their previous therapy.
topic fixed combination
glaucoma
intraocular pressure
ocular hypertension
primary open angle glaucoma
prostaglandin
prostamide
timolol
url http://www.ijo.cn/en_publish/2016/1/20160112.pdf
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AT kevinjasher bimatoprosttimololfixedcombinationbtfcinpatientswithprimaryopenangleglaucomaorocularhypertensioningreece
AT dimitriospapaconstantinou bimatoprosttimololfixedcombinationbtfcinpatientswithprimaryopenangleglaucomaorocularhypertensioningreece
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